pax_global_header00006660000000000000000000000064130115123040014500gustar00rootroot0000000000000052 comment=f2d04eeaecf9acfd0e269f68fd560f8a4f3288d6 Quorum-1.1.1/000077500000000000000000000000001301151230400127705ustar00rootroot00000000000000Quorum-1.1.1/.gitignore000066400000000000000000000001441301151230400147570ustar00rootroot00000000000000Makefile.in aclocal.m4 autom4te.cache config.h.in configure depcomp install-sh missing config.h.in~ Quorum-1.1.1/.gitmod000066400000000000000000000000101301151230400142430ustar00rootroot00000000000000develop Quorum-1.1.1/AUTHORS000066400000000000000000000001131301151230400140330ustar00rootroot00000000000000Guillaume Marcais Aleksey Zimin Quorum-1.1.1/COPYING000066400000000000000000001045131301151230400140270ustar00rootroot00000000000000 GNU GENERAL PUBLIC LICENSE Version 3, 29 June 2007 Copyright (C) 2007 Free Software Foundation, Inc. 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Copyright (C) This program is free software: you can redistribute it and/or modify it under the terms of the GNU General Public License as published by the Free Software Foundation, either version 3 of the License, or (at your option) any later version. This program is distributed in the hope that it will be useful, but WITHOUT ANY WARRANTY; without even the implied warranty of MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the GNU General Public License for more details. You should have received a copy of the GNU General Public License along with this program. If not, see . Also add information on how to contact you by electronic and paper mail. If the program does terminal interaction, make it output a short notice like this when it starts in an interactive mode: Copyright (C) This program comes with ABSOLUTELY NO WARRANTY; for details type `show w'. This is free software, and you are welcome to redistribute it under certain conditions; type `show c' for details. The hypothetical commands `show w' and `show c' should show the appropriate parts of the General Public License. Of course, your program's commands might be different; for a GUI interface, you would use an "about box". You should also get your employer (if you work as a programmer) or school, if any, to sign a "copyright disclaimer" for the program, if necessary. For more information on this, and how to apply and follow the GNU GPL, see . The GNU General Public License does not permit incorporating your program into proprietary programs. If your program is a subroutine library, you may consider it more useful to permit linking proprietary applications with the library. If this is what you want to do, use the GNU Lesser General Public License instead of this License. But first, please read . Quorum-1.1.1/ChangeLog000066400000000000000000000000001301151230400145300ustar00rootroot00000000000000Quorum-1.1.1/INSTALL000066400000000000000000000366001301151230400140260ustar00rootroot00000000000000Installation Instructions ************************* Copyright (C) 1994-1996, 1999-2002, 2004-2011 Free Software Foundation, Inc. Copying and distribution of this file, with or without modification, are permitted in any medium without royalty provided the copyright notice and this notice are preserved. This file is offered as-is, without warranty of any kind. Basic Installation ================== Briefly, the shell commands `./configure; make; make install' should configure, build, and install this package. The following more-detailed instructions are generic; see the `README' file for instructions specific to this package. Some packages provide this `INSTALL' file but do not implement all of the features documented below. The lack of an optional feature in a given package is not necessarily a bug. More recommendations for GNU packages can be found in *note Makefile Conventions: (standards)Makefile Conventions. The `configure' shell script attempts to guess correct values for various system-dependent variables used during compilation. It uses those values to create a `Makefile' in each directory of the package. It may also create one or more `.h' files containing system-dependent definitions. Finally, it creates a shell script `config.status' that you can run in the future to recreate the current configuration, and a file `config.log' containing compiler output (useful mainly for debugging `configure'). It can also use an optional file (typically called `config.cache' and enabled with `--cache-file=config.cache' or simply `-C') that saves the results of its tests to speed up reconfiguring. Caching is disabled by default to prevent problems with accidental use of stale cache files. If you need to do unusual things to compile the package, please try to figure out how `configure' could check whether to do them, and mail diffs or instructions to the address given in the `README' so they can be considered for the next release. If you are using the cache, and at some point `config.cache' contains results you don't want to keep, you may remove or edit it. The file `configure.ac' (or `configure.in') is used to create `configure' by a program called `autoconf'. You need `configure.ac' if you want to change it or regenerate `configure' using a newer version of `autoconf'. The simplest way to compile this package is: 1. `cd' to the directory containing the package's source code and type `./configure' to configure the package for your system. Running `configure' might take a while. While running, it prints some messages telling which features it is checking for. 2. Type `make' to compile the package. 3. Optionally, type `make check' to run any self-tests that come with the package, generally using the just-built uninstalled binaries. 4. Type `make install' to install the programs and any data files and documentation. When installing into a prefix owned by root, it is recommended that the package be configured and built as a regular user, and only the `make install' phase executed with root privileges. 5. Optionally, type `make installcheck' to repeat any self-tests, but this time using the binaries in their final installed location. This target does not install anything. Running this target as a regular user, particularly if the prior `make install' required root privileges, verifies that the installation completed correctly. 6. You can remove the program binaries and object files from the source code directory by typing `make clean'. To also remove the files that `configure' created (so you can compile the package for a different kind of computer), type `make distclean'. There is also a `make maintainer-clean' target, but that is intended mainly for the package's developers. If you use it, you may have to get all sorts of other programs in order to regenerate files that came with the distribution. 7. Often, you can also type `make uninstall' to remove the installed files again. In practice, not all packages have tested that uninstallation works correctly, even though it is required by the GNU Coding Standards. 8. Some packages, particularly those that use Automake, provide `make distcheck', which can by used by developers to test that all other targets like `make install' and `make uninstall' work correctly. This target is generally not run by end users. Compilers and Options ===================== Some systems require unusual options for compilation or linking that the `configure' script does not know about. Run `./configure --help' for details on some of the pertinent environment variables. You can give `configure' initial values for configuration parameters by setting variables in the command line or in the environment. Here is an example: ./configure CC=c99 CFLAGS=-g LIBS=-lposix *Note Defining Variables::, for more details. Compiling For Multiple Architectures ==================================== You can compile the package for more than one kind of computer at the same time, by placing the object files for each architecture in their own directory. To do this, you can use GNU `make'. `cd' to the directory where you want the object files and executables to go and run the `configure' script. `configure' automatically checks for the source code in the directory that `configure' is in and in `..'. This is known as a "VPATH" build. With a non-GNU `make', it is safer to compile the package for one architecture at a time in the source code directory. After you have installed the package for one architecture, use `make distclean' before reconfiguring for another architecture. On MacOS X 10.5 and later systems, you can create libraries and executables that work on multiple system types--known as "fat" or "universal" binaries--by specifying multiple `-arch' options to the compiler but only a single `-arch' option to the preprocessor. Like this: ./configure CC="gcc -arch i386 -arch x86_64 -arch ppc -arch ppc64" \ CXX="g++ -arch i386 -arch x86_64 -arch ppc -arch ppc64" \ CPP="gcc -E" CXXCPP="g++ -E" This is not guaranteed to produce working output in all cases, you may have to build one architecture at a time and combine the results using the `lipo' tool if you have problems. Installation Names ================== By default, `make install' installs the package's commands under `/usr/local/bin', include files under `/usr/local/include', etc. You can specify an installation prefix other than `/usr/local' by giving `configure' the option `--prefix=PREFIX', where PREFIX must be an absolute file name. You can specify separate installation prefixes for architecture-specific files and architecture-independent files. If you pass the option `--exec-prefix=PREFIX' to `configure', the package uses PREFIX as the prefix for installing programs and libraries. Documentation and other data files still use the regular prefix. In addition, if you use an unusual directory layout you can give options like `--bindir=DIR' to specify different values for particular kinds of files. Run `configure --help' for a list of the directories you can set and what kinds of files go in them. In general, the default for these options is expressed in terms of `${prefix}', so that specifying just `--prefix' will affect all of the other directory specifications that were not explicitly provided. The most portable way to affect installation locations is to pass the correct locations to `configure'; however, many packages provide one or both of the following shortcuts of passing variable assignments to the `make install' command line to change installation locations without having to reconfigure or recompile. The first method involves providing an override variable for each affected directory. For example, `make install prefix=/alternate/directory' will choose an alternate location for all directory configuration variables that were expressed in terms of `${prefix}'. Any directories that were specified during `configure', but not in terms of `${prefix}', must each be overridden at install time for the entire installation to be relocated. The approach of makefile variable overrides for each directory variable is required by the GNU Coding Standards, and ideally causes no recompilation. However, some platforms have known limitations with the semantics of shared libraries that end up requiring recompilation when using this method, particularly noticeable in packages that use GNU Libtool. The second method involves providing the `DESTDIR' variable. For example, `make install DESTDIR=/alternate/directory' will prepend `/alternate/directory' before all installation names. The approach of `DESTDIR' overrides is not required by the GNU Coding Standards, and does not work on platforms that have drive letters. On the other hand, it does better at avoiding recompilation issues, and works well even when some directory options were not specified in terms of `${prefix}' at `configure' time. Optional Features ================= If the package supports it, you can cause programs to be installed with an extra prefix or suffix on their names by giving `configure' the option `--program-prefix=PREFIX' or `--program-suffix=SUFFIX'. Some packages pay attention to `--enable-FEATURE' options to `configure', where FEATURE indicates an optional part of the package. They may also pay attention to `--with-PACKAGE' options, where PACKAGE is something like `gnu-as' or `x' (for the X Window System). The `README' should mention any `--enable-' and `--with-' options that the package recognizes. For packages that use the X Window System, `configure' can usually find the X include and library files automatically, but if it doesn't, you can use the `configure' options `--x-includes=DIR' and `--x-libraries=DIR' to specify their locations. Some packages offer the ability to configure how verbose the execution of `make' will be. For these packages, running `./configure --enable-silent-rules' sets the default to minimal output, which can be overridden with `make V=1'; while running `./configure --disable-silent-rules' sets the default to verbose, which can be overridden with `make V=0'. Particular systems ================== On HP-UX, the default C compiler is not ANSI C compatible. If GNU CC is not installed, it is recommended to use the following options in order to use an ANSI C compiler: ./configure CC="cc -Ae -D_XOPEN_SOURCE=500" and if that doesn't work, install pre-built binaries of GCC for HP-UX. HP-UX `make' updates targets which have the same time stamps as their prerequisites, which makes it generally unusable when shipped generated files such as `configure' are involved. Use GNU `make' instead. On OSF/1 a.k.a. Tru64, some versions of the default C compiler cannot parse its `' header file. The option `-nodtk' can be used as a workaround. If GNU CC is not installed, it is therefore recommended to try ./configure CC="cc" and if that doesn't work, try ./configure CC="cc -nodtk" On Solaris, don't put `/usr/ucb' early in your `PATH'. This directory contains several dysfunctional programs; working variants of these programs are available in `/usr/bin'. So, if you need `/usr/ucb' in your `PATH', put it _after_ `/usr/bin'. On Haiku, software installed for all users goes in `/boot/common', not `/usr/local'. It is recommended to use the following options: ./configure --prefix=/boot/common Specifying the System Type ========================== There may be some features `configure' cannot figure out automatically, but needs to determine by the type of machine the package will run on. Usually, assuming the package is built to be run on the _same_ architectures, `configure' can figure that out, but if it prints a message saying it cannot guess the machine type, give it the `--build=TYPE' option. TYPE can either be a short name for the system type, such as `sun4', or a canonical name which has the form: CPU-COMPANY-SYSTEM where SYSTEM can have one of these forms: OS KERNEL-OS See the file `config.sub' for the possible values of each field. If `config.sub' isn't included in this package, then this package doesn't need to know the machine type. If you are _building_ compiler tools for cross-compiling, you should use the option `--target=TYPE' to select the type of system they will produce code for. If you want to _use_ a cross compiler, that generates code for a platform different from the build platform, you should specify the "host" platform (i.e., that on which the generated programs will eventually be run) with `--host=TYPE'. Sharing Defaults ================ If you want to set default values for `configure' scripts to share, you can create a site shell script called `config.site' that gives default values for variables like `CC', `cache_file', and `prefix'. `configure' looks for `PREFIX/share/config.site' if it exists, then `PREFIX/etc/config.site' if it exists. Or, you can set the `CONFIG_SITE' environment variable to the location of the site script. A warning: not all `configure' scripts look for a site script. Defining Variables ================== Variables not defined in a site shell script can be set in the environment passed to `configure'. However, some packages may run configure again during the build, and the customized values of these variables may be lost. In order to avoid this problem, you should set them in the `configure' command line, using `VAR=value'. For example: ./configure CC=/usr/local2/bin/gcc causes the specified `gcc' to be used as the C compiler (unless it is overridden in the site shell script). Unfortunately, this technique does not work for `CONFIG_SHELL' due to an Autoconf bug. Until the bug is fixed you can use this workaround: CONFIG_SHELL=/bin/bash /bin/bash ./configure CONFIG_SHELL=/bin/bash `configure' Invocation ====================== `configure' recognizes the following options to control how it operates. `--help' `-h' Print a summary of all of the options to `configure', and exit. `--help=short' `--help=recursive' Print a summary of the options unique to this package's `configure', and exit. The `short' variant lists options used only in the top level, while the `recursive' variant lists options also present in any nested packages. `--version' `-V' Print the version of Autoconf used to generate the `configure' script, and exit. `--cache-file=FILE' Enable the cache: use and save the results of the tests in FILE, traditionally `config.cache'. FILE defaults to `/dev/null' to disable caching. `--config-cache' `-C' Alias for `--cache-file=config.cache'. `--quiet' `--silent' `-q' Do not print messages saying which checks are being made. To suppress all normal output, redirect it to `/dev/null' (any error messages will still be shown). `--srcdir=DIR' Look for the package's source code in directory DIR. Usually `configure' can determine that directory automatically. `--prefix=DIR' Use DIR as the installation prefix. *note Installation Names:: for more details, including other options available for fine-tuning the installation locations. `--no-create' `-n' Run the configure checks, but stop before creating any output files. `configure' also accepts some other, not widely useful, options. Run `configure --help' for more details. Quorum-1.1.1/Makefile.am000066400000000000000000000070331301151230400150270ustar00rootroot00000000000000ACLOCAL_AMFLAGS=-I m4 AM_CPPFLAGS = -I$(srcdir)/include -I$(srcdir) $(JELLYFISH2_0_CFLAGS) AM_CXXFLAGS = -Wall -g -O2 -std=c++0x AM_LDFLAGS = $(STATIC_FLAGS) LDADD = $(JELLYFISH2_0_LIBS) # Yaggo automatic rules with silencing V_YAGGO = $(V_YAGGO_$(V)) V_YAGGO_ = $(V_YAGGO_$(AM_DEFAULT_VERBOSITY)) V_YAGGO_0 = @echo " YAGGO " $@; .yaggo.hpp: @echo yaggo $< $@ $(V_YAGGO)$(YAGGO) --license $(srcdir)/header-license -o $@ $< YAGGO_SOURCES = src/error_correct_reads_cmdline.hpp \ src/create_database_cmdline.hpp \ src/merge_mate_pairs_cmdline.hpp \ src/split_mate_pairs_cmdline.hpp BUILT_SOURCES = $(YAGGO_SOURCES) noinst_HEADERS = $(YAGGO_SOURCES) CLEANFILES = EXTRA_DIST = bin_PROGRAMS = quorum_error_correct_reads quorum_create_database \ merge_mate_pairs split_mate_pairs quorum_error_correct_reads_SOURCES = src/error_correct_reads.cc \ src/err_log.cc quorum_create_database_SOURCES = src/create_database.cc merge_mate_pairs_SOURCES = src/merge_mate_pairs.cc split_mate_pairs_SOURCES = src/split_mate_pairs.cc noinst_HEADERS += src/error_correct_reads.hpp \ src/error_correct_reads.hpp src/verbose_log.hpp \ src/kmer.hpp src/mer_database.hpp src/err_log.hpp noinst_HEADERS += include/gzip_stream.hpp include/misc.hpp \ include/jflib/locks_pthread.hpp \ include/jflib/pool.hpp \ include/jflib/multiplexed_io.hpp ############################### # Adapter database generation # ############################### dist_data_DATA = data/adapter.jf DISTCLEANFILES = data/adapter.jf SUFFIXES = .jf .fa .fa.jf: $(AM_V_GEN)mkdir -p $(@D); $(JELLYFISH) count -m 24 -s 5k -C -t 10 -o $@ $< perl_scripts = quorum libs_scripts = $(patsubst %,.libs/%,$(perl_scripts)) bin_SCRIPTS = $(libs_scripts) noinst_SCRIPTS = $(perl_scripts) CLEANFILES += $(libs_scripts) $(perl_scripts) EXTRA_DIST += $(patsubst %,src/%.in,$(perl_scripts)) if RELATIVE_PATHS quorum_bindir=$$dir else quorum_bindir=$(bindir) endif if HAVE_RELATIVE_JF_PATH quorum_jellyfish=$$dir/$(RELATIVE_JF_PATH) local_quorum_jellyfish = $(shell realpath "$(bindir)/$(RELATIVE_JF_PATH)") else quorum_jellyfish=$(JELLYFISH) local_quorum_jellyfish = $(quorum_jellyfish) endif inst_subst = sed -e 's|[@]JELLYFISH[@]|$(quorum_jellyfish)|g' \ -e 's|[@]bindir[@]|$(quorum_bindir)|g' \ -e 's|[@]JF_LIB_PATH[@]|$(JF_LIB_PATH)|g' \ -e 's|[@]PACKAGE_VERSION[@]|$(PACKAGE_VERSION)|g' \ -e 's|[@]JELLYFISH_VERSION[@]|$(JELLYFISH_VERSION)|g' local_subst = sed -e 's|[@]JELLYFISH[@]|$(quorum_jellyfish)|g' \ -e 's|[@]bindir[@]|$(abs_builddir)|g' \ -e 's|[@]JF_LIB_PATH[@]|$(JF_LIB_PATH)|g' \ -e 's|[@]PACKAGE_VERSION[@]|$(PACKAGE_VERSION)|g' \ -e 's|[@]JELLYFISH_VERSION[@]|$(JELLYFISH_VERSION)|g' .libs/%: src/%.in Makefile @mkdir -p $(dir $@) && $(inst_subst) < $< > $@ %: src/%.in Makefile $(AM_V_GEN)$(local_subst) < $< > $@ && chmod a+x $@ ############## # Unit tests # ############## TESTS = all_tests check_PROGRAMS = all_tests query_mer_database histo_mer_database all_tests_SOURCES = unit_tests/test_mer_database.cc all_tests_CXXFLAGS = $(AM_CXXFLAGS) -I$(srcdir)/unit_tests/gtest/include -I$(srcdir)/unit_tests all_tests_LDADD = libgtest_main.la $(LDADD) noinst_HEADERS += unit_tests/test_misc.hpp query_mer_database_SOURCES = src/query_mer_database.cc histo_mer_database_SOURCES = src/histo_mer_database.cc include gtest.mk -include $(srcdir)/local.mk Quorum-1.1.1/NEWS000066400000000000000000000000311301151230400134610ustar00rootroot00000000000000* Initial release 0.1.0. Quorum-1.1.1/README000077700000000000000000000000001301151230400151222README.mdustar00rootroot00000000000000Quorum-1.1.1/README.md000066400000000000000000000073461301151230400142610ustar00rootroot00000000000000# Platform Quorum has been tested on Linux with gcc 4.4 to gcc 4.7. # Installation You should download the latest release distribution tar ball from the [releases section](https://github.com/gmarcais/Quorum/releases). If compiling from the github tree code, you will need `autoconf`, `automake` and `yaggo`. You can download `yaggo` from the [github release page](https://github.com/gmarcais/yaggo/releases) and copy the `yaggo` problem into your `PATH`. Quorum requires [Jellyfish](https://github.com/gmarcais/Jellyfish/releases) to be installed. For Quorum to compile `pkg-config` must find Jellyfish. The following command must pring "OK": ~~~ pkg-config --exists jellyfish-2.0 && echo OK ~~~ If not, set the variable `PKG_CONFIG_PATH` appropriately. If installing from the github tree, first run `autoreconf -fi`. Then install the usual way: ~~~ ./configure --prefix=/path/where/to/install make make install ~~~ The last command may need to be run as root, if installing in a system directory. # Usage Only one switch (`-s`) is required to run Quorum. This switch specify the size of the Jellyfish hash and it must be large enough so that all k-mers will fit into memory. With Illumina reads, a good estimate for this size is: (G + k * n) / 0.8 where G is the estimated genome size, k is the k-mer length (24 by default) and n is the number of reads. If the chosen size is too small, quorum will stop with the error message: "Failed: Increase the size parameter". For example, for a bacteria with 2 million Illumina reads in files read1.fastq and read2.fastq, the command would be: ~~~ quorum -s 50M read1.fastq read2.fastq ~~~ The output corrected file is called by default `quorum_corrected.fa`. #Output format The correction made are appended to the header line in the fasta format. For example, the following 101 bases long read: ~~~ @1204 GACCGGGCATGGGCTGAGCCTGTTCGGGAAGCTGACGGAGCCGGAAGAGGCCGGGATCGACCCTTCCGCCCCGCCCGCCGACTGGGTCGACCGGCCGGGCG ~~~ is corrected to: ~~~ >1204 86:sub:T-C 91:3_trunc 62:5_trunc CTTCCGCCCCGCCCGCCGACTGGGCCGAC ~~~ The coordinate system is 0-based in the original reads (like a C or Perl array). Here, at base 86 a substitution was made from T to C. The 5\_trunc is the index of the first base (0 if not specified) and the 3\_trunc is the index after the last base (read length if not specified). Hence, the length of the corrected reads is computed as 3\_trunc - 5\_trunc (29 in this example). The uncorrected and corrected reads align as follows: ~~~ 0 62 86 91 101 | | | | | GACCGGGCATGGGCTGAGCCTGTTCGGGAAGCTGACGGAGCCGGAAGAGGCCGGGATCGACCCTTCCGCCCCGCCCGCCGACTGGGTCGACCGGCCGGGCG CTTCCGCCCCGCCCGCCGACTGGGCCGAC ~~~ # Switches Other useful switches include (see `quorum --help` for a short description of all of them). * `--threads NUMBER` Number of threads to use. * `--kmer-len LENGTH` Length of k-mer to use. Defaults to 24. This is limited to 31. * `--contaminant FILE` Pass in a fasta or fastq file of contaminant sequences. The error correction program will truncate any reads which contains a k-mer present in the contaminant sequences. * `--prefix NAME` By default, all output file have the form `quorum_*`. This can be changed with this switch. * `--min-q-char ASCII` This is the ASCII value of the base of quality encoding. If not specified, it is auto-detected: the first 1,000 reads of the first file are read and the minimum quality value seen in these reads is used for min-q-char. An error is raised if this auto-detected base is not one of the standard value (33, 59 or 64). Quorum-1.1.1/build-aux/000077500000000000000000000000001301151230400146625ustar00rootroot00000000000000Quorum-1.1.1/build-aux/.gitignore000066400000000000000000000001071301151230400166500ustar00rootroot00000000000000# Ignore everything in this directory * # Except this file !.gitignore Quorum-1.1.1/build/000077500000000000000000000000001301151230400140675ustar00rootroot00000000000000Quorum-1.1.1/build/.gitignore000066400000000000000000000001071301151230400160550ustar00rootroot00000000000000# Ignore everything in this directory * # Except this file !.gitignore Quorum-1.1.1/configure.ac000066400000000000000000000050151301151230400152570ustar00rootroot00000000000000AC_INIT([quorum], [1.1.1], [gmarcais@cs.cmu.edu]) AC_CONFIG_AUX_DIR([build-aux]) AC_CONFIG_SRCDIR([src/error_correct_reads.hpp]) AC_CONFIG_HEADERS([config.h]) AC_CONFIG_MACRO_DIR([m4]) AM_INIT_AUTOMAKE([subdir-objects foreign]) AM_SILENT_RULES([yes]) # Compile using libtool to get the path to jellyfish added to exec LT_INIT # Checks for programs. AC_LANG(C++) AC_PROG_CXX # Checks for libraries. AC_CHECK_LIB([pthread], [pthread_create]) AC_CHECK_LIB([rt], [clock_gettime]) # Checks for header files. AC_CHECK_HEADERS([stdlib.h string.h]) # Check for yaggo AC_ARG_VAR([YAGGO], [Yaggo switch parser generator]) AS_IF([test "x$YAGGO" = "x"], [AC_PATH_PROG([YAGGO], [yaggo], [false])]) # Get jellyfish compile flags && executable PKG_CHECK_MODULES([JELLYFISH2_0], [jellyfish-2.0]) JELLYFISH_VERSION=$(pkg-config --modversion jellyfish-2.0) AC_SUBST([JELLYFISH_VERSION]) AC_ARG_VAR([JELLYFISH], [Jellyfish executable absolute path (default to looking in PATH)]) AS_IF([test "x$JELLYFISH" = "x"], [AC_PATH_PROG([JELLYFISH], [jellyfish], [false])]) AC_ARG_VAR([JF_LIB_PATH], [Append this path to LD_LIBRARY_PATH in quorum]) # --enable-all-static AC_ARG_ENABLE([all-static], [AC_HELP_STRING([--enable-all-static], [create statically linked executable])]) STATIC_FLAGS= AS_IF([test "x$enable_all_static" = xyes], [AC_SUBST([STATIC_FLAGS], [-all-static])]) # --enable-relative-paths AC_ARG_ENABLE([relative-paths], [AC_HELP_STRING([--enable-relative-paths], [store relative paths in quorum Perl script])]) AM_CONDITIONAL([RELATIVE_PATHS], [test x$enable_relative_paths = xyes]) # --with-relative-jf-path AC_ARG_WITH([relative-jf-path], [AC_HELP_STRING([--with-relative-jf-path], [relative path from quorum to jellyfish (use an absolute path if not given. default to "." if given with no argument)])], [case "$withval" in (yes) with_relative_jf_path="jellyfish" ;; (no) with_relative_jf_path= ;; (*) with_relative_jf_path=$withval/jellyfish ;; esac], [with_relative_jf_path= ]) AC_SUBST([RELATIVE_JF_PATH], $with_relative_jf_path) AM_CONDITIONAL([HAVE_RELATIVE_JF_PATH], [test x$with_relative_jf_path != x]) AC_CHECK_TYPE([__int128], [AC_DEFINE([HAVE_INT128], [1], [Define if type __int128 is supported])]) # Check the version of strerror_r AC_FUNC_STRERROR_R # Checks for typedefs, structures, and compiler characteristics. AC_HEADER_STDBOOL AC_TYPE_SIZE_T AC_TYPE_SSIZE_T AC_CHECK_TYPES([ptrdiff_t]) # Checks for library functions. AC_CHECK_FUNCS([]) AC_OUTPUT([Makefile]) Quorum-1.1.1/data/000077500000000000000000000000001301151230400137015ustar00rootroot00000000000000Quorum-1.1.1/data/adapter.fa000066400000000000000000001261741301151230400156440ustar00rootroot00000000000000>1 GATCGGAAGAGCTCGTATGCCGTCTTCTGCTTG >2 ACACTCTTTCCCTACACGACGCTCTTCCGATCT >3 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >4 CAAGCAGAAGACGGCATACGAGCTCTTCCGATCT >5 GATCGGAAGAGCGGTTCAGCAGGAATGCCGAG >6 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >7 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >0 AAACTCTTTCCCTACACGACGCTCTTCCGATCT >1 AAAGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >2 AAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >3 AAAGCAGAAGACGGCATACGAGCTCTTCCGATCT >4 AACGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >5 AAGGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >6 AATAATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >7 AATCATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >8 AATCGGAAGAGCGGTTCAGCAGGAATGCCGAG >9 AATCGGAAGAGCTCGTATGCCGTCTTCTGCTTG >10 AATGAAACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >11 AATGACACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >12 AATGAGACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >13 AATGATAAGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >14 AATGATACAGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >15 AATGATACCGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >16 AATGATACGACGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >17 AATGATACGCCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >18 AATGATACGGAGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >19 AATGATACGGCAACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >20 AATGATACGGCCACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >21 AATGATACGGCGAACACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >22 AATGATACGGCGACAACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >23 AATGATACGGCGACCAACGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >24 AATGATACGGCGACCACAGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >25 AATGATACGGCGACCACCAAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >26 AATGATACGGCGACCACCCAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >27 AATGATACGGCGACCACCGAAATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >28 AATGATACGGCGACCACCGACATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >29 AATGATACGGCGACCACCGAGAACTACACTCTTTCCCTACACGACGCTCTTCCGATCT >30 AATGATACGGCGACCACCGAGACCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >31 AATGATACGGCGACCACCGAGAGCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >32 AATGATACGGCGACCACCGAGATATACACTCTTTCCCTACACGACGCTCTTCCGATCT >33 AATGATACGGCGACCACCGAGATCAACACTCTTTCCCTACACGACGCTCTTCCGATCT >34 AATGATACGGCGACCACCGAGATCCACACTCTTTCCCTACACGACGCTCTTCCGATCT >35 AATGATACGGCGACCACCGAGATCGACACTCTTTCCCTACACGACGCTCTTCCGATCT >36 AATGATACGGCGACCACCGAGATCTAAACTCTTTCCCTACACGACGCTCTTCCGATCT >37 AATGATACGGCGACCACCGAGATCTACAATCTTTCCCTACACGACGCTCTTCCGATCT >38 AATGATACGGCGACCACCGAGATCTACACACTTTCCCTACACGACGCTCTTCCGATCT >39 AATGATACGGCGACCACCGAGATCTACACCCTTTCCCTACACGACGCTCTTCCGATCT >40 AATGATACGGCGACCACCGAGATCTACACGCTTTCCCTACACGACGCTCTTCCGATCT >41 AATGATACGGCGACCACCGAGATCTACACTATTTCCCTACACGACGCTCTTCCGATCT >42 AATGATACGGCGACCACCGAGATCTACACTCATTCCCTACACGACGCTCTTCCGATCT >43 AATGATACGGCGACCACCGAGATCTACACTCCTTCCCTACACGACGCTCTTCCGATCT >44 AATGATACGGCGACCACCGAGATCTACACTCGTTCCCTACACGACGCTCTTCCGATCT >45 AATGATACGGCGACCACCGAGATCTACACTCTATCCCTACACGACGCTCTTCCGATCT >46 AATGATACGGCGACCACCGAGATCTACACTCTCTCCCTACACGACGCTCTTCCGATCT >47 AATGATACGGCGACCACCGAGATCTACACTCTGTCCCTACACGACGCTCTTCCGATCT >48 AATGATACGGCGACCACCGAGATCTACACTCTTACCCTACACGACGCTCTTCCGATCT >49 AATGATACGGCGACCACCGAGATCTACACTCTTCCCCTACACGACGCTCTTCCGATCT >50 AATGATACGGCGACCACCGAGATCTACACTCTTGCCCTACACGACGCTCTTCCGATCT >51 AATGATACGGCGACCACCGAGATCTACACTCTTTACCTACACGACGCTCTTCCGATCT >52 AATGATACGGCGACCACCGAGATCTACACTCTTTCACTACACGACGCTCTTCCGATCT >53 AATGATACGGCGACCACCGAGATCTACACTCTTTCCATACACGACGCTCTTCCGATCT >54 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCAACACGACGCTCTTCCGATCT >55 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCCACACGACGCTCTTCCGATCT >56 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCGACACGACGCTCTTCCGATCT >57 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTAAACGACGCTCTTCCGATCT >58 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACAAGACGCTCTTCCGATCT >59 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACAACGCTCTTCCGATCT >60 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACCACGCTCTTCCGATCT >61 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGAAGCTCTTCCGATCT >62 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACACTCTTCCGATCT >63 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACCCTCTTCCGATCT >64 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGATCTTCCGATCT >65 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCACTTCCGATCT >66 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCCCTTCCGATCT >67 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCGCTTCCGATCT >68 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTATTCCGATCT >69 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCATCCGATCT >70 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCCTCCGATCT >71 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCGTCCGATCT >72 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTACCGATCT >73 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTCCCGATCT >74 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTGCCGATCT >75 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTACGATCT >76 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCAGATCT >77 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCAATCT >78 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCCATCT >79 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGAACT >80 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGACCT >81 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGAGCT >82 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATAT >83 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCA >84 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCC >85 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCG >86 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >87 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATGT >88 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATTT >89 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGCTCT >90 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGGTCT >91 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGTTCT >92 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCTATCT >93 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCGGATCT >94 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCTGATCT >95 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTGCGATCT >96 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTTCGATCT >97 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTGTTCCGATCT >98 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTTTTCCGATCT >99 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGGTCTTCCGATCT >100 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGTTCTTCCGATCT >101 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACTCTCTTCCGATCT >102 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGAGGCTCTTCCGATCT >103 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGATGCTCTTCCGATCT >104 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGCCGCTCTTCCGATCT >105 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGGCGCTCTTCCGATCT >106 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGTCGCTCTTCCGATCT >107 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACTACGCTCTTCCGATCT >108 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACAGGACGCTCTTCCGATCT >109 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACATGACGCTCTTCCGATCT >110 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACCCGACGCTCTTCCGATCT >111 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACGCGACGCTCTTCCGATCT >112 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACTCGACGCTCTTCCGATCT >113 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTAGACGACGCTCTTCCGATCT >114 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTATACGACGCTCTTCCGATCT >115 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTCCACGACGCTCTTCCGATCT >116 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTGCACGACGCTCTTCCGATCT >117 AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTTCACGACGCTCTTCCGATCT >118 AATGATACGGCGACCACCGAGATCTACACTCTTTCCGTACACGACGCTCTTCCGATCT >119 AATGATACGGCGACCACCGAGATCTACACTCTTTCCTTACACGACGCTCTTCCGATCT >120 AATGATACGGCGACCACCGAGATCTACACTCTTTCGCTACACGACGCTCTTCCGATCT >121 AATGATACGGCGACCACCGAGATCTACACTCTTTCTCTACACGACGCTCTTCCGATCT >122 AATGATACGGCGACCACCGAGATCTACACTCTTTGCCTACACGACGCTCTTCCGATCT >123 AATGATACGGCGACCACCGAGATCTACACTCTTTTCCTACACGACGCTCTTCCGATCT >124 AATGATACGGCGACCACCGAGATCTACACTGTTTCCCTACACGACGCTCTTCCGATCT >125 AATGATACGGCGACCACCGAGATCTACACTTTTTCCCTACACGACGCTCTTCCGATCT >126 AATGATACGGCGACCACCGAGATCTACAGTCTTTCCCTACACGACGCTCTTCCGATCT >127 AATGATACGGCGACCACCGAGATCTACATTCTTTCCCTACACGACGCTCTTCCGATCT >128 AATGATACGGCGACCACCGAGATCTACCCTCTTTCCCTACACGACGCTCTTCCGATCT >129 AATGATACGGCGACCACCGAGATCTACGCTCTTTCCCTACACGACGCTCTTCCGATCT >130 AATGATACGGCGACCACCGAGATCTACTCTCTTTCCCTACACGACGCTCTTCCGATCT >131 AATGATACGGCGACCACCGAGATCTAGACTCTTTCCCTACACGACGCTCTTCCGATCT >132 AATGATACGGCGACCACCGAGATCTATACTCTTTCCCTACACGACGCTCTTCCGATCT >133 AATGATACGGCGACCACCGAGATCTCCACTCTTTCCCTACACGACGCTCTTCCGATCT >134 AATGATACGGCGACCACCGAGATCTGCACTCTTTCCCTACACGACGCTCTTCCGATCT >135 AATGATACGGCGACCACCGAGATCTTCACTCTTTCCCTACACGACGCTCTTCCGATCT >136 AATGATACGGCGACCACCGAGATGTACACTCTTTCCCTACACGACGCTCTTCCGATCT >137 AATGATACGGCGACCACCGAGATTTACACTCTTTCCCTACACGACGCTCTTCCGATCT >138 AATGATACGGCGACCACCGAGCTCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >139 AATGATACGGCGACCACCGAGGTCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >140 AATGATACGGCGACCACCGAGTTCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >141 AATGATACGGCGACCACCGATATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >142 AATGATACGGCGACCACCGCGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >143 AATGATACGGCGACCACCGGGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >144 AATGATACGGCGACCACCGTGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >145 AATGATACGGCGACCACCTAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >146 AATGATACGGCGACCACGGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >147 AATGATACGGCGACCACTGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >148 AATGATACGGCGACCAGCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >149 AATGATACGGCGACCATCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >150 AATGATACGGCGACCCCCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >151 AATGATACGGCGACCGCCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >152 AATGATACGGCGACCTCCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >153 AATGATACGGCGACGACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >154 AATGATACGGCGACTACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >155 AATGATACGGCGAGCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >156 AATGATACGGCGATCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >157 AATGATACGGCGCCCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >158 AATGATACGGCGGCCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >159 AATGATACGGCGTCCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >160 AATGATACGGCTACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >161 AATGATACGGGGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >162 AATGATACGGTGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >163 AATGATACGTCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >164 AATGATACTGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >165 AATGATAGGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >166 AATGATATGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >167 AATGATCCGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >168 AATGATGCGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >169 AATGATTCGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >170 AATGCTACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >171 AATGGTACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >172 AATGTTACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >173 AATTATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >174 ACAATCTTTCCCTACACGACGCTCTTCCGATCT >175 ACACACTTTCCCTACACGACGCTCTTCCGATCT >176 ACACCCTTTCCCTACACGACGCTCTTCCGATCT >177 ACACGCTTTCCCTACACGACGCTCTTCCGATCT >178 ACACTATTTCCCTACACGACGCTCTTCCGATCT >179 ACACTCATTCCCTACACGACGCTCTTCCGATCT >180 ACACTCCTTCCCTACACGACGCTCTTCCGATCT >181 ACACTCGTTCCCTACACGACGCTCTTCCGATCT >182 ACACTCTATCCCTACACGACGCTCTTCCGATCT >183 ACACTCTCTCCCTACACGACGCTCTTCCGATCT >184 ACACTCTGTCCCTACACGACGCTCTTCCGATCT >185 ACACTCTTACCCTACACGACGCTCTTCCGATCT >186 ACACTCTTCCCCTACACGACGCTCTTCCGATCT >187 ACACTCTTGCCCTACACGACGCTCTTCCGATCT >188 ACACTCTTTACCTACACGACGCTCTTCCGATCT >189 ACACTCTTTCACTACACGACGCTCTTCCGATCT >190 ACACTCTTTCCATACACGACGCTCTTCCGATCT >191 ACACTCTTTCCCAACACGACGCTCTTCCGATCT >192 ACACTCTTTCCCCACACGACGCTCTTCCGATCT >193 ACACTCTTTCCCGACACGACGCTCTTCCGATCT >194 ACACTCTTTCCCTAAACGACGCTCTTCCGATCT >195 ACACTCTTTCCCTACAAGACGCTCTTCCGATCT >196 ACACTCTTTCCCTACACAACGCTCTTCCGATCT >197 ACACTCTTTCCCTACACCACGCTCTTCCGATCT >198 ACACTCTTTCCCTACACGAAGCTCTTCCGATCT >199 ACACTCTTTCCCTACACGACACTCTTCCGATCT >200 ACACTCTTTCCCTACACGACCCTCTTCCGATCT >201 ACACTCTTTCCCTACACGACGATCTTCCGATCT >202 ACACTCTTTCCCTACACGACGCACTTCCGATCT >203 ACACTCTTTCCCTACACGACGCCCTTCCGATCT >204 ACACTCTTTCCCTACACGACGCGCTTCCGATCT >205 ACACTCTTTCCCTACACGACGCTATTCCGATCT >206 ACACTCTTTCCCTACACGACGCTCATCCGATCT >207 ACACTCTTTCCCTACACGACGCTCCTCCGATCT >208 ACACTCTTTCCCTACACGACGCTCGTCCGATCT >209 ACACTCTTTCCCTACACGACGCTCTACCGATCT >210 ACACTCTTTCCCTACACGACGCTCTCCCGATCT >211 ACACTCTTTCCCTACACGACGCTCTGCCGATCT >212 ACACTCTTTCCCTACACGACGCTCTTACGATCT >213 ACACTCTTTCCCTACACGACGCTCTTCAGATCT >214 ACACTCTTTCCCTACACGACGCTCTTCCAATCT >215 ACACTCTTTCCCTACACGACGCTCTTCCCATCT >216 ACACTCTTTCCCTACACGACGCTCTTCCGAACT >217 ACACTCTTTCCCTACACGACGCTCTTCCGACCT >218 ACACTCTTTCCCTACACGACGCTCTTCCGAGCT >219 ACACTCTTTCCCTACACGACGCTCTTCCGATAT >220 ACACTCTTTCCCTACACGACGCTCTTCCGATCA >221 ACACTCTTTCCCTACACGACGCTCTTCCGATCC >222 ACACTCTTTCCCTACACGACGCTCTTCCGATCG >223 ACACTCTTTCCCTACACGACGCTCTTCCGATCT >224 ACACTCTTTCCCTACACGACGCTCTTCCGATGT >225 ACACTCTTTCCCTACACGACGCTCTTCCGATTT >226 ACACTCTTTCCCTACACGACGCTCTTCCGCTCT >227 ACACTCTTTCCCTACACGACGCTCTTCCGGTCT >228 ACACTCTTTCCCTACACGACGCTCTTCCGTTCT >229 ACACTCTTTCCCTACACGACGCTCTTCCTATCT >230 ACACTCTTTCCCTACACGACGCTCTTCGGATCT >231 ACACTCTTTCCCTACACGACGCTCTTCTGATCT >232 ACACTCTTTCCCTACACGACGCTCTTGCGATCT >233 ACACTCTTTCCCTACACGACGCTCTTTCGATCT >234 ACACTCTTTCCCTACACGACGCTGTTCCGATCT >235 ACACTCTTTCCCTACACGACGCTTTTCCGATCT >236 ACACTCTTTCCCTACACGACGGTCTTCCGATCT >237 ACACTCTTTCCCTACACGACGTTCTTCCGATCT >238 ACACTCTTTCCCTACACGACTCTCTTCCGATCT >239 ACACTCTTTCCCTACACGAGGCTCTTCCGATCT >240 ACACTCTTTCCCTACACGATGCTCTTCCGATCT >241 ACACTCTTTCCCTACACGCCGCTCTTCCGATCT >242 ACACTCTTTCCCTACACGGCGCTCTTCCGATCT >243 ACACTCTTTCCCTACACGTCGCTCTTCCGATCT >244 ACACTCTTTCCCTACACTACGCTCTTCCGATCT >245 ACACTCTTTCCCTACAGGACGCTCTTCCGATCT >246 ACACTCTTTCCCTACATGACGCTCTTCCGATCT >247 ACACTCTTTCCCTACCCGACGCTCTTCCGATCT >248 ACACTCTTTCCCTACGCGACGCTCTTCCGATCT >249 ACACTCTTTCCCTACTCGACGCTCTTCCGATCT >250 ACACTCTTTCCCTAGACGACGCTCTTCCGATCT >251 ACACTCTTTCCCTATACGACGCTCTTCCGATCT >252 ACACTCTTTCCCTCCACGACGCTCTTCCGATCT >253 ACACTCTTTCCCTGCACGACGCTCTTCCGATCT >254 ACACTCTTTCCCTTCACGACGCTCTTCCGATCT >255 ACACTCTTTCCGTACACGACGCTCTTCCGATCT >256 ACACTCTTTCCTTACACGACGCTCTTCCGATCT >257 ACACTCTTTCGCTACACGACGCTCTTCCGATCT >258 ACACTCTTTCTCTACACGACGCTCTTCCGATCT >259 ACACTCTTTGCCTACACGACGCTCTTCCGATCT >260 ACACTCTTTTCCTACACGACGCTCTTCCGATCT >261 ACACTGTTTCCCTACACGACGCTCTTCCGATCT >262 ACACTTTTTCCCTACACGACGCTCTTCCGATCT >263 ACAGTCTTTCCCTACACGACGCTCTTCCGATCT >264 ACATTCTTTCCCTACACGACGCTCTTCCGATCT >265 ACCCTCTTTCCCTACACGACGCTCTTCCGATCT >266 ACGCTCTTTCCCTACACGACGCTCTTCCGATCT >267 ACTCTCTTTCCCTACACGACGCTCTTCCGATCT >268 ACTGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >269 AGACTCTTTCCCTACACGACGCTCTTCCGATCT >270 AGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >271 AGTGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >272 ATACTCTTTCCCTACACGACGCTCTTCCGATCT >273 ATTGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >274 CAAACAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >275 CAAACAGAAGACGGCATACGAGCTCTTCCGATCT >276 CAACCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >277 CAACCAGAAGACGGCATACGAGCTCTTCCGATCT >278 CAAGAAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >279 CAAGAAGAAGACGGCATACGAGCTCTTCCGATCT >280 CAAGCAAAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >281 CAAGCAAAAGACGGCATACGAGCTCTTCCGATCT >282 CAAGCACAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >283 CAAGCACAAGACGGCATACGAGCTCTTCCGATCT >284 CAAGCAGAAAACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >285 CAAGCAGAAAACGGCATACGAGCTCTTCCGATCT >286 CAAGCAGAACACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >287 CAAGCAGAACACGGCATACGAGCTCTTCCGATCT >288 CAAGCAGAAGAAGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >289 CAAGCAGAAGAAGGCATACGAGCTCTTCCGATCT >290 CAAGCAGAAGACAGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >291 CAAGCAGAAGACAGCATACGAGCTCTTCCGATCT >292 CAAGCAGAAGACCGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >293 CAAGCAGAAGACCGCATACGAGCTCTTCCGATCT >294 CAAGCAGAAGACGACATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >295 CAAGCAGAAGACGACATACGAGCTCTTCCGATCT >296 CAAGCAGAAGACGCCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >297 CAAGCAGAAGACGCCATACGAGCTCTTCCGATCT >298 CAAGCAGAAGACGGAATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >299 CAAGCAGAAGACGGAATACGAGCTCTTCCGATCT >300 CAAGCAGAAGACGGCAAACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >301 CAAGCAGAAGACGGCAAACGAGCTCTTCCGATCT >302 CAAGCAGAAGACGGCACACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >303 CAAGCAGAAGACGGCACACGAGCTCTTCCGATCT >304 CAAGCAGAAGACGGCAGACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >305 CAAGCAGAAGACGGCAGACGAGCTCTTCCGATCT >306 CAAGCAGAAGACGGCATAAGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >307 CAAGCAGAAGACGGCATAAGAGCTCTTCCGATCT >308 CAAGCAGAAGACGGCATACAAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >309 CAAGCAGAAGACGGCATACAAGCTCTTCCGATCT >310 CAAGCAGAAGACGGCATACCAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >311 CAAGCAGAAGACGGCATACCAGCTCTTCCGATCT >312 CAAGCAGAAGACGGCATACGAAATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >313 CAAGCAGAAGACGGCATACGAACTCTTCCGATCT >314 CAAGCAGAAGACGGCATACGACATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >315 CAAGCAGAAGACGGCATACGACCTCTTCCGATCT >316 CAAGCAGAAGACGGCATACGAGAACGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >317 CAAGCAGAAGACGGCATACGAGACCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >318 CAAGCAGAAGACGGCATACGAGAGCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >319 CAAGCAGAAGACGGCATACGAGATAGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >320 CAAGCAGAAGACGGCATACGAGATCAGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >321 CAAGCAGAAGACGGCATACGAGATCCGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >322 CAAGCAGAAGACGGCATACGAGATCGATCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >323 CAAGCAGAAGACGGCATACGAGATCGCTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >324 CAAGCAGAAGACGGCATACGAGATCGGACTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >325 CAAGCAGAAGACGGCATACGAGATCGGCCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >326 CAAGCAGAAGACGGCATACGAGATCGGGCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >327 CAAGCAGAAGACGGCATACGAGATCGGTATCGGCATTCCTGCTGAACCGCTCTTCCGATCT >328 CAAGCAGAAGACGGCATACGAGATCGGTCACGGCATTCCTGCTGAACCGCTCTTCCGATCT >329 CAAGCAGAAGACGGCATACGAGATCGGTCCCGGCATTCCTGCTGAACCGCTCTTCCGATCT >330 CAAGCAGAAGACGGCATACGAGATCGGTCGCGGCATTCCTGCTGAACCGCTCTTCCGATCT >331 CAAGCAGAAGACGGCATACGAGATCGGTCTAGGCATTCCTGCTGAACCGCTCTTCCGATCT >332 CAAGCAGAAGACGGCATACGAGATCGGTCTCAGCATTCCTGCTGAACCGCTCTTCCGATCT >333 CAAGCAGAAGACGGCATACGAGATCGGTCTCCGCATTCCTGCTGAACCGCTCTTCCGATCT >334 CAAGCAGAAGACGGCATACGAGATCGGTCTCGACATTCCTGCTGAACCGCTCTTCCGATCT >335 CAAGCAGAAGACGGCATACGAGATCGGTCTCGCCATTCCTGCTGAACCGCTCTTCCGATCT >336 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGAATTCCTGCTGAACCGCTCTTCCGATCT >337 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCAATCCTGCTGAACCGCTCTTCCGATCT >338 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCACTCCTGCTGAACCGCTCTTCCGATCT >339 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCAGTCCTGCTGAACCGCTCTTCCGATCT >340 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATACCTGCTGAACCGCTCTTCCGATCT >341 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATCCCTGCTGAACCGCTCTTCCGATCT >342 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATGCCTGCTGAACCGCTCTTCCGATCT >343 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTACTGCTGAACCGCTCTTCCGATCT >344 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCATGCTGAACCGCTCTTCCGATCT >345 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCAGCTGAACCGCTCTTCCGATCT >346 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCCGCTGAACCGCTCTTCCGATCT >347 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCGGCTGAACCGCTCTTCCGATCT >348 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTACTGAACCGCTCTTCCGATCT >349 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTCCTGAACCGCTCTTCCGATCT >350 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGATGAACCGCTCTTCCGATCT >351 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCAGAACCGCTCTTCCGATCT >352 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCCGAACCGCTCTTCCGATCT >353 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCGGAACCGCTCTTCCGATCT >354 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTAAACCGCTCTTCCGATCT >355 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTCAACCGCTCTTCCGATCT >356 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAAACGCTCTTCCGATCT >357 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACAGCTCTTCCGATCT >358 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCACTCTTCCGATCT >359 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCCCTCTTCCGATCT >360 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGATCTTCCGATCT >361 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCACTTCCGATCT >362 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCCCTTCCGATCT >363 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCGCTTCCGATCT >364 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTATTCCGATCT >365 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCATCCGATCT >366 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCCTCCGATCT >367 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCGTCCGATCT >368 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTACCGATCT >369 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTCCCGATCT >370 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTGCCGATCT >371 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTACGATCT >372 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCAGATCT >373 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCAATCT >374 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCCATCT >375 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGAACT >376 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGACCT >377 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGAGCT >378 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATAT >379 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCA >380 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCC >381 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCG >382 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >383 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATGT >384 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATTT >385 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGCTCT >386 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGGTCT >387 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGTTCT >388 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCTATCT >389 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCGGATCT >390 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCTGATCT >391 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTGCGATCT >392 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTTCGATCT >393 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTGTTCCGATCT >394 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTTTTCCGATCT >395 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGGTCTTCCGATCT >396 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGTTCTTCCGATCT >397 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCTCTCTTCCGATCT >398 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACGGCTCTTCCGATCT >399 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACTGCTCTTCCGATCT >400 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAAGCGCTCTTCCGATCT >401 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAATCGCTCTTCCGATCT >402 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGACCCGCTCTTCCGATCT >403 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAGCCGCTCTTCCGATCT >404 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGATCCGCTCTTCCGATCT >405 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGCACCGCTCTTCCGATCT >406 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGGACCGCTCTTCCGATCT >407 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGTACCGCTCTTCCGATCT >408 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTTAACCGCTCTTCCGATCT >409 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGGTGAACCGCTCTTCCGATCT >410 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGTTGAACCGCTCTTCCGATCT >411 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTTCTGAACCGCTCTTCCGATCT >412 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCGTGCTGAACCGCTCTTCCGATCT >413 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCTTGCTGAACCGCTCTTCCGATCT >414 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTGCTGCTGAACCGCTCTTCCGATCT >415 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTTCTGCTGAACCGCTCTTCCGATCT >416 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCCTTCCTGCTGAACCGCTCTTCCGATCT >417 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCGTTCCTGCTGAACCGCTCTTCCGATCT >418 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCTTTCCTGCTGAACCGCTCTTCCGATCT >419 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGGATTCCTGCTGAACCGCTCTTCCGATCT >420 CAAGCAGAAGACGGCATACGAGATCGGTCTCGGTATTCCTGCTGAACCGCTCTTCCGATCT >421 CAAGCAGAAGACGGCATACGAGATCGGTCTCGTCATTCCTGCTGAACCGCTCTTCCGATCT >422 CAAGCAGAAGACGGCATACGAGATCGGTCTCTGCATTCCTGCTGAACCGCTCTTCCGATCT >423 CAAGCAGAAGACGGCATACGAGATCGGTCTGGGCATTCCTGCTGAACCGCTCTTCCGATCT >424 CAAGCAGAAGACGGCATACGAGATCGGTCTTGGCATTCCTGCTGAACCGCTCTTCCGATCT >425 CAAGCAGAAGACGGCATACGAGATCGGTGTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >426 CAAGCAGAAGACGGCATACGAGATCGGTTTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >427 CAAGCAGAAGACGGCATACGAGATCGTTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >428 CAAGCAGAAGACGGCATACGAGATCTGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >429 CAAGCAGAAGACGGCATACGAGATCTTCCGATCT >430 CAAGCAGAAGACGGCATACGAGATGGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >431 CAAGCAGAAGACGGCATACGAGATTGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >432 CAAGCAGAAGACGGCATACGAGCACTTCCGATCT >433 CAAGCAGAAGACGGCATACGAGCCCTTCCGATCT >434 CAAGCAGAAGACGGCATACGAGCGCTTCCGATCT >435 CAAGCAGAAGACGGCATACGAGCTATTCCGATCT >436 CAAGCAGAAGACGGCATACGAGCTCATCCGATCT >437 CAAGCAGAAGACGGCATACGAGCTCCTCCGATCT >438 CAAGCAGAAGACGGCATACGAGCTCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >439 CAAGCAGAAGACGGCATACGAGCTCGTCCGATCT >440 CAAGCAGAAGACGGCATACGAGCTCTACCGATCT >441 CAAGCAGAAGACGGCATACGAGCTCTCCCGATCT >442 CAAGCAGAAGACGGCATACGAGCTCTGCCGATCT >443 CAAGCAGAAGACGGCATACGAGCTCTTACGATCT >444 CAAGCAGAAGACGGCATACGAGCTCTTCAGATCT >445 CAAGCAGAAGACGGCATACGAGCTCTTCCAATCT >446 CAAGCAGAAGACGGCATACGAGCTCTTCCCATCT >447 CAAGCAGAAGACGGCATACGAGCTCTTCCGAACT >448 CAAGCAGAAGACGGCATACGAGCTCTTCCGACCT >449 CAAGCAGAAGACGGCATACGAGCTCTTCCGAGCT >450 CAAGCAGAAGACGGCATACGAGCTCTTCCGATAT >451 CAAGCAGAAGACGGCATACGAGCTCTTCCGATCA >452 CAAGCAGAAGACGGCATACGAGCTCTTCCGATCC >453 CAAGCAGAAGACGGCATACGAGCTCTTCCGATCG >454 CAAGCAGAAGACGGCATACGAGCTCTTCCGATCT >455 CAAGCAGAAGACGGCATACGAGCTCTTCCGATGT >456 CAAGCAGAAGACGGCATACGAGCTCTTCCGATTT >457 CAAGCAGAAGACGGCATACGAGCTCTTCCGCTCT >458 CAAGCAGAAGACGGCATACGAGCTCTTCCGGTCT >459 CAAGCAGAAGACGGCATACGAGCTCTTCCGTTCT >460 CAAGCAGAAGACGGCATACGAGCTCTTCCTATCT >461 CAAGCAGAAGACGGCATACGAGCTCTTCGGATCT >462 CAAGCAGAAGACGGCATACGAGCTCTTCTGATCT >463 CAAGCAGAAGACGGCATACGAGCTCTTGCGATCT >464 CAAGCAGAAGACGGCATACGAGCTCTTTCGATCT >465 CAAGCAGAAGACGGCATACGAGCTGTTCCGATCT >466 CAAGCAGAAGACGGCATACGAGCTTTTCCGATCT >467 CAAGCAGAAGACGGCATACGAGGTCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >468 CAAGCAGAAGACGGCATACGAGGTCTTCCGATCT >469 CAAGCAGAAGACGGCATACGAGTTCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >470 CAAGCAGAAGACGGCATACGAGTTCTTCCGATCT >471 CAAGCAGAAGACGGCATACGATATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >472 CAAGCAGAAGACGGCATACGATCTCTTCCGATCT >473 CAAGCAGAAGACGGCATACGCGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >474 CAAGCAGAAGACGGCATACGCGCTCTTCCGATCT >475 CAAGCAGAAGACGGCATACGGGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >476 CAAGCAGAAGACGGCATACGGGCTCTTCCGATCT >477 CAAGCAGAAGACGGCATACGTGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >478 CAAGCAGAAGACGGCATACGTGCTCTTCCGATCT >479 CAAGCAGAAGACGGCATACTAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >480 CAAGCAGAAGACGGCATACTAGCTCTTCCGATCT >481 CAAGCAGAAGACGGCATAGGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >482 CAAGCAGAAGACGGCATAGGAGCTCTTCCGATCT >483 CAAGCAGAAGACGGCATATGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >484 CAAGCAGAAGACGGCATATGAGCTCTTCCGATCT >485 CAAGCAGAAGACGGCATCCGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >486 CAAGCAGAAGACGGCATCCGAGCTCTTCCGATCT >487 CAAGCAGAAGACGGCATGCGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >488 CAAGCAGAAGACGGCATGCGAGCTCTTCCGATCT >489 CAAGCAGAAGACGGCATTCGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >490 CAAGCAGAAGACGGCATTCGAGCTCTTCCGATCT >491 CAAGCAGAAGACGGCCTACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >492 CAAGCAGAAGACGGCCTACGAGCTCTTCCGATCT >493 CAAGCAGAAGACGGCGTACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >494 CAAGCAGAAGACGGCGTACGAGCTCTTCCGATCT >495 CAAGCAGAAGACGGCTTACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >496 CAAGCAGAAGACGGCTTACGAGCTCTTCCGATCT >497 CAAGCAGAAGACGGGATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >498 CAAGCAGAAGACGGGATACGAGCTCTTCCGATCT >499 CAAGCAGAAGACGGTATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >500 CAAGCAGAAGACGGTATACGAGCTCTTCCGATCT >501 CAAGCAGAAGACGTCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >502 CAAGCAGAAGACGTCATACGAGCTCTTCCGATCT >503 CAAGCAGAAGACTGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >504 CAAGCAGAAGACTGCATACGAGCTCTTCCGATCT >505 CAAGCAGAAGAGGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >506 CAAGCAGAAGAGGGCATACGAGCTCTTCCGATCT >507 CAAGCAGAAGATGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >508 CAAGCAGAAGATGGCATACGAGCTCTTCCGATCT >509 CAAGCAGAAGCCGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >510 CAAGCAGAAGCCGGCATACGAGCTCTTCCGATCT >511 CAAGCAGAAGGCGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >512 CAAGCAGAAGGCGGCATACGAGCTCTTCCGATCT >513 CAAGCAGAAGTCGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >514 CAAGCAGAAGTCGGCATACGAGCTCTTCCGATCT >515 CAAGCAGAATACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >516 CAAGCAGAATACGGCATACGAGCTCTTCCGATCT >517 CAAGCAGACGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >518 CAAGCAGACGACGGCATACGAGCTCTTCCGATCT >519 CAAGCAGAGGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >520 CAAGCAGAGGACGGCATACGAGCTCTTCCGATCT >521 CAAGCAGATGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >522 CAAGCAGATGACGGCATACGAGCTCTTCCGATCT >523 CAAGCAGCAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >524 CAAGCAGCAGACGGCATACGAGCTCTTCCGATCT >525 CAAGCAGGAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >526 CAAGCAGGAGACGGCATACGAGCTCTTCCGATCT >527 CAAGCAGTAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >528 CAAGCAGTAGACGGCATACGAGCTCTTCCGATCT >529 CAAGCATAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >530 CAAGCATAAGACGGCATACGAGCTCTTCCGATCT >531 CAAGCCGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >532 CAAGCCGAAGACGGCATACGAGCTCTTCCGATCT >533 CAAGCGGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >534 CAAGCGGAAGACGGCATACGAGCTCTTCCGATCT >535 CAAGCTGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >536 CAAGCTGAAGACGGCATACGAGCTCTTCCGATCT >537 CAAGGAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >538 CAAGGAGAAGACGGCATACGAGCTCTTCCGATCT >539 CAAGTAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >540 CAAGTAGAAGACGGCATACGAGCTCTTCCGATCT >541 CAATCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >542 CAATCAGAAGACGGCATACGAGCTCTTCCGATCT >543 CACGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >544 CACGCAGAAGACGGCATACGAGCTCTTCCGATCT >545 CAGGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >546 CAGGCAGAAGACGGCATACGAGCTCTTCCGATCT >547 CAGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >548 CATCGGAAGAGCGGTTCAGCAGGAATGCCGAG >549 CATCGGAAGAGCTCGTATGCCGTCTTCTGCTTG >550 CATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >551 CATGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >552 CATGCAGAAGACGGCATACGAGCTCTTCCGATCT >553 CCACTCTTTCCCTACACGACGCTCTTCCGATCT >554 CCAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >555 CCAGCAGAAGACGGCATACGAGCTCTTCCGATCT >556 CCGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >557 CGAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >558 CGAGCAGAAGACGGCATACGAGCTCTTCCGATCT >559 CGATCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >560 CGCTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >561 CGGACTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >562 CGGCCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >563 CGGGCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >564 CGGTATCGGCATTCCTGCTGAACCGCTCTTCCGATCT >565 CGGTCACGGCATTCCTGCTGAACCGCTCTTCCGATCT >566 CGGTCCCGGCATTCCTGCTGAACCGCTCTTCCGATCT >567 CGGTCGCGGCATTCCTGCTGAACCGCTCTTCCGATCT >568 CGGTCTAGGCATTCCTGCTGAACCGCTCTTCCGATCT >569 CGGTCTCAGCATTCCTGCTGAACCGCTCTTCCGATCT >570 CGGTCTCCGCATTCCTGCTGAACCGCTCTTCCGATCT >571 CGGTCTCGACATTCCTGCTGAACCGCTCTTCCGATCT >572 CGGTCTCGCCATTCCTGCTGAACCGCTCTTCCGATCT >573 CGGTCTCGGAATTCCTGCTGAACCGCTCTTCCGATCT >574 CGGTCTCGGCAATCCTGCTGAACCGCTCTTCCGATCT >575 CGGTCTCGGCACTCCTGCTGAACCGCTCTTCCGATCT >576 CGGTCTCGGCAGTCCTGCTGAACCGCTCTTCCGATCT >577 CGGTCTCGGCATACCTGCTGAACCGCTCTTCCGATCT >578 CGGTCTCGGCATCCCTGCTGAACCGCTCTTCCGATCT >579 CGGTCTCGGCATGCCTGCTGAACCGCTCTTCCGATCT >580 CGGTCTCGGCATTACTGCTGAACCGCTCTTCCGATCT >581 CGGTCTCGGCATTCATGCTGAACCGCTCTTCCGATCT >582 CGGTCTCGGCATTCCAGCTGAACCGCTCTTCCGATCT >583 CGGTCTCGGCATTCCCGCTGAACCGCTCTTCCGATCT >584 CGGTCTCGGCATTCCGGCTGAACCGCTCTTCCGATCT >585 CGGTCTCGGCATTCCTACTGAACCGCTCTTCCGATCT >586 CGGTCTCGGCATTCCTCCTGAACCGCTCTTCCGATCT >587 CGGTCTCGGCATTCCTGATGAACCGCTCTTCCGATCT >588 CGGTCTCGGCATTCCTGCAGAACCGCTCTTCCGATCT >589 CGGTCTCGGCATTCCTGCCGAACCGCTCTTCCGATCT >590 CGGTCTCGGCATTCCTGCGGAACCGCTCTTCCGATCT >591 CGGTCTCGGCATTCCTGCTAAACCGCTCTTCCGATCT >592 CGGTCTCGGCATTCCTGCTCAACCGCTCTTCCGATCT >593 CGGTCTCGGCATTCCTGCTGAAACGCTCTTCCGATCT >594 CGGTCTCGGCATTCCTGCTGAACAGCTCTTCCGATCT >595 CGGTCTCGGCATTCCTGCTGAACCACTCTTCCGATCT >596 CGGTCTCGGCATTCCTGCTGAACCCCTCTTCCGATCT >597 CGGTCTCGGCATTCCTGCTGAACCGATCTTCCGATCT >598 CGGTCTCGGCATTCCTGCTGAACCGCACTTCCGATCT >599 CGGTCTCGGCATTCCTGCTGAACCGCCCTTCCGATCT >600 CGGTCTCGGCATTCCTGCTGAACCGCGCTTCCGATCT >601 CGGTCTCGGCATTCCTGCTGAACCGCTATTCCGATCT >602 CGGTCTCGGCATTCCTGCTGAACCGCTCATCCGATCT >603 CGGTCTCGGCATTCCTGCTGAACCGCTCCTCCGATCT >604 CGGTCTCGGCATTCCTGCTGAACCGCTCGTCCGATCT >605 CGGTCTCGGCATTCCTGCTGAACCGCTCTACCGATCT >606 CGGTCTCGGCATTCCTGCTGAACCGCTCTCCCGATCT >607 CGGTCTCGGCATTCCTGCTGAACCGCTCTGCCGATCT >608 CGGTCTCGGCATTCCTGCTGAACCGCTCTTACGATCT >609 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCAGATCT >610 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCAATCT >611 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCCATCT >612 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGAACT >613 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGACCT >614 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGAGCT >615 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATAT >616 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCA >617 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCC >618 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCG >619 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >620 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATGT >621 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATTT >622 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGCTCT >623 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGGTCT >624 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGTTCT >625 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCTATCT >626 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCGGATCT >627 CGGTCTCGGCATTCCTGCTGAACCGCTCTTCTGATCT >628 CGGTCTCGGCATTCCTGCTGAACCGCTCTTGCGATCT >629 CGGTCTCGGCATTCCTGCTGAACCGCTCTTTCGATCT >630 CGGTCTCGGCATTCCTGCTGAACCGCTGTTCCGATCT >631 CGGTCTCGGCATTCCTGCTGAACCGCTTTTCCGATCT >632 CGGTCTCGGCATTCCTGCTGAACCGGTCTTCCGATCT >633 CGGTCTCGGCATTCCTGCTGAACCGTTCTTCCGATCT >634 CGGTCTCGGCATTCCTGCTGAACCTCTCTTCCGATCT >635 CGGTCTCGGCATTCCTGCTGAACGGCTCTTCCGATCT >636 CGGTCTCGGCATTCCTGCTGAACTGCTCTTCCGATCT >637 CGGTCTCGGCATTCCTGCTGAAGCGCTCTTCCGATCT >638 CGGTCTCGGCATTCCTGCTGAATCGCTCTTCCGATCT >639 CGGTCTCGGCATTCCTGCTGACCCGCTCTTCCGATCT >640 CGGTCTCGGCATTCCTGCTGAGCCGCTCTTCCGATCT >641 CGGTCTCGGCATTCCTGCTGATCCGCTCTTCCGATCT >642 CGGTCTCGGCATTCCTGCTGCACCGCTCTTCCGATCT >643 CGGTCTCGGCATTCCTGCTGGACCGCTCTTCCGATCT >644 CGGTCTCGGCATTCCTGCTGTACCGCTCTTCCGATCT >645 CGGTCTCGGCATTCCTGCTTAACCGCTCTTCCGATCT >646 CGGTCTCGGCATTCCTGGTGAACCGCTCTTCCGATCT >647 CGGTCTCGGCATTCCTGTTGAACCGCTCTTCCGATCT >648 CGGTCTCGGCATTCCTTCTGAACCGCTCTTCCGATCT >649 CGGTCTCGGCATTCGTGCTGAACCGCTCTTCCGATCT >650 CGGTCTCGGCATTCTTGCTGAACCGCTCTTCCGATCT >651 CGGTCTCGGCATTGCTGCTGAACCGCTCTTCCGATCT >652 CGGTCTCGGCATTTCTGCTGAACCGCTCTTCCGATCT >653 CGGTCTCGGCCTTCCTGCTGAACCGCTCTTCCGATCT >654 CGGTCTCGGCGTTCCTGCTGAACCGCTCTTCCGATCT >655 CGGTCTCGGCTTTCCTGCTGAACCGCTCTTCCGATCT >656 CGGTCTCGGGATTCCTGCTGAACCGCTCTTCCGATCT >657 CGGTCTCGGTATTCCTGCTGAACCGCTCTTCCGATCT >658 CGGTCTCGTCATTCCTGCTGAACCGCTCTTCCGATCT >659 CGGTCTCTGCATTCCTGCTGAACCGCTCTTCCGATCT >660 CGGTCTGGGCATTCCTGCTGAACCGCTCTTCCGATCT >661 CGGTCTTGGCATTCCTGCTGAACCGCTCTTCCGATCT >662 CGGTGTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >663 CGGTTTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >664 CGTTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >665 CTAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >666 CTAGCAGAAGACGGCATACGAGCTCTTCCGATCT >667 CTGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >668 GAACGGAAGAGCGGTTCAGCAGGAATGCCGAG >669 GAACGGAAGAGCTCGTATGCCGTCTTCTGCTTG >670 GAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >671 GAAGCAGAAGACGGCATACGAGCTCTTCCGATCT >672 GACCGGAAGAGCGGTTCAGCAGGAATGCCGAG >673 GACCGGAAGAGCTCGTATGCCGTCTTCTGCTTG >674 GAGCGGAAGAGCGGTTCAGCAGGAATGCCGAG >675 GAGCGGAAGAGCTCGTATGCCGTCTTCTGCTTG >676 GATAGGAAGAGCGGTTCAGCAGGAATGCCGAG >677 GATAGGAAGAGCTCGTATGCCGTCTTCTGCTTG >678 GATCAGAAGAGCGGTTCAGCAGGAATGCCGAG >679 GATCAGAAGAGCTCGTATGCCGTCTTCTGCTTG >680 GATCCGAAGAGCGGTTCAGCAGGAATGCCGAG >681 GATCCGAAGAGCTCGTATGCCGTCTTCTGCTTG >682 GATCGAAAGAGCGGTTCAGCAGGAATGCCGAG >683 GATCGAAAGAGCTCGTATGCCGTCTTCTGCTTG >684 GATCGCAAGAGCGGTTCAGCAGGAATGCCGAG >685 GATCGCAAGAGCTCGTATGCCGTCTTCTGCTTG >686 GATCGGAAAAGCGGTTCAGCAGGAATGCCGAG >687 GATCGGAAAAGCTCGTATGCCGTCTTCTGCTTG >688 GATCGGAACAGCGGTTCAGCAGGAATGCCGAG >689 GATCGGAACAGCTCGTATGCCGTCTTCTGCTTG >690 GATCGGAAGAACGGTTCAGCAGGAATGCCGAG >691 GATCGGAAGAACTCGTATGCCGTCTTCTGCTTG >692 GATCGGAAGACCGGTTCAGCAGGAATGCCGAG >693 GATCGGAAGACCTCGTATGCCGTCTTCTGCTTG >694 GATCGGAAGAGAGGTTCAGCAGGAATGCCGAG >695 GATCGGAAGAGATCGTATGCCGTCTTCTGCTTG >696 GATCGGAAGAGCACGTATGCCGTCTTCTGCTTG >697 GATCGGAAGAGCAGTTCAGCAGGAATGCCGAG >698 GATCGGAAGAGCCCGTATGCCGTCTTCTGCTTG >699 GATCGGAAGAGCCGTTCAGCAGGAATGCCGAG >700 GATCGGAAGAGCGATTCAGCAGGAATGCCGAG >701 GATCGGAAGAGCGCGTATGCCGTCTTCTGCTTG >702 GATCGGAAGAGCGCTTCAGCAGGAATGCCGAG >703 GATCGGAAGAGCGGATCAGCAGGAATGCCGAG >704 GATCGGAAGAGCGGCTCAGCAGGAATGCCGAG >705 GATCGGAAGAGCGGGTCAGCAGGAATGCCGAG >706 GATCGGAAGAGCGGTACAGCAGGAATGCCGAG >707 GATCGGAAGAGCGGTCCAGCAGGAATGCCGAG >708 GATCGGAAGAGCGGTGCAGCAGGAATGCCGAG >709 GATCGGAAGAGCGGTTAAGCAGGAATGCCGAG >710 GATCGGAAGAGCGGTTCAACAGGAATGCCGAG >711 GATCGGAAGAGCGGTTCACCAGGAATGCCGAG >712 GATCGGAAGAGCGGTTCAGAAGGAATGCCGAG >713 GATCGGAAGAGCGGTTCAGCAAGAATGCCGAG >714 GATCGGAAGAGCGGTTCAGCACGAATGCCGAG >715 GATCGGAAGAGCGGTTCAGCAGAAATGCCGAG >716 GATCGGAAGAGCGGTTCAGCAGCAATGCCGAG >717 GATCGGAAGAGCGGTTCAGCAGGAAAGCCGAG >718 GATCGGAAGAGCGGTTCAGCAGGAACGCCGAG >719 GATCGGAAGAGCGGTTCAGCAGGAAGGCCGAG >720 GATCGGAAGAGCGGTTCAGCAGGAATACCGAG >721 GATCGGAAGAGCGGTTCAGCAGGAATCCCGAG >722 GATCGGAAGAGCGGTTCAGCAGGAATGACGAG >723 GATCGGAAGAGCGGTTCAGCAGGAATGCAGAG >724 GATCGGAAGAGCGGTTCAGCAGGAATGCCAAG >725 GATCGGAAGAGCGGTTCAGCAGGAATGCCCAG >726 GATCGGAAGAGCGGTTCAGCAGGAATGCCGAA >727 GATCGGAAGAGCGGTTCAGCAGGAATGCCGAC >728 GATCGGAAGAGCGGTTCAGCAGGAATGCCGAG >729 GATCGGAAGAGCGGTTCAGCAGGAATGCCGAT >730 GATCGGAAGAGCGGTTCAGCAGGAATGCCGCG >731 GATCGGAAGAGCGGTTCAGCAGGAATGCCGGG >732 GATCGGAAGAGCGGTTCAGCAGGAATGCCGTG >733 GATCGGAAGAGCGGTTCAGCAGGAATGCCTAG >734 GATCGGAAGAGCGGTTCAGCAGGAATGCGGAG >735 GATCGGAAGAGCGGTTCAGCAGGAATGCTGAG >736 GATCGGAAGAGCGGTTCAGCAGGAATGGCGAG >737 GATCGGAAGAGCGGTTCAGCAGGAATGTCGAG >738 GATCGGAAGAGCGGTTCAGCAGGAATTCCGAG >739 GATCGGAAGAGCGGTTCAGCAGGACTGCCGAG >740 GATCGGAAGAGCGGTTCAGCAGGAGTGCCGAG >741 GATCGGAAGAGCGGTTCAGCAGGATTGCCGAG >742 GATCGGAAGAGCGGTTCAGCAGGCATGCCGAG >743 GATCGGAAGAGCGGTTCAGCAGGGATGCCGAG >744 GATCGGAAGAGCGGTTCAGCAGGTATGCCGAG >745 GATCGGAAGAGCGGTTCAGCAGTAATGCCGAG >746 GATCGGAAGAGCGGTTCAGCATGAATGCCGAG >747 GATCGGAAGAGCGGTTCAGCCGGAATGCCGAG >748 GATCGGAAGAGCGGTTCAGCGGGAATGCCGAG >749 GATCGGAAGAGCGGTTCAGCTGGAATGCCGAG >750 GATCGGAAGAGCGGTTCAGGAGGAATGCCGAG >751 GATCGGAAGAGCGGTTCAGTAGGAATGCCGAG >752 GATCGGAAGAGCGGTTCATCAGGAATGCCGAG >753 GATCGGAAGAGCGGTTCCGCAGGAATGCCGAG >754 GATCGGAAGAGCGGTTCGGCAGGAATGCCGAG >755 GATCGGAAGAGCGGTTCTGCAGGAATGCCGAG >756 GATCGGAAGAGCGGTTGAGCAGGAATGCCGAG >757 GATCGGAAGAGCGGTTTAGCAGGAATGCCGAG >758 GATCGGAAGAGCGTTTCAGCAGGAATGCCGAG >759 GATCGGAAGAGCTAGTATGCCGTCTTCTGCTTG >760 GATCGGAAGAGCTCATATGCCGTCTTCTGCTTG >761 GATCGGAAGAGCTCCTATGCCGTCTTCTGCTTG >762 GATCGGAAGAGCTCGAATGCCGTCTTCTGCTTG >763 GATCGGAAGAGCTCGCATGCCGTCTTCTGCTTG >764 GATCGGAAGAGCTCGGATGCCGTCTTCTGCTTG >765 GATCGGAAGAGCTCGTAAGCCGTCTTCTGCTTG >766 GATCGGAAGAGCTCGTACGCCGTCTTCTGCTTG >767 GATCGGAAGAGCTCGTAGGCCGTCTTCTGCTTG >768 GATCGGAAGAGCTCGTATACCGTCTTCTGCTTG >769 GATCGGAAGAGCTCGTATCCCGTCTTCTGCTTG >770 GATCGGAAGAGCTCGTATGACGTCTTCTGCTTG >771 GATCGGAAGAGCTCGTATGCAGTCTTCTGCTTG >772 GATCGGAAGAGCTCGTATGCCATCTTCTGCTTG >773 GATCGGAAGAGCTCGTATGCCCTCTTCTGCTTG >774 GATCGGAAGAGCTCGTATGCCGACTTCTGCTTG >775 GATCGGAAGAGCTCGTATGCCGCCTTCTGCTTG >776 GATCGGAAGAGCTCGTATGCCGGCTTCTGCTTG >777 GATCGGAAGAGCTCGTATGCCGTATTCTGCTTG >778 GATCGGAAGAGCTCGTATGCCGTCATCTGCTTG >779 GATCGGAAGAGCTCGTATGCCGTCCTCTGCTTG >780 GATCGGAAGAGCTCGTATGCCGTCGTCTGCTTG >781 GATCGGAAGAGCTCGTATGCCGTCTACTGCTTG >782 GATCGGAAGAGCTCGTATGCCGTCTCCTGCTTG >783 GATCGGAAGAGCTCGTATGCCGTCTGCTGCTTG >784 GATCGGAAGAGCTCGTATGCCGTCTTATGCTTG >785 GATCGGAAGAGCTCGTATGCCGTCTTCAGCTTG >786 GATCGGAAGAGCTCGTATGCCGTCTTCCGCTTG >787 GATCGGAAGAGCTCGTATGCCGTCTTCGGCTTG >788 GATCGGAAGAGCTCGTATGCCGTCTTCTACTTG >789 GATCGGAAGAGCTCGTATGCCGTCTTCTCCTTG >790 GATCGGAAGAGCTCGTATGCCGTCTTCTGATTG >791 GATCGGAAGAGCTCGTATGCCGTCTTCTGCATG >792 GATCGGAAGAGCTCGTATGCCGTCTTCTGCCTG >793 GATCGGAAGAGCTCGTATGCCGTCTTCTGCGTG >794 GATCGGAAGAGCTCGTATGCCGTCTTCTGCTAG >795 GATCGGAAGAGCTCGTATGCCGTCTTCTGCTCG >796 GATCGGAAGAGCTCGTATGCCGTCTTCTGCTGG >797 GATCGGAAGAGCTCGTATGCCGTCTTCTGCTTA >798 GATCGGAAGAGCTCGTATGCCGTCTTCTGCTTC >799 GATCGGAAGAGCTCGTATGCCGTCTTCTGCTTG >800 GATCGGAAGAGCTCGTATGCCGTCTTCTGCTTT >801 GATCGGAAGAGCTCGTATGCCGTCTTCTGGTTG >802 GATCGGAAGAGCTCGTATGCCGTCTTCTGTTTG >803 GATCGGAAGAGCTCGTATGCCGTCTTCTTCTTG >804 GATCGGAAGAGCTCGTATGCCGTCTTGTGCTTG >805 GATCGGAAGAGCTCGTATGCCGTCTTTTGCTTG >806 GATCGGAAGAGCTCGTATGCCGTGTTCTGCTTG >807 GATCGGAAGAGCTCGTATGCCGTTTTCTGCTTG >808 GATCGGAAGAGCTCGTATGCCTTCTTCTGCTTG >809 GATCGGAAGAGCTCGTATGCGGTCTTCTGCTTG >810 GATCGGAAGAGCTCGTATGCTGTCTTCTGCTTG >811 GATCGGAAGAGCTCGTATGGCGTCTTCTGCTTG >812 GATCGGAAGAGCTCGTATGTCGTCTTCTGCTTG >813 GATCGGAAGAGCTCGTATTCCGTCTTCTGCTTG >814 GATCGGAAGAGCTCGTCTGCCGTCTTCTGCTTG >815 GATCGGAAGAGCTCGTGTGCCGTCTTCTGCTTG >816 GATCGGAAGAGCTCGTTTGCCGTCTTCTGCTTG >817 GATCGGAAGAGCTCTTATGCCGTCTTCTGCTTG >818 GATCGGAAGAGCTGGTATGCCGTCTTCTGCTTG >819 GATCGGAAGAGCTGTTCAGCAGGAATGCCGAG >820 GATCGGAAGAGCTTGTATGCCGTCTTCTGCTTG >821 GATCGGAAGAGGGGTTCAGCAGGAATGCCGAG >822 GATCGGAAGAGGTCGTATGCCGTCTTCTGCTTG >823 GATCGGAAGAGTGGTTCAGCAGGAATGCCGAG >824 GATCGGAAGAGTTCGTATGCCGTCTTCTGCTTG >825 GATCGGAAGATCGGTTCAGCAGGAATGCCGAG >826 GATCGGAAGATCTCGTATGCCGTCTTCTGCTTG >827 GATCGGAAGCGCGGTTCAGCAGGAATGCCGAG >828 GATCGGAAGCGCTCGTATGCCGTCTTCTGCTTG >829 GATCGGAAGGGCGGTTCAGCAGGAATGCCGAG >830 GATCGGAAGGGCTCGTATGCCGTCTTCTGCTTG >831 GATCGGAAGTGCGGTTCAGCAGGAATGCCGAG >832 GATCGGAAGTGCTCGTATGCCGTCTTCTGCTTG >833 GATCGGAATAGCGGTTCAGCAGGAATGCCGAG >834 GATCGGAATAGCTCGTATGCCGTCTTCTGCTTG >835 GATCGGACGAGCGGTTCAGCAGGAATGCCGAG >836 GATCGGACGAGCTCGTATGCCGTCTTCTGCTTG >837 GATCGGAGGAGCGGTTCAGCAGGAATGCCGAG >838 GATCGGAGGAGCTCGTATGCCGTCTTCTGCTTG >839 GATCGGATGAGCGGTTCAGCAGGAATGCCGAG >840 GATCGGATGAGCTCGTATGCCGTCTTCTGCTTG >841 GATCGGCAGAGCGGTTCAGCAGGAATGCCGAG >842 GATCGGCAGAGCTCGTATGCCGTCTTCTGCTTG >843 GATCGGGAGAGCGGTTCAGCAGGAATGCCGAG >844 GATCGGGAGAGCTCGTATGCCGTCTTCTGCTTG >845 GATCGGTAGAGCGGTTCAGCAGGAATGCCGAG >846 GATCGGTAGAGCTCGTATGCCGTCTTCTGCTTG >847 GATCGTAAGAGCGGTTCAGCAGGAATGCCGAG >848 GATCGTAAGAGCTCGTATGCCGTCTTCTGCTTG >849 GATCTGAAGAGCGGTTCAGCAGGAATGCCGAG >850 GATCTGAAGAGCTCGTATGCCGTCTTCTGCTTG >851 GATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >852 GATGGGAAGAGCGGTTCAGCAGGAATGCCGAG >853 GATGGGAAGAGCTCGTATGCCGTCTTCTGCTTG >854 GATTGGAAGAGCGGTTCAGCAGGAATGCCGAG >855 GATTGGAAGAGCTCGTATGCCGTCTTCTGCTTG >856 GCACTCTTTCCCTACACGACGCTCTTCCGATCT >857 GCTCGGAAGAGCGGTTCAGCAGGAATGCCGAG >858 GCTCGGAAGAGCTCGTATGCCGTCTTCTGCTTG >859 GGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >860 GGTCGGAAGAGCGGTTCAGCAGGAATGCCGAG >861 GGTCGGAAGAGCTCGTATGCCGTCTTCTGCTTG >862 GTTCGGAAGAGCGGTTCAGCAGGAATGCCGAG >863 GTTCGGAAGAGCTCGTATGCCGTCTTCTGCTTG >864 TAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT >865 TAAGCAGAAGACGGCATACGAGCTCTTCCGATCT >866 TATCGGAAGAGCGGTTCAGCAGGAATGCCGAG >867 TATCGGAAGAGCTCGTATGCCGTCTTCTGCTTG >868 TATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT >869 TCACTCTTTCCCTACACGACGCTCTTCCGATCT >870 TGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT Quorum-1.1.1/gtest.mk000077500000000000000000000010571301151230400144550ustar00rootroot00000000000000############################## # Gtest build. ############################## # Build rules for libraries. check_LTLIBRARIES = libgtest.la libgtest_main.la libgtest_la_SOURCES = unit_tests/gtest/src/gtest-all.cc libgtest_main_la_SOURCES = unit_tests/gtest/src/gtest_main.cc libgtest_main_la_LIBADD = libgtest.la libgtest_la_CXXFLAGS = -I$(srcdir)/unit_tests libgtest_main_la_CXXFLAGS = -I$(srcdir)/unit_tests GTEST_SRC = unit_tests/gtest/src/gtest-all.cc \ unit_tests/gtest/src/gtest_main.cc \ unit_tests/gtest/gtest.h EXTRA_DIST += $(GTEST_SRC) Quorum-1.1.1/header-license000066400000000000000000000013311301151230400155610ustar00rootroot00000000000000/* Quorum * Copyright (C) 2012 Genome group at University of Maryland. * * This program is free software: you can redistribute it and/or * modify it under the terms of the GNU General Public License as * published by the Free Software Foundation, either version 3 of the * License, or (at your option) any later version. * * This program is distributed in the hope that it will be useful, but * WITHOUT ANY WARRANTY; without even the implied warranty of * MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the GNU * General Public License for more details. * * You should have received a copy of the GNU General Public License * along with this program. If not, see . */ Quorum-1.1.1/include/000077500000000000000000000000001301151230400144135ustar00rootroot00000000000000Quorum-1.1.1/include/gzip_stream.hpp000066400000000000000000000017121301151230400174510ustar00rootroot00000000000000#ifndef __GZIP_STREAM__ #define __GZIP_STREAM__ #include #include #include #include template > class basic_gzipstream : public std::ostream { typedef __gnu_cxx::stdio_filebuf<_CharT> stdbuf; public: basic_gzipstream(const char *filename) : std::ostream(open_gzip(filename)), closed(false) { } virtual ~basic_gzipstream() { close(); delete rdbuf(); } void close() { if(!closed) { flush(); pclose(((stdbuf*)rdbuf())->file()); closed = true; } } private: static stdbuf *open_gzip(const char *filename) { std::string command("gzip -1 > '"); command += filename; command += "'"; FILE *f = popen(command.c_str(), "w"); if(!f) throw std::runtime_error("popen failed"); return new stdbuf(f, std::ios::out); } bool closed; }; typedef basic_gzipstream gzipstream; #endif Quorum-1.1.1/include/jflib/000077500000000000000000000000001301151230400155015ustar00rootroot00000000000000Quorum-1.1.1/include/jflib/locks_pthread.hpp000066400000000000000000000115001301151230400210310ustar00rootroot00000000000000/* This file is part of Jflib. Jflib is free software: you can redistribute it and/or modify it under the terms of the GNU General Public License as published by the Free Software Foundation, either version 3 of the License, or (at your option) any later version. Jflib is distributed in the hope that it will be useful, but WITHOUT ANY WARRANTY; without even the implied warranty of MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the GNU General Public License for more details. You should have received a copy of the GNU General Public License along with Jflib. If not, see . */ #ifndef _JFLIB_LOCKS_PTHREAD_H_ #define _JFLIB_LOCKS_PTHREAD_H_ #include #include namespace jflib { namespace locks{ namespace pthread { class cond { pthread_mutex_t _mutex; pthread_cond_t _cond; public: cond() { pthread_mutex_init(&_mutex, NULL); pthread_cond_init(&_cond, NULL); } ~cond() { pthread_cond_destroy(&_cond); pthread_mutex_destroy(&_mutex); } inline void lock() { pthread_mutex_lock(&_mutex); } inline void unlock() { pthread_mutex_unlock(&_mutex); } inline void wait() { pthread_cond_wait(&_cond, &_mutex); } inline void signal() { pthread_cond_signal(&_cond); } inline void broadcast() { pthread_cond_broadcast(&_cond); } inline int timedwait(struct timespec *abstime) { return pthread_cond_timedwait(&_cond, &_mutex, abstime); } inline int timedwait(time_t seconds) { struct timespec curtime; clock_gettime(CLOCK_REALTIME, &curtime); curtime.tv_sec += seconds; return timedwait(&curtime); } }; class mutex { pthread_mutex_t _mutex; public: mutex() { pthread_mutex_init(&_mutex, NULL); } ~mutex() { pthread_mutex_destroy(&_mutex); } inline void lock() { pthread_mutex_lock(&_mutex); } inline void unlock() { pthread_mutex_unlock(&_mutex); } inline bool try_lock() { return !pthread_mutex_trylock(&_mutex); } }; class mutex_lock { mutex& m_; public: explicit mutex_lock(mutex& m) : m_(m) { m_.lock(); } ~mutex_lock() { m_.unlock(); } }; class Semaphore { int _value, _wakeups; cond _cv; public: Semaphore(int value) : _value(value), _wakeups(0) { // nothing to do } ~Semaphore() {} inline void wait() { _cv.lock(); _value--; if (_value < 0) { do { _cv.wait(); } while(_wakeups < 1); _wakeups--; } _cv.unlock(); } inline void signal() { _cv.lock(); _value++; if(_value <= 0) { _wakeups++; _cv.signal(); } _cv.unlock(); } }; #if defined(_POSIX_BARRIERS) && (_POSIX_BARRIERS - 20012L) >= 0 class barrier { pthread_barrier_t _barrier; public: barrier(unsigned count) { pthread_barrier_init(&_barrier, NULL, count); } ~barrier() { pthread_barrier_destroy(&_barrier); } inline int wait() { return pthread_barrier_wait(&_barrier); } }; #else # ifndef PTHREAD_BARRIER_SERIAL_THREAD # define PTHREAD_BARRIER_SERIAL_THREAD 1 # endif class barrier { int count; // required # of threads int current; // current # of threads that have passed thru mutex barlock; // protect current Semaphore barrier1; // implement the barrier Semaphore barrier2; public: barrier(unsigned cnt) : count(cnt), current(0), barrier1(0), barrier2(0) { } ~barrier() {} inline int wait() { int ret = 0; barlock.lock(); current += 1; if(current == count) { ret = PTHREAD_BARRIER_SERIAL_THREAD; for(int i=0; i. */ #ifndef _JFLIB_MULTIPLEXED_IO_H_ #define _JFLIB_MULTIPLEXED_IO_H_ #include #include #include #include #include #include #include namespace jflib { /** Output multiplexer class. Multiple threads write to a pool of * buffers which are then written by a single thread to an * ostream. Similar to asynchronous IO, potentially easier to use. * * This works in 2 steps: first create the o_multiplexer based on an * `std::ostream`. This will setup the pool/FIFO. Then, each thread creates * an `omstream` based on the `o_multiplexer`. Each of this `omstream` * obtain and send buffers to the ostream using the pool. To ensure * that the output is not interleaved with other threads output, * there is a `end_record()` (or `<< endr`) method which marks the * end of a record that can be send to the underlying ostream and * written as one atomic operation. A `sync()` operation (or `<< * std::flush`) implies an end of record as well. * * An example: * ~~~{.cc} * std::ofstream file("/path/to/file"); // Open file for output * jflib::o_multiplexer multiplexer(file); // Create multiplexer to file * * // In each thread * jflib::omstream out(multiplexer); // Create my multiplexed ostream * out << "Hello world!\n" << "How are you doing?\n" << endr; * ~~~ * * The two lines are guaranteed to not be interleaved with output * from other thread. They are an atomic record. */ class o_multiplexer { class buffer; class multiplexedbuf; typedef pool buffer_pool; struct writer_info { std::ostream *os; buffer_pool *pool; writer_info(std::ostream *_os, buffer_pool *_pool) : os(_os), pool(_pool) { } }; public: /** Constructor based on an ostream `os` and `nb_buffers` of size * `buffer_size`. * @param os Underlying stream to write to. * * @param nb_buffers For reliable performance, there should be * more nb_buffers than threads that will create omstream, * otherwise there will always be threads waiting on getting a * buffer. Probably, 2 to 3 times the number of threads. * * @param buffer_size The size of a buffer should be larger than * the record length. If not, the buffer get enlarged (size * doubled) when a record does not fit into a buffer. */ o_multiplexer(std::ostream *os, size_t nb_buffers, size_t buffer_size) : _os(os), _pool(nb_buffers), _info(_os, &_pool), _writer_started(false) { for(buffer_pool::iterator it = _pool.begin(); it != _pool.end(); ++it) { if(!it->resize(buffer_size)) throw std::runtime_error("Failed to allocate memory for buffers"); } int res = pthread_create(&_writer_id, 0, writer_loop, (void*)&_info); if(res) throw std::runtime_error("Failed to create the writer thread"); _writer_started = true; } /** Destructor. Sync is called on the underlying ostream, but it * is otherwise not changed (not closed or destroyed) by this * destructor. */ virtual ~o_multiplexer() { close(); } /** Tell the writer thread to stop after the pool is empty. To be * safe, this should be called after every threads with an * omstream() associated have are done writing to the * stream. Unspecified behavior if a thread writes after close has * been called. * * @todo should we implement a safe version that waits for every * omstream object to be destroyed? */ void close() { _pool.close_A_to_B(); if(_writer_started) { pthread_join(_writer_id, 0); _writer_started = false; } _os->flush(); } private: static void *writer_loop(void *_d) { writer_info *d = (writer_info*)_d; while(true) { buffer_pool::elt e(d->pool->get_B()); if(e.is_empty()) break; if(e->write_len() > 0) d->os->write(e->base(), e->write_len()); if(e->do_sync()) d->os->flush(); } d->os->flush(); return 0; } class buffer { public: buffer() : _write_len(0), _sync(false), _data(0), _end(0) { } buffer(size_t size) : _write_len(0), _sync(false), _data((char*)malloc(size)), _end(_data + size) { if(!_data) throw std::runtime_error("Failed to allocate multiplexer::buffer"); } ~buffer() { free(_data); } char *base() const { return _data; } char *end() const { return _end; } std::streamsize write_len() const { return _write_len; } void set_write_len(std::streamsize s) { _write_len = s; } bool do_sync() const { return _sync; } void set_do_sync(bool sync) { _sync = sync; } size_t size() const { return _end - _data; } char *resize(size_t min_size = 0) { const size_t csize = size(); if(!min_size) min_size = 2 * csize; if(min_size <= csize) return _data; if(min_size == 0) min_size = 4096; char *ndata = (char*)realloc(_data, min_size); if(!ndata) return 0; _data = ndata; _end = _data + min_size; return _data; } private: std::streamsize _write_len; bool _sync; char *_data; char *_end; }; class basebuf : public std::streambuf { protected: basebuf() { } public: virtual ~basebuf() { } virtual void end_record() { } }; class closedbuf : public basebuf { public: closedbuf() { } virtual ~closedbuf() { } }; class multiplexedbuf : public basebuf { public: multiplexedbuf(buffer_pool *pool) : _pool(pool), _closed(false) { update_buffer(); } virtual ~multiplexedbuf() { } /** Send a sync signal. A sync implies the end of a record. */ virtual int sync() { if(_closed) return -1; size_t s = pptr() - pbase(); if(s == 0) return 0; _elt->set_write_len(s); _elt->set_do_sync(true); // Release and get new buffer if(!update_buffer()) return -1; return 0; } void end_record() { if(_closed) return; size_t clen = pptr() - pbase(); if(clen == 0) return; _elt->set_write_len(clen); ++_nbr; if(2 * clen >= (size_t)(epptr() - pptr()) * _nbr) { _elt->set_do_sync(false); update_buffer(); } } virtual int overflow(int c) { if(_closed) return EOF; if(_nbr == 0) { // No record in its entirety ptrdiff_t old_size = _elt->end() - _elt->base(); if(!_elt->resize()) return EOF; setp(_elt->base(), _elt->end()); pbump(old_size); } else { // Save part not in a record and release rest. ptrdiff_t in_buf = pptr() - pbase(); if(_elt->write_len() < in_buf) { size_t extra = in_buf - _elt->write_len(); if(!_overflow_buffer.resize(extra)) return EOF; memcpy(_overflow_buffer.base(), pptr() - extra, extra); _overflow_buffer.set_write_len(extra); } else _overflow_buffer.set_write_len(0); _elt->set_do_sync(false); if(!update_buffer()) return EOF; if(_overflow_buffer.write_len() > 0) { const char* nbase = _elt->resize(2 * _overflow_buffer.write_len()); if(!nbase) return EOF; setp(_elt->base(), _elt->end()); memcpy(pbase(), _overflow_buffer.base(), _overflow_buffer.write_len()); pbump(_overflow_buffer.write_len()); } } if(c != EOF) { *pptr() = c; pbump(1); } return !EOF; } private: // Release the current buffer and update it with a new one, // unless the stream is closed. bool update_buffer() { if(!_closed) _closed = _pool->is_closed_B_to_A(); if(_closed) { _elt.release(); setp(0, 0); } else { _elt = _pool->get_A(); _elt->set_write_len(0); setp(_elt->base(), _elt->end()); } _nbr = 0; return !_closed; } buffer_pool *_pool; bool _closed; unsigned int _nbr; // number of records buffer_pool::elt _elt; buffer _overflow_buffer; }; friend class omstream; multiplexedbuf *new_multiplexedbuf() { return new multiplexedbuf(&_pool); } std::ostream *_os; buffer_pool _pool; writer_info _info; pthread_t _writer_id; bool _writer_started; }; /** Multiplexed ostream. */ class omstream : public std::ostream { public: omstream(o_multiplexer &om) : std::ostream(om.new_multiplexedbuf()) { } virtual ~omstream() { rdbuf()->pubsync(); delete rdbuf(); } /** Mark the end of a record */ void end_record() { ((o_multiplexer::basebuf*)rdbuf())->end_record(); } /** Close this ostream */ void close() { rdbuf()->pubsync(); delete rdbuf(new o_multiplexer::closedbuf()); } private: }; struct endrT { }; static const endrT endr = { }; } jflib::omstream &operator<<(jflib::omstream &os, const jflib::endrT &rhs) { os.end_record(); return os; } #endif /* _JFLIB_MULTIPLEXED_IO_H_ */ Quorum-1.1.1/include/jflib/pool.hpp000066400000000000000000000125721301151230400171720ustar00rootroot00000000000000#ifndef _JFLIB_POOL_H_ #define _JFLIB_POOL_H_ #include #include #include #include namespace jflib { /** Fixed size pool of objects with lock-free access. Conceptually, * there are two sides: A and B. There are 2 FIFOs in opposite * direction between A and B. One "get" an element from one side * (say A) and then "release" it. This correspond to dequeue from * the queue B->A then enqueueing into A->B. To get an element can * block if the queue is empty but to release never does. * * The class itself manages 'size' elements in the queues and are * initialized with 'value'. Initially, all the elements are in the * B->A queue. * * The elements of type T in the pool should not be accessed * unless one has the obtained the elt object and has not released * (or destructed) it. * * WARNING: The iterator on the elements does not check any of this * and is not thread-safe. */ template class pool { class side; public: // typedef typename std::vector Tvec; typedef T* iterator; pool(size_t size) : size_(size), elts_(new T[size]), B2A(size, elts_), A2B(size, elts_) { B2A.other_ = &A2B; A2B.other_ = &B2A; for(uint32_t i = 0; i < size_; ++i) B2A.fifo_.enqueue(i); } virtual ~pool() { delete [] elts_; } size_t size() const { return size_; } /** Get the side A. Used to get an element from side A. */ side &get_A() { return B2A; } /** Get the side B. Used to get an element from side B. */ side &get_B() { return A2B; } void close_A_to_B() { A2B.fifo_.close(); A2B.signal(true); } void close_B_to_A() { B2A.fifo_.close(); B2A.signal(true); } bool is_closed_A_to_B() const { return A2B.fifo_.is_closed(); } bool is_closed_B_to_A() const { return B2A.fifo_.is_closed(); } /** Iterators on the elements. Unlike other */ T* begin() { return elts_; } T* end() { return elts_ + size_; } /** A wrapper around an element of type T. The element can be * obtained with operator* or operator->. release() is called by * the destructor to requeue the element in to the double * fifo. When the double fifo is empty and closed, the element * obtained is_empty() method returns true. */ class elt { public: elt() : i_(cbT::guard), v_(0), s_(0) { } elt(side &s) : i_(s.get()), v_(s[i_]), s_(s.other_) { } ~elt() { release(); } elt &operator=(side &s) { release(); i_ = s.get(); v_ = s[i_]; s_ = s.other_; return *this; } void release() { if(v_) s_->release(i_); v_ = 0; } bool is_empty() const { return v_ == 0; } T &operator*() { return *v_; } T *operator->() { return v_; } friend class pool; private: elt(const elt &rhs) { } elt &operator=(const elt &rhs) { } uint32_t i_; // Index of stored value T *v_; // Stored value side *s_; // Side to release to }; static const elt closed; private: typedef circular_buffer cbT; /** A circular buffer with a conditional variable to wait in the * empty event and a pointer to the other direction circular * buffer. Every method is private and are accessible only by its * friends :) */ class side { private: friend class pool; friend class elt; enum State { NONE, WAITING, CLOSED }; side(size_t size, T* elts) : fifo_(2*size), state_(NONE), other_(0), elts_(elts) { } uint32_t get(); T *operator[](uint32_t i); void release(uint32_t i); void signal(bool force = false); cbT fifo_; CV cond_; State state_; side *other_; T *elts_; }; size_t size_; T* elts_; side B2A; // Manages queue from B->A side A2B; // Manages queue from A->B }; } template uint32_t jflib::pool::side::get() { bool last_attempt = false; uint32_t res = fifo_.dequeue(); while(res == cbT::guard) { cond_.lock(); switch(a_load(state_)) { case CLOSED: if(last_attempt) { cond_.unlock(); return cbT::guard; } else { last_attempt = true; break; } case NONE: a_store(state_, WAITING); break; case WAITING: break; } res = fifo_.dequeue(); if(res == cbT::guard) { if(last_attempt) { cond_.unlock(); break; } } else { cond_.unlock(); break; } do { cond_.timedwait(5); } while(a_load(state_) == WAITING); cond_.unlock(); } return res; } template T * jflib::pool::side::operator[](uint32_t i) { if(i == cbT::guard) return 0; return &elts_[i]; } template void jflib::pool::side::release(uint32_t i) { while(!fifo_.enqueue(i)) ; signal(); } template void jflib::pool::side::signal(bool close) { if(a_load(state_) != NONE || close) { cond_.lock(); a_store(state_, close ? CLOSED : NONE); cond_.broadcast(); cond_.unlock(); } } #endif /* _JFLIB_POOL_H_ */ Quorum-1.1.1/include/misc.hpp000066400000000000000000000026111301151230400160570ustar00rootroot00000000000000#ifndef __MISC_HPP__ #define __MISC_HPP__ //#define _GNU_SOURCE #include #include #include // IO manipulator for substrings class substr { public: const char * const _str; size_t const _len; substr(const char *str, size_t len) : _str(str), _len(len) {} substr(const char *str, const char *end) : _str(str), _len(end > str ? end - str : 0) {} }; inline bool is_base(const char c) { switch(c) { case 'A': case 'C': case 'G': case 'T': case 'a': case 'c': case 'g': case 't': return true; default: return false; } } inline bool not_base(const char c) { return !is_base(c); } inline std::ostream & operator<<(std::ostream &os, const substr &ss) { assert(std::count_if(ss._str, ss._str+ss._len, not_base) == 0); return os.write(ss._str, ss._len); } template int getFldsFromLine(char *line, T &res) { char *saveptr; res.clear(); char *tok = strtok_r(line, " \t\n", &saveptr); while(tok) { res.push_back(tok); tok = strtok_r(0, " \t\n", &saveptr); } return res.size(); } template int appendFldsFromLine(char *line, T &res) { char *saveptr; int numFlds = 0; char *tok = strtok_r(line, " \t\n", &saveptr); while(tok) { res.push_back(tok); ++numFlds; tok = strtok_r(0, " \t\n", &saveptr); } return numFlds; } #include #define BREAKPOINT raise(SIGINT); #endif Quorum-1.1.1/local.mk000066400000000000000000000007601301151230400144160ustar00rootroot00000000000000# Build the easy install script bin_SCRIPTS += quorum_easy_install quorum_easy_install: quorum_easy_install.in Makefile $(do_subst) < $< > $@ chmod +x $@ distcheck: quorum_easy_install dist: quorum_easy_install AM_CXXFLAGS += -Werror # Count lines of code .PHONY: cloc cloc: cloc --force-lang="Ruby,yaggo" --force-lang="make,am" --force-lang="make,mk" \ --exclude-dir="gtest" --ignored=cloc_ignored_src_files \ $(srcdir)/src $(srcdir)/include \ $(srcdir)/Makefile.am $(srcdir)/*.mk Quorum-1.1.1/m4/000077500000000000000000000000001301151230400133105ustar00rootroot00000000000000Quorum-1.1.1/m4/.gitignore000066400000000000000000000001071301151230400152760ustar00rootroot00000000000000# Ignore everything in this directory * # Except this file !.gitignore Quorum-1.1.1/paper/000077500000000000000000000000001301151230400140775ustar00rootroot00000000000000Quorum-1.1.1/paper/.gitignore000066400000000000000000000000501301151230400160620ustar00rootroot00000000000000*.aux *.bbl *.blg *.log bmc_article.pdf Quorum-1.1.1/paper/bmc_article.bib000077500000000000000000012406031301151230400170320ustar00rootroot00000000000000Automatically generated by Mendeley 1.5.2 Any changes to this file will be lost if it is regenerated by Mendeley. @article{Yang2012, abstract = {Error Correction is important for most next-generation sequencing applications because highly accurate sequenced reads will likely lead to higher quality results. Many techniques for error correction of sequencing data from next-gen platforms have been developed in the recent years. However, compared with the fast development of sequencing technologies, there is a lack of standardized evaluation procedure for different error-correction methods, making it difficult to assess their relative merits and demerits. In this article, we provide a comprehensive review of many error-correction methods, and establish a common set of benchmark data and evaluation criteria to provide a comparative assessment. We present experimental results on quality, run-time, memory usage and scalability of several error-correction methods. Apart from providing explicit recommendations useful to practitioners, the review serves to identify the current state of the art and promising directions for future research. Availability: All error-correction programs used in this article are downloaded from hosting websites. The evaluation tool kit is publicly available at: http://aluru-sun.ece.iastate.edu/doku.php?id=ecr.}, author = {Yang, X and Chockalingam, S P and Aluru, S}, doi = {10.1093/bib/bbs015}, file = {:home/gus/Documents/Mendeley Desktop/Yang, Chockalingam, Aluru\_2012\_A survey of error-correction methods for next-generation sequencing.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Yang, Chockalingam, Aluru\_2012\_A survey of error-correction methods for next-generation sequencing(2).pdf:pdf}, isbn = {1467546314774054}, issn = {14675463}, journal = {Briefings in Bioinformatics}, keywords = {error correction,next generation sequencing,sequence analysis}, pages = {bbs015--}, publisher = {Oxford University Press}, title = {{A survey of error-correction methods for next-generation sequencing}}, url = {http://bib.oxfordjournals.org/cgi/doi/10.1093/bib/bbs015 http://bib.oxfordjournals.org/content/early/2012/04/06/bib.bbs015.short}, year = {2012} } @article{Purcell2005, abstract = {We present the first non-blocking hashtable based on open addressing that provides the following benefits: it combines good cache locality, accessing a single cacheline if there are no collisions, with short straight-line code; it needs no storage overhead for pointers and memory allocator schemes, having instead an overhead of two words per bucket; it does not need to periodically reorganise or replicate the table; and it does not need garbage collection, even with arbitrary-sized keys. Open problems include resizing the table and replacing, rather than erasing, entries. The result is a highly-concurrent set algorithm that approaches or outperforms the best externally- chained implementations we tested, with fixed memory costs and no need to select or fine-tune a garbage collector or locking strategy.}, author = {Purcell, Chris and Harris, Tim}, file = {:home/gus/Documents/Mendeley Desktop/Purcell, Harris\_2005\_Non-blocking hatables with open addressing.pdf:pdf}, journal = {University of Cambridge Technical Report}, keywords = {hash table,lock free}, number = {639}, title = {{Non-blocking hatables with open addressing}}, year = {2005} } @article{Hallett2004, author = {Hallett, M T}, file = {:home/gus/Documents/Mendeley Desktop/Hallett\_2004\_Identifying Lateral Gene Transfers.pdf:pdf}, keywords = {blocking loop}, mendeley-tags = {blocking loop}, pages = {1--29}, title = {{Identifying Lateral Gene Transfers}}, year = {2004} } @article{Wetzel2011, abstract = {Next-generation sequencing technologies allow genomes to be sequenced more quickly and less expensively than ever before. However, as sequencing technology has improved, the difficulty of de novo genome assembly has increased, due in large part to the shorter reads generated by the new technologies. The use of mated sequences (referred to as mate-pairs) is a standard means of disambiguating assemblies to obtain a more complete picture of the genome without resorting to manual finishing. Here, we examine the effectiveness of mate-pair information in resolving repeated sequences in the DNA (a paramount issue to overcome). While it has been empirically accepted that mate-pairs improve assemblies, and a variety of assemblers use mate-pairs in the context of repeat resolution, the effectiveness of mate-pairs in this context has not been systematically evaluated in previous literature.}, author = {Wetzel, Joshua and Kingsford, Carl and Pop, Mihai}, doi = {10.1186/1471-2105-12-95}, file = {:home/gus/Documents/Mendeley Desktop/Wetzel, Kingsford, Pop\_2011\_Assessing the benefits of using mate-pairs to resolve repeats in de novo short-read prokaryotic assemblies.pdf:pdf}, issn = {1471-2105}, journal = {BMC bioinformatics}, keywords = {Bacteria,Bacteria: classification,Bacteria: genetics,Bacterial,DNA,DNA: methods,Genome, Bacterial,High-Throughput Nucleotide Sequencing,High-Throughput Nucleotide Sequencing: methods,Sequence Analysis, DNA,Sequence Analysis, DNA: methods}, month = jan, number = {1}, pages = {95}, pmid = {21486487}, title = {{Assessing the benefits of using mate-pairs to resolve repeats in de novo short-read prokaryotic assemblies.}}, url = {http://www.biomedcentral.com/1471-2105/12/95}, volume = {12}, year = {2011} } @article{Panda2010, annote = {10.1038/nature08696}, author = {Li, Ruiqiang and Fan, Wei and Tian, Geng and Zhu, Hongmei and He, Lin and Cai, Jing and Huang, Quanfei and Cai, Qingle and Li, Bo and Bai, Yinqi and Zhang, Zhihe and Zhang, Yaping and Wang, Wen and Li, Jun and Wei, Fuwen and Li, Heng and Jian, Min and Li, Jianwen and Zhang, Zhaolei and Nielsen, Rasmus and Li, Dawei and Gu, Wanjun and Yang, Zhentao and Xuan, Zhaoling and Ryder, Oliver A and Leung, Frederick Chi-Ching and Zhou, Yan and Cao, Jianjun and Sun, Xiao and Fu, Yonggui and Fang, Xiaodong and Guo, Xiaosen and Wang, Bo and Hou, Rong and Shen, Fujun and Mu, Bo and Ni, Peixiang and Lin, Runmao and Qian, Wubin and Wang, Guodong and Yu, Chang and Nie, Wenhui and Wang, Jinhuan and Wu, Zhigang and Liang, Huiqing and Min, Jiumeng and Wu, Qi and Cheng, Shifeng and Ruan, Jue and Wang, Mingwei and Shi, Zhongbin and Wen, Ming and Liu, Binghang and Ren, Xiaoli and Zheng, Huisong and Dong, Dong and Cook, Kathleen and Shan, Gao and Zhang, Hao and Kosiol, Carolin and Xie, Xueying and Lu, Zuhong and Zheng, Hancheng and Li, Yingrui and Steiner, Cynthia C and Lam, Tommy Tsan-Yuk and Lin, Siyuan and Zhang, Qinghui and Li, Guoqing and Tian, Jing and Gong, Timing and Liu, Hongde and Zhang, Dejin and Fang, Lin and Ye, Chen and Zhang, Juanbin and Hu, Wenbo and Xu, Anlong and Ren, Yuanyuan and Zhang, Guojie and Bruford, Michael W and Li, Qibin and Ma, Lijia and Guo, Yiran and An, Na and Hu, Yujie and Zheng, Yang and Shi, Yongyong and Li, Zhiqiang and Liu, Qing and Chen, Yanling and Zhao, Jing and Qu, Ning and Zhao, Shancen and Tian, Feng and Wang, Xiaoling and Wang, Haiyin and Xu, Lizhi and Liu, Xiao and Vinar, Tomas and Wang, Yajun and Lam, Tak-Wah and Yiu, Siu-Ming and Liu, Shiping and Zhang, Hemin and Li, Desheng and Huang, Yan and Wang, Xia and Yang, Guohua and Jiang, Zhi and Wang, Junyi and Qin, Nan and Li, Li and Li, Jingxiang and Bolund, Lars and Kristiansen, Karsten and Wong, Gane Ka-Shu and Olson, Maynard and Zhang, Xiuqing and Li, Songgang and Yang, Huanming and Wang, Jian and Wang, Jun}, doi = {http://dx.doi.org/10.1038/nature08696}, issn = {0028-0836}, journal = {Nature}, number = {7279}, pages = {311--317}, publisher = {Macmillan Publishers Limited. All rights reserved}, title = {{The sequence and de novo assembly of the giant panda genome}}, volume = {463}, year = {2010} } @article{Gibbs2012, author = {Gibbs, Richard A and Rogers, Jeffrey}, doi = {10.1038/483164a}, file = {:home/gus/Documents/Mendeley Desktop/Gibbs, Rogers\_2012\_Genomics Gorilla gorilla gorilla.pdf:pdf}, issn = {1476-4687}, journal = {Nature}, month = mar, number = {7388}, pages = {164--5}, pmid = {22398552}, publisher = {Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.}, shorttitle = {Nature}, title = {{Genomics: Gorilla gorilla gorilla.}}, url = {http://dx.doi.org/10.1038/483164a}, volume = {483}, year = {2012} } @article{Manber1990, author = {Manber, Udi and Myers, Gene}, file = {:home/gus/Documents/Mendeley Desktop/Manber, Myers\_1990\_Suffix arrays a new method for on-line string searches.pdf:pdf}, isbn = {0-89871-251-3}, month = jan, pages = {319--327}, title = {{Suffix arrays: a new method for on-line string searches}}, url = {http://dl.acm.org/citation.cfm?id=320176.320218}, year = {1990} } @article{Kim:2007uq, abstract = {One of the main goals in genome sequencing projects is to determine a haploid consensus sequence even when clone libraries are constructed from homologous chromosomes. However, it has been noticed that haplotypes can be inferred from genome assemblies by investigating phase conservation in sequenced reads. In this study, we seek to infer haplotypes, a diploid consensus sequence, from the genome assembly of an organism, Ciona intestinalis. The Ciona intestinalis genome is an ideal resource from which haplotypes can be inferred because of the high polymorphism rate (1.2\%). The haplotype estimation scheme consists of polymorphism detection and phase estimation. The core step of our method is a Gibbs sampling procedure. The mate-pair information from two-end sequenced clone inserts is exploited to provide long-range continuity. We estimate the polymorphism rate of Ciona intestinalis to be 1.2\% and 1.5\%, according to two different polymorphism counting schemes. The distribution of heterozygosity number is well fit by a compound Poisson distribution. The N50 length of haplotype segments is 37.9 kb in our assembly, while the N50 scaffold length of the Ciona intestinalis assembly is 190 kb. We also infer diploid gene sequences from haplotype segments. According to our reconstruction, 85.4\% of predicted gene sequences are continuously covered by single haplotype segments. Our results indicate 97\% accuracy in haplotype estimation, based on a simulated data set. We conduct a comparative analysis with Ciona savignyi, and discover interesting patterns of conserved DNA elements in chordates.}, author = {Kim, Jong Hyun and Waterman, Michael S and Li, Lei M}, doi = {10.1101/gr.5894107}, file = {:home/gus/Documents/Mendeley Desktop/Kim, Waterman, Li\_2007\_Diploid genome reconstruction of Ciona intestinalis and comparative analysis with Ciona savignyi.pdf:pdf}, journal = {Genome Res}, month = jul, number = {7}, pages = {1101--1110}, pmid = {17567986}, title = {{Diploid genome reconstruction of Ciona intestinalis and comparative analysis with Ciona savignyi}}, volume = {17}, year = {2007} } @article{Ilie2011b, abstract = {High-throughput sequencing technologies produce very large amounts of data and sequencing errors constitute one of the major problems in analyzing such data. Current algorithms for correcting these errors are not very accurate and do not automatically adapt to the given data.}, author = {Ilie, Lucian and Fazayeli, Farideh and Ilie, Silvana}, file = {:home/gus/Documents/Mendeley Desktop/Ilie, Fazayeli, Ilie\_2011\_HiTEC accurate error correction in high-throughput sequencing data.pdf:pdf}, institution = {Department of Computer Science, University of Western Ontario, London, ON N6A 5B7, Canada. ilie@csd.uwo.ca}, journal = {Bioinformatics}, number = {3}, pages = {295--302}, pmid = {21115437}, title = {{HiTEC: accurate error correction in high-throughput sequencing data.}}, url = {http://www.ncbi.nlm.nih.gov/pubmed/21115437 http://bioinformatics.oxfordjournals.org/content/27/3/295.short}, volume = {27}, year = {2011} } @article{Florea:2010kx, author = {Florea, Liliana and Souvorov, Alexander and Salzberg, Steven}, doi = {10.1186/gb-2010-11-s1-p13}, issn = {1465-6906}, journal = {Genome Biology}, number = {Suppl 1}, pages = {P13}, title = {{Genes and genomes, an imperfect world: comparison of gene annotations of two Bos taurus draft assemblies}}, url = {http://genomebiology.com/2010/11/S1/P13}, volume = {11}, year = {2010} } @article{Stranneheim2010, abstract = {New generation sequencing technologies producing increasingly complex datasets demand new efficient and specialized sequence analysis algorithms. Often, it is only the 'novel' sequences in a complex dataset that are of interest and the superfluous sequences need to be removed.}, author = {Stranneheim, Henrik and K\"{a}ller, Max and Allander, Tobias and Andersson, Bj\"{o}rn and Arvestad, Lars and Lundeberg, Joakim}, doi = {10.1093/bioinformatics/btq230}, file = {:home/gus/Documents/Mendeley Desktop/Stranneheim et al.\_2010\_Classification of DNA sequences using Bloom filters.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,DNA,Genome,Humans,Metagenome,Mitochondrial,Respiratory System,Respiratory System: microbiology,Sensitivity and Specificity,Sequence Analysis}, month = jul, number = {13}, pages = {1595--600}, pmid = {20472541}, title = {{Classification of DNA sequences using Bloom filters.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/26/13/1595}, volume = {26}, year = {2010} } @article{Vinson:2005kx, abstract = {Whole-genome assembly is now used routinely to obtain high-quality draft sequence for the genomes of species with low levels of polymorphism. However, genome assembly remains extremely challenging for highly polymorphic species. The difficulty arises because two divergent haplotypes are sequenced together, making it difficult to distinguish alleles at the same locus from paralogs at different loci. We present here a method for assembling highly polymorphic diploid genomes that involves assembling the two haplotypes separately and then merging them to obtain a reference sequence. Our method was developed to assemble the genome of the sea squirt Ciona savignyi, which was sequenced to a depth of 12.7 x from a single wild individual. By comparing finished clones of the two haplotypes we determined that the sequenced individual had an extremely high heterozygosity rate, averaging 4.6\% with significant regional variation and rearrangements at all physical scales. Applied to these data, our method produced a reference assembly covering 157 Mb, with N50 contig and scaffold sizes of 47 kb and 989 kb, respectively. Alignment of ESTs indicates that 88\% of loci are present at least once and 81\% exactly once in the reference assembly. Our method represented loci in a single copy more reliably and achieved greater contiguity than a conventional whole-genome assembly method.}, author = {Vinson, Jade P and Jaffe, David B and O'Neill, Keith and Karlsson, Elinor K and Stange-Thomann, Nicole and Anderson, Scott and Mesirov, Jill P and Satoh, Nori and Satou, Yutaka and Nusbaum, Chad and Birren, Bruce and Galagan, James E and Lander, Eric S}, doi = {10.1101/gr.3722605}, journal = {Genome Res}, month = aug, number = {8}, pages = {1127--1135}, pmid = {16077012}, title = {{Assembly of polymorphic genomes: algorithms and application to Ciona savignyi}}, volume = {15}, year = {2005} } @misc{TheMendeleySupportTeam2011a, abstract = {A quick introduction to Mendeley. Learn how Mendeley creates your personal digital library, how to organize and annotate documents, how to collaborate and share with colleagues, and how to generate citations and bibliographies.}, address = {London}, author = {{The Mendeley Support Team}}, booktitle = {Mendeley Desktop}, file = {:home/gus/Documents/Mendeley Desktop/The Mendeley Support Team\_2011\_Getting Started with Mendeley.pdf:pdf}, keywords = {Mendeley,how-to,user manual}, pages = {1--16}, publisher = {Mendeley Ltd.}, title = {{Getting Started with Mendeley}}, url = {http://www.mendeley.com}, year = {2011} } @article{Salzberg2011, abstract = {New sequencing technology has dramatically altered the landscape of whole-genome sequencing, allowing scientists to initiate numerous projects to decode the genomes of previously unsequenced organisms. The lowest-cost technology can generate deep coverage of most species, including mammals, in just a few days. The sequence data generated by one of these projects consists of millions or billions of short DNA sequences (reads) that range from 50-150 nucleotides in length. These sequences must then be assembled de novo before most genome analyses can begin. Unfortunately, genome assembly remains a very difficult problem, made more difficult by shorter reads and unreliable long-range linking information. In this study, we evaluated several of the leading de novo assembly algorithms on four different short-read data sets, all generated by Illumina sequencers. Our results describe the relative performance of the different assemblers as well as other significant differences in assembly difficulty that appear to be inherent in the genomes themselves. Three overarching conclusions are apparent: first, that data quality, rather than the assembler itself, has a dramatic affect on the quality of an assembled genome; second, that the degree of contiguity of an assembly varies enormously among different assemblers and different genomes; and third, that the correctness of an assembly also varies widely, and is not well correlated with statistics on contiguity. In order to enable others to replicate our results, all of our data and methods are freely available, as are all assemblers used in this study.}, author = {Salzberg, S. L. and Phillippy, A. M. and Zimin, A. V. and Puiu, D. and Magoc, T. and Koren, S. and Treangen, T. and Schatz, M. C. and Delcher, A. L. and Roberts, M. and Marcais, G. and Pop, M. and Yorke, J. A.}, doi = {10.1101/gr.131383.111}, file = {:home/gus/Documents/Mendeley Desktop/Salzberg et al.\_2011\_GAGE A critical evaluation of genome assemblies and assembly algorithms(2).pdf:pdf}, issn = {1088-9051}, journal = {Genome Research}, month = dec, pages = {gr.131383.111--}, title = {{GAGE: A critical evaluation of genome assemblies and assembly algorithms}}, url = {http://genome.cshlp.org/cgi/content/abstract/gr.131383.111v1}, year = {2011} } @inproceedings{Kanevsky, abstract = {Given a graph G with n vertices and m edges, a k-connectivity query for vertices v' and v" of G asks whether there exist k disjoint paths between v' and v". The authors consider the problem of performing k-connectivity queries for k\⩽4. First, they present a static data structure that answers such queries in O(1) time. Next, they consider the problem of performing queries intermixed with online updates that insert vertices and edges. For triconnected graphs they give a dynamic data structure that supports queries and updates in time O($\alpha$( l,n)) amortized, where n is the current number of vertices of the graph and l is the total number of operations performed ($\alpha$(l, n) denotes the slowly growing Ackermann function inverse). For general graphs, a sequence of l operations takes total time O(n log n +l). All of the above data structures use space O(n), proportional to the number of vertices of the graph. The results also yield an efficient algorithm for testing whether graph G is four-connected that runs in O(n$\alpha$(n, n)+m) time using O(n+m) space}, author = {Kanevsky, A. and Tamassia, R. and {Di Battista}, G. and Chen, J.}, booktitle = {[1991] Proceedings 32nd Annual Symposium of Foundations of Computer Science}, doi = {10.1109/SFCS.1991.185451}, isbn = {0-8186-2445-0}, pages = {793--801}, publisher = {IEEE Comput. Soc. Press}, title = {{On-line maintenance of the four-connected components of a graph}}, url = {http://ieeexplore.ieee.org/xpl/freeabs\_all.jsp?arnumber=185451} } @article{Jin, abstract = {Phylogenies-the evolutionary histories of groups of organisms-play a major role in representing the interrelationships among biological entities. Many methods for reconstructing and studying such phylogenies have been proposed, almost all of which assume that the underlying history of a given set of species can be represented by a binary tree. Although many biological processes can be effectively modeled and summarized in this fashion, others cannot: recombination, hybrid speciation, and horizontal gene transfer result in networks of relationships rather than trees of relationships. In previous works, we formulated a maximum parsimony (MP) criterion for reconstructing and evaluating phylogenetic networks, and demonstrated its quality on biological as well as synthetic data sets. In this paper, we provide further theoretical results as well as a very fast heuristic algorithm for the MP criterion of phylogenetic networks. In particular, we provide a novel combinatorial definition of phylogenetic networks in terms of "forbidden cycles," and provide detailed hardness and hardness of approximation proofs for the "small" MP problem. We demonstrate the performance of our heuristic in terms of time and accuracy on both biological and synthetic data sets. Finally, we explain the difference between our model and a similar one formulated by Nguyen et al., and describe the implications of this difference on the hardness and approximation results.}, author = {Jin, Guohua and Nakhleh, Luay and Snir, Sagi and Tuller, Tamir}, doi = {10.1109/TCBB.2008.119}, file = {:home/gus/Documents/Mendeley Desktop/Jin et al.\_Unknown\_Parsimony score of phylogenetic networks hardness results and a linear-time heuristic.pdf:pdf}, issn = {1557-9964}, journal = {IEEE/ACM transactions on computational biology and bioinformatics / IEEE, ACM}, keywords = {Algorithms,Archaea,Archaea: genetics,Cyclooxygenase 2,Cyclooxygenase 2: genetics,Genetic,Models,Phylogeny,Plant Proteins,Plant Proteins: genetics,Plants,Plants: genetics,Ribosomal Proteins,Ribosomal Proteins: genetics,blocking loop}, mendeley-tags = {blocking loop}, number = {3}, pages = {495--505}, pmid = {19644176}, title = {{Parsimony score of phylogenetic networks: hardness results and a linear-time heuristic.}}, url = {http://ieeexplore.ieee.org/xpl/freeabs\_all.jsp?arnumber=4668337}, volume = {6} } @article{Schatz2010, abstract = {Second-generation sequencing technology can now be used to sequence an entire human genome in a matter of days and at low cost. Sequence read lengths, initially very short, have rapidly increased since the technology first appeared, and we now are seeing a growing number of efforts to sequence large genomes de novo from these short reads. In this Perspective, we describe the issues associated with short-read assembly, the different types of data produced by second-gen sequencers, and the latest assembly algorithms designed for these data. We also review the genomes that have been assembled recently from short reads and make recommendations for sequencing strategies that will yield a high-quality assembly.}, author = {Schatz, Michael C and Delcher, Arthur L and Salzberg, Steven L}, doi = {10.1101/gr.101360.109}, file = {:home/gus/Documents/Mendeley Desktop/Schatz, Delcher, Salzberg\_2010\_Assembly of large genomes using second-generation sequencing.pdf:pdf}, issn = {1549-5469}, journal = {Genome research}, keywords = {Algorithms,Base Sequence,Genome, Human,Genomics,Genomics: methods,Humans,Sequence Analysis, DNA,Sequence Analysis, DNA: methods}, month = sep, number = {9}, pages = {1165--73}, pmid = {20508146}, title = {{Assembly of large genomes using second-generation sequencing.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2928494\&tool=pmcentrez\&rendertype=abstract}, volume = {20}, year = {2010} } @article{Zerbino2009a, abstract = {Despite the short length of their reads, micro-read sequencing technologies have shown their usefulness for de novo sequencing. However, especially in eukaryotic genomes, complex repeat patterns are an obstacle to large assemblies.}, author = {Zerbino, Daniel R and McEwen, Gayle K and Margulies, Elliott H and Birney, Ewan}, doi = {10.1371/journal.pone.0008407}, file = {:home/gus/Documents/Mendeley Desktop/Zerbino, McEwen\_2009\_Pebble and rock band heuristic resolution of repeats and scaffolding in the velvet short-read de novo assembler.pdf:pdf}, issn = {1932-6203}, journal = {PloS one}, keywords = {Algorithms,Animals,Chromosomes, Artificial, Bacterial,Chromosomes, Artificial, Bacterial: genetics,Computer Simulation,Ferrets,Ferrets: genetics,Pseudomonas syringae,Pseudomonas syringae: genetics,Repetitive Sequences, Nucleic Acid,Repetitive Sequences, Nucleic Acid: genetics,Sequence Analysis, DNA,Sequence Analysis, DNA: instrumentation,Sequence Analysis, DNA: methods}, month = jan, number = {12}, pages = {e8407}, pmid = {20027311}, title = {{Pebble and rock band: heuristic resolution of repeats and scaffolding in the velvet short-read de novo assembler.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2793427\&tool=pmcentrez\&rendertype=abstract}, volume = {4}, year = {2009} } @article{Lander1988, abstract = {Results from physical mapping projects have recently been reported for the genomes of Escherichia coli, Saccharomyces cerevisiae, and Caenorhabditis elegans, and similar projects are currently being planned for other organisms. In such projects, the physical map is assembled by first "fingerprinting" a large number of clones chosen at random from a recombinant library and then inferring overlaps between clones with sufficiently similar fingerprints. Although the basic approach is the same, there are many possible choices for the fingerprint used to characterize the clones and the rules for declaring overlap. In this paper, we derive simple formulas showing how the progress of a physical mapping project is affected by the nature of the fingerprinting scheme. Using these formulas, we discuss the analytic considerations involved in selecting an appropriate fingerprinting scheme for a particular project.}, author = {Lander, E S and Waterman, M S}, file = {:home/gus/Documents/Mendeley Desktop/Lander, Waterman\_1988\_Genomic mapping by fingerprinting random clones a mathematical analysis.pdf:pdf}, issn = {0888-7543}, journal = {Genomics}, keywords = {Animals,Caenorhabditis,Caenorhabditis: genetics,Chromosome Mapping,Cloning,Escherichia coli,Escherichia coli: genetics,Mathematics,Molecular,Nucleotide Mapping,Saccharomyces cerevisiae,Saccharomyces cerevisiae: genetics}, month = apr, number = {3}, pages = {231--9}, pmid = {3294162}, title = {{Genomic mapping by fingerprinting random clones: a mathematical analysis.}}, url = {http://www.ncbi.nlm.nih.gov/pubmed/3294162}, volume = {2}, year = {1988} } @article{Miller1998, author = {Miller, Peter}, file = {:home/gus/Documents/Mendeley Desktop/Miller\_1998\_Recursive make considered harmful.pdf:pdf}, journal = {AUUGN Journal of AUUG Inc}, number = {1}, pages = {14--25}, title = {{Recursive make considered harmful}}, url = {http://www.unix-ag.uni-kl.de/svn/kbibtex/kbibtex/tags/release-0.1/admin/unsermake/doc/auug97.pdf}, volume = {19}, year = {1998} } @article{Manber1990, annote = { From Duplicate 1 ( Suffix arrays: a new method for on-line string searches - Manber, Udi; Myers, Gene ) }, author = {Manber, Udi and Myers, Gene}, file = {:home/gus/Documents/Mendeley Desktop/Manber, Myers\_1990\_Suffix arrays a new method for on-line string searches(2).pdf:pdf;:home/gus/Documents/Mendeley Desktop/Manber, Myers\_1990\_Suffix arrays a new method for on-line string searches.pdf:pdf}, isbn = {0-89871-251-3}, journal = {Proceedings of the first annual ACM-SIAM \ldots}, month = jan, pages = {319--327}, title = {{Suffix arrays: a new method for on-line string searches}}, url = {http://portal.acm.org/citation.cfm?id=320218 http://dl.acm.org/citation.cfm?id=320176.320218}, year = {1990} } @article{Rhrissorrakrai2011, abstract = {ABSTRACT: BACKGROUND: Graphical models of network associations are useful for both visualizing and integrating multiple types of association data. Identifying modules, or groups of functionally related gene products, is an important challenge in analyzing biological networks. However, existing tools to identify modules are insufficient when applied to dense networks of experimentally derived interaction data. To address this problem, we have developed an agglomerative clustering method that is able to identify highly modular sets of gene products within highly interconnected molecular interaction networks. RESULTS: MINE outperforms MCODE, CFinder, NEMO, SPICi, and MCL in identifying non-exclusive, high modularity clusters when applied to the C. elegans protein-protein interaction network. The algorithm generally achieves superior geometric accuracy and modularity for annotated functional categories. In comparison with the most closely related algorithm, MCODE, the top clusters identified by MINE are consistently of higher density and MINE is less likely to designate overlapping modules as a single unit. MINE offers a high level of granularity with a small number of adjustable parameters, enabling users to fine-tune cluster results for input networks with differing topological properties. CONCLUSIONS: MINE was created in response to the challenge of discovering high quality modules of gene products within highly interconnected biological networks. The algorithm allows a high degree of flexibility and user-customisation of results with few adjustable parameters. MINE outperforms several popular clustering algorithms in identifying modules with high modularity and obtains good overall recall and precision of functional annotations in protein-protein interaction networks from both S. cerevisiae and C. elegans.}, author = {Rhrissorrakrai, Kahn and Gunsalus, Kristin C}, doi = {10.1186/1471-2105-12-192}, issn = {1471-2105}, journal = {BMC bioinformatics}, month = may, number = {1}, pages = {192}, pmid = {21605434}, title = {{MINE: Module Identification in NEtworks.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3123237\&tool=pmcentrez\&rendertype=abstract}, volume = {12}, year = {2011} } @article{Yang2011, abstract = {High-throughput short read sequencing is revolutionizing genomics and systems biology research by enabling cost-effective deep coverage sequencing of genomes and transcriptomes. Error detection and correction are crucial to many short read sequencing applications including de novo genome sequencing, genome resequencing, and digital gene expression analysis. Short read error detection is typically carried out by counting the observed frequencies of kmers in reads and validating those with frequencies exceeding a threshold. In case of genomes with high repeat content, an erroneous kmer may be frequently observed if it has few nucleotide differences with valid kmers with multiple occurrences in the genome. Error detection and correction were mostly applied to genomes with low repeat content and this remains a challenging problem for genomes with high repeat content.}, author = {Yang, Xiao and Aluru, Srinivas and Dorman, Karin S}, doi = {10.1186/1471-2105-12-S1-S52}, file = {:home/gus/Documents/Mendeley Desktop//Yang, Aluru, Dorman\_2011\_Repeat-aware modeling and correction of short read errors.pdf:pdf}, issn = {1471-2105}, journal = {BMC bioinformatics}, keywords = {Algorithms,Computational Biology,Computational Biology: methods,Genomics,Genomics: methods,High-Throughput Nucleotide Sequencing,High-Throughput Nucleotide Sequencing: methods,Likelihood Functions,Models,Software,Statistical}, month = jan, number = {Suppl 1}, pages = {S52}, pmid = {21342585}, title = {{Repeat-aware modeling and correction of short read errors.}}, url = {http://www.biomedcentral.com/1471-2105/12/S1/S52}, volume = {12 Suppl 1}, year = {2011} } @inproceedings{Ortiz2010, abstract = {Popular sorting algorithms do not translate well into hardware implementations. Instead, hardware-based solutions like sorting networks and linear sorters exploit parallelism to increase sorting efficiency. Linear sorters, built from identical nodes with simple control, have less area and latency than sorting networks, but they are limited in their throughput. We present a system composed of multiple linear sorters acting in parallel in order to increase throughput. Interleaving is used to increase bandwidth and allow sorting of multiple values per clock cycle, and the amount of interleaving and depth of the linear sorters can be adapted to suit specific applications. Implementation of this system into a Field Programmable Gate Array (FPGA) results in a speedup of 68 compared to quicksort running in a MicroBlaze processor.}, author = {Ortiz, Jorge and Andrews, David}, booktitle = {2010 IEEE International Symposium on Parallel \& Distributed Processing, Workshops and Phd Forum (IPDPSW)}, doi = {10.1109/IPDPSW.2010.5470730}, file = {:home/gus/Documents/Mendeley Desktop/Ortiz, Andrews\_2010\_A configurable high-throughput linear sorter system.pdf:pdf}, isbn = {978-1-4244-6533-0}, month = apr, pages = {1--8}, publisher = {IEEE}, title = {{A configurable high-throughput linear sorter system}}, url = {http://ieeexplore.ieee.org/lpdocs/epic03/wrapper.htm?arnumber=5470730}, year = {2010} } @article{dohm2008substantial, author = {Dohm, J.C. and Lottaz, C. and Borodina, T. and Himmelbauer, H.}, file = {:home/gus/Documents/Mendeley Desktop/Dohm et al.\_2008\_Substantial biases in ultra-short read data sets from high-throughput DNA sequencing.pdf:pdf}, journal = {Nucleic acids research}, number = {16}, pages = {e105}, publisher = {Oxford Univ Press}, title = {{Substantial biases in ultra-short read data sets from high-throughput DNA sequencing}}, url = {http://nar.oxfordjournals.org/content/36/16/e105.short}, volume = {36}, year = {2008} } @article{Zerbino2008, abstract = {We have developed a new set of algorithms, collectively called "Velvet," to manipulate de Bruijn graphs for genomic sequence assembly. A de Bruijn graph is a compact representation based on short words (k-mers) that is ideal for high coverage, very short read (25-50 bp) data sets. Applying Velvet to very short reads and paired-ends information only, one can produce contigs of significant length, up to 50-kb N50 length in simulations of prokaryotic data and 3-kb N50 on simulated mammalian BACs. When applied to real Solexa data sets without read pairs, Velvet generated contigs of approximately 8 kb in a prokaryote and 2 kb in a mammalian BAC, in close agreement with our simulated results without read-pair information. Velvet represents a new approach to assembly that can leverage very short reads in combination with read pairs to produce useful assemblies.}, author = {Zerbino, Daniel R and Birney, Ewan}, doi = {10.1101/gr.074492.107}, file = {:home/gus/Documents/Mendeley Desktop/Zerbino, Birney\_2008\_Velvet algorithms for de novo short read assembly using de Bruijn graphs.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Animals,Chromosomes, Artificial, Bacterial,Computational Biology,Computational Biology: methods,Computer Simulation,Genome, Bacterial,Genome, Human,Genomics,Humans,Mammals,Mammals: genetics,Sequence Analysis, DNA,Sequence Analysis, DNA: methods,Sequence Analysis, DNA: standards,Streptococcus,Streptococcus: genetics}, month = may, number = {5}, pages = {821--9}, pmid = {18349386}, title = {{Velvet: algorithms for de novo short read assembly using de Bruijn graphs.}}, url = {http://genome.cshlp.org/cgi/content/abstract/18/5/821}, volume = {18}, year = {2008} } @article{Butler:2008kx, abstract = {New DNA sequencing technologies deliver data at dramatically lower costs but demand new analytical methods to take full advantage of the very short reads that they produce. We provide an initial, theoretical solution to the challenge of de novo assembly from whole-genome shotgun "microreads." For 11 genomes of sizes up to 39 Mb, we generated high-quality assemblies from 80x coverage by paired 30-base simulated reads modeled after real Illumina-Solexa reads. The bacterial genomes of Campylobacter jejuni and Escherichia coli assemble optimally, yielding single perfect contigs, and larger genomes yield assemblies that are highly connected and accurate. Assemblies are presented in a graph form that retains intrinsic ambiguities such as those arising from polymorphism, thereby providing information that has been absent from previous genome assemblies. For both C. jejuni and E. coli, this assembly graph is a single edge encompassing the entire genome. Larger genomes produce more complicated graphs, but the vast majority of the bases in their assemblies are present in long edges that are nearly always perfect. We describe a general method for genome assembly that can be applied to all types of DNA sequence data, not only short read data, but also conventional sequence reads.}, author = {Butler, Jonathan and MacCallum, Iain and Kleber, Michael and Shlyakhter, Ilya a and Belmonte, Matthew K and Lander, Eric S and Nusbaum, Chad and Jaffe, David B}, doi = {10.1101/gr.7337908}, file = {:home/gus/Documents/Mendeley Desktop/Butler et al.\_2008\_ALLPATHS de novo assembly of whole-genome shotgun microreads.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Bacterial,Bacterial: genetics,Campylobacter jejuni,Campylobacter jejuni: genetics,Computational Biology,Computational Biology: methods,Computer Simulation,DNA,DNA: methods,DNA: standards,Escherichia coli,Escherichia coli: genetics,Genome,Reproducibility of Results,Sequence Analysis}, month = may, number = {5}, pages = {810--20}, pmid = {18340039}, title = {{ALLPATHS: de novo assembly of whole-genome shotgun microreads.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2336810\&tool=pmcentrez\&rendertype=abstract}, volume = {18}, year = {2008} } @article{Ilie2011a, author = {Ilie, L}, file = {:home/gus/Documents/Mendeley Desktop/Ilie, Fazayeli, Ilie\_2011\_HiTEC accurate error correction in high-throughput sequencing data.pdf:pdf}, journal = {Bioinformatics}, title = {{HiTEC: accurate error correction in high-throughput sequencing data}}, url = {http://bioinformatics.oxfordjournals.org/content/27/3/295.short}, year = {2011} } @article{Drmanac2010, abstract = {Genome sequencing of large numbers of individuals promises to advance the understanding, treatment, and prevention of human diseases, among other applications. We describe a genome sequencing platform that achieves efficient imaging and low reagent consumption with combinatorial probe anchor ligation chemistry to independently assay each base from patterned nanoarrays of self-assembling DNA nanoballs. We sequenced three human genomes with this platform, generating an average of 45- to 87-fold coverage per genome and identifying 3.2 to 4.5 million sequence variants per genome. Validation of one genome data set demonstrates a sequence accuracy of about 1 false variant per 100 kilobases. The high accuracy, affordable cost of \$4400 for sequencing consumables, and scalability of this platform enable complete human genome sequencing for the detection of rare variants in large-scale genetic studies.}, author = {Drmanac, Radoje and Sparks, Andrew B and Callow, Matthew J and Halpern, Aaron L and Burns, Norman L and Kermani, Bahram G and Carnevali, Paolo and Nazarenko, Igor and Nilsen, Geoffrey B and Yeung, George and Dahl, Fredrik and Fernandez, Andres and Staker, Bryan and Pant, Krishna P and Baccash, Jonathan and Borcherding, Adam P and Brownley, Anushka and Cedeno, Ryan and Chen, Linsu and Chernikoff, Dan and Cheung, Alex and Chirita, Razvan and Curson, Benjamin and Ebert, Jessica C and Hacker, Coleen R and Hartlage, Robert and Hauser, Brian and Huang, Steve and Jiang, Yuan and Karpinchyk, Vitali and Koenig, Mark and Kong, Calvin and Landers, Tom and Le, Catherine and Liu, Jia and McBride, Celeste E and Morenzoni, Matt and Morey, Robert E and Mutch, Karl and Perazich, Helena and Perry, Kimberly and Peters, Brock A and Peterson, Joe and Pethiyagoda, Charit L and Pothuraju, Kaliprasad and Richter, Claudia and Rosenbaum, Abraham M and Roy, Shaunak and Shafto, Jay and Sharanhovich, Uladzislau and Shannon, Karen W and Sheppy, Conrad G and Sun, Michel and Thakuria, Joseph V and Tran, Anne and Vu, Dylan and Zaranek, Alexander Wait and Wu, Xiaodi and Drmanac, Snezana and Oliphant, Arnold R and Banyai, William C and Martin, Bruce and Ballinger, Dennis G and Church, George M and Reid, Clifford A}, doi = {10.1126/science.1181498}, file = {:home/gus/Documents/Mendeley Desktop/Drmanac et al.\_2010\_Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays.pdf:pdf}, issn = {1095-9203}, journal = {Science (New York, N.Y.)}, keywords = {Base Sequence,Computational Biology,Costs and Cost Analysis,DNA,DNA: chemistry,DNA: economics,DNA: genetics,DNA: instrumentation,DNA: methods,DNA: standards,Databases,Genome,Genomic Library,Genotype,Haplotypes,Human,Human Genome Project,Humans,Male,Microarray Analysis,Nanostructures,Nanotechnology,Nucleic Acid,Nucleic Acid Amplification Techniques,Polymorphism,Sequence Analysis,Single Nucleotide,Software}, month = jan, number = {5961}, pages = {78--81}, pmid = {19892942}, title = {{Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays.}}, url = {http://www.sciencemag.org/content/327/5961/78.abstract}, volume = {327}, year = {2010} } @article{yang2010reptile, author = {Yang, X. and Dorman, K.S. and Aluru, S.}, file = {:home/gus/Documents/Mendeley Desktop/Yang, Dorman, Aluru\_2010\_Reptile representative tiling for short read error correction.pdf:pdf}, journal = {Bioinformatics}, number = {20}, pages = {2526}, publisher = {Oxford Univ Press}, title = {{Reptile: representative tiling for short read error correction}}, url = {http://bioinformatics.oxfordjournals.org/content/26/20/2526.short}, volume = {26}, year = {2010} } @article{Li2003, abstract = {In shotgun sequencing projects, the genome or BAC length is not always known. We approach estimating genome length by first estimating the repeat structure of the genome or BAC, sometimes of interest in its own right, on the basis of a set of random reads from a genome project. Moreover, we can find the consensus for repeat families before assembly. Our methods are based on the l-tuple content of the reads.}, author = {Li, Xiaoman and Waterman, Michael S}, doi = {10.1101/gr.1251803}, file = {:home/gus/Documents/Mendeley Desktop/Li, Waterman\_2003\_Estimating the repeat structure and length of DNA sequences using L-tuples.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Artificial,Bacterial,Bacterial: genetics,Base Composition,Chromosome Mapping,Chromosome Mapping: statistics \& numerical data,Chromosomes,Computational Biology,Computational Biology: statistics \& numerical data,Computer Simulation,Computer Simulation: statistics \& numerical data,Consensus Sequence,DNA,Mathematical Computing,Nucleic Acid,Nucleic Acid: genetics,Poisson Distribution,Repetitive Sequences,Software}, month = aug, number = {8}, pages = {1916--22}, pmid = {12902383}, title = {{Estimating the repeat structure and length of DNA sequences using L-tuples.}}, url = {http://genome.cshlp.org/cgi/content/abstract/13/8/1916}, volume = {13}, year = {2003} } @inproceedings{Cheriyan1991, address = {New York, New York, USA}, author = {Cheriyan, Joseph and Thurimella, Ramakrishna}, booktitle = {Proceedings of the twenty-third annual ACM symposium on Theory of computing - STOC '91}, doi = {10.1145/103418.103460}, file = {:home/gus/Documents/Mendeley Desktop/Cheriyan, Thurimella\_1991\_Algorithms for parallel k -vertex connectivity and sparse certificates.pdf:pdf}, isbn = {0897913973}, month = jan, pages = {391--401}, publisher = {ACM Press}, title = {{Algorithms for parallel k -vertex connectivity and sparse certificates}}, url = {http://dl.acm.org/citation.cfm?id=103418.103460}, year = {1991} } @article{Michael1996, address = {New York, New York, USA}, author = {Michael, Maged M. and Scott, Michael L.}, doi = {10.1145/248052.248106}, file = {:home/gus/Documents/Mendeley Desktop/Michael, Scott\_1996\_Simple, fast, and practical non-blocking and blocking concurrent queue algorithms.pdf:pdf}, isbn = {0897918002}, journal = {Proceedings of the fifteenth annual ACM symposium on Principles of distributed computing - PODC '96}, keywords = {compare and swap,concurrent queue,lock-free,multiprogramming,non-blocking}, pages = {267--275}, publisher = {ACM Press}, title = {{Simple, fast, and practical non-blocking and blocking concurrent queue algorithms}}, url = {http://portal.acm.org/citation.cfm?doid=248052.248106}, year = {1996} } @article{Medvedev2011, abstract = {The continuing improvements to high-throughput sequencing (HTS) platforms have begun to unfold a myriad of new applications. As a result, error correction of sequencing reads remains an important problem. Though several tools do an excellent job of correcting datasets where the reads are sampled close to uniformly, the problem of correcting reads coming from drastically non-uniform datasets, such as those from single-cell sequencing, remains open.}, author = {Medvedev, Paul and Scott, Eric and Kakaradov, Boyko and Pevzner, Pavel}, doi = {10.1093/bioinformatics/btr208}, file = {:home/gus/Documents/Mendeley Desktop/Medvedev et al.\_2011\_Error correction of high-throughput sequencing datasets with non-uniform coverage.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, month = jul, number = {13}, pages = {i137--i141}, pmid = {21685062}, title = {{Error correction of high-throughput sequencing datasets with non-uniform coverage.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3117386\&tool=pmcentrez\&rendertype=abstract}, volume = {27}, year = {2011} } @article{Kim:2007uq, abstract = {One of the main goals in genome sequencing projects is to determine a haploid consensus sequence even when clone libraries are constructed from homologous chromosomes. However, it has been noticed that haplotypes can be inferred from genome assemblies by investigating phase conservation in sequenced reads. In this study, we seek to infer haplotypes, a diploid consensus sequence, from the genome assembly of an organism, Ciona intestinalis. The Ciona intestinalis genome is an ideal resource from which haplotypes can be inferred because of the high polymorphism rate (1.2\%). The haplotype estimation scheme consists of polymorphism detection and phase estimation. The core step of our method is a Gibbs sampling procedure. The mate-pair information from two-end sequenced clone inserts is exploited to provide long-range continuity. We estimate the polymorphism rate of Ciona intestinalis to be 1.2\% and 1.5\%, according to two different polymorphism counting schemes. The distribution of heterozygosity number is well fit by a compound Poisson distribution. The N50 length of haplotype segments is 37.9 kb in our assembly, while the N50 scaffold length of the Ciona intestinalis assembly is 190 kb. We also infer diploid gene sequences from haplotype segments. According to our reconstruction, 85.4\% of predicted gene sequences are continuously covered by single haplotype segments. Our results indicate 97\% accuracy in haplotype estimation, based on a simulated data set. We conduct a comparative analysis with Ciona savignyi, and discover interesting patterns of conserved DNA elements in chordates.}, author = {Kim, Jong Hyun and Waterman, Michael S and Li, Lei M}, doi = {10.1101/gr.5894107}, file = {:home/gus/Documents/Mendeley Desktop/Kim, Waterman, Li\_2007\_Diploid genome reconstruction of Ciona intestinalis and comparative analysis with Ciona savignyi.pdf:pdf}, journal = {Genome Res}, month = jul, number = {7}, pages = {1101--1110}, pmid = {17567986}, title = {{Diploid genome reconstruction of Ciona intestinalis and comparative analysis with Ciona savignyi}}, volume = {17}, year = {2007} } @article{Schroder2009, abstract = {MOTIVATION: Second-generation sequencing technologies produce a massive amount of short reads in a single experiment. However, sequencing errors can cause major problems when using this approach for de novo sequencing applications. Moreover, existing error correction methods have been designed and optimized for shotgun sequencing. Therefore, there is an urgent need for the design of fast and accurate computational methods and tools for error correction of large amounts of short read data. RESULTS: We present SHREC, a new algorithm for correcting errors in short-read data that uses a generalized suffix trie on the read data as the underlying data structure. Our results show that the method can identify erroneous reads with sensitivity and specificity of over 99\% and 96\% for simulated data with error rates of up to 3\% as well as for real data. Furthermore, it achieves an error correction accuracy of over 80\% for simulated data and over 88\% for real data. These results are clearly superior to previously published approaches. SHREC is available as an efficient open-source Java implementation that allows processing of 10 million of short reads on a standard workstation.}, author = {Schr\"{o}der, Jan and Schr\"{o}der, Heiko and Puglisi, Simon J and Sinha, Ranjan and Schmidt, Bertil}, doi = {10.1093/bioinformatics/btp379}, file = {:home/gus/Documents/Mendeley Desktop/Schr\"{o}der et al.\_2009\_SHREC a short-read error correction method.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Schr\"{o}der et al.\_2009\_SHREC a short-read error correction method(2).pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,Computational Biology,Computational Biology: methods,DNA,DNA: genetics,DNA: methods,Databases,Error correction,Genome,Genome: genetics,Nucleic Acid,Research Design,Sequence Analysis,Time Factors}, mendeley-tags = {Error correction}, month = sep, number = {17}, pages = {2157--63}, pmid = {19542152}, title = {{SHREC: a short-read error correction method.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/25/17/2157}, volume = {25}, year = {2009} } @inproceedings{sundell2003fast, author = {Sundell, H. and Tsigas, P.}, booktitle = {Parallel and Distributed Processing Symposium, 2003. Proceedings. International}, file = {:home/gus/Documents/Mendeley Desktop/Sundell, Tsigas\_2003\_Fast and lock-free concurrent priority queues for multi-thread systems.pdf:pdf}, pages = {11--pp}, publisher = {IEEE}, title = {{Fast and lock-free concurrent priority queues for multi-thread systems}}, url = {http://ieeexplore.ieee.org/xpls/abs\_all.jsp?arnumber=1213189}, year = {2003} } @article{Zerbino2009a, abstract = {Despite the short length of their reads, micro-read sequencing technologies have shown their usefulness for de novo sequencing. However, especially in eukaryotic genomes, complex repeat patterns are an obstacle to large assemblies.}, author = {Zerbino, Daniel R DR and McEwen, GK Gayle K and Margulies, Elliott H and Birney, Ewan}, doi = {10.1371/journal.pone.0008407}, file = {:home/gus/Documents/Mendeley Desktop/Zerbino, McEwen\_2009\_Pebble and rock band heuristic resolution of repeats and scaffolding in the velvet short-read de novo assembler.pdf:pdf}, issn = {1932-6203}, journal = {PloS one}, keywords = {Algorithms,Animals,Artificial,Bacterial,Bacterial: genetics,Chromosomes,Computer Simulation,DNA,DNA: instrumentation,DNA: methods,Ferrets,Ferrets: genetics,Nucleic Acid,Nucleic Acid: genetics,Pseudomonas syringae,Pseudomonas syringae: genetics,Repetitive Sequences,Sequence Analysis}, month = jan, number = {12}, pages = {e8407}, pmid = {20027311}, title = {{Pebble and rock band: heuristic resolution of repeats and scaffolding in the velvet short-read de novo assembler}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2793427\&tool=pmcentrez\&rendertype=abstract http://dx.plos.org/10.1371/journal.pone.0008407}, volume = {4}, year = {2009} } @misc{TheMendeleySupportTeam2011, abstract = {A quick introduction to Mendeley. Learn how Mendeley creates your personal digital library, how to organize and annotate documents, how to collaborate and share with colleagues, and how to generate citations and bibliographies.}, address = {London}, author = {{The Mendeley Support Team}}, booktitle = {Mendeley Desktop}, file = {:home/gus/Documents/Mendeley Desktop/The Mendeley Support Team\_2011\_Getting Started with Mendeley.pdf:pdf}, keywords = {Mendeley,how-to,user manual}, pages = {1--16}, publisher = {Mendeley Ltd.}, title = {{Getting Started with Mendeley}}, url = {http://www.mendeley.com}, year = {2011} } @article{Yang2011a, abstract = {High-throughput short read sequencing is revolutionizing genomics and systems biology research by enabling cost-effective deep coverage sequencing of genomes and transcriptomes. Error detection and correction are crucial to many short read sequencing applications including de novo genome sequencing, genome resequencing, and digital gene expression analysis. Short read error detection is typically carried out by counting the observed frequencies of kmers in reads and validating those with frequencies exceeding a threshold. In case of genomes with high repeat content, an erroneous kmer may be frequently observed if it has few nucleotide differences with valid kmers with multiple occurrences in the genome. Error detection and correction were mostly applied to genomes with low repeat content and this remains a challenging problem for genomes with high repeat content.}, author = {Yang, Xiao and Aluru, Srinivas and Dorman, Karin S}, doi = {10.1186/1471-2105-12-S1-S52}, file = {:home/gus/Documents/Mendeley Desktop//Yang, Aluru, Dorman\_2011\_Repeat-aware modeling and correction of short read errors.pdf:pdf}, issn = {1471-2105}, journal = {BMC bioinformatics}, keywords = {Algorithms,Computational Biology,Computational Biology: methods,Genomics,Genomics: methods,High-Throughput Nucleotide Sequencing,High-Throughput Nucleotide Sequencing: methods,Likelihood Functions,Models, Statistical,Software,Statistical}, month = jan, pages = {S52}, pmid = {21342585}, title = {{Repeat-aware modeling and correction of short read errors.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3044310\&tool=pmcentrez\&rendertype=abstract}, volume = {12 Suppl 1}, year = {2011} } @article{Kim:2007uq, abstract = {One of the main goals in genome sequencing projects is to determine a haploid consensus sequence even when clone libraries are constructed from homologous chromosomes. However, it has been noticed that haplotypes can be inferred from genome assemblies by investigating phase conservation in sequenced reads. In this study, we seek to infer haplotypes, a diploid consensus sequence, from the genome assembly of an organism, Ciona intestinalis. The Ciona intestinalis genome is an ideal resource from which haplotypes can be inferred because of the high polymorphism rate (1.2\%). The haplotype estimation scheme consists of polymorphism detection and phase estimation. The core step of our method is a Gibbs sampling procedure. The mate-pair information from two-end sequenced clone inserts is exploited to provide long-range continuity. We estimate the polymorphism rate of Ciona intestinalis to be 1.2\% and 1.5\%, according to two different polymorphism counting schemes. The distribution of heterozygosity number is well fit by a compound Poisson distribution. The N50 length of haplotype segments is 37.9 kb in our assembly, while the N50 scaffold length of the Ciona intestinalis assembly is 190 kb. We also infer diploid gene sequences from haplotype segments. According to our reconstruction, 85.4\% of predicted gene sequences are continuously covered by single haplotype segments. Our results indicate 97\% accuracy in haplotype estimation, based on a simulated data set. We conduct a comparative analysis with Ciona savignyi, and discover interesting patterns of conserved DNA elements in chordates.}, author = {Kim, Jong Hyun and Waterman, Michael S and Li, Lei M}, doi = {10.1101/gr.5894107}, journal = {Genome Res}, month = jul, number = {7}, pages = {1101--1110}, pmid = {17567986}, title = {{Diploid genome reconstruction of Ciona intestinalis and comparative analysis with Ciona savignyi}}, volume = {17}, year = {2007} } @inproceedings{michael2002safe, author = {Michael, M.M.}, booktitle = {Proceedings of the twenty-first annual symposium on Principles of distributed computing}, file = {:home/gus/Documents/Mendeley Desktop/Michael\_2002\_Safe memory reclamation for dynamic lock-free objects using atomic reads and writes.pdf:pdf}, pages = {21--30}, publisher = {ACM}, title = {{Safe memory reclamation for dynamic lock-free objects using atomic reads and writes}}, url = {http://portal.acm.org/citation.cfm?id=571829}, year = {2002} } @article{Langmead2009, abstract = {Bowtie is an ultrafast, memory-efficient alignment program for aligning short DNA sequence reads to large genomes. For the human genome, Burrows-Wheeler indexing allows Bowtie to align more than 25 million reads per CPU hour with a memory footprint of approximately 1.3 gigabytes. Bowtie extends previous Burrows-Wheeler techniques with a novel quality-aware backtracking algorithm that permits mismatches. Multiple processor cores can be used simultaneously to achieve even greater alignment speeds. Bowtie is open source (http://bowtie.cbcb.umd.edu).}, author = {Langmead, Ben and Trapnell, Cole and Pop, Mihai and Salzberg, Steven L}, doi = {10.1186/gb-2009-10-3-r25}, file = {:home/gus/Documents/Mendeley Desktop/Langmead et al.\_2009\_Ultrafast and memory-efficient alignment of short DNA sequences to the human genome.pdf:pdf}, issn = {1465-6914}, journal = {Genome biology}, keywords = {Algorithms,Base Sequence,Genome,Human,Human: genetics,Humans,Sequence Alignment,Sequence Alignment: methods}, month = jan, number = {3}, pages = {R25}, pmid = {19261174}, title = {{Ultrafast and memory-efficient alignment of short DNA sequences to the human genome.}}, url = {http://genomebiology.com/2009/10/3/R25}, volume = {10}, year = {2009} } @incollection{Hart2008, address = {New York}, author = {Hart, John P.}, booktitle = {Current Northeast Paleoethnobotany II}, chapter = {7}, editor = {Hart, John P.}, file = {:home/gus/Documents/Mendeley Desktop/Hart\_2008\_Evolving the three sisters the changing histories of maize, bean, and squash in new york and the greater northeast.pdf:pdf}, pages = {87--100}, publisher = {New York State Museum Bulletin 512}, title = {{Evolving the three sisters: the changing histories of maize, bean, and squash in new york and the greater northeast}}, year = {2008} } @article{Farach1997, author = {Farach, M.}, file = {:home/gus/Documents/Mendeley Desktop/Farach\_1997\_Optimal suffix tree construction with large alphabets.pdf:pdf}, isbn = {0-8186-8197-7}, keywords = {combinatorial pattern matching,data structure,integer alphabet,integer alphabets,large alphabets,pattern matching,sorting,suffix tree}, month = oct, pages = {137}, title = {{Optimal suffix tree construction with large alphabets}}, url = {http://dl.acm.org/citation.cfm?id=795663.796326}, year = {1997} } @article{Gonzalez-Porta2011, abstract = {DNA arrays have been widely used to perform transcriptome-wide analysis of gene expression, and many methods have been developed to measure gene expression variability and to compare gene expression between conditions. Because RNA-seq is also becoming increasingly popular for transcriptome characterization, the possibility exists for further quantification of individual alternative transcript isoforms, and therefore for estimating the relative ratios of alternative splice forms within a given gene. Changes in splicing ratios, even without changes in overall gene expression, may have important phenotypic effects. Here we have developed statistical methodology to measure variability in splicing ratios within conditions, to compare it between conditions, and to identify genes with condition-specific splicing ratios. Furthermore, we have developed methodology to deconvolute the relative contribution of variability in gene expression versus variability in splicing ratios to the overall variability of transcript abundances. As a proof of concept, we have applied this methodology to estimates of transcript abundances obtained from RNA-seq experiments in lymphoblastoid cells from Caucasian and Yoruban individuals. We have found that protein-coding genes exhibit low splicing variability within populations, with many genes exhibiting constant ratios across individuals. When comparing these two populations, we have found that up to 10\% of the studied protein-coding genes exhibit population-specific splicing ratios. We estimate that ∼60\% of the total variability observed in the abundance of transcript isoforms can be explained by variability in transcription. A large fraction of the remaining variability can likely result from variability in splicing. Finally, we also detected that variability in splicing is uncommon without variability in transcription.}, author = {Gonz\`{a}lez-Porta, Mar and Calvo, Miquel and Sammeth, Michael and Guig\'{o}, Roderic}, doi = {10.1101/gr.121947.111}, file = {:home/gus/Documents/Mendeley Desktop/Gonz\`{a}lez-Porta et al.\_2011\_Estimation of alternative splicing variability in human populations.pdf:pdf}, issn = {1549-5469}, journal = {Genome research}, month = dec, number = {3}, pages = {528--538}, pmid = {22113879}, title = {{Estimation of alternative splicing variability in human populations.}}, url = {http://genome.cshlp.org/cgi/content/abstract/22/3/528}, volume = {22}, year = {2011} } @article{Bloom1970, author = {Bloom, Burton H.}, doi = {10.1145/362686.362692}, file = {:home/gus/Documents/Mendeley Desktop/Bloom\_1970\_Spacetime trade-offs in hash coding with allowable errors.pdf:pdf}, issn = {00010782}, journal = {Communications of the ACM}, keywords = {Bloom filter,hash addressing,hash coding,retrieval efficiency,retrieval trade-offs,scatter storage,searching,storage efficiency,storage layout}, mendeley-tags = {Bloom filter}, month = jul, number = {7}, pages = {422--426}, title = {{Space/time trade-offs in hash coding with allowable errors}}, url = {http://dl.acm.org/citation.cfm?id=362686.362692}, volume = {13}, year = {1970} } @inproceedings{Gao2004, author = {Gao, H. and Groote, J.F. F and Hesselink, W.H. H}, booktitle = {18th International Parallel and Distributed Processing Symposium}, doi = {10.1109/IPDPS.2004.1302969}, file = {:home/gus/Documents/Mendeley Desktop/Gao, Groote, Hesselink\_Unknown\_Almost wait-free resizable hashtables.pdf:pdf}, isbn = {0769521320}, number = {C}, pages = {50--58}, publisher = {Ieee}, title = {{Almost wait-free resizable hashtables}}, url = {http://ieeexplore.ieee.org/lpdocs/epic03/wrapper.htm?arnumber=1302969}, volume = {00}, year = {2004} } @article{nagarajan2009parametric, author = {Nagarajan, N. and Pop, M.}, file = {:home/gus/Documents/Mendeley Desktop/Nagarajan, Pop\_2009\_Parametric complexity of sequence assembly theory and applications to next generation sequencing.pdf:pdf}, journal = {Journal of computational biology}, number = {7}, pages = {897--908}, publisher = {Mary Ann Liebert, Inc. 140 Huguenot Street, 3rd Floor New Rochelle, NY 10801 USA}, title = {{Parametric complexity of sequence assembly: theory and applications to next generation sequencing}}, url = {http://www.liebertonline.com/doi/abs/10.1089/cmb.2009.0005}, volume = {16}, year = {2009} } @article{Kawrykow2012, abstract = {Background Comparative genomics, or the study of the relationships of genome structure and function across different species, offers a powerful tool for studying evolution, annotating genomes, and understanding the causes of various genetic disorders. However, aligning multiple sequences of DNA, an essential intermediate step for most types of analyses, is a difficult computational task. In parallel, citizen science, an approach that takes advantage of the fact that the human brain is exquisitely tuned to solving specific types of problems, is becoming increasingly popular. There, instances of hard computational problems are dispatched to a crowd of non-expert human game players and solutions are sent back to a central server. Methodology/Principal Findings We introduce Phylo, a human-based computing framework applying “crowd sourcing†techniques to solve the Multiple Sequence Alignment (MSA) problem. The key idea of Phylo is to convert the MSA problem into a casual game that can be played by ordinary web users with a minimal prior knowledge of the biological context. We applied this strategy to improve the alignment of the promoters of disease-related genes from up to 44 vertebrate species. Since the launch in November 2010, we received more than 350,000 solutions submitted from more than 12,000 registered users. Our results show that solutions submitted contributed to improving the accuracy of up to 70\% of the alignment blocks considered. Conclusions/Significance We demonstrate that, combined with classical algorithms, crowd computing techniques can be successfully used to help improving the accuracy of MSA. More importantly, we show that an NP-hard computational problem can be embedded in casual game that can be easily played by people without significant scientific training. This suggests that citizen science approaches can be used to exploit the billions of “human-brain peta-flops†of computation that are spent every day playing games. Phylo is available at: http://phylo.cs.mcgill.ca.}, author = {Kawrykow, Alexander and Roumanis, Gary and Kam, Alfred and Kwak, Daniel and Leung, Clarence and Wu, Chu and Zarour, Eleyine and Sarmenta, Luis and Blanchette, Mathieu and Waldisp\"{u}hl, J\'{e}r\^{o}me}, doi = {10.1371/journal.pone.0031362}, editor = {Michalak, Pawel}, file = {:home/gus/Documents/Mendeley Desktop/Kawrykow et al.\_2012\_Phylo A Citizen Science Approach for Improving Multiple Sequence Alignment.pdf:pdf}, issn = {1932-6203}, journal = {PLoS ONE}, keywords = {Biology,Computational Biology,Computer Science,Computer applications,Computing methods,Evolutionary Biology,Genetics,Genetics and Genomics,Genomics,Organismal evolution,Research Article}, month = mar, number = {3}, pages = {e31362}, publisher = {Public Library of Science}, title = {{Phylo: A Citizen Science Approach for Improving Multiple Sequence Alignment}}, url = {http://dx.plos.org/10.1371/journal.pone.0031362}, volume = {7}, year = {2012} } @article{shi2010parallel, author = {Shi, H. and Schmidt, B. and Liu, W. and M\"{u}ller-Wittig, W.}, file = {:home/gus/Documents/Mendeley Desktop/Shi et al.\_2010\_A parallel algorithm for error correction in high-throughput short-read data on CUDA-enabled graphics hardware.pdf:pdf}, journal = {Journal of Computational Biology}, number = {4}, pages = {603--615}, publisher = {Mary Ann Liebert, Inc. 140 Huguenot Street, 3rd Floor New Rochelle, NY 10801 USA}, title = {{A parallel algorithm for error correction in high-throughput short-read data on CUDA-enabled graphics hardware}}, url = {http://www.liebertonline.com/doi/abs/10.1089/cmb.2009.0062}, volume = {17}, year = {2010} } @article{Marcais2011, abstract = {Counting the number of occurrences of every k-mer (substring of length k) in a long string is a central subproblem in many applications, including genome assembly, error correction of sequencing reads, fast multiple sequence alignment and repeat detection. Recently, the deep sequence coverage generated by next-generation sequencing technologies has caused the amount of sequence to be processed during a genome project to grow rapidly, and has rendered current k-mer counting tools too slow and memory intensive. At the same time, large multicore computers have become commonplace in research facilities allowing for a new parallel computational paradigm.}, author = {Mar\c{c}ais, Guillaume and Kingsford, Carl}, doi = {10.1093/bioinformatics/btr011}, file = {:home/gus/Documents/Mendeley Desktop/Mar\c{c}ais, Kingsford\_2011\_A fast, lock-free approach for efficient parallel counting of occurrences of k-mers.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Mar\c{c}ais, Kingsford\_2011\_A fast, lock-free approach for efficient parallel counting of occurrences of k-mers(2).pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,Animals,Base Sequence,Computational Biology,Computational Biology: methods,DNA,DNA: methods,Genome,Humans,Sequence Alignment,Sequence Analysis,Software}, month = mar, number = {6}, pages = {764--70}, pmid = {21217122}, title = {{A fast, lock-free approach for efficient parallel counting of occurrences of k-mers.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/27/6/764}, volume = {27}, year = {2011} } @article{Maccallum:2009vn, abstract = {We demonstrate that genome sequences approaching finished quality can be generated from short paired reads. Using 36 base (fragment) and 26 base (jumping) reads from five microbial genomes of varied GC composition and sizes up to 40 Mb, ALLPATHS2 generated assemblies with long, accurate contigs and scaffolds. Velvet and EULER-SR were less accurate. For example, for Escherichia coli, the fraction of 10-kb stretches that were perfect was 99.8\% (ALLPATHS2), 68.7\% (Velvet), and 42.1\% (EULER-SR).}, author = {Maccallum, Iain and Przybylski, Dariusz and Gnerre, Sante and Burton, Joshua and Shlyakhter, Ilya and Gnirke, Andreas and Malek, Joel and McKernan, Kevin and Ranade, Swati and Shea, Terrance P and Williams, Louise and Young, Sarah and Nusbaum, Chad and Jaffe, David B}, doi = {10.1186/gb-2009-10-10-r103}, file = {:home/gus/Documents/Mendeley Desktop//Maccallum et al.\_2009\_ALLPATHS 2 small genomes assembled accurately and with high continuity from short paired reads.pdf:pdf}, issn = {1465-6914}, journal = {Genome biology}, keywords = {Bacteria,Bacteria: genetics,Base Pairing,Base Pairing: genetics,Fungi,Fungi: genetics,Genome,Genome: genetics,Genomics,Genomics: methods,Reproducibility of Results,Software}, month = jan, number = {10}, pages = {R103}, pmid = {19796385}, title = {{ALLPATHS 2: small genomes assembled accurately and with high continuity from short paired reads.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2784318\&tool=pmcentrez\&rendertype=abstract}, volume = {10}, year = {2009} } @article{Roberts2004, abstract = {MOTIVATION: Comparison of nucleic acid and protein sequences is a fundamental tool of modern bioinformatics. A dominant method of such string matching is the 'seed-and-extend' approach, in which occurrences of short subsequences called 'seeds' are used to search for potentially longer matches in a large database of sequences. Each such potential match is then checked to see if it extends beyond the seed. To be effective, the seed-and-extend approach needs to catalogue seeds from virtually every substring in the database of search strings. Projects such as mammalian genome assemblies and large-scale protein matching, however, have such large sequence databases that the resulting list of seeds cannot be stored in RAM on a single computer. This significantly slows the matching process. RESULTS: We present a simple and elegant method in which only a small fraction of seeds, called 'minimizers', needs to be stored. Using minimizers can speed up string-matching computations by a large factor while missing only a small fraction of the matches found using all seeds.}, author = {Roberts, Michael and Hayes, Wayne and Hunt, Brian R and Mount, Stephen M and Yorke, James A}, doi = {10.1093/bioinformatics/bth408}, file = {:home/gus/Documents/Mendeley Desktop/Roberts et al.\_2004\_Reducing storage requirements for biological sequence comparison.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Roberts et al.\_2004\_Reducing storage requirements for biological sequence comparison(3).pdf:pdf}, issn = {1367-4803}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,Computer-Assisted,Databases,Genetic,Information Storage and Retrieval,Information Storage and Retrieval: methods,Numerical Analysis,Sequence Alignment,Sequence Alignment: methods,Sequence Analysis,Sequence Analysis: methods}, month = dec, number = {18}, pages = {3363--9}, pmid = {15256412}, title = {{Reducing storage requirements for biological sequence comparison.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/20/18/3363}, volume = {20}, year = {2004} } @article{Ilie2011c, abstract = {Multiple spaced seeds represent the current state-of-the-art for similarity search in bioinformatics, with applications in various areas such as sequence alignment, read mapping, oligonucleotide design, etc. We present SpEED, a software program that computes highly sensitive multiple spaced seeds. SpEED can be several orders of magnitude faster and computes better seeds than the existing leading software programs.}, author = {Ilie, Lucian and Ilie, Silvana and {Mansouri Bigvand}, Anahita}, doi = {10.1093/bioinformatics/btr368}, file = {:home/gus/Documents/Mendeley Desktop/Ilie, Ilie, Mansouri Bigvand\_2011\_SpEED fast computation of sensitive spaced seeds.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, month = sep, number = {17}, pages = {2433--4}, pmid = {21690104}, title = {{SpEED: fast computation of sensitive spaced seeds.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/27/17/2433}, volume = {27}, year = {2011} } @misc{JeffGilchrist2008, abstract = {In this paper, we present parallel algorithms for lossless data compression based on the Burrows-Wheeler Transform (BWT) block-sorting technique. We investigate the performance of using data parallelism and task parallelism for both multi-threaded and message-passing programming. The output produced by the parallel algorithms is fully compatible with their sequential counterparts. To balance the workload among processors we develop a task scheduling strategy. An extensive set of experiments is performed with a shared memory NUMA system using up to 120 processors and on a distributed memory cluster using up to 100 processors. Our experimental results show that significant speedup can be achieved with both data parallel and task parallel methodologies. These algorithms will greatly reduce the amount of time it takes to compress large amounts of data while the compressed data remains in a form that users without access to multiple processor systems can still use.}, author = {{Jeff Gilchrist} and {Aysegul Cuhadar}}, booktitle = {International Journal of Web and Grid Services}, doi = {10.1504/IJWGS.2008.018498}, file = {:home/gus/Documents/Mendeley Desktop/Jeff Gilchrist, Aysegul Cuhadar\_2008\_Parallel lossless data compression using the Burrows-Wheeler Transform.html:html}, keywords = {BWT,Burrows-Wheeler Transform,MPI,bzip2,data parallelism,distributed computing,lossless data compression,message passing interface,multi-threading,parallel computing,task parallelism,task scheduling.,workload balance}, pages = {117--135}, title = {{Parallel lossless data compression using the Burrows-Wheeler Transform}}, url = {http://www.inderscience.com/search/index.php?action=record\&rec\_id=18498\&prevQuery=\&ps=10\&m=or}, urldate = {11/10/11}, volume = {4}, year = {2008} } @article{Anders2010, abstract = {High-throughput sequencing assays such as RNA-Seq, ChIP-Seq or barcode counting provide quantitative readouts in the form of count data. To infer differential signal in such data correctly and with good statistical power, estimation of data variability throughout the dynamic range and a suitable error model are required. We propose a method based on the negative binomial distribution, with variance and mean linked by local regression and present an implementation, DESeq, as an R/Bioconductor package.}, author = {Anders, Simon and Huber, Wolfgang}, doi = {10.1186/gb-2010-11-10-r106}, file = {:home/gus/Documents/Mendeley Desktop/Anders, Huber\_2010\_Differential expression analysis for sequence count data.pdf:pdf}, issn = {1465-6914}, journal = {Genome biology}, keywords = {Animals,Binomial Distribution,Chromatin Immunoprecipitation,Chromatin Immunoprecipitation: methods,Computational Biology,Computational Biology: methods,Drosophila,Drosophila: genetics,Gene Expression Profiling,Gene Expression Profiling: methods,High-Throughput Nucleotide Sequencing,High-Throughput Nucleotide Sequencing: methods,Linear Models,Models, Genetic,Saccharomyces cerevisiae,Saccharomyces cerevisiae: genetics,Sequence Analysis, RNA,Sequence Analysis, RNA: methods,Stem Cells,Tissue Culture Techniques}, month = jan, number = {10}, pages = {R106}, pmid = {20979621}, title = {{Differential expression analysis for sequence count data.}}, url = {http://genomebiology.com/2010/11/10/R106}, volume = {11}, year = {2010} } @article{10.1371/journal.pone.0005350, abstract = {

The success of genome-wide association (GWA) studies for the detection of sequence variation affecting complex traits in human has spurred interest in the use of large-scale high-density single nucleotide polymorphism (SNP) genotyping for the identification of quantitative trait loci (QTL) and for marker-assisted selection in model and agricultural species. A cost-effective and efficient approach for the development of a custom genotyping assay interrogating 54,001 SNP loci to support GWA applications in cattle is described. A novel algorithm for achieving a compressed inter-marker interval distribution proved remarkably successful, with median interval of 37 kb and maximum predicted gap of \<350 kb. The assay was tested on a panel of 576 animals from 21 cattle breeds and six outgroup species and revealed that from 39,765 to 46,492 SNP are polymorphic within individual breeds (average minor allele frequency (MAF) ranging from 0.24 to 0.27). The assay also identified 79 putative copy number variants in cattle. Utility for GWA was demonstrated by localizing known variation for coat color and the presence/absence of horns to their correct genomic locations. The combination of SNP selection and the novel spacing algorithm allows an efficient approach for the development of high-density genotyping platforms in species having full or even moderate quality draft sequence. Aspects of the approach can be exploited in species which lack an available genome sequence. The BovineSNP50 assay described here is commercially available from Illumina and provides a robust platform for mapping disease genes and QTL in cattle.

}, author = {K., Lakshmi and T., Lawley Cynthia and D., Schnabel Robert and F., Taylor Jeremy and F., Allan Mark and P., Heaton Michael and Jeff, O'Connell and S., Moore Stephen and L., Smith Timothy P and S., Sonstegard Tad and Matukumalli, Van Tassell Curtis P}, doi = {10.1371/journal.pone.0005350}, journal = {PLoS ONE}, number = {4}, pages = {e5350}, publisher = {Public Library of Science}, title = {{Development and Characterization of a High Density SNP Genotyping Assay for Cattle}}, url = {http://dx.doi.org/10.1371/journal.pone.0005350}, volume = {4}, year = {2009} } @article{Dean2008, author = {Dean, Jeffrey and Ghemawat, Sanjay}, doi = {10.1145/1327452.1327492}, file = {:home/gus/Documents/Mendeley Desktop/Dean, Ghemawat\_2008\_MapReduce.pdf:pdf}, issn = {00010782}, journal = {Communications of the ACM}, month = jan, number = {1}, pages = {107}, title = {{MapReduce}}, url = {http://dl.acm.org/citation.cfm?id=1327452.1327492}, volume = {51}, year = {2008} } @article{Hernandez2008, abstract = {Novel high-throughput DNA sequencing technologies allow researchers to characterize a bacterial genome during a single experiment and at a moderate cost. However, the increase in sequencing throughput that is allowed by using such platforms is obtained at the expense of individual sequence read length, which must be assembled into longer contigs to be exploitable. This study focuses on the Illumina sequencing platform that produces millions of very short sequences that are 35 bases in length. We propose a de novo assembler software that is dedicated to process such data. Based on a classical overlap graph representation and on the detection of potentially spurious reads, our software generates a set of accurate contigs of several kilobases that cover most of the bacterial genome. The assembly results were validated by comparing data sets that were obtained experimentally for Staphylococcus aureus strain MW2 and Helicobacter acinonychis strain Sheeba with that of their published genomes acquired by conventional sequencing of 1.5- to 3.0-kb fragments. We also provide indications that the broad coverage achieved by high-throughput sequencing might allow for the detection of clonal polymorphisms in the set of DNA molecules being sequenced.}, author = {Hernandez, David and Fran\c{c}ois, Patrice and Farinelli, Laurent and Oster\aa s, Magne and Schrenzel, Jacques}, doi = {10.1101/gr.072033.107}, file = {:home/gus/Documents/Mendeley Desktop/Hernandez et al.\_2008\_De novo bacterial genome sequencing millions of very short reads assembled on a desktop computer.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Chromosome Mapping,Genome, Bacterial,Genome, Bacterial: genetics,Helicobacter,Helicobacter: classification,Helicobacter: genetics,Microcomputers,Polymorphism, Genetic,Reproducibility of Results,Sequence Analysis, DNA,Sequence Analysis, DNA: economics,Sequence Analysis, DNA: instrumentation,Sequence Analysis, DNA: methods,Software,Staphylococcus aureus,Staphylococcus aureus: classification,Staphylococcus aureus: genetics}, month = may, number = {5}, pages = {802--9}, pmid = {18332092}, title = {{De novo bacterial genome sequencing: millions of very short reads assembled on a desktop computer.}}, url = {http://genome.cshlp.org/cgi/content/abstract/18/5/802}, volume = {18}, year = {2008} } @article{Schatz:2010uq, abstract = {Second-generation sequencing technology can now be used to sequence an entire human genome in a matter of days and at low cost. Sequence read lengths, initially very short, have rapidly increased since the technology first appeared, and we now are seeing a growing number of efforts to sequence large genomes de novo from these short reads. In this Perspective, we describe the issues associated with short-read assembly, the different types of data produced by second-gen sequencers, and the latest assembly algorithms designed for these data. We also review the genomes that have been assembled recently from short reads and make recommendations for sequencing strategies that will yield a high-quality assembly.}, author = {Schatz, Michael C and Delcher, Arthur L and Salzberg, Steven L}, doi = {10.1101/gr.101360.109}, file = {:home/gus/Documents/Mendeley Desktop/Schatz, Delcher, Salzberg\_2010\_Assembly of large genomes using second-generation sequencing.pdf:pdf}, issn = {1549-5469}, journal = {Genome research}, keywords = {Algorithms,Base Sequence,DNA,DNA: methods,Genome,Genomics,Genomics: methods,Human,Humans,Sequence Analysis}, month = sep, number = {9}, pages = {1165--73}, pmid = {20508146}, title = {{Assembly of large genomes using second-generation sequencing.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2928494\&tool=pmcentrez\&rendertype=abstract}, volume = {20}, year = {2010} } @article{Grabherr2011, abstract = {Massively parallel sequencing of cDNA has enabled deep and efficient probing of transcriptomes. Current approaches for transcript reconstruction from such data often rely on aligning reads to a reference genome, and are thus unsuitable for samples with a partial or missing reference genome. Here we present the Trinity method for de novo assembly of full-length transcripts and evaluate it on samples from fission yeast, mouse and whitefly, whose reference genome is not yet available. By efficiently constructing and analyzing sets of de Bruijn graphs, Trinity fully reconstructs a large fraction of transcripts, including alternatively spliced isoforms and transcripts from recently duplicated genes. Compared with other de novo transcriptome assemblers, Trinity recovers more full-length transcripts across a broad range of expression levels, with a sensitivity similar to methods that rely on genome alignments. Our approach provides a unified solution for transcriptome reconstruction in any sample, especially in the absence of a reference genome.}, author = {Grabherr, Manfred G and Haas, Brian J and Yassour, Moran and Levin, Joshua Z and Thompson, Dawn A and Amit, Ido and Adiconis, Xian and Fan, Lin and Raychowdhury, Raktima and Zeng, Qiandong and Chen, Zehua and Mauceli, Evan and Hacohen, Nir and Gnirke, Andreas and Rhind, Nicholas and di Palma, Federica and Birren, Bruce W and Nusbaum, Chad and Lindblad-Toh, Kerstin and Friedman, Nir and Regev, Aviv}, doi = {10.1038/nbt.1883}, file = {:home/gus/Documents/Mendeley Desktop/Grabherr et al.\_2011\_Full-length transcriptome assembly from RNA-Seq data without a reference genome.pdf:pdf}, issn = {1546-1696}, journal = {Nature biotechnology}, month = may, number = {7}, pages = {644--652}, pmid = {21572440}, publisher = {Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.}, shorttitle = {Nat Biotech}, title = {{Full-length transcriptome assembly from RNA-Seq data without a reference genome.}}, url = {http://dx.doi.org/10.1038/nbt.1883}, volume = {29}, year = {2011} } @article{Ruffalo2011, abstract = {Motivation: The advent of next-generation sequencing (NGS) techniques presents many novel opportunities for many applications in life sciences. The vast number of short reads produced by these techniques, however, pose significant computational challenges. The first step in many types of genomic analysis is the mapping of short reads to a reference genome, and several groups have developed dedicated algorithms and software packages to perform this function. As the developers of these packages optimize their algorithms with respect to various considerations, the relative merits of different software packages remain unclear. However, for scientists who generate and use NGS data for their specific research projects, an important consideration is choosing the software that is most suitable for their application. Results: With a view to comparing existing short read alignment software, we develop a simulation and evaluation suite, SEAL, which simulates NGS runs for different configurations of various factors, including sequencing error, indels and coverage. We also develop criteria to compare the performances of software with disparate output structure (e.g. some packages return a single alignment while some return multiple possible alignments). Using these criteria, we comprehensively evaluate the performances of Bowtie, BWA, mr- and mrsFAST, Novoalign, SHRiMP and SOAPv2, with regard to accuracy and runtime. Conclusion: We expect that the results presented here will be useful to investigators in choosing the alignment software that is most suitable for their specific research aims. Our results also provide insights into the factors that should be considered to use alignment results effectively. SEAL can also be used to evaluate the performance of algorithms that use deep sequencing data for various purposes (e.g. identification of genomic variants). Availability: SEAL is available as open source at http://compbio.case.edu/seal/. Contact: matthew.ruffalo@case.edu Supplementary information: Supplementary data are available at Bioinformatics online.}, author = {Ruffalo, M. and LaFramboise, T. and Koyuturk, M.}, doi = {10.1093/bioinformatics/btr477}, file = {:home/gus/Documents/Mendeley Desktop/Ruffalo, LaFramboise, Koyuturk\_2011\_Comparative analysis of algorithms for next-generation sequencing read alignment.pdf:pdf}, issn = {1367-4803}, journal = {Bioinformatics}, month = aug, number = {20}, pages = {2790--2796}, title = {{Comparative analysis of algorithms for next-generation sequencing read alignment}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/27/20/2790}, volume = {27}, year = {2011} } @article{Almeida2007, author = {Almeida, Paulo S\'{e}rgio and Baquero, Carlos and Pregui\c{c}a, Nuno and Hutchison, David}, issn = {0020-0190}, journal = {Information Processing Letters}, keywords = {Bloom filters,Data structures,Distributed systems,Randomized algorithms}, month = mar, number = {6}, pages = {255--261}, title = {{Scalable Bloom Filters}}, url = {http://www.sciencedirect.com/science/article/pii/S0020019006003127}, volume = {101}, year = {2007} } @inproceedings{Chazelle:2004:BFE:982792.982797, address = {Philadelphia, PA, USA}, author = {Chazelle, Bernard and Kilian, Joe and Rubinfeld, Ronitt and Tal, Ayellet}, booktitle = {Proceedings of the fifteenth annual ACM-SIAM symposium on Discrete algorithms}, isbn = {0-89871-558-X}, pages = {30--39}, publisher = {Society for Industrial and Applied Mathematics}, series = {SODA '04}, title = {{The Bloomier filter: an efficient data structure for static support lookup tables}}, url = {http://dl.acm.org/citation.cfm?id=982792.982797}, year = {2004} } @article{Schatz:2010uq, abstract = {Second-generation sequencing technology can now be used to sequence an entire human genome in a matter of days and at low cost. Sequence read lengths, initially very short, have rapidly increased since the technology first appeared, and we now are seeing a growing number of efforts to sequence large genomes de novo from these short reads. In this Perspective, we describe the issues associated with short-read assembly, the different types of data produced by second-gen sequencers, and the latest assembly algorithms designed for these data. We also review the genomes that have been assembled recently from short reads and make recommendations for sequencing strategies that will yield a high-quality assembly.}, author = {Schatz, Michael C and Delcher, Arthur L and Salzberg, Steven L}, doi = {10.1101/gr.101360.109}, journal = {Genome Res}, month = sep, number = {9}, pages = {1165--1173}, pmid = {20508146}, title = {{Assembly of large genomes using second-generation sequencing}}, volume = {20}, year = {2010} } @article{Zimin2009, abstract = {The genome of the domestic cow, Bos taurus, was sequenced using a mixture of hierarchical and whole-genome shotgun sequencing methods.}, author = {Zimin, Aleksey V and Delcher, Arthur L and Florea, Liliana and Kelley, David R and Schatz, Michael C and Puiu, Daniela and Hanrahan, Finnian and Pertea, Geo and {Van Tassell}, Curtis P and Sonstegard, Tad S and Mar\c{c}ais, Guillaume and Roberts, Michael and Subramanian, Poorani and Yorke, James a and Salzberg, Steven L}, doi = {10.1186/gb-2009-10-4-r42}, file = {:home/gus/Documents/Mendeley Desktop/Zimin et al.\_2009\_A whole-genome assembly of the domestic cow, Bos taurus.pdf:pdf}, issn = {1465-6914}, journal = {Genome biology}, keywords = {Animals,Cattle,Cattle: genetics,Chromosome Mapping,Female,Genome,Genome, Human,Genome, Human: genetics,Genome: genetics,Genomics,Humans,Male,Sequence Analysis, DNA,Sequence Analysis, DNA: methods,Sequence Analysis, DNA: statistics \& numerical dat,Synteny,Y Chromosome,Y Chromosome: genetics}, month = jan, number = {4}, pages = {R42}, pmid = {19393038}, title = {{A whole-genome assembly of the domestic cow, Bos taurus.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2688933\&tool=pmcentrez\&rendertype=abstract}, volume = {10}, year = {2009} } @article{Gao, author = {Gao, H. and Groote, J.F. and Hesselink, W.H.}, doi = {10.1109/IPDPS.2004.1302969}, file = {:home/gus/Documents/Mendeley Desktop/Gao, Groote, Hesselink\_Unknown\_Almost wait-free resizable hashtables.pdf:pdf}, isbn = {0-7695-2132-0}, journal = {18th International Parallel and Distributed Processing Symposium, 2004. Proceedings.}, pages = {50--58}, publisher = {Ieee}, title = {{Almost wait-free resizable hashtables}}, url = {http://ieeexplore.ieee.org/lpdocs/epic03/wrapper.htm?arnumber=1302969} } @article{medvedev2007computability, author = {Medvedev, P. and Georgiou, K. and Myers, G. and Brudno, M.}, file = {:home/gus/Documents/Mendeley Desktop/Medvedev et al.\_2007\_Computability of models for sequence assembly.pdf:pdf}, journal = {Algorithms in Bioinformatics}, pages = {289--301}, publisher = {Springer}, title = {{Computability of models for sequence assembly}}, url = {http://www.springerlink.com/index/H711368771048H21.pdf}, year = {2007} } @article{Butler2008, abstract = {New DNA sequencing technologies deliver data at dramatically lower costs but demand new analytical methods to take full advantage of the very short reads that they produce. We provide an initial, theoretical solution to the challenge of de novo assembly from whole-genome shotgun "microreads." For 11 genomes of sizes up to 39 Mb, we generated high-quality assemblies from 80x coverage by paired 30-base simulated reads modeled after real Illumina-Solexa reads. The bacterial genomes of Campylobacter jejuni and Escherichia coli assemble optimally, yielding single perfect contigs, and larger genomes yield assemblies that are highly connected and accurate. Assemblies are presented in a graph form that retains intrinsic ambiguities such as those arising from polymorphism, thereby providing information that has been absent from previous genome assemblies. For both C. jejuni and E. coli, this assembly graph is a single edge encompassing the entire genome. Larger genomes produce more complicated graphs, but the vast majority of the bases in their assemblies are present in long edges that are nearly always perfect. We describe a general method for genome assembly that can be applied to all types of DNA sequence data, not only short read data, but also conventional sequence reads.}, author = {Butler, Jonathan and MacCallum, Iain and Kleber, Michael and Shlyakhter, Ilya a and Belmonte, Matthew K and Lander, Eric S and Nusbaum, Chad and Jaffe, David B}, doi = {10.1101/gr.7337908}, file = {:home/gus/Documents/Mendeley Desktop/Butler et al.\_2008\_ALLPATHS de novo assembly of whole-genome shotgun microreads.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Campylobacter jejuni,Campylobacter jejuni: genetics,Computational Biology,Computational Biology: methods,Computer Simulation,Escherichia coli,Escherichia coli: genetics,Genome, Bacterial,Genome, Bacterial: genetics,Reproducibility of Results,Sequence Analysis, DNA,Sequence Analysis, DNA: methods,Sequence Analysis, DNA: standards}, month = may, number = {5}, pages = {810--20}, pmid = {18340039}, title = {{ALLPATHS: de novo assembly of whole-genome shotgun microreads.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2336810\&tool=pmcentrez\&rendertype=abstract}, volume = {18}, year = {2008} } @article{Miller:2010ys, abstract = {The emergence of next-generation sequencing platforms led to resurgence of research in whole-genome shotgun assembly algorithms and software. DNA sequencing data from the Roche 454, Illumina/Solexa, and ABI SOLiD platforms typically present shorter read lengths, higher coverage, and different error profiles compared with Sanger sequencing data. Since 2005, several assembly software packages have been created or revised specifically for de novo assembly of next-generation sequencing data. This review summarizes and compares the published descriptions of packages named SSAKE, SHARCGS, VCAKE, Newbler, Celera Assembler, Euler, Velvet, ABySS, AllPaths, and SOAPdenovo. More generally, it compares the two standard methods known as the de Bruijn graph approach and the overlap/layout/consensus approach to assembly.}, author = {Miller, Jason R and Koren, Sergey and Sutton, Granger}, doi = {10.1016/j.ygeno.2010.03.001}, journal = {Genomics}, month = jun, number = {6}, pages = {315--327}, pmid = {20211242}, title = {{Assembly algorithms for next-generation sequencing data}}, volume = {95}, year = {2010} } @misc{TheMendeleySupportTeam2011a, abstract = {A quick introduction to Mendeley. Learn how Mendeley creates your personal digital library, how to organize and annotate documents, how to collaborate and share with colleagues, and how to generate citations and bibliographies.}, address = {London}, author = {{The Mendeley Support Team}}, booktitle = {Mendeley Desktop}, file = {:home/gus/Documents/Mendeley Desktop/The Mendeley Support Team\_2011\_Getting Started with Mendeley.pdf:pdf}, keywords = {Mendeley,how-to,user manual}, pages = {1--16}, publisher = {Mendeley Ltd.}, title = {{Getting Started with Mendeley}}, url = {http://www.mendeley.com}, year = {2011} } @article{Reed2004, abstract = {A family of probability densities, which has proved useful in modelling the size distributions of various phenomens, including incomes and earnings, human settlement sizes, oil-field volumes and particle sizes, is introduced. The distribution, named herein as the double Pareto-lognormal or dPlN distribution, arises as that of the state of a geometric Brownian motion (GBM), with lognormally distributed initial state, after an exponentially distributed length of time (or equivalently as the distribution of the killed state of such a GBM with constant killing rate). A number of phenomena can be viewed as resulting from such a process (e.g., incomes, settlement sizes), which explains the good fit. Properties of the distribution are derived and estimation methods discussed. The distribution exhibits Paretian power-law) behaviour in both tails, and when plotted on logarithmic axes, its density exhibits hyperbolic-type behaviour.}, author = {Reed, William J. and Jorgensen, Murray}, file = {:home/gus/Documents/Mendeley Desktop/Reed, Jorgensen\_2004\_The double Pareto-lognormal distribution—a new parametric model for size distributions.pdf:pdf}, journal = {Communications in Statistics-Theory \ldots}, number = {8}, pages = {1733--1753}, title = {{The double Pareto-lognormal distribution—a new parametric model for size distributions}}, url = {http://www.tandfonline.com/doi/abs/10.1081/STA-120037438}, volume = {33}, year = {2004} } @article{michael2004hazard, author = {Michael, M.M.}, file = {:home/gus/Documents/Mendeley Desktop/Michael\_2004\_Hazard pointers Safe memory reclamation for lock-free objects.pdf:pdf}, journal = {Parallel and Distributed Systems, IEEE Transactions on}, number = {6}, pages = {491--504}, publisher = {IEEE}, title = {{Hazard pointers: Safe memory reclamation for lock-free objects}}, url = {http://ieeexplore.ieee.org/xpls/abs\_all.jsp?arnumber=1291819}, volume = {15}, year = {2004} } @article{Phenix2011, abstract = {Inferring regulatory and metabolic network models from quantitative genetic interaction data remains a major challenge in systems biology. Here, we present a novel quantitative model for interpreting epistasis within pathways responding to an external signal. The model provides the basis of an experimental method to determine the architecture of such pathways, and establishes a new set of rules to infer the order of genes within them. The method also allows the extraction of quantitative parameters enabling a new level of information to be added to genetic network models. It is applicable to any system where the impact of combinatorial loss-of-function mutations can be quantified with sufficient accuracy. We test the method by conducting a systematic analysis of a thoroughly characterized eukaryotic gene network, the galactose utilization pathway in Saccharomyces cerevisiae. For this purpose, we quantify the effects of single and double gene deletions on two phenotypic traits, fitness and reporter gene expression. We show that applying our method to fitness traits reveals the order of metabolic enzymes and the effects of accumulating metabolic intermediates. Conversely, the analysis of expression traits reveals the order of transcriptional regulatory genes, secondary regulatory signals and their relative strength. Strikingly, when the analyses of the two traits are combined, the method correctly infers ∼80\% of the known relationships without any false positives.}, author = {Phenix, Hilary and Morin, Katy and Batenchuk, Cory and Parker, Jacob and Abedi, Vida and Yang, Liu and Tepliakova, Lioudmila and Perkins, Theodore J and K\ae rn, Mads}, doi = {10.1371/journal.pcbi.1002048}, editor = {Ohler, Uwe}, file = {:home/gus/Documents/Mendeley Desktop/Phenix et al.\_2011\_Quantitative epistasis analysis and pathway inference from genetic interaction data.pdf:pdf}, issn = {1553-7358}, journal = {PLoS computational biology}, keywords = {Biology,Computational Biology,Functional genomics,Gene expression,Gene regulation,Genomics,Metabolic networks,Molecular genetics,Regulatory networks,Research Article,Signaling networks,Systems biology}, month = may, number = {5}, pages = {e1002048}, pmid = {21589890}, publisher = {Public Library of Science}, title = {{Quantitative epistasis analysis and pathway inference from genetic interaction data.}}, url = {http://dx.plos.org/10.1371/journal.pcbi.1002048}, volume = {7}, year = {2011} } @article{Pugh1990, author = {Pugh, William}, doi = {10.1145/78973.78977}, issn = {00010782}, journal = {Communications of the ACM}, keywords = {data structures,searching,trees}, month = jun, number = {6}, pages = {668--676}, title = {{Skip lists: a probabilistic alternative to balanced trees}}, url = {http://dl.acm.org/citation.cfm?id=78973.78977}, volume = {33}, year = {1990} } @inproceedings{Fomitchev2004, address = {New York, New York, USA}, annote = {http://drdobbs.com/parallel/208801371}, author = {Fomitchev, Mikhail and Ruppert, Eric}, booktitle = {Proceedings of the twenty-third annual ACM symposium on Principles of distributed computing - PODC '04}, doi = {10.1145/1011767.1011776}, file = {:home/gus/Documents/Mendeley Desktop/Fomitchev, Ruppert\_2004\_Lock-free linked lists and skip lists.pdf:pdf}, isbn = {1581138024}, keywords = {amortized analysis,analysis,distributed,efficient,fault-tolerant,linked list,lock-free,skip list}, month = jul, pages = {50}, publisher = {ACM Press}, title = {{Lock-free linked lists and skip lists}}, url = {http://dl.acm.org/citation.cfm?id=1011767.1011776}, year = {2004} } @article{Au2010, abstract = {Alternative splicing is a prevalent post-transcriptional process, which is not only important to normal cellular function but is also involved in human diseases. The newly developed second generation sequencing technique provides high-throughput data (RNA-seq data) to study alternative splicing events in different types of cells. Here, we present a computational method, SpliceMap, to detect splice junctions from RNA-seq data. This method does not depend on any existing annotation of gene structures and is capable of finding novel splice junctions with high sensitivity and specificity. It can handle long reads (50-100 nt) and can exploit paired-read information to improve mapping accuracy. Several parameters are included in the output to indicate the reliability of the predicted junction and help filter out false predictions. We applied SpliceMap to analyze 23 million paired 50-nt reads from human brain tissue. The results show at this depth of sequencing, RNA-seq can support reliable detection of splice junctions except for those that are present at very low level. Compared to current methods, SpliceMap can achieve 12\% higher sensitivity without sacrificing specificity.}, author = {Au, Kin Fai and Jiang, Hui and Lin, Lan and Xing, Yi and Wong, Wing Hung}, doi = {10.1093/nar/gkq211}, file = {:home/gus/Documents/Mendeley Desktop/Au et al.\_2010\_Detection of splice junctions from paired-end RNA-seq data by SpliceMap.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Au et al.\_2010\_Detection of splice junctions from paired-end RNA-seq data by SpliceMap(2).pdf:pdf}, issn = {1362-4962}, journal = {Nucleic acids research}, keywords = {Algorithms,Alternative Splicing,Computational Biology,Computational Biology: methods,Humans,Polymerase Chain Reaction,RNA,RNA Splice Sites,Sequence Analysis,Software}, month = aug, number = {14}, pages = {4570--8}, pmid = {20371516}, title = {{Detection of splice junctions from paired-end RNA-seq data by SpliceMap.}}, url = {http://nar.oxfordjournals.org/cgi/content/abstract/gkq211v1}, volume = {38}, year = {2010} } @inproceedings{Lin2010, address = {New York, New York, USA}, author = {Lin, Jimmy and Schatz, Michael}, booktitle = {Proceedings of the Eighth Workshop on Mining and Learning with Graphs - MLG '10}, doi = {10.1145/1830252.1830263}, file = {:home/gus/Documents/Mendeley Desktop/Lin, Schatz\_2010\_Design patterns for efficient graph algorithms in MapReduce.pdf:pdf}, isbn = {9781450302142}, month = jul, pages = {78--85}, publisher = {ACM Press}, title = {{Design patterns for efficient graph algorithms in MapReduce}}, url = {http://dl.acm.org/citation.cfm?id=1830252.1830263}, year = {2010} } @book{Colden1755, address = {London}, author = {Colden, Cadwallader}, edition = {3rd editio}, file = {:home/gus/Documents/Mendeley Desktop/Colden\_1755\_The History of the Five Indian Nations of Canada.jpeg:jpeg}, pages = {Vol. II 18--24}, title = {{The History of the Five Indian Nations of Canada}}, url = {http://america.eb.com/america/article?articleId=385137\&query=Iroquois}, year = {1755} } @article{Zerbino2008, abstract = {We have developed a new set of algorithms, collectively called "Velvet," to manipulate de Bruijn graphs for genomic sequence assembly. A de Bruijn graph is a compact representation based on short words (k-mers) that is ideal for high coverage, very short read (25-50 bp) data sets. Applying Velvet to very short reads and paired-ends information only, one can produce contigs of significant length, up to 50-kb N50 length in simulations of prokaryotic data and 3-kb N50 on simulated mammalian BACs. When applied to real Solexa data sets without read pairs, Velvet generated contigs of approximately 8 kb in a prokaryote and 2 kb in a mammalian BAC, in close agreement with our simulated results without read-pair information. Velvet represents a new approach to assembly that can leverage very short reads in combination with read pairs to produce useful assemblies.}, author = {Zerbino, Daniel R and Birney, Ewan}, doi = {10.1101/gr.074492.107}, file = {:home/gus/Documents/Mendeley Desktop/Zerbino, Birney\_2008\_Velvet algorithms for de novo short read assembly using de Bruijn graphs.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Animals,Artificial,Bacterial,Chromosomes,Computational Biology,Computational Biology: methods,Computer Simulation,DNA,DNA: methods,DNA: standards,Genome,Genomics,Human,Humans,Mammals,Mammals: genetics,Sequence Analysis,Streptococcus,Streptococcus: genetics}, month = may, number = {5}, pages = {821--9}, pmid = {18349386}, title = {{Velvet: algorithms for de novo short read assembly using de Bruijn graphs}}, url = {http://genome.cshlp.org/content/18/5/821.short http://genome.cshlp.org/cgi/content/abstract/18/5/821}, volume = {18}, year = {2008} } @article{Kao2011, abstract = {Developing accurate, scalable algorithms to improve data quality is an important computational challenge associated with recent advances in high-throughput sequencing technology. In this study, a novel error-correction algorithm, called ECHO, is introduced for correcting base-call errors in short-reads, without the need of a reference genome. Unlike most previous methods, ECHO does not require the user to specify parameters of which optimal values are typically unknown a priori. ECHO automatically sets the parameters in the assumed model and estimates error characteristics specific to each sequencing run, while maintaining a running time that is within the range of practical use. ECHO is based on a probabilistic model and is able to assign a quality score to each corrected base. Furthermore, it explicitly models heterozygosity in diploid genomes and provides a reference-free method for detecting bases that originated from heterozygous sites. On both real and simulated data, ECHO is able to improve the accuracy of previous error-correction methods by several folds to an order of magnitude, depending on the sequence coverage depth and the position in the read. The improvement is most pronounced toward the end of the read, where previous methods become noticeably less effective. Using a whole-genome yeast data set, it is demonstrated here that ECHO is capable of coping with nonuniform coverage. Also, it is shown that using ECHO to perform error correction as a preprocessing step considerably facilitates de novo assembly, particularly in the case of low-to-moderate sequence coverage depth.}, author = {Kao, Wei-Chun and Chan, Andrew H and Song, Yun S}, doi = {10.1101/gr.111351.110}, file = {:home/gus/Documents/Mendeley Desktop/Kao, Chan, Song\_2011\_ECHO A reference-free short-read error correction algorithm.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Kao, Chan, Song\_2011\_ECHO A reference-free short-read error correction algorithm(2).pdf:pdf}, issn = {1549-5469}, journal = {Genome research}, month = may, number = {7}, pages = {1181--1192}, pmid = {21482625}, title = {{ECHO: A reference-free short-read error correction algorithm.}}, url = {http://genome.cshlp.org/cgi/content/abstract/21/7/1181}, volume = {21}, year = {2011} } @article{Chin2011, abstract = {Recent advances in genome technologies and the ensuing outpouring of genomic information related to cancer have accelerated the convergence of discovery science and clinical medicine. Successful examples of translating cancer genomics into therapeutics and diagnostics reinforce its potential to make possible personalized cancer medicine. However, the bottlenecks along the path of converting a genome discovery into a tangible clinical endpoint are numerous and formidable. In this Perspective, we emphasize the importance of establishing the biological relevance of a cancer genomic discovery in realizing its clinical potential and discuss some of the major obstacles to moving from the bench to the bedside.}, author = {Chin, Lynda and Andersen, Jannik N and Futreal, P Andrew}, doi = {10.1038/nm.2323}, file = {:home/gus/Documents/Mendeley Desktop/Chin, Andersen, Futreal\_2011\_Cancer genomics from discovery science to personalized medicine.pdf:pdf}, issn = {1546-170X}, journal = {Nature medicine}, keywords = {Genomics,Humans,Individualized Medicine,Neoplasms,Neoplasms: genetics,Neoplasms: therapy}, language = {en}, month = mar, number = {3}, pages = {297--303}, pmid = {21383744}, publisher = {Nature Publishing Group}, title = {{Cancer genomics: from discovery science to personalized medicine.}}, url = {http://www.nature.com/nm/journal/v17/n3/full/nm.2323.html?WT.ec\_id=NM-201103}, volume = {17}, year = {2011} } @article{Zhao2011, author = {Zhao, Z and Yin, J and Li, Y}, file = {:home/gus/Documents/Mendeley Desktop/Zhao, Yin, Li\_2011\_An efficient hybrid approach to correcting errors in short reads.pdf:pdf}, journal = {Modeling Decision for Artificial \ldots}, title = {{An efficient hybrid approach to correcting errors in short reads}}, url = {http://www.springerlink.com/index/P53757J416772662.pdf}, year = {2011} } @article{Li01082009, abstract = {Summary: SOAP2 is a significantly improved version of the short oligonucleotide alignment program that both reduces computer memory usage and increases alignment speed at an unprecedented rate. We used a Burrows Wheeler Transformation (BWT) compression index to substitute the seed strategy for indexing the reference sequence in the main memory. We tested it on the whole human genome and found that this new algorithm reduced memory usage from 14.7 to 5.4 GB and improved alignment speed by 20‚\{\"{A}\}\{\`{\i}\}30 times. SOAP2 is compatible with both single- and paired-end reads. Additionally, this tool now supports multiple text and compressed file formats. A consensus builder has also been developed for consensus assembly and SNP detection from alignment of short reads on a reference genome.Availability: http://soap.genomics.org.cnContact: soap@genomics.org.cn}, author = {Li, Ruiqiang and Yu, Chang and Li, Yingrui and Lam, Tak-Wah and Yiu, Siu-Ming and Kristiansen, Karsten and Wang, Jun}, doi = {10.1093/bioinformatics/btp336}, file = {:home/gus/Documents/Mendeley Desktop/Li et al.\_2009\_SOAP2 an improved ultrafast tool for short read alignment.pdf:pdf}, journal = {Bioinformatics}, number = {15}, pages = {1966--1967}, title = {{SOAP2: an improved ultrafast tool for short read alignment}}, url = {http://bioinformatics.oxfordjournals.org/content/25/15/1966.abstract}, volume = {25}, year = {2009} } @inproceedings{ferragina2004alphabet, author = {Ferragina, P. and Manzini, G. and M\"{a}kinen, V. and Navarro, G.}, booktitle = {String Processing and Information Retrieval}, file = {:home/gus/Documents/Mendeley Desktop/Ferragina et al.\_2004\_An alphabet-friendly FM-index.pdf:pdf}, pages = {228--228}, publisher = {Springer}, title = {{An alphabet-friendly FM-index}}, url = {http://www.springerlink.com/index/P95U67K0XV0X382E.pdf}, year = {2004} } @article{Roberts12122004, abstract = {Motivation: Comparison of nucleic acid and protein sequences is a fundamental tool of modern bioinformatics. A dominant method of such string matching is the ‘seed-and-extend’ approach, in which occurrences of short subsequences called ‘seeds’ are used to search for potentially longer matches in a large database of sequences. Each such potential match is then checked to see if it extends beyond the seed. To be effective, the seed-and-extend approach needs to catalogue seeds from virtually every substring in the database of search strings. Projects such as mammalian genome assemblies and large-scale protein matching, however, have such large sequence databases that the resulting list of seeds cannot be stored in RAM on a single computer. This significantly slows the matching process.Results: We present a simple and elegant method in which only a small fraction of seeds, called ‘minimizers’, needs to be stored. Using minimizers can speed up string-matching computations by a large factor while missing only a small fraction of the matches found using all seeds.}, author = {Roberts, Michael and Hayes, Wayne and Hunt, Brian R and Mount, Stephen M and Yorke, James A}, doi = {10.1093/bioinformatics/bth408}, journal = {Bioinformatics}, number = {18}, pages = {3363--3369}, title = {{Reducing storage requirements for biological sequence comparison}}, url = {http://bioinformatics.oxfordjournals.org/content/20/18/3363.abstract}, volume = {20}, year = {2004} } @article{Richter2008, abstract = {The new research field of metagenomics is providing exciting insights into various, previously unclassified ecological systems. Next-generation sequencing technologies are producing a rapid increase of environmental data in public databases. There is great need for specialized software solutions and statistical methods for dealing with complex metagenome data sets.}, author = {Richter, Daniel C and Ott, Felix and Auch, Alexander F and Schmid, Ramona and Huson, Daniel H}, doi = {10.1371/journal.pone.0003373}, editor = {Field, Dawn}, file = {:home/gus/Documents/Mendeley Desktop/Richter et al.\_2008\_MetaSim a sequencing simulator for genomics and metagenomics.pdf:pdf}, issn = {1932-6203}, journal = {PloS one}, keywords = {Databases, Genetic,Genomics,Models, Theoretical,User-Computer Interface}, month = jan, number = {10}, pages = {e3373}, pmid = {18841204}, publisher = {Public Library of Science}, title = {{MetaSim: a sequencing simulator for genomics and metagenomics.}}, url = {http://dx.plos.org/10.1371/journal.pone.0003373}, volume = {3}, year = {2008} } @article{Brown2012, abstract = {Deep shotgun sequencing and analysis of genomes, transcriptomes, amplified single-cell genomes, and metagenomes enable the sensitive investigation of a wide range of biological phenomena. However, it is increasingly difficult to deal with the volume of data emerging from deep short-read sequencers, in part because of random and systematic sampling variation as well as a high sequencing error rate. These challenges have led to the development of entire new classes of short-read mapping tools, as well as new \{$\backslash$em de novo\} assemblers. Even newer assembly strategies for dealing with transcriptomes, single-cell genomes, and metagenomes have also emerged. Despite these advances, algorithms and compute capacity continue to be challenged by the continued improvements in sequencing technology throughput. We here describe an approach we term digital normalization, a single-pass computational algorithm that discards redundant data and both sampling variation and the number of errors present in deep sequencing data sets. Digital normalization substantially reduces the size of data sets and accordingly decreases the memory and time requirements for \{$\backslash$em de novo\} sequence assembly, all without significantly impacting content of the generated contigs. In doing so, it converts high random coverage to low systematic coverage. Digital normalization is an effective and efficient approach to normalizing coverage, removing errors, and reducing data set size for shotgun sequencing data sets. It is particularly useful for reducing the compute requirements for \{$\backslash$em de novo\} sequence assembly. We demonstrate this for the assembly of microbial genomes, amplified single-cell genomic data, and transcriptomic data. The software is freely available for use and modification.}, annote = {I am skeptical about this paper: - As they mention at the end of the paper, they only tested on bacterial genome with low amount of repeats. This is conceptually a big drawback for a paper whose purpose is to reduce the amount of data to tackle large projects. Assembling E. coli is not a challenge anymore. - Given that the coverage of most part of the genome is now made uniform, we lost a big indicator to detect repeat regions. The Celera assembler and others will likely collapse many copies of repeat regions and have many more mis-assemblies as a result. Which does not show up in the E. coli dataset. - I disagree with the claim that "Digital normalization retains information while discarding both data and errors" is beneficial. When looking at their own data (Table 1.) I see the following trend. For a mer length of k, one base error creates usually around k erroneous k-mers. Hence the error rate can be estimated as the number of k-mers in the reads minus the number of true k-mers, divided by the number of reads. For E. coli in Table 1 they kept a tenth of the reads while reducing the number of erroneous k-mers by only half. Hence the error rate in the reads that are kept is approximately 5 times HIGHER. This trend of higher error rate in the kept reads is even worse in the three-pass procedure (Table 2.). They reduced the number of erroneous k-mers in absolute value but increased it in proportion. Is it really a good operation? Actually, based on this, I would go the other way around. I would count k-mers in the remaining 90\% of the reads (the discarded ones), which have a lower error rate (approximately half the original error rate). I would then used these k-mers to do error correction on ALL of the reads.}, archivePrefix = {arXiv}, arxivId = {1203.4802}, author = {Brown, C. Titus and Howe, Adina and Zhang, Qingpeng and Pyrkosz, Alexis B. and Brom, Timothy H.}, eprint = {1203.4802}, file = {:home/gus/Documents/Mendeley Desktop/Brown et al.\_2012\_A single pass approach to reducing sampling variation, removing errors, and scaling \{em de novo\} assembly of shotgun sequences.pdf:pdf}, month = mar, title = {{A single pass approach to reducing sampling variation, removing errors, and scaling \{$\backslash$em de novo\} assembly of shotgun sequences}}, url = {http://arxiv.org/abs/1203.4802}, year = {2012} } @article{Pugh1990, author = {Pugh, William}, doi = {10.1145/78973.78977}, file = {:home/gus/Documents/Mendeley Desktop//Pugh\_1990\_Skip lists a probabilistic alternative to balanced trees.pdf:pdf}, issn = {00010782}, journal = {Communications of the ACM}, keywords = {data structures,searching,trees}, month = jun, number = {6}, pages = {668--676}, publisher = {ACM}, title = {{Skip lists: a probabilistic alternative to balanced trees}}, url = {http://dl.acm.org/citation.cfm?id=78973.78977 http://dl.acm.org/citation.cfm?id=78977,}, volume = {33}, year = {1990} } @misc{TheMendeleySupportTeam2011, abstract = {A quick introduction to Mendeley. Learn how Mendeley creates your personal digital library, how to organize and annotate documents, how to collaborate and share with colleagues, and how to generate citations and bibliographies.}, address = {London}, author = {{The Mendeley Support Team}}, booktitle = {Mendeley Desktop}, file = {:home/gus/Documents/Mendeley Desktop/The Mendeley Support Team\_2011\_Getting Started with Mendeley.pdf:pdf}, keywords = {Mendeley,how-to,user manual}, pages = {1--16}, publisher = {Mendeley Ltd.}, title = {{Getting Started with Mendeley}}, url = {http://www.mendeley.com}, year = {2011} } @article{Li2009, abstract = {The enormous amount of short reads generated by the new DNA sequencing technologies call for the development of fast and accurate read alignment programs. A first generation of hash table-based methods has been developed, including MAQ, which is accurate, feature rich and fast enough to align short reads from a single individual. However, MAQ does not support gapped alignment for single-end reads, which makes it unsuitable for alignment of longer reads where indels may occur frequently. The speed of MAQ is also a concern when the alignment is scaled up to the resequencing of hundreds of individuals.}, author = {Li, Heng and Durbin, Richard}, doi = {10.1093/bioinformatics/btp324}, file = {:home/gus/Documents/Mendeley Desktop/Li, Durbin\_2009\_Fast and accurate short read alignment with Burrows-Wheeler transform.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,Genomics,Genomics: methods,Sequence Alignment,Sequence Alignment: methods,Sequence Analysis, DNA,Sequence Analysis, DNA: methods,Software}, month = jul, number = {14}, pages = {1754--60}, pmid = {19451168}, title = {{Fast and accurate short read alignment with Burrows-Wheeler transform.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/25/14/1754}, volume = {25}, year = {2009} } @article{Maccallum2009, abstract = {We demonstrate that genome sequences approaching finished quality can be generated from short paired reads. Using 36 base (fragment) and 26 base (jumping) reads from five microbial genomes of varied GC composition and sizes up to 40 Mb, ALLPATHS2 generated assemblies with long, accurate contigs and scaffolds. Velvet and EULER-SR were less accurate. For example, for Escherichia coli, the fraction of 10-kb stretches that were perfect was 99.8\% (ALLPATHS2), 68.7\% (Velvet), and 42.1\% (EULER-SR).}, author = {Maccallum, Iain and Przybylski, Dariusz and Gnerre, Sante and Burton, Joshua and Shlyakhter, Ilya and Gnirke, Andreas and Malek, Joel and McKernan, Kevin and Ranade, Swati and Shea, Terrance P and Williams, Louise and Young, Sarah and Nusbaum, Chad and Jaffe, David B}, doi = {10.1186/gb-2009-10-10-r103}, file = {:home/gus/Documents/Mendeley Desktop//Maccallum et al.\_2009\_ALLPATHS 2 small genomes assembled accurately and with high continuity from short paired reads.pdf:pdf}, issn = {1465-6914}, journal = {Genome biology}, keywords = {Bacteria,Bacteria: genetics,Base Pairing,Base Pairing: genetics,Fungi,Fungi: genetics,Genome,Genome: genetics,Genomics,Genomics: methods,Reproducibility of Results,Software}, month = jan, number = {10}, pages = {R103}, pmid = {19796385}, title = {{ALLPATHS 2: small genomes assembled accurately and with high continuity from short paired reads.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2784318\&tool=pmcentrez\&rendertype=abstract}, volume = {10}, year = {2009} } @article{Heyn2012, author = {Heyn, Holger and Li, Ning and Ferreira, Humberto J and Moran, Sebastian and Pisano, David G and Gomez, Antonio and Diez, Javier}, doi = {10.1073/pnas.1120658109}, file = {:home/gus/Documents/Mendeley Desktop/Heyn et al.\_2012\_Distinct DNA methylomes of newborns and centenarians.pdf:pdf}, journal = {PNAS}, title = {{Distinct DNA methylomes of newborns and centenarians}}, year = {2012} } @article{PETER1991, abstract = {We extend the notion of randomness (in the version introduced by Schnorr) to computable Probability Spaces and compare it to a dynamical notion of randomness: typicality. Roughly, a point is typical for some dynamic, if it follows the statistical behavior of the system (Birkhoff’s pointwise ergodic theorem). We prove that a point is Schnorr random if and only if it is typical for every mixing computable dynamics. To prove the result we develop some tools for the theory of computable probability spaces (for example, morphisms) that are expected to have other applications.}, author = {PETER, GACS and HOYRUP, MATHIEU and CRISTOBAL, ROJAS}, file = {:home/gus/Documents/Mendeley Desktop/PETER, HOYRUP, CRISTOBAL\_1991\_Randomness on computable probability spaces—a dynamical point of view.pdf:pdf}, journal = {Theory of Computing Systems}, keywords = {Birkhoff’s ergodic theorem,Computability,Schnorr Randomness,computable measures}, mendeley-tags = {Computability}, pages = {1--18}, title = {{Randomness on computable probability spaces—a dynamical point of view}}, url = {http://www.springerlink.com/index/3q774874623m0nm6.pdf}, year = {1991} } @article{Ding2012, author = {Ding, Li and Ley, Timothy J. and Larson, David E. and Miller, Christopher A. and Koboldt, Daniel C. and Welch, John S. and Ritchey, Julie K. and Young, Margaret A. and Lamprecht, Tamara and McLellan, Michael D. and McMichael, Joshua F. and Wallis, John W. and Lu, Charles and Shen, Dong and Harris, Christopher C. and Dooling, David J. and Fulton, Robert S. and Fulton, Lucinda L. and Chen, Ken and Schmidt, Heather and Kalicki-Veizer, Joelle and Magrini, Vincent J. and Cook, Lisa and McGrath, Sean D. and Vickery, Tammi L. and Wendl, Michael C. and Heath, Sharon and Watson, Mark A. and Link, Daniel C. and Tomasson, Michael H. and Shannon, William D. and Payton, Jacqueline E. and Kulkarni, Shashikant and Westervelt, Peter and Walter, Matthew J. and Graubert, Timothy A. and Mardis, Elaine R. and Wilson, Richard K. and DiPersio, John F.}, doi = {10.1038/nature10738}, file = {:home/gus/Documents/Mendeley Desktop/Ding et al.\_2012\_Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing(2).pdf:pdf;:home/gus/Documents/Mendeley Desktop/Ding et al.\_2012\_Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing.pdf:pdf}, issn = {0028-0836}, journal = {Nature}, month = jan, number = {7382}, pages = {506--510}, publisher = {Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.}, shorttitle = {Nature}, title = {{Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing}}, url = {http://dx.doi.org/10.1038/nature10738}, volume = {481}, year = {2012} } @article{Jaffe2003, abstract = {We previously described the whole-genome assembly program Arachne, presenting assemblies of simulated data for small to mid-sized genomes. Here we describe algorithmic adaptations to the program, allowing for assembly of mammalian-size genomes, and also improving the assembly of smaller genomes. Three principal changes were simultaneously made and applied to the assembly of the mouse genome, during a six-month period of development: (1) Supercontigs (scaffolds) were iteratively broken and rejoined using several criteria, yielding a 64-fold increase in length (N50), and apparent elimination of all global misjoins; (2) gaps between contigs in supercontigs were filled (partially or completely) by insertion of reads, as suggested by pairing within the supercontig, increasing the N50 contig length by 50\%; (3) memory usage was reduced fourfold. The outcome of this mouse assembly and its analysis are described in (Mouse Genome Sequencing Consortium 2002).}, author = {Jaffe, David B and Butler, Jonathan and Gnerre, Sante and Mauceli, Evan and Lindblad-Toh, Kerstin and Mesirov, Jill P and Zody, Michael C and Lander, Eric S}, doi = {10.1101/gr.828403}, file = {:home/gus/Documents/Mendeley Desktop/Jaffe et al.\_2003\_Whole-genome sequence assembly for mammalian genomes Arachne 2.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Animals,Computational Biology,Computational Biology: methods,Contig Mapping,Contig Mapping: methods,Genome,Humans,Mice,Software}, month = jan, number = {1}, pages = {91--6}, pmid = {12529310}, title = {{Whole-genome sequence assembly for mammalian genomes: Arachne 2.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=430950\&tool=pmcentrez\&rendertype=abstract}, volume = {13}, year = {2003} } @article{Koren2007, abstract = {Protein-protein interaction (PPI) networks have become prevalent recently as high-throughput experiment data has become available. Many network growth models have been proposed to reproduce the properties of the networks. We present a stochastic sampling method for capturing network topology properties and use it to infer the model that best matches the observed topology. We apply the method to three real networks, Caenorhabditis elegans, Drosophila melanogaster, and Saccharomyces cerevisiae. We show that using the current protein-interaction networks, the models are not consistent across organisms.}, author = {Koren, Sergey and Mar\c{c}ais, Guillaume}, file = {:home/gus/Documents/Mendeley Desktop/Koren, Mar\c{c}ais\_2007\_Network Comparison Using Stochastic Sampling and its Applications.pdf:pdf}, keywords = {PPI,Random walks}, pages = {1--8}, title = {{Network Comparison Using Stochastic Sampling and its Applications}}, year = {2007} } @article{Peterlongo2011, abstract = {Background: The analysis of next-generation sequencing data from large genomes is a timely research topic. Sequencers are producing billions of short sequence fragments from newly sequenced organisms. Computational methods for reconstructing sequences (whole-genome assemblers) are typically employed to process such data. However, one of the main drawback of these methods is the high memory requirement. Results: We present Mapsembler, an iterative targeted assembler which processes large datasets of reads on commodity hardware. Mapsembler checks for the presence of given regions of interest in the reads and reconstructs their neighborhood, either as a plain sequence (consensus) or as a graph (full sequence structure). We introduce new algorithms to retrieve homologues of a sequence from reads and construct an extension graph. Conclusions: Mapsembler is the rst software that enables de novo discovery around a region of interest of gene homologues, SNPs, exon skipping as well as other structural events, directly from raw sequencing reads. Compared to traditional assembly software, memory requirement and execution time of Mapsembler are considerably lower, as data indexing is localized. Mapsembler can be used at http://mapsembler.genouest.org}, author = {Peterlongo, Pierre and Chikhi, Rayan}, file = {:home/gus/Documents/Mendeley Desktop/Peterlongo, Chikhi\_2011\_Mapsembler, targeted assembly of larges genomes on a desktop computer.pdf:pdf}, keywords = {NGS,algorithms,bioinformatics,genome,light memory usage,targeted assembly}, month = mar, title = {{Mapsembler, targeted assembly of larges genomes on a desktop computer}}, url = {http://hal.inria.fr/inria-00577218/ http://hal.inria.fr/docs/00/57/72/18/PDF/RR-7565.pdf}, year = {2011} } @article{Nagaraj2007, abstract = {Expressed sequence tag (EST) sequencing projects are underway for numerous organisms, generating millions of short, single-pass nucleotide sequence reads, accumulating in EST databases. Extensive computational strategies have been developed to organize and analyse both small- and large-scale EST data for gene discovery, transcript and single nucleotide polymorphism analysis as well as functional annotation of putative gene products. We provide an overview of the significance of ESTs in the genomic era, their properties and the applications of ESTs. Methods adopted for each step of EST analysis by various research groups have been compared. Challenges that lie ahead in organizing and analysing the ever increasing EST data have also been identified. The most appropriate software tools for EST pre-processing, clustering and assembly, database matching and functional annotation have been compiled (available online from http://biolinfo.org/EST). We propose a road map for EST analysis to accelerate the effective analyses of EST data sets. An investigation of EST analysis platforms reveals that they all terminate prior to downstream functional annotation including gene ontologies, motif/pattern analysis and pathway mapping.}, author = {Nagaraj, Shivashankar H and Gasser, Robin B and Ranganathan, Shoba}, doi = {10.1093/bib/bbl015}, file = {:home/gus/Documents/Mendeley Desktop/Nagaraj, Gasser, Ranganathan\_2007\_A hitchhiker's guide to expressed sequence tag (EST) analysis.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Nagaraj, Gasser, Ranganathan\_2007\_A hitchhiker's guide to expressed sequence tag (EST) analysis(2).pdf:pdf}, issn = {1467-5463}, journal = {Briefings in bioinformatics}, keywords = {Animals,Complementary,Complementary: chemistry,Consensus Sequence,Consensus Sequence: genetics,DNA,Databases,Expressed Sequence Tags,Genetic,Genetic: standards,Genomics,Genomics: methods,Humans,Nucleic Acid,Nucleic Acid: standards,RNA,Software,Untranslated Regions,Untranslated Regions: chemistry}, mendeley-tags = {RNA}, month = jan, number = {1}, pages = {6--21}, pmid = {16772268}, title = {{A hitchhiker's guide to expressed sequence tag (EST) analysis.}}, url = {http://bib.oxfordjournals.org/cgi/content/abstract/8/1/6}, volume = {8}, year = {2007} } @article{Maccallum:2009vn, abstract = {We demonstrate that genome sequences approaching finished quality can be generated from short paired reads. Using 36 base (fragment) and 26 base (jumping) reads from five microbial genomes of varied GC composition and sizes up to 40 Mb, ALLPATHS2 generated assemblies with long, accurate contigs and scaffolds. Velvet and EULER-SR were less accurate. For example, for Escherichia coli, the fraction of 10-kb stretches that were perfect was 99.8\% (ALLPATHS2), 68.7\% (Velvet), and 42.1\% (EULER-SR).}, author = {Maccallum, Iain and Przybylski, Dariusz and Gnerre, Sante and Burton, Joshua and Shlyakhter, Ilya and Gnirke, Andreas and Malek, Joel and McKernan, Kevin and Ranade, Swati and Shea, Terrance P and Williams, Louise and Young, Sarah and Nusbaum, Chad and Jaffe, David B}, doi = {10.1186/gb-2009-10-10-r103}, file = {:home/gus/Documents/Mendeley Desktop//Maccallum et al.\_2009\_ALLPATHS 2 small genomes assembled accurately and with high continuity from short paired reads.pdf:pdf}, journal = {Genome Biol}, number = {10}, pages = {R103}, pmid = {19796385}, title = {{ALLPATHS 2: small genomes assembled accurately and with high continuity from short paired reads}}, volume = {10}, year = {2009} } @article{Yang2011, abstract = {High-throughput short read sequencing is revolutionizing genomics and systems biology research by enabling cost-effective deep coverage sequencing of genomes and transcriptomes. Error detection and correction are crucial to many short read sequencing applications including de novo genome sequencing, genome resequencing, and digital gene expression analysis. Short read error detection is typically carried out by counting the observed frequencies of kmers in reads and validating those with frequencies exceeding a threshold. In case of genomes with high repeat content, an erroneous kmer may be frequently observed if it has few nucleotide differences with valid kmers with multiple occurrences in the genome. Error detection and correction were mostly applied to genomes with low repeat content and this remains a challenging problem for genomes with high repeat content.}, author = {Yang, Xiao and Aluru, Srinivas and Dorman, Karin S}, doi = {10.1186/1471-2105-12-S1-S52}, file = {:home/gus/Documents/Mendeley Desktop//Yang, Aluru, Dorman\_2011\_Repeat-aware modeling and correction of short read errors.pdf:pdf}, issn = {1471-2105}, journal = {BMC bioinformatics}, keywords = {Algorithms,Computational Biology,Computational Biology: methods,Genomics,Genomics: methods,High-Throughput Nucleotide Sequencing,High-Throughput Nucleotide Sequencing: methods,Likelihood Functions,Models,Software,Statistical}, month = jan, number = {Suppl 1}, pages = {S52}, pmid = {21342585}, title = {{Repeat-aware modeling and correction of short read errors.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3044310\&tool=pmcentrez\&rendertype=abstract http://www.biomedcentral.com/1471-2105/12/S1/S52}, volume = {12 Suppl 1}, year = {2011} } @incollection{springerlink:10.1007/978-3-642-23038-7_21, annote = {10.1007/978-3-642-23038-7\_21}, author = {Patro, Rob and Sefer, Emre and Malin, Justin and Mar\c{c}ais, Guillaume and Navlakha, Saket and Kingsford, Carl}, booktitle = {Algorithms in Bioinformatics}, editor = {Przytycka, Teresa and Sagot, Marie-France}, file = {:home/gus/Documents/Mendeley Desktop/Patro et al.\_2011\_Parsimonious Reconstruction of Network Evolution.pdf:pdf}, isbn = {978-3-642-23037-0}, pages = {237--249}, publisher = {Springer Berlin / Heidelberg}, series = {Lecture Notes in Computer Science}, title = {{Parsimonious Reconstruction of Network Evolution}}, url = {http://dx.doi.org/10.1007/978-3-642-23038-7\_21}, volume = {6833}, year = {2011} } @article{Rumble2009, abstract = {The development of Next Generation Sequencing technologies, capable of sequencing hundreds of millions of short reads (25-70 bp each) in a single run, is opening the door to population genomic studies of non-model species. In this paper we present SHRiMP - the SHort Read Mapping Package: a set of algorithms and methods to map short reads to a genome, even in the presence of a large amount of polymorphism. Our method is based upon a fast read mapping technique, separate thorough alignment methods for regular letter-space as well as AB SOLiD (color-space) reads, and a statistical model for false positive hits. We use SHRiMP to map reads from a newly sequenced Ciona savignyi individual to the reference genome. We demonstrate that SHRiMP can accurately map reads to this highly polymorphic genome, while confirming high heterozygosity of C. savignyi in this second individual. SHRiMP is freely available at http://compbio.cs.toronto.edu/shrimp.}, author = {Rumble, Stephen M and Lacroute, Phil and Dalca, Adrian V and Fiume, Marc and Sidow, Arend and Brudno, Michael}, doi = {10.1371/journal.pcbi.1000386}, file = {:home/gus/Documents/Mendeley Desktop/Rumble et al.\_2009\_SHRiMP accurate mapping of short color-space reads.pdf:pdf}, issn = {1553-7358}, journal = {PLoS computational biology}, keywords = {Algorithms,Animals,Chromosome Mapping,Chromosome Mapping: methods,Computer Simulation,Models, Statistical,Reproducibility of Results,Sequence Alignment,Sequence Alignment: methods,Sequence Analysis, DNA,Sequence Analysis, DNA: methods,Software,Urochordata,Urochordata: genetics}, month = may, number = {5}, pages = {e1000386}, pmid = {19461883}, title = {{SHRiMP: accurate mapping of short color-space reads.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2678294\&tool=pmcentrez\&rendertype=abstract}, volume = {5}, year = {2009} } @article{Simpson2010, abstract = {MOTIVATION: Sequence assembly is a difficult problem whose importance has grown again recently as the cost of sequencing has dramatically dropped. Most new sequence assembly software has started by building a de Bruijn graph, avoiding the overlap-based methods used previously because of the computational cost and complexity of these with very large numbers of short reads. Here, we show how to use suffix array-based methods that have formed the basis of recent very fast sequence mapping algorithms to find overlaps and generate assembly string graphs asymptotically faster than previously described algorithms. RESULTS: Standard overlap assembly methods have time complexity O(N(2)), where N is the sum of the lengths of the reads. We use the Ferragina-Manzini index (FM-index) derived from the Burrows-Wheeler transform to find overlaps of length at least tau among a set of reads. As well as an approach that finds all overlaps then implements transitive reduction to produce a string graph, we show how to output directly only the irreducible overlaps, significantly shrinking memory requirements and reducing compute time to O(N), independent of depth. Overlap-based assembly methods naturally handle mixed length read sets, including capillary reads or long reads promised by the third generation sequencing technologies. The algorithms we present here pave the way for overlap-based assembly approaches to be developed that scale to whole vertebrate genome de novo assembly.}, author = {Simpson, Jared T and Durbin, Richard}, doi = {10.1093/bioinformatics/btq217}, file = {:home/gus/Documents/Mendeley Desktop/Simpson, Durbin\_2010\_Efficient construction of an assembly string graph using the FM-index.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,Genomics,Genomics: methods,Sequence Analysis, DNA,Sequence Analysis, DNA: methods,Software}, month = jun, number = {12}, pages = {i367--73}, pmid = {20529929}, title = {{Efficient construction of an assembly string graph using the FM-index.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/26/12/i367}, volume = {26}, year = {2010} } @article{Kashtan2005, abstract = {Biological networks have an inherent simplicity: they are modular with a design that can be separated into units that perform almost independently. Furthermore, they show reuse of recurring patterns termed network motifs. Little is known about the evolutionary origin of these properties. Current models of biological evolution typically produce networks that are highly nonmodular and lack understandable motifs. Here, we suggest a possible explanation for the origin of modularity and network motifs in biology. We use standard evolutionary algorithms to evolve networks. A key feature in this study is evolution under an environment (evolutionary goal) that changes in a modular fashion. That is, we repeatedly switch between several goals, each made of a different combination of subgoals. We find that such "modularly varying goals" lead to the spontaneous evolution of modular network structure and network motifs. The resulting networks rapidly evolve to satisfy each of the different goals. Such switching between related goals may represent biological evolution in a changing environment that requires different combinations of a set of basic biological functions. The present study may shed light on the evolutionary forces that promote structural simplicity in biological networks and offers ways to improve the evolutionary design of engineered systems.}, author = {Kashtan, Nadav and Alon, Uri}, doi = {10.1073/pnas.0503610102}, file = {:home/gus/Documents/Mendeley Desktop/Kashtan, Alon\_2005\_Spontaneous evolution of modularity and network motifs.pdf:pdf}, issn = {0027-8424}, journal = {Proceedings of the National Academy of Sciences of the United States of America}, keywords = {Algorithms,Biological Evolution,Computer Simulation,Neural Networks (Computer)}, month = sep, number = {39}, pages = {13773--8}, pmid = {16174729}, title = {{Spontaneous evolution of modularity and network motifs.}}, url = {http://www.pnas.org/cgi/content/abstract/102/39/13773}, volume = {102}, year = {2005} } @article{Li2011, author = {Li, Yingrui and Zheng, Hancheng and Luo, Ruibang and Wu, Honglong and Zhu, Hongmei and Li, Ruiqiang and Cao, Hongzhi and Wu, Boxin and Huang, Shujia and Shao, Haojing and Ma, Hanzhou and Zhang, Fan and Feng, Shuijian and Zhang, Wei and Du, Hongli and Tian, Geng and Li, Jingxiang and Zhang, Xiuqing and Li, Songgang and Bolund, Lars and Kristiansen, Karsten and de Smith, Adam J and Blakemore, Alexandra I F and Coin, Lachlan J M and Yang, Huanming and Wang, Jian and Wang, Jun}, doi = {10.1038/nbt.1904}, file = {:home/gus/Documents/Mendeley Desktop/Li et al.\_2011\_Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly.pdf:pdf}, issn = {1087-0156}, journal = {Nature Biotechnology}, month = jul, number = {8}, pages = {723--730}, publisher = {Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.}, shorttitle = {Nat Biotech}, title = {{Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly}}, url = {http://dx.doi.org/10.1038/nbt.1904}, volume = {29}, year = {2011} } @article{Gnerre:2011zr, abstract = {Massively parallel DNA sequencing technologies are revolutionizing genomics by making it possible to generate billions of relatively short (\~{}100-base) sequence reads at very low cost. Whereas such data can be readily used for a wide range of biomedical applications, it has proven difficult to use them to generate high-quality de novo genome assemblies of large, repeat-rich vertebrate genomes. To date, the genome assemblies generated from such data have fallen far short of those obtained with the older (but much more expensive) capillary-based sequencing approach. Here, we report the development of an algorithm for genome assembly, ALLPATHS-LG, and its application to massively parallel DNA sequence data from the human and mouse genomes, generated on the Illumina platform. The resulting draft genome assemblies have good accuracy, short-range contiguity, long-range connectivity, and coverage of the genome. In particular, the base accuracy is high (≥99.95\%) and the scaffold sizes (N50 size = 11.5 Mb for human and 7.2 Mb for mouse) approach those obtained with capillary-based sequencing. The combination of improved sequencing technology and improved computational methods should now make it possible to increase dramatically the de novo sequencing of large genomes. The ALLPATHS-LG program is available at http://www.broadinstitute.org/science/programs/genome-biology/crd.}, annote = { From Duplicate 2 ( High-quality draft assemblies of mammalian genomes from massively parallel sequence data - Gnerre, Sante; Maccallum, Iain; Przybylski, Dariusz; Ribeiro, Filipe J; Burton, Joshua N; Walker, Bruce J; Sharpe, Ted; Hall, Giles; Shea, Terrance P; Sykes, Sean; Berlin, Aaron M; Aird, Daniel; Costello, Maura; Daza, Riza; Williams, Louise; Nicol, Robert; Gnirke, Andreas; Nusbaum, Chad; Lander, Eric S; Jaffe, David B ) }, author = {Gnerre, Sante and Maccallum, Iain and Przybylski, Dariusz and Ribeiro, Filipe J and Burton, Joshua N and Walker, Bruce J and Sharpe, Ted and Hall, Giles and Shea, Terrance P and Sykes, Sean and Berlin, Aaron M and Aird, Daniel and Costello, Maura and Daza, Riza and Williams, Louise and Nicol, Robert and Gnirke, Andreas and Nusbaum, Chad and Lander, Eric S and Jaffe, David B}, doi = {10.1073/pnas.1017351108}, file = {:home/gus/Documents/Mendeley Desktop/Gnerre et al.\_2011\_High-quality draft assemblies of mammalian genomes from massively parallel sequence data.pdf:pdf}, issn = {1091-6490}, journal = {Proc Natl Acad Sci U S A}, keywords = {Algorithms,Animals,DNA,DNA: methods,Genome,Genome: genetics,Genomics,Genomics: methods,Humans,Internet,Mice,Reproducibility of Results,Sequence Analysis,Software}, month = jan, number = {4}, pages = {1513--1518}, pmid = {21187386}, title = {{High-quality draft assemblies of mammalian genomes from massively parallel sequence data}}, url = {http://www.pnas.org/cgi/content/abstract/108/4/1513}, volume = {108}, year = {2011} } @article{Chaisson2009, abstract = {Increasing read length is currently viewed as the crucial condition for fragment assembly with next-generation sequencing technologies. However, introducing mate-paired reads (separated by a gap of length, GapLength) opens a possibility to transform short mate-pairs into long mate-reads of length approximately GapLength, and thus raises the question as to whether the read length (as opposed to GapLength) even matters. We describe a new tool, EULER-USR, for assembling mate-paired short reads and use it to analyze the question of whether the read length matters. We further complement the ongoing experimental efforts to maximize read length by a new computational approach for increasing the effective read length. While the common practice is to trim the error-prone tails of the reads, we present an approach that substitutes trimming with error correction using repeat graphs. An important and counterintuitive implication of this result is that one may extend sequencing reactions that degrade with length "past their prime" to where the error rate grows above what is normally acceptable for fragment assembly.}, author = {Chaisson, Mark J and Brinza, Dumitru and Pevzner, Pavel A}, doi = {10.1101/gr.079053.108}, file = {:home/gus/Documents/Mendeley Desktop/Chaisson, Brinza, Pevzner\_2009\_De novo fragment assembly with short mate-paired reads Does the read length matter.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Bacterial,Base Pairing,Base Pairing: physiology,Base Sequence,Base Sequence: physiology,Bias (Epidemiology),Biological,Chromosome Mapping,Chromosome Mapping: methods,Computational Biology,Computational Biology: methods,DNA,DNA: methods,Escherichia coli,Escherichia coli: genetics,Genetic Markers,Genome,Models,Sequence Alignment,Sequence Alignment: methods,Sequence Analysis}, month = feb, number = {2}, pages = {336--46}, pmid = {19056694}, title = {{De novo fragment assembly with short mate-paired reads: Does the read length matter?}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2652199\&tool=pmcentrez\&rendertype=abstract}, volume = {19}, year = {2009} } @article{Maccallum:2009vn, abstract = {We demonstrate that genome sequences approaching finished quality can be generated from short paired reads. Using 36 base (fragment) and 26 base (jumping) reads from five microbial genomes of varied GC composition and sizes up to 40 Mb, ALLPATHS2 generated assemblies with long, accurate contigs and scaffolds. Velvet and EULER-SR were less accurate. For example, for Escherichia coli, the fraction of 10-kb stretches that were perfect was 99.8\% (ALLPATHS2), 68.7\% (Velvet), and 42.1\% (EULER-SR).}, author = {Maccallum, Iain and Przybylski, Dariusz and Gnerre, Sante and Burton, Joshua and Shlyakhter, Ilya and Gnirke, Andreas and Malek, Joel and McKernan, Kevin and Ranade, Swati and Shea, Terrance P and Williams, Louise and Young, Sarah and Nusbaum, Chad and Jaffe, David B}, doi = {10.1186/gb-2009-10-10-r103}, file = {:home/gus/Documents/Mendeley Desktop//Maccallum et al.\_2009\_ALLPATHS 2 small genomes assembled accurately and with high continuity from short paired reads.pdf:pdf}, issn = {1465-6914}, journal = {Genome biology}, keywords = {Bacteria,Bacteria: genetics,Base Pairing,Base Pairing: genetics,Fungi,Fungi: genetics,Genome,Genome: genetics,Genomics,Genomics: methods,Reproducibility of Results,Software}, month = jan, number = {10}, pages = {R103}, pmid = {19796385}, title = {{ALLPATHS 2: small genomes assembled accurately and with high continuity from short paired reads.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2784318\&tool=pmcentrez\&rendertype=abstract}, volume = {10}, year = {2009} } @article{Ilie2011, abstract = {High-throughput sequencing technologies produce very large amounts of data and sequencing errors constitute one of the major problems in analyzing such data. Current algorithms for correcting these errors are not very accurate and do not automatically adapt to the given data.}, author = {Ilie, Lucian and Fazayeli, Farideh and Ilie, Silvana}, institution = {Department of Computer Science, University of Western Ontario, London, ON N6A 5B7, Canada. ilie@csd.uwo.ca}, journal = {Bioinformatics}, number = {3}, pages = {295--302}, pmid = {21115437}, title = {{HiTEC: accurate error correction in high-throughput sequencing data.}}, url = {http://www.ncbi.nlm.nih.gov/pubmed/21115437}, volume = {27}, year = {2011} } @article{Butler:2008kx, abstract = {New DNA sequencing technologies deliver data at dramatically lower costs but demand new analytical methods to take full advantage of the very short reads that they produce. We provide an initial, theoretical solution to the challenge of de novo assembly from whole-genome shotgun "microreads." For 11 genomes of sizes up to 39 Mb, we generated high-quality assemblies from 80x coverage by paired 30-base simulated reads modeled after real Illumina-Solexa reads. The bacterial genomes of Campylobacter jejuni and Escherichia coli assemble optimally, yielding single perfect contigs, and larger genomes yield assemblies that are highly connected and accurate. Assemblies are presented in a graph form that retains intrinsic ambiguities such as those arising from polymorphism, thereby providing information that has been absent from previous genome assemblies. For both C. jejuni and E. coli, this assembly graph is a single edge encompassing the entire genome. Larger genomes produce more complicated graphs, but the vast majority of the bases in their assemblies are present in long edges that are nearly always perfect. We describe a general method for genome assembly that can be applied to all types of DNA sequence data, not only short read data, but also conventional sequence reads.}, author = {Butler, Jonathan and MacCallum, Iain and Kleber, Michael and Shlyakhter, Ilya a and Belmonte, Matthew K and Lander, Eric S and Nusbaum, Chad and Jaffe, David B}, doi = {10.1101/gr.7337908}, file = {:home/gus/Documents/Mendeley Desktop/Butler et al.\_2008\_ALLPATHS de novo assembly of whole-genome shotgun microreads.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Bacterial,Bacterial: genetics,Campylobacter jejuni,Campylobacter jejuni: genetics,Computational Biology,Computational Biology: methods,Computer Simulation,DNA,DNA: methods,DNA: standards,Escherichia coli,Escherichia coli: genetics,Genome,Reproducibility of Results,Sequence Analysis}, month = may, number = {5}, pages = {810--20}, pmid = {18340039}, title = {{ALLPATHS: de novo assembly of whole-genome shotgun microreads.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2336810\&tool=pmcentrez\&rendertype=abstract}, volume = {18}, year = {2008} } @incollection{CLR, author = {Cormen, T. and Leiserson, C. and Rivest, R.}, chapter = {12}, publisher = {MIT Press}, title = {{Introduction to Algorithms}}, year = {1990} } @article{Gilchrist2007, author = {Gilchrist, Jeff}, doi = {10.1109/AINA.2007.109}, file = {:home/gus/Documents/Mendeley Desktop/Gilchrist\_2007\_Parallel lossless data compression based on the burrows-wheeler transform.pdf:pdf}, isbn = {0-7695-2846-5}, issn = {1550-445X}, journal = {21st International Conference on Advanced Networking and Applications (AINA '07)}, month = may, pages = {877--884}, publisher = {Ieee}, title = {{Parallel lossless data compression based on the burrows-wheeler transform}}, url = {http://ieeexplore.ieee.org/lpdocs/epic03/wrapper.htm?arnumber=4220984 http://www.computer.org/portal/web/csdl/doi/10.1109/AINA.2007.109}, year = {2007} } @article{Baker2012, author = {Baker, Monya}, doi = {10.1038/nmeth.1858}, file = {:home/gus/Documents/Mendeley Desktop/Baker\_2012\_Structural variation the genome's hidden architecture.pdf:pdf}, issn = {1548-7091}, journal = {Nature Methods}, month = jan, number = {2}, pages = {133--137}, publisher = {Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.}, shorttitle = {Nat Meth}, title = {{Structural variation: the genome's hidden architecture}}, url = {http://dx.doi.org/10.1038/nmeth.1858}, volume = {9}, year = {2012} } @article{Huttenhower2006, abstract = {MOTIVATION: The diverse microarray datasets that have become available over the past several years represent a rich opportunity and challenge for biological data mining. Many supervised and unsupervised methods have been developed for the analysis of individual microarray datasets. However, integrated analysis of multiple datasets can provide a broader insight into genetic regulation of specific biological pathways under a variety of conditions. RESULTS: To aid in the analysis of such large compendia of microarray experiments, we present Microarray Experiment Functional Integration Technology (MEFIT), a scalable Bayesian framework for predicting functional relationships from integrated microarray datasets. Furthermore, MEFIT predicts these functional relationships within the context of specific biological processes. All results are provided in the context of one or more specific biological functions, which can be provided by a biologist or drawn automatically from catalogs such as the Gene Ontology (GO). Using MEFIT, we integrated 40 Saccharomyces cerevisiae microarray datasets spanning 712 unique conditions. In tests based on 110 biological functions drawn from the GO biological process ontology, MEFIT provided a 5\% or greater performance increase for 54 functions, with a 5\% or more decrease in performance in only two functions.}, annote = {MEFIT. Better correlation / aggregation for micro-array data.}, author = {Huttenhower, Curtis and Hibbs, Matt and Myers, Chad and Troyanskaya, Olga G}, doi = {10.1093/bioinformatics/btl492}, file = {:home/gus/Documents/Mendeley Desktop/Huttenhower et al.\_2006\_A scalable method for integration and functional analysis of multiple microarray datasets.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,Bayes Theorem,Databases, Genetic,Gene Expression Profiling,Gene Expression Profiling: methods,Information Storage and Retrieval,Information Storage and Retrieval: methods,Saccharomyces cerevisiae,Saccharomyces cerevisiae Proteins,Saccharomyces cerevisiae Proteins: metabolism,Saccharomyces cerevisiae: metabolism,Systems Integration}, month = dec, number = {23}, pages = {2890--7}, pmid = {17005538}, title = {{A scalable method for integration and functional analysis of multiple microarray datasets.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/22/23/2890}, volume = {22}, year = {2006} } @article{Melsted2011, abstract = {BACKGROUND:Counting k-mers (substrings of length k in DNA sequence data) is an essential component of many methods in bioinformatics, including for genome and transcriptome assembly, for metagenomic sequencing, and for error correction of sequence reads. Although simple in principle, counting k-mers in large modern sequence data sets can easily overwhelm the memory capacity of standard computers. In current data sets, a large fraction - often more than 50\% - of the storage capacity may be spent on storing k-mers that contain sequencing errors and which are typically observed only a single time in the data. These singleton k-mers are uninformative for many algorithms without some kind of error correction.RESULTS:We present a new method that identifies all the k-mers that occur more than once in a DNA sequence data set. Our method does this using a Bloom filter, a probabilistic data structure that stores all the observed k-mers implicitly in memory with greatly reduced memory requirements. We then make a second sweep through the data to provide exact counts of all nonunique k-mers. For example data sets, we report up to 50\% savings in memory usage compared to current software, with modest costs in computational speed. This approach may reduce memory requirements for any algorithm that starts by counting k-mers in sequence data with errors.CONCLUSIONS:A reference implementation for this methodology, BFCounter, is written in C++ and is GPL licensed. It is available for free download at http://pritch.bsd.uchicago.edu/software.html}, author = {Melsted, Pall and Pritchard, Jonathan K}, doi = {10.1186/1471-2105-12-333}, file = {:home/gus/Documents/Mendeley Desktop/Melsted, Pritchard\_2011\_Efficient counting of k-mers in DNA sequences using a Bloom Filter.pdf:pdf}, issn = {1471-2105}, journal = {BMC Bioinformatics}, number = {1}, pages = {333}, title = {{Efficient counting of k-mers in DNA sequences using a Bloom Filter}}, url = {http://www.biomedcentral.com/1471-2105/12/333}, volume = {12}, year = {2011} } @article{salmela2011correcting, author = {Salmela, L. and Schr\"{o}der, J.}, file = {:home/gus/Documents/Mendeley Desktop/Salmela, Schr\"{o}der\_2011\_Correcting errors in short reads by multiple alignments.pdf:pdf}, journal = {Bioinformatics}, number = {11}, pages = {1455}, publisher = {Oxford Univ Press}, title = {{Correcting errors in short reads by multiple alignments}}, url = {http://bioinformatics.oxfordjournals.org/content/27/11/1455.short}, volume = {27}, year = {2011} } @article{Rhrissorrakrai2011a, abstract = {ABSTRACT: BACKGROUND: Graphical models of network associations are useful for both visualizing and integrating multiple types of association data. Identifying modules, or groups of functionally related gene products, is an important challenge in analyzing biological networks. However, existing tools to identify modules are insufficient when applied to dense networks of experimentally derived interaction data. To address this problem, we have developed an agglomerative clustering method that is able to identify highly modular sets of gene products within highly interconnected molecular interaction networks. RESULTS: MINE outperforms MCODE, CFinder, NEMO, SPICi, and MCL in identifying non-exclusive, high modularity clusters when applied to the C. elegans protein-protein interaction network. The algorithm generally achieves superior geometric accuracy and modularity for annotated functional categories. In comparison with the most closely related algorithm, MCODE, the top clusters identified by MINE are consistently of higher density and MINE is less likely to designate overlapping modules as a single unit. MINE offers a high level of granularity with a small number of adjustable parameters, enabling users to fine-tune cluster results for input networks with differing topological properties. CONCLUSIONS: MINE was created in response to the challenge of discovering high quality modules of gene products within highly interconnected biological networks. The algorithm allows a high degree of flexibility and user-customisation of results with few adjustable parameters. MINE outperforms several popular clustering algorithms in identifying modules with high modularity and obtains good overall recall and precision of functional annotations in protein-protein interaction networks from both S. cerevisiae and C. elegans.}, author = {Rhrissorrakrai, Kahn and Gunsalus, Kristin C}, doi = {10.1186/1471-2105-12-192}, file = {:home/gus/Documents/Mendeley Desktop/Rhrissorrakrai, Gunsalus\_2011\_MINE Module Identification in NEtworks.pdf:pdf}, issn = {1471-2105}, journal = {BMC bioinformatics}, month = may, number = {1}, pages = {192}, pmid = {21605434}, title = {{MINE: Module Identification in NEtworks.}}, url = {http://www.biomedcentral.com/1471-2105/12/192}, volume = {12}, year = {2011} } @article{Navlakha2011, abstract = {What proteins interacted in a long-extinct ancestor of yeast? How have different members of a protein complex assembled together over time? Our ability to answer such questions has been limited by the unavailability of ancestral protein-protein interaction (PPI) networks. To overcome this limitation, we propose several novel algorithms to reconstruct the growth history of a present-day network. Our likelihood-based method finds a probable previous state of the graph by applying an assumed growth model backwards in time. This approach retains node identities so that the history of individual nodes can be tracked. Using this methodology, we estimate protein ages in the yeast PPI network that are in good agreement with sequence-based estimates of age and with structural features of protein complexes. Further, by comparing the quality of the inferred histories for several different growth models (duplication-mutation with complementarity, forest fire, and preferential attachment), we provide additional evidence that a duplication-based model captures many features of PPI network growth better than models designed to mimic social network growth. From the reconstructed history, we model the arrival time of extant and ancestral interactions and predict that complexes have significantly re-wired over time and that new edges tend to form within existing complexes. We also hypothesize a distribution of per-protein duplication rates, track the change of the network's clustering coefficient, and predict paralogous relationships between extant proteins that are likely to be complementary to the relationships inferred using sequence alone. Finally, we infer plausible parameters for the model, thereby predicting the relative probability of various evolutionary events. The success of these algorithms indicates that parts of the history of the yeast PPI are encoded in its present-day form.}, author = {Navlakha, Saket and Kingsford, Carl}, doi = {10.1371/journal.pcbi.1001119}, editor = {Bader, Joel S.}, file = {:home/gus/Documents/Mendeley Desktop/Navlakha, Kingsford\_2011\_Network archaeology uncovering ancient networks from present-day interactions.pdf:pdf}, issn = {1553-7358}, journal = {PLoS computational biology}, keywords = {Computational Biology/Systems Biology,Computer Science,Molecular Biology/Bioinformatics,Research Article}, month = apr, number = {4}, pages = {e1001119}, pmid = {21533211}, publisher = {Public Library of Science}, title = {{Network archaeology: uncovering ancient networks from present-day interactions.}}, url = {http://dx.plos.org/10.1371/journal.pcbi.1001119}, volume = {7}, year = {2011} } @article{Goya2010, abstract = {Motivation: Next-generation sequencing (NGS) has enabled whole genome and transcriptome single nucleotide variant (SNV) discovery in cancer. NGS produces millions of short sequence reads that, once aligned to a reference genome sequence, can be interpreted for the presence of SNVs. Although tools exist for SNV discovery from NGS data, none are specifically suited to work with data from tumors, where altered ploidy and tumor cellularity impact the statistical expectations of SNV discovery. Results: We developed three implementations of a probabilistic Binomial mixture model, called SNVMix, designed to infer SNVs from NGS data from tumors to address this problem. The first models allelic counts as observations and infers SNVs and model parameters using an expectation maximization (EM) algorithm and is therefore capable of adjusting to deviation of allelic frequencies inherent in genomically unstable tumor genomes. The second models nucleotide and mapping qualities of the reads by probabilistically weighting the contribution of a read/nucleotide to the inference of a SNV based on the confidence we have in the base call and the read alignment. The third combines filtering out low-quality data in addition to probabilistic weighting of the qualities. We quantitatively evaluated these approaches on 16 ovarian cancer RNASeq datasets with matched genotyping arrays and a human breast cancer genome sequenced to >40 (haploid) coverage with ground truth data and show systematically that the SNVMix models outperform competing approaches. Availability: Software and data are available at http://compbio.bccrc.ca Contact: sshahbccrc.ca Supplemantary information: Supplementary data are available at Bioinformatics online.}, author = {Goya, Rodrigo and Sun, Mark G F and Morin, Ryan D and Leung, Gillian and Ha, Gavin and Wiegand, Kimberley C and Senz, Janine and Crisan, Anamaria and Marra, Marco A and Hirst, Martin and Huntsman, David and Murphy, Kevin P and Aparicio, Sam and Shah, Sohrab P}, file = {:home/gus/Documents/Mendeley Desktop/Goya et al.\_2010\_SNVMix predicting single nucleotide variants from next-generation sequencing of tumors.pdf:pdf}, institution = {Department of Molecular Oncology Breast Cancer Research Program, British Columbia Cancer Research Centre, Vancouver, BC, Canada.}, journal = {Bioinformatics}, number = {6}, pages = {730--736}, publisher = {Oxford University Press}, title = {{SNVMix: predicting single nucleotide variants from next-generation sequencing of tumors}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2832826\&tool=pmcentrez\&rendertype=abstract}, volume = {26}, year = {2010} } @article{trigger1978iroquois, author = {Trigger, B.}, journal = {Pennsylvania Archaeologist}, pages = {55--65}, title = {{Iroquois matriliny}}, url = {http://scholar.google.com/scholar?hl=fr\&q=Iroquoian+Matriliny\&btnG=Rechercher\&lr=\&as\_ylo=\&as\_vis=0\#0}, volume = {48}, year = {1978} } @article{dalloul2010multi, author = {Dalloul, R.A. and Long, J.A. and Zimin, A.V. and Aslam, L. and Beal, K. and Bouffard, P. and Burt, D.W. and Crasta, O. and Crooijmans, R.P.M.A. and Cooper, K. and Others}, file = {:home/gus/Documents/Mendeley Desktop/Dalloul et al.\_2010\_Multi-platform next-generation sequencing of the domestic turkey (Meleagris gallopavo) genome assembly and analysis.pdf:pdf}, journal = {PLoS biology}, number = {9}, pages = {e1000475}, title = {{Multi-platform next-generation sequencing of the domestic turkey (Meleagris gallopavo): genome assembly and analysis}}, url = {http://dx.plos.org/10.1371/journal.pbio.1000475}, volume = {8}, year = {2010} } @article{Li01022010, abstract = {Next-generation massively parallel DNA sequencing technologies provide ultrahigh throughput at a substantially lower unit data cost; however, the data are very short read length sequences, making de novo assembly extremely challenging. Here, we describe a novel method for de novo assembly of large genomes from short read sequences. We successfully assembled both the Asian and African human genome sequences, achieving an N50 contig size of 7.4 and 5.9 kilobases (kb) and scaffold of 446.3 and 61.9 kb, respectively. The development of this de novo short read assembly method creates new opportunities for building reference sequences and carrying out accurate analyses of unexplored genomes in a cost-effective way.}, author = {Li, Ruiqiang and Zhu, Hongmei and Ruan, Jue and Qian, Wubin and Fang, Xiaodong and Shi, Zhongbin and Li, Yingrui and Li, Shengting and Shan, Gao and Kristiansen, Karsten and Li, Songgang and Yang, Huanming and Wang, Jian and Wang, Jun}, doi = {10.1101/gr.097261.109}, file = {:home/gus/Documents/Mendeley Desktop/Li et al.\_2010\_De novo assembly of human genomes with massively parallel short read sequencing.pdf:pdf}, journal = {Genome Research}, number = {2}, pages = {265--272}, title = {{De novo assembly of human genomes with massively parallel short read sequencing}}, url = {http://genome.cshlp.org/content/20/2/265.abstract}, volume = {20}, year = {2010} } @article{Zerbino2009, author = {Zerbino, DR and McEwen, GK}, file = {:home/gus/Documents/Mendeley Desktop/Zerbino, McEwen\_2009\_Pebble and rock band heuristic resolution of repeats and scaffolding in the velvet short-read de novo assembler.pdf:pdf}, journal = {PloS one}, title = {{Pebble and rock band: heuristic resolution of repeats and scaffolding in the velvet short-read de novo assembler}}, url = {http://dx.plos.org/10.1371/journal.pone.0008407}, year = {2009} } @inproceedings{Chazelle:2004:BFE:982792.982797, address = {Philadelphia, PA, USA}, author = {Chazelle, Bernard and Kilian, Joe and Rubinfeld, Ronitt and Tal, Ayellet}, booktitle = {Proceedings of the fifteenth annual ACM-SIAM symposium on Discrete algorithms}, file = {:home/gus/Documents/Mendeley Desktop/Chazelle et al.\_2004\_The Bloomier filter an efficient data structure for static support lookup tables.pdf:pdf}, isbn = {0-89871-558-X}, pages = {30--39}, publisher = {Society for Industrial and Applied Mathematics}, series = {SODA '04}, title = {{The Bloomier filter: an efficient data structure for static support lookup tables}}, url = {http://dl.acm.org/citation.cfm?id=982797 http://dl.acm.org/citation.cfm?id=982792.982797}, year = {2004} } @inproceedings{Gao2004, author = {Gao, H and Groote, J F and Hesselink, W H}, booktitle = {18th International Parallel and Distributed Processing Symposium}, doi = {10.1109/IPDPS.2004.1302969}, isbn = {0769521320}, number = {C}, pages = {50--58}, publisher = {Ieee}, title = {{Almost wait-free resizable hashtables}}, url = {http://ieeexplore.ieee.org/lpdocs/epic03/wrapper.htm?arnumber=1302969}, volume = {00}, year = {2004} } @article{Butler:2008kx, abstract = {New DNA sequencing technologies deliver data at dramatically lower costs but demand new analytical methods to take full advantage of the very short reads that they produce. We provide an initial, theoretical solution to the challenge of de novo assembly from whole-genome shotgun "microreads." For 11 genomes of sizes up to 39 Mb, we generated high-quality assemblies from 80x coverage by paired 30-base simulated reads modeled after real Illumina-Solexa reads. The bacterial genomes of Campylobacter jejuni and Escherichia coli assemble optimally, yielding single perfect contigs, and larger genomes yield assemblies that are highly connected and accurate. Assemblies are presented in a graph form that retains intrinsic ambiguities such as those arising from polymorphism, thereby providing information that has been absent from previous genome assemblies. For both C. jejuni and E. coli, this assembly graph is a single edge encompassing the entire genome. Larger genomes produce more complicated graphs, but the vast majority of the bases in their assemblies are present in long edges that are nearly always perfect. We describe a general method for genome assembly that can be applied to all types of DNA sequence data, not only short read data, but also conventional sequence reads.}, author = {Butler, Jonathan and MacCallum, Iain and Kleber, Michael and Shlyakhter, Ilya A and Belmonte, Matthew K and Lander, Eric S and Nusbaum, Chad and Jaffe, David B}, doi = {10.1101/gr.7337908}, file = {:home/gus/Documents/Mendeley Desktop/Butler et al.\_2008\_ALLPATHS de novo assembly of whole-genome shotgun microreads.pdf:pdf}, journal = {Genome Res}, month = may, number = {5}, pages = {810--820}, pmid = {18340039}, title = {{ALLPATHS: de novo assembly of whole-genome shotgun microreads}}, volume = {18}, year = {2008} } @article{Dayarian:2010ly, abstract = {High throughput sequencing (HTS) platforms produce gigabases of short read (<100 bp) data per run. While these short reads are adequate for resequencing applications, de novo assembly of moderate size genomes from such reads remains a significant challenge. These limitations could be partially overcome by utilizing mate pair technology, which provides pairs of short reads separated by a known distance along the genome.}, author = {Dayarian, Adel and Michael, Todd P and Sengupta, Anirvan M}, doi = {10.1186/1471-2105-11-345}, journal = {BMC Bioinformatics}, pages = {345}, pmid = {20576136}, title = {{SOPRA: Scaffolding algorithm for paired reads via statistical optimization}}, volume = {11}, year = {2010} } @article{Pevzner:2001uq, abstract = {For the last 20 years, fragment assembly in DNA sequencing followed the "overlap-layout-consensus" paradigm that is used in all currently available assembly tools. Although this approach proved useful in assembling clones, it faces difficulties in genomic shotgun assembly. We abandon the classical "overlap-layout-consensus" approach in favor of a new euler algorithm that, for the first time, resolves the 20-year-old "repeat problem" in fragment assembly. Our main result is the reduction of the fragment assembly to a variation of the classical Eulerian path problem that allows one to generate accurate solutions of large-scale sequencing problems. euler, in contrast to the celera assembler, does not mask such repeats but uses them instead as a powerful fragment assembly tool.}, author = {Pevzner, P A and Tang, H and Waterman, M S}, doi = {10.1073/pnas.171285098}, file = {:home/gus/Documents/Mendeley Desktop/Pevzner, Tang, Waterman\_2001\_An Eulerian path approach to DNA fragment assembly.pdf:pdf}, journal = {Proc Natl Acad Sci U S A}, month = aug, number = {17}, pages = {9748--9753}, pmid = {11504945}, title = {{An Eulerian path approach to DNA fragment assembly}}, volume = {98}, year = {2001} } @article{mt2006science, author = {{Mt Pleasant}, J. and Staller, JE and Tykot, RH and Benz, BF}, journal = {Histories of Maize: Multidisciplinary approaches to the prehistory, linguistics, biogeography, domestication, and evolution of maize. Elsevier, San Diego}, pages = {529--537}, title = {{The science behind the three sisters mound system: an agronomic assessment of an indigenous agricultural system in the Northeast}}, url = {http://scholar.google.com/scholar?hl=fr\&q=The+Science+Behind+the+Three+Sisters+Mound+System:+An+Agronomic+Assessment+of+an+Indigenous+Agricultural+System+in+the+Northeast.\&btnG=Rechercher\&lr=\&as\_ylo=\&as\_vis=0\#0}, year = {2006} } @article{Kurtz2008, abstract = {The challenges of accurate gene prediction and enumeration are further aggravated in large genomes that contain highly repetitive transposable elements (TEs). Yet TEs play a substantial role in genome evolution and are themselves an important subject of study. Repeat annotation, based on counting occurrences of k-mers, has been previously used to distinguish TEs from low-copy genic regions; but currently available software solutions are impractical due to high memory requirements or specialization for specific user-tasks.}, author = {Kurtz, Stefan and Narechania, Apurva and Stein, Joshua C and Ware, Doreen}, doi = {10.1186/1471-2164-9-517}, file = {:home/gus/Documents/Mendeley Desktop/Kurtz et al.\_2008\_A new method to compute K-mer frequencies and its application to annotate large repetitive plant genomes.pdf:pdf}, issn = {1471-2164}, journal = {BMC genomics}, keywords = {Computational Biology,Computational Biology: methods,DNA Transposable Elements,Genome, Plant,Genomics,Genomics: methods,Methods,Oryza sativa,Software,Sorghum,Zea mays}, month = jan, pages = {517}, pmid = {18976482}, title = {{A new method to compute K-mer frequencies and its application to annotate large repetitive plant genomes.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2613927\&tool=pmcentrez\&rendertype=abstract}, volume = {9}, year = {2008} } @article{Gnerre2011, abstract = {Massively parallel DNA sequencing technologies are revolutionizing genomics by making it possible to generate billions of relatively short (\~{}100-base) sequence reads at very low cost. Whereas such data can be readily used for a wide range of biomedical applications, it has proven difficult to use them to generate high-quality de novo genome assemblies of large, repeat-rich vertebrate genomes. To date, the genome assemblies generated from such data have fallen far short of those obtained with the older (but much more expensive) capillary-based sequencing approach. Here, we report the development of an algorithm for genome assembly, ALLPATHS-LG, and its application to massively parallel DNA sequence data from the human and mouse genomes, generated on the Illumina platform. The resulting draft genome assemblies have good accuracy, short-range contiguity, long-range connectivity, and coverage of the genome. In particular, the base accuracy is high (≥99.95\%) and the scaffold sizes (N50 size = 11.5 Mb for human and 7.2 Mb for mouse) approach those obtained with capillary-based sequencing. The combination of improved sequencing technology and improved computational methods should now make it possible to increase dramatically the de novo sequencing of large genomes. The ALLPATHS-LG program is available at http://www.broadinstitute.org/science/programs/genome-biology/crd.}, author = {Gnerre, Sante and Maccallum, Iain and Przybylski, Dariusz and Ribeiro, Filipe J and Burton, Joshua N and Walker, Bruce J and Sharpe, Ted and Hall, Giles and Shea, Terrance P and Sykes, Sean and Berlin, Aaron M and Aird, Daniel and Costello, Maura and Daza, Riza and Williams, Louise and Nicol, Robert and Gnirke, Andreas and Nusbaum, Chad and Lander, Eric S and Jaffe, David B}, doi = {10.1073/pnas.1017351108}, file = {:home/gus/Documents/Mendeley Desktop/Gnerre et al.\_2011\_High-quality draft assemblies of mammalian genomes from massively parallel sequence data.pdf:pdf}, issn = {1091-6490}, journal = {Proceedings of the National Academy of Sciences of the United States of America}, keywords = {Algorithms,Animals,Genome,Genome: genetics,Genomics,Genomics: methods,Humans,Internet,Mice,Reproducibility of Results,Sequence Analysis, DNA,Sequence Analysis, DNA: methods,Software}, month = jan, number = {4}, pages = {1513--8}, pmid = {21187386}, title = {{High-quality draft assemblies of mammalian genomes from massively parallel sequence data.}}, url = {http://www.pnas.org/cgi/content/abstract/108/4/1513}, volume = {108}, year = {2011} } @article{Berger2011, abstract = {Prostate cancer is the second most common cause of male cancer deaths in the United States. However, the full range of prostate cancer genomic alterations is incompletely characterized. Here we present the complete sequence of seven primary human prostate cancers and their paired normal counterparts. Several tumours contained complex chains of balanced (that is, 'copy-neutral') rearrangements that occurred within or adjacent to known cancer genes. Rearrangement breakpoints were enriched near open chromatin, androgen receptor and ERG DNA binding sites in the setting of the ETS gene fusion TMPRSS2-ERG, but inversely correlated with these regions in tumours lacking ETS fusions. This observation suggests a link between chromatin or transcriptional regulation and the genesis of genomic aberrations. Three tumours contained rearrangements that disrupted CADM2, and four harboured events disrupting either PTEN (unbalanced events), a prostate tumour suppressor, or MAGI2 (balanced events), a PTEN interacting protein not previously implicated in prostate tumorigenesis. Thus, genomic rearrangements may arise from transcriptional or chromatin aberrancies and engage prostate tumorigenic mechanisms.}, author = {Berger, Michael F and Lawrence, Michael S and Demichelis, Francesca and Drier, Yotam and Cibulskis, Kristian and Sivachenko, Andrey Y and Sboner, Andrea and Esgueva, Raquel and Pflueger, Dorothee and Sougnez, Carrie and Onofrio, Robert and Carter, Scott L and Park, Kyung and Habegger, Lukas and Ambrogio, Lauren and Fennell, Timothy and Parkin, Melissa and Saksena, Gordon and Voet, Douglas and Ramos, Alex H and Pugh, Trevor J and Wilkinson, Jane and Fisher, Sheila and Winckler, Wendy and Mahan, Scott and Ardlie, Kristin and Baldwin, Jennifer and Simons, Jonathan W and Kitabayashi, Naoki and MacDonald, Theresa Y and Kantoff, Philip W and Chin, Lynda and Gabriel, Stacey B and Gerstein, Mark B and Golub, Todd R and Meyerson, Matthew and Tewari, Ashutosh and Lander, Eric S and Getz, Gad and Rubin, Mark A and Garraway, Levi A}, doi = {10.1038/nature09744}, file = {:home/gus/Documents/Mendeley Desktop/Berger et al.\_2011\_The genomic complexity of primary human prostate cancer.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Berger et al.\_2011\_The genomic complexity of primary human prostate cancer(2).pdf:pdf}, isbn = {doi:10.1038/nature09744}, issn = {1476-4687}, journal = {Nature}, keywords = {Carrier Proteins,Carrier Proteins: genetics,Case-Control Studies,Cell Adhesion Molecules,Cell Adhesion Molecules: genetics,Chromatin,Chromatin: genetics,Chromatin: metabolism,Chromosome Aberrations,Chromosome Breakpoints,Epigenesis, Genetic,Epigenesis, Genetic: genetics,Gene Expression Regulation, Neoplastic,Genetic,Genetic: genetics,Genome, Human,Genome, Human: genetics,Human,Human: genetics,Humans,Male,Neoplastic,PTEN Phosphohydrolase,PTEN Phosphohydrolase: genetics,PTEN Phosphohydrolase: metabolism,Prostatic Neoplasms,Prostatic Neoplasms: genetics,Recombination, Genetic,Recombination, Genetic: genetics,Signal Transduction,Signal Transduction: genetics,Transcription, Genetic}, language = {en}, month = feb, number = {7333}, pages = {214--20}, pmid = {21307934}, publisher = {Nature Publishing Group}, title = {{The genomic complexity of primary human prostate cancer.}}, url = {http://www.nature.com/nature/journal/v470/n7333//full/nature09744.html}, volume = {470}, year = {2011} } @article{Zabet2012, abstract = {Motivation: Transcription factors (TFs) are proteins that regulate gene activity by binding to specific sites on the DNA. Understanding the way these molecules locate their target site is of great importance in understanding gene regulation. We developed a comprehensive computational model of this process and estimated the model parameters in (Zabet and Adryan, 2011). Results: GRiP is a highly versatile implementation of this model and simulates the search process in a computationally efficient way. This program aims to provide researchers in the field with a flexible and highly customisable simulation framework. Its features include representation of DNA sequence, TFs and the interaction between TFs and the DNA (facilitated diffusion mechanism), or between various TFs (cooperative behaviour). The software will record both information on the dynamics associated with the search process (locations of molecules) and also steady state results (affinity landscape, occupancy-bias, collision hotspots). Availability: http://logic.sysbiol.cam.ac.uk/grip Supplementary information: Additional information and data is presented in the Supplementary Material which is available at Bioinformatics online. Contact: n.r.zabet@gen.cam.ac.uk}, author = {Zabet, N. R. and Adryan, B.}, doi = {10.1093/bioinformatics/bts132}, file = {:home/gus/Documents/Mendeley Desktop/Zabet, Adryan\_2012\_GRiP a computational tool to simulate transcription factor binding in prokaryotes.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Zabet, Adryan\_2012\_GRiP a computational tool to simulate transcription factor binding in prokaryotes(2).pdf:pdf}, issn = {1367-4803}, journal = {Bioinformatics}, month = mar, pages = {bts132--}, title = {{GRiP: a computational tool to simulate transcription factor binding in prokaryotes}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/bts132v1}, year = {2012} } @article{Ladan-Mozes2007, author = {Ladan-Mozes, Edya and Shavit, Nir}, doi = {10.1007/s00446-007-0050-0}, file = {:home/gus/Documents/Mendeley Desktop/Ladan-Mozes, Shavit\_2007\_An optimistic approach to lock-free FIFO queues.pdf:pdf}, issn = {0178-2770}, journal = {Distributed Computing}, month = nov, number = {5}, pages = {323--341}, title = {{An optimistic approach to lock-free FIFO queues}}, url = {http://www.springerlink.com/index/10.1007/s00446-007-0050-0}, volume = {20}, year = {2007} } @article{Trapnell2009, abstract = {A new protocol for sequencing the messenger RNA in a cell, known as RNA-Seq, generates millions of short sequence fragments in a single run. These fragments, or 'reads', can be used to measure levels of gene expression and to identify novel splice variants of genes. However, current software for aligning RNA-Seq data to a genome relies on known splice junctions and cannot identify novel ones. TopHat is an efficient read-mapping algorithm designed to align reads from an RNA-Seq experiment to a reference genome without relying on known splice sites.}, author = {Trapnell, Cole and Pachter, Lior and Salzberg, Steven L}, doi = {10.1093/bioinformatics/btp120}, file = {:home/gus/Documents/Mendeley Desktop/Trapnell, Pachter, Salzberg\_2009\_TopHat discovering splice junctions with RNA-Seq.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Trapnell, Pachter, Salzberg\_2009\_TopHat discovering splice junctions with RNA-Seq(2).pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,Gene Expression Profiling,Gene Expression Profiling: methods,Genetic,Messenger,Models,RNA,RNA Splicing,RNA Splicing: genetics,Sequence Alignment,Sequence Analysis,Software}, month = may, number = {9}, pages = {1105--11}, pmid = {19289445}, title = {{TopHat: discovering splice junctions with RNA-Seq.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/25/9/1105}, volume = {25}, year = {2009} } @article{Simpson2009, abstract = {Widespread adoption of massively parallel deoxyribonucleic acid (DNA) sequencing instruments has prompted the recent development of de novo short read assembly algorithms. A common shortcoming of the available tools is their inability to efficiently assemble vast amounts of data generated from large-scale sequencing projects, such as the sequencing of individual human genomes to catalog natural genetic variation. To address this limitation, we developed ABySS (Assembly By Short Sequences), a parallelized sequence assembler. As a demonstration of the capability of our software, we assembled 3.5 billion paired-end reads from the genome of an African male publicly released by Illumina, Inc. Approximately 2.76 million contigs > or =100 base pairs (bp) in length were created with an N50 size of 1499 bp, representing 68\% of the reference human genome. Analysis of these contigs identified polymorphic and novel sequences not present in the human reference assembly, which were validated by alignment to alternate human assemblies and to other primate genomes.}, author = {Simpson, Jared T and Wong, Kim and Jackman, Shaun D and Schein, Jacqueline E and Jones, Steven J M and Birol, Inan\c{c}}, doi = {10.1101/gr.089532.108}, file = {:home/gus/Documents/Mendeley Desktop/Simpson et al.\_2009\_ABySS a parallel assembler for short read sequence data.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Animals,Computational Biology,Computational Biology: methods,Contig Mapping,Escherichia coli K12,Escherichia coli K12: genetics,Genetic Variation,Genome, Human,Humans,Polymorphism, Genetic,Reproducibility of Results,Sequence Analysis, DNA,Sequence Analysis, DNA: methods,Software}, month = jun, number = {6}, pages = {1117--23}, pmid = {19251739}, title = {{ABySS: a parallel assembler for short read sequence data.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2694472\&tool=pmcentrez\&rendertype=abstract}, volume = {19}, year = {2009} } @article{Chor2009, abstract = {The empirical frequencies of DNA k-mers in whole genome sequences provide an interesting perspective on genomic complexity, and the availability of large segments of genomic sequence from many organisms means that analysis of k-mers with non-trivial lengths is now possible.}, author = {Chor, Benny and Horn, David and Goldman, Nick and Levy, Yaron and Massingham, Tim}, doi = {10.1186/gb-2009-10-10-r108}, file = {:home/gus/Documents/Mendeley Desktop/Chor et al.\_2009\_Genomic DNA k-mer spectra models and modalities.pdf:pdf}, issn = {1465-6914}, journal = {Genome biology}, keywords = {Animals,Base Composition,Base Composition: genetics,Chickens,Chickens: genetics,Computer Simulation,CpG Islands,CpG Islands: genetics,DNA,DNA: genetics,Genome,Genome: genetics,Humans,Markov Chains,Models, Genetic,Zebrafish,Zebrafish: genetics}, month = jan, number = {10}, pages = {R108}, pmid = {19814784}, title = {{Genomic DNA k-mer spectra: models and modalities.}}, url = {http://genomebiology.com/2009/10/10/R108}, volume = {10}, year = {2009} } @article{Roberts12122004, abstract = {Motivation: Comparison of nucleic acid and protein sequences is a fundamental tool of modern bioinformatics. A dominant method of such string matching is the ‘seed-and-extend’ approach, in which occurrences of short subsequences called ‘seeds’ are used to search for potentially longer matches in a large database of sequences. Each such potential match is then checked to see if it extends beyond the seed. To be effective, the seed-and-extend approach needs to catalogue seeds from virtually every substring in the database of search strings. Projects such as mammalian genome assemblies and large-scale protein matching, however, have such large sequence databases that the resulting list of seeds cannot be stored in RAM on a single computer. This significantly slows the matching process.Results: We present a simple and elegant method in which only a small fraction of seeds, called ‘minimizers’, needs to be stored. Using minimizers can speed up string-matching computations by a large factor while missing only a small fraction of the matches found using all seeds.}, author = {Roberts, Michael and Hayes, Wayne and Hunt, Brian R and Mount, Stephen M and Yorke, James A}, doi = {10.1093/bioinformatics/bth408}, file = {:home/gus/Documents/Mendeley Desktop/Roberts et al.\_2004\_Reducing storage requirements for biological sequence comparison(2).pdf:pdf}, issn = {1367-4803}, journal = {Bioinformatics}, keywords = {Algorithms,Computer-Assisted,Databases,Genetic,Information Storage and Retrieval,Information Storage and Retrieval: methods,Numerical Analysis,Sequence Alignment,Sequence Alignment: methods,Sequence Analysis,Sequence Analysis: methods}, month = dec, number = {18}, pages = {3363--3369}, pmid = {15256412}, title = {{Reducing storage requirements for biological sequence comparison}}, url = {http://bioinformatics.oxfordjournals.org/content/20/18/3363.short}, volume = {20}, year = {2004} } @inproceedings{Martinez2005, author = {Martinez, J. and Cumplido, R. and Feregrino, C.}, booktitle = {2005 International Conference on Reconfigurable Computing and FPGAs (ReConFig'05)}, doi = {10.1109/RECONFIG.2005.9}, isbn = {0-7695-2456-7}, month = sep, pages = {17--17}, publisher = {IEEE}, title = {{An FPGA Parallel Sorting Architecture for the Burrows Wheeler Transform}}, url = {http://dl.acm.org/citation.cfm?id=1114693.1115262}, year = {2005} } @article{zhao2011psaec, author = {Zhao, Z. and Yin, J. and Zhan, Y. and Xiong, W. and Li, Y. and Liu, F.}, file = {:home/gus/Documents/Mendeley Desktop/Zhao et al.\_2011\_PSAEC An Improved Algorithm for Short Read Error Correction Using Partial Suffix Arrays.pdf:pdf}, journal = {Frontiers in Algorithmics and Algorithmic Aspects in Information and Management}, pages = {220--232}, publisher = {Springer}, title = {{PSAEC: An Improved Algorithm for Short Read Error Correction Using Partial Suffix Arrays}}, url = {http://www.springerlink.com/index/9L77826718445828.pdf}, year = {2011} } @article{Li2008, abstract = {New sequencing technologies promise a new era in the use of DNA sequence. However, some of these technologies produce very short reads, typically of a few tens of base pairs, and to use these reads effectively requires new algorithms and software. In particular, there is a major issue in efficiently aligning short reads to a reference genome and handling ambiguity or lack of accuracy in this alignment. Here we introduce the concept of mapping quality, a measure of the confidence that a read actually comes from the position it is aligned to by the mapping algorithm. We describe the software MAQ that can build assemblies by mapping shotgun short reads to a reference genome, using quality scores to derive genotype calls of the consensus sequence of a diploid genome, e.g., from a human sample. MAQ makes full use of mate-pair information and estimates the error probability of each read alignment. Error probabilities are also derived for the final genotype calls, using a Bayesian statistical model that incorporates the mapping qualities, error probabilities from the raw sequence quality scores, sampling of the two haplotypes, and an empirical model for correlated errors at a site. Both read mapping and genotype calling are evaluated on simulated data and real data. MAQ is accurate, efficient, versatile, and user-friendly. It is freely available at http://maq.sourceforge.net.}, author = {Li, Heng and Ruan, Jue and Durbin, Richard}, doi = {10.1101/gr.078212.108}, file = {:home/gus/Documents/Mendeley Desktop/Li, Ruan, Durbin\_2008\_Mapping short DNA sequencing reads and calling variants using mapping quality scores.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Li, Ruan, Durbin\_2008\_Mapping short DNA sequencing reads and calling variants using mapping quality scores(2).pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Bacterial,Bacterial: genetics,Bayes Theorem,Chromosome Mapping,Chromosome Mapping: statistics \& numerical data,Computer Simulation,DNA,DNA: genetics,DNA: statistics \& numerical dat,Diploidy,Genome,Human,Humans,Polymorphism,Reproducibility of Results,Salmonella paratyphi A,Salmonella paratyphi A: genetics,Sequence Alignment,Sequence Alignment: statistics \& numerical data,Sequence Analysis,Single Nucleotide,Software}, month = nov, number = {11}, pages = {1851--8}, pmid = {18714091}, title = {{Mapping short DNA sequencing reads and calling variants using mapping quality scores.}}, url = {http://genome.cshlp.org/cgi/content/abstract/18/11/1851}, volume = {18}, year = {2008} } @article{Kumar2011, abstract = {To catalog protein-altering mutations that may drive the development of prostate cancers and their progression to metastatic disease systematically, we performed whole-exome sequencing of 23 prostate cancers derived from 16 different lethal metastatic tumors and three high-grade primary carcinomas. All tumors were propagated in mice as xenografts, designated the LuCaP series, to model phenotypic variation, such as responses to cancer-directed therapeutics. Although corresponding normal tissue was not available for most tumors, we were able to take advantage of increasingly deep catalogs of human genetic variation to remove most germline variants. On average, each tumor genome contained [\~{}]200 novel nonsynonymous variants, of which the vast majority was specific to individual carcinomas. A subset of genes was recurrently altered across tumors derived from different individuals, including TP53, DLK2, GPC6, and SDF4. Unexpectedly, three prostate cancer genomes exhibited substantially higher mutation frequencies, with 2,000-4,000 novel coding variants per exome. A comparison of castration-resistant and castration-sensitive pairs of tumor lines derived from the same prostate cancer highlights mutations in the Wnt pathway as potentially contributing to the development of castration resistance. Collectively, our results indicate that point mutations arising in coding regions of advanced prostate cancers are common but, with notable exceptions, very few genes are mutated in a substantial fraction of tumors. We also report a previously undescribed subtype of prostate cancers exhibiting "hypermutated" genomes, with potential implications for resistance to cancer therapeutics. Our results also suggest that increasingly deep catalogs of human germline variation may challenge the necessity of sequencing matched tumor-normal pairs.}, author = {Kumar, A. and White, T. A. and MacKenzie, A. P. and Clegg, N. and Lee, C. and Dumpit, R. F. and Coleman, I. and Ng, S. B. and Salipante, S. J. and Rieder, M. J. and Nickerson, D. A. and Corey, E. and Lange, P. H. and Morrissey, C. and Vessella, R. L. and Nelson, P. S. and Shendure, J.}, doi = {10.1073/pnas.1108745108}, file = {:home/gus/Documents/Mendeley Desktop/Kumar et al.\_2011\_Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancers.pdf:pdf}, issn = {0027-8424}, journal = {Proceedings of the National Academy of Sciences}, month = sep, number = {41}, pages = {17087--17092}, title = {{Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancers}}, url = {http://www.pnas.org/cgi/content/abstract/108/41/17087}, volume = {108}, year = {2011} } @article{Pop:2009fk, abstract = {Research into genome assembly algorithms has experienced a resurgence due to new challenges created by the development of next generation sequencing technologies. Several genome assemblers have been published in recent years specifically targeted at the new sequence data; however, the ever-changing technological landscape leads to the need for continued research. In addition, the low cost of next generation sequencing data has led to an increased use of sequencing in new settings. For example, the new field of metagenomics relies on large-scale sequencing of entire microbial communities instead of isolate genomes, leading to new computational challenges. In this article, we outline the major algorithmic approaches for genome assembly and describe recent developments in this domain.}, author = {Pop, Mihai}, doi = {10.1093/bib/bbp026}, journal = {Brief Bioinform}, month = jul, number = {4}, pages = {354--366}, pmid = {19482960}, title = {{Genome assembly reborn: recent computational challenges}}, volume = {10}, year = {2009} } @article{Brummitt2012, abstract = {Understanding how interdependence among systems affects cascading behaviors is increasingly important across many fields of science and engineering. Inspired by cascades of load shedding in coupled electric grids and other infrastructure, we study the Bak-Tang-Wiesenfeld sandpile model on modular random graphs and on graphs based on actual, interdependent power grids. Starting from two isolated networks, adding some connectivity between them is beneficial, for it suppresses the largest cascades in each system. Too much interconnectivity, however, becomes detrimental for two reasons. First, interconnections open pathways for neighboring networks to inflict large cascades. Second, as in real infrastructure, new interconnections increase capacity and total possible load, which fuels even larger cascades. Using a multitype branching process and simulations we show these effects and estimate the optimal level of interconnectivity that balances their trade-offs. Such equilibria could allow, for example, power grid owners to minimize the largest cascades in their grid. We also show that asymmetric capacity among interdependent networks affects the optimal connectivity that each prefers and may lead to an arms race for greater capacity. Our multitype branching process framework provides building blocks for better prediction of cascading processes on modular random graphs and on multitype networks in general.}, author = {Brummitt, Charles D and D'Souza, Raissa M and Leicht, E A}, doi = {10.1073/pnas.1110586109}, file = {:home/gus/Documents/Mendeley Desktop/Brummitt, D'Souza, Leicht\_2012\_Suppressing cascades of load in interdependent networks.pdf:pdf}, issn = {1091-6490}, journal = {Proceedings of the National Academy of Sciences of the United States of America}, month = feb, number = {12}, pages = {E680--689}, pmid = {22355144}, title = {{Suppressing cascades of load in interdependent networks.}}, url = {http://www.pnas.org/cgi/content/abstract/109/12/E680}, volume = {109}, year = {2012} } @article{Schuenemann2011, abstract = {Although investigations of medieval plague victims have identified Yersinia pestis as the putative etiologic agent of the pandemic, methodological limitations have prevented large-scale genomic investigations to evaluate changes in the pathogen's virulence over time. We screened over 100 skeletal remains from Black Death victims of the East Smithfield mass burial site (1348-1350, London, England). Recent methods of DNA enrichment coupled with high-throughput DNA sequencing subsequently permitted reconstruction of ten full human mitochondrial genomes (16 kb each) and the full pPCP1 (9.6 kb) virulence-associated plasmid at high coverage. Comparisons of molecular damage profiles between endogenous human and Y. pestis DNA confirmed its authenticity as an ancient pathogen, thus representing the longest contiguous genomic sequence for an ancient pathogen to date. Comparison of our reconstructed plasmid against modern Y. pestis shows identity with several isolates matching the Medievalis biovar; however, our chromosomal sequences indicate the victims were infected with a Y. pestis variant that has not been previously reported. Our data reveal that the Black Death in medieval Europe was caused by a variant of Y. pestis that may no longer exist, and genetic data carried on its pPCP1 plasmid were not responsible for the purported epidemiological differences between ancient and modern forms of Y. pestis infections.}, author = {Schuenemann, V. J. and Bos, K. and DeWitte, S. and Schmedes, S. and Jamieson, J. and Mittnik, A. and Forrest, S. and Coombes, B. K. and Wood, J. W. and Earn, D. J. D. and White, W. and Krause, J. and Poinar, H. N.}, doi = {10.1073/pnas.1105107108}, file = {:home/gus/Documents/Mendeley Desktop/Schuenemann et al.\_2011\_PNAS Plus Targeted enrichment of ancient pathogens yielding the pPCP1 plasmid of Yersinia pestis from victims of the Black Death.pdf:pdf}, issn = {0027-8424}, journal = {Proceedings of the National Academy of Sciences}, month = aug, pages = {1105107108--}, title = {{PNAS Plus: Targeted enrichment of ancient pathogens yielding the pPCP1 plasmid of Yersinia pestis from victims of the Black Death}}, url = {http://www.pnas.org/cgi/content/abstract/1105107108v1}, year = {2011} } @article{Ferragina2000, author = {Ferragina, P. and Manzini, G.}, file = {:home/gus/Documents/Mendeley Desktop/Ferragina, Manzini\_2000\_Opportunistic data structures with applications.pdf:pdf}, isbn = {0-7695-0850-2}, keywords = {Glimpse tool,computational complexity,data compression,data indexing,data set,data structures,database indexing,database theory,entropy,opportunistic data structures,query performance,search,sublinear query time complexity,sublinear space complexity,succinct suffix array,suffix array data structures,suffix tree data structures}, month = nov, pages = {390}, title = {{Opportunistic data structures with applications}}, url = {http://dl.acm.org/citation.cfm?id=795666.796543 http://www.di.unipi.it/~ferragin/Libraries/fmindexV2/index.html}, year = {2000} } @article{David2011, abstract = {We report on a major update (version 2) of the original SHort Read Mapping Program (SHRiMP). SHRiMP2 primarily targets mapping sensitivity, and is able to achieve high accuracy at a very reasonable speed. SHRiMP2 supports both letter space and color space (AB/SOLiD) reads, enables for direct alignment of paired reads and uses parallel computation to fully utilize multi-core architectures. AVAILABILITY: SHRiMP2 executables and source code are freely available at: http://compbio.cs.toronto.edu/shrimp/.}, author = {David, Matei and Dzamba, Misko and Lister, Dan and Ilie, Lucian and Brudno, Michael}, doi = {10.1093/bioinformatics/btr046}, file = {:home/gus/Documents/Mendeley Desktop/David et al.\_2011\_SHRiMP2 sensitive yet practical SHort Read Mapping.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,Chromosome Mapping,DNA,Genetic,Genomics,Genomics: methods,Polymorphism,Sequence Alignment,Sequence Analysis,Software}, month = apr, number = {7}, pages = {1011--2}, pmid = {21278192}, title = {{SHRiMP2: sensitive yet practical SHort Read Mapping.}}, url = {http://www.ncbi.nlm.nih.gov/pubmed/21278192}, volume = {27}, year = {2011} } @article{Chong1993, author = {Chong, Ka Wong and Lam, Tak Wah}, file = {:home/gus/Documents/Mendeley Desktop/Chong, Lam\_1993\_Finding connected components in O (log n loglog n ) time on the EREW PRAM.pdf:pdf}, isbn = {0-89871-313-7}, month = jan, pages = {11--20}, title = {{Finding connected components in O (log n loglog n ) time on the EREW PRAM}}, url = {http://dl.acm.org/citation.cfm?id=313559.313575}, year = {1993} } @article{Rogers2012, abstract = {ABSTRACT: We propose a method for predicting splice graphs that enhances curated gene models using evidence from RNA-Seq and EST alignments. Results obtained using RNA-Seq experiments in Arabidopsis thaliana show that predictions made by our SpliceGrapher method are more consistent with current gene models than predictions made by TAU and Cufflinks. Furthermore, analysis of plant and human data indicates that the machine learning approach used by SpliceGrapher is useful for discriminating between real and spurious splice sites, and can improve the reliability of detection of alternative splicing. SpliceGrapher is available for download at http://SpliceGrapher.sf.net.}, author = {Rogers, Mark F and Thomas, Julie and Reddy, Anireddy Sn and Ben-Hur, Asa}, doi = {10.1186/gb-2012-13-1-r4}, issn = {1465-6914}, journal = {Genome biology}, month = jan, number = {1}, pages = {R4}, pmid = {22293517}, title = {{SpliceGrapher: detecting patterns of alternative splicing from RNA-Seq data in the context of gene models and EST data.}}, url = {http://genomebiology.com/2012/13/1/R4}, volume = {13}, year = {2012} } @article{Manber1990, author = {Manber, Udi and Myers, Gene}, file = {:home/gus/Documents/Mendeley Desktop/Manber, Myers\_1990\_Suffix arrays a new method for on-line string searches.pdf:pdf}, isbn = {0-89871-251-3}, journal = {Proceedings of the first annual ACM-SIAM \ldots}, month = jan, pages = {319--327}, title = {{Suffix arrays: a new method for on-line string searches}}, url = {http://portal.acm.org/citation.cfm?id=320218 http://dl.acm.org/citation.cfm?id=320176.320218}, year = {1990} } @article{Venter2001, author = {Venter, JC and Adams, MD and Myers, EW}, file = {:home/gus/Documents/Mendeley Desktop/Venter, Adams, Myers\_2001\_The sequence of the human genome.pdf:pdf}, journal = {Science's \ldots}, title = {{The sequence of the human genome}}, url = {http://stke.sciencemag.org/cgi/content/abstract/sci;291/5507/1304}, year = {2001} } @techreport{Drepper2007, author = {Drepper, Ulrich}, file = {:home/gus/Documents/Mendeley Desktop/Drepper\_2007\_What Every Programmer Should Know About Memory.pdf:pdf}, keywords = {Cache,Memory,lock free}, title = {{What Every Programmer Should Know About Memory}}, year = {2007} } @article{Almeida2007, author = {Almeida, Paulo S\'{e}rgio PS and Baquero, Carlos and Pregui\c{c}a, Nuno and Hutchison, David}, file = {:home/gus/Documents/Mendeley Desktop//Almeida et al.\_2007\_Scalable Bloom Filters.pdf:pdf}, issn = {0020-0190}, journal = {Information Processing Letters}, keywords = {Distributed systems,Randomized algorithms,bloom filters,data structures,dis-,expected,lower false positive rates,require more state}, month = mar, number = {6}, pages = {255--261}, title = {{Scalable Bloom Filters}}, url = {http://www.sciencedirect.com/science/article/pii/S0020019006003127}, volume = {101}, year = {2007} } @article{Liu2012, abstract = {SUMMARY: SOAP3 is the first short read alignment tool that leverages the multi-processors in a graphic processing unit (GPU) to achieve a drastic improvement in speed. We adapted the compressed full-text index (BWT) used by SOAP2 in view of the advantages and disadvantages of GPU. When tested with millions of Illumina Hiseq 2000 length-100bp reads, SOAP3 takes less than 30 seconds to align a million read pairs onto the human reference genome and is at least 7.5 and 20 times faster than BWA and Bowtie, respectively. For aligning reads with up to 4 mismatches, SOAP3 aligns slightly more reads than BWA and Bowtie; this is because SOAP3, unlike BWA and Bowtie, is not heuristic-based and always reports all answers. AVAILABILITY: SOAP3 is available at: http://www.cs.hku.hk/2bwt-tools/soap3; and http://soap.genomics.org.cn/soap3.html. CONTACT: liruiqiang@gmail.com, twlam@cs.hku.hk.}, author = {Liu, Chi-Man and Wong, Thomas and Wu, Edward and Luo, Ruibang and Yiu, Siu-Ming and Li, Yingrui and Wang, B and Yu, C and Chu, X and Zhao, K and Li, Ruiqiang and Lam, Tak-Wah}, doi = {10.1093/bioinformatics/bts061}, file = {:home/gus/Documents/Mendeley Desktop/Liu et al.\_2012\_SOAP3 Ultra-fast GPU-based parallel alignment tool for short reads.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, month = jan, number = {6}, pages = {878--879}, pmid = {22285832}, title = {{SOAP3: Ultra-fast GPU-based parallel alignment tool for short reads.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/28/6/878}, volume = {28}, year = {2012} } @book{Menon2011, address = {New York, New York, USA}, author = {Menon, Rohith K. and Bhat, Goutham P. and Schatz, Michael C.}, booktitle = {Proceedings of the second international workshop on MapReduce and its applications - MapReduce '11}, doi = {10.1145/1996092.1996104}, file = {:home/gus/Documents/Mendeley Desktop/Menon, Bhat, Schatz\_2011\_Rapid parallel genome indexing with MapReduce.pdf:pdf}, isbn = {9781450307000}, keywords = {DNA sequence analysis,MapReduce,burrows-wheeler transform,cloud computing,parallel suffix array construction}, month = jun, pages = {51}, publisher = {ACM Press}, title = {{Rapid parallel genome indexing with MapReduce}}, url = {http://dl.acm.org/citation.cfm?id=1996092.1996104}, year = {2011} } @article{Nakamura2011, abstract = {We identified the sequence-specific starting positions of consecutive miscalls in the mapping of reads obtained from the Illumina Genome Analyser (GA). Detailed analysis of the miscall pattern indicated that the underlying mechanism involves sequence-specific interference of the base elongation process during sequencing. The two major sequence patterns that trigger this sequence-specific error (SSE) are: (i) inverted repeats and (ii) GGC sequences. We speculate that these sequences favor dephasing by inhibiting single-base elongation, by: (i) folding single-stranded DNA and (ii) altering enzyme preference. This phenomenon is a major cause of sequence coverage variability and of the unfavorable bias observed for population-targeted methods such as RNA-seq and ChIP-seq. Moreover, SSE is a potential cause of false single-nucleotide polymorphism (SNP) calls and also significantly hinders de novo assembly. This article highlights the importance of recognizing SSE and its underlying mechanisms in the hope of enhancing the potential usefulness of the Illumina sequencers.}, author = {Nakamura, Kensuke and Oshima, Taku and Morimoto, Takuya and Ikeda, Shun and Yoshikawa, Hirofumi and Shiwa, Yuh and Ishikawa, Shu and Linak, Margaret C and Hirai, Aki and Takahashi, Hiroki and Altaf-Ul-Amin, Md and Ogasawara, Naotake and Kanaya, Shigehiko}, doi = {10.1093/nar/gkr344}, file = {:home/gus/Documents/Mendeley Desktop/Nakamura et al.\_2011\_Sequence-specific error profile of Illumina sequencers.pdf:pdf}, issn = {1362-4962}, journal = {Nucleic acids research}, month = may, number = {13}, pages = {e90--}, pmid = {21576222}, title = {{Sequence-specific error profile of Illumina sequencers.}}, url = {http://nar.oxfordjournals.org/cgi/content/abstract/39/13/e90}, volume = {39}, year = {2011} } @article{Edgar2004, abstract = {We describe MUSCLE, a new computer program for creating multiple alignments of protein sequences. Elements of the algorithm include fast distance estimation using kmer counting, progressive alignment using a new profile function we call the log-expectation score, and refinement using tree-dependent restricted partitioning. The speed and accuracy of MUSCLE are compared with T-Coffee, MAFFT and CLUSTALW on four test sets of reference alignments: BAliBASE, SABmark, SMART and a new benchmark, PREFAB. MUSCLE achieves the highest, or joint highest, rank in accuracy on each of these sets. Without refinement, MUSCLE achieves average accuracy statistically indistinguishable from T-Coffee and MAFFT, and is the fastest of the tested methods for large numbers of sequences, aligning 5000 sequences of average length 350 in 7 min on a current desktop computer. The MUSCLE program, source code and PREFAB test data are freely available at http://www.drive5. com/muscle.}, author = {Edgar, Robert C}, doi = {10.1093/nar/gkh340}, file = {:home/gus/Documents/Mendeley Desktop/Edgar\_2004\_MUSCLE multiple sequence alignment with high accuracy and high throughput.pdf:pdf}, issn = {1362-4962}, journal = {Nucleic acids research}, keywords = {Algorithms,Amino Acid Motifs,Amino Acid Sequence,Internet,Molecular Sequence Data,Reproducibility of Results,Sequence Alignment,Sequence Alignment: methods,Sequence Analysis, Protein,Sequence Analysis, Protein: methods,Software,Time Factors}, month = jan, number = {5}, pages = {1792--7}, pmid = {15034147}, title = {{MUSCLE: multiple sequence alignment with high accuracy and high throughput.}}, url = {http://nar.oxfordjournals.org/cgi/content/abstract/32/5/1792}, volume = {32}, year = {2004} } @article{Manber1990, author = {Manber, Udi and Myers, Gene}, file = {:home/gus/Documents/Mendeley Desktop/Manber, Myers\_1990\_Suffix arrays a new method for on-line string searches(2).pdf:pdf;:home/gus/Documents/Mendeley Desktop/Manber, Myers\_1990\_Suffix arrays a new method for on-line string searches.pdf:pdf}, isbn = {0-89871-251-3}, journal = {Proceedings of the first annual ACM-SIAM \ldots}, month = jan, pages = {319--327}, title = {{Suffix arrays: a new method for on-line string searches}}, url = {http://portal.acm.org/citation.cfm?id=320218 http://dl.acm.org/citation.cfm?id=320176.320218}, year = {1990} } @article{Trapnell2010, abstract = {High-throughput mRNA sequencing (RNA-Seq) promises simultaneous transcript discovery and abundance estimation. However, this would require algorithms that are not restricted by prior gene annotations and that account for alternative transcription and splicing. Here we introduce such algorithms in an open-source software program called Cufflinks. To test Cufflinks, we sequenced and analyzed >430 million paired 75-bp RNA-Seq reads from a mouse myoblast cell line over a differentiation time series. We detected 13,692 known transcripts and 3,724 previously unannotated ones, 62\% of which are supported by independent expression data or by homologous genes in other species. Over the time series, 330 genes showed complete switches in the dominant transcription start site (TSS) or splice isoform, and we observed more subtle shifts in 1,304 other genes. These results suggest that Cufflinks can illuminate the substantial regulatory flexibility and complexity in even this well-studied model of muscle development and that it can improve transcriptome-based genome annotation.}, author = {Trapnell, Cole and Williams, Brian A and Pertea, Geo and Mortazavi, Ali and Kwan, Gordon and van Baren, Marijke J and Salzberg, Steven L and Wold, Barbara J and Pachter, Lior}, doi = {10.1038/nbt.1621}, issn = {1546-1696}, journal = {Nature biotechnology}, keywords = {Algorithms,Animals,Cell Differentiation,Cell Differentiation: genetics,Cell Line,Gene Expression Profiling,Gene Expression Profiling: methods,Genome,Messenger,Messenger: analysis,Messenger: genetics,Messenger: metabolism,Mice,Oligonucleotide Array Sequence Analysis,Oligonucleotide Array Sequence Analysis: methods,Protein Isoforms,Protein Isoforms: genetics,Protein Isoforms: metabolism,Proto-Oncogene Proteins c-myc,Proto-Oncogene Proteins c-myc: genetics,Proto-Oncogene Proteins c-myc: metabolism,RNA,RNA: methods,Sequence Analysis,Software}, month = may, number = {5}, pages = {511--5}, pmid = {20436464}, publisher = {Nature Publishing Group}, shorttitle = {Nat Biotech}, title = {{Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation.}}, url = {http://dx.doi.org/10.1038/nbt.1621}, volume = {28}, year = {2010} } @article{Gnerre:2011zr, abstract = {Massively parallel DNA sequencing technologies are revolutionizing genomics by making it possible to generate billions of relatively short (\~{}100-base) sequence reads at very low cost. Whereas such data can be readily used for a wide range of biomedical applications, it has proven difficult to use them to generate high-quality de novo genome assemblies of large, repeat-rich vertebrate genomes. To date, the genome assemblies generated from such data have fallen far short of those obtained with the older (but much more expensive) capillary-based sequencing approach. Here, we report the development of an algorithm for genome assembly, ALLPATHS-LG, and its application to massively parallel DNA sequence data from the human and mouse genomes, generated on the Illumina platform. The resulting draft genome assemblies have good accuracy, short-range contiguity, long-range connectivity, and coverage of the genome. In particular, the base accuracy is high (≥99.95\%) and the scaffold sizes (N50 size = 11.5 Mb for human and 7.2 Mb for mouse) approach those obtained with capillary-based sequencing. The combination of improved sequencing technology and improved computational methods should now make it possible to increase dramatically the de novo sequencing of large genomes. The ALLPATHS-LG program is available at http://www.broadinstitute.org/science/programs/genome-biology/crd.}, author = {Gnerre, Sante and Maccallum, Iain and Przybylski, Dariusz and Ribeiro, Filipe J and Burton, Joshua N and Walker, Bruce J and Sharpe, Ted and Hall, Giles and Shea, Terrance P and Sykes, Sean and Berlin, Aaron M and Aird, Daniel and Costello, Maura and Daza, Riza and Williams, Louise and Nicol, Robert and Gnirke, Andreas and Nusbaum, Chad and Lander, Eric S and Jaffe, David B}, doi = {10.1073/pnas.1017351108}, journal = {Proc Natl Acad Sci U S A}, month = jan, number = {4}, pages = {1513--1518}, pmid = {21187386}, title = {{High-quality draft assemblies of mammalian genomes from massively parallel sequence data}}, volume = {108}, year = {2011} } @article{Marsaglia2003, abstract = {Description of a class of simple, extremely fast random number generators (RNGs) with periods 2 k - 1 for k = 32, 64, 96, 128, 160, 192. These RNGs seem to pass tests of randomness very well.}, author = {Marsaglia, George}, file = {:home/gus/Documents/Mendeley Desktop/Marsaglia\_2003\_Xorshift RNGs.pdf:pdf}, issn = {15487660}, journal = {Journal Of Statistical Software}, number = {14}, pages = {1--6}, publisher = {American Statistical Association}, title = {{Xorshift RNGs}}, url = {http://www.jstatsoft.org/v08/i14/paper}, volume = {8}, year = {2003} } @article{herlihy2002repeat, author = {Herlihy, M. and Luchangco, V. and Moir, M.}, file = {:home/gus/Documents/Mendeley Desktop/Herlihy, Luchangco, Moir\_2002\_The repeat offender problem A mechanism for supporting dynamic-sized lock-free data structures.pdf:pdf}, publisher = {Sun Microsystems, Inc.}, title = {{The repeat offender problem: A mechanism for supporting dynamic-sized lock-free data structures}}, url = {http://portal.acm.org/citation.cfm?id=1698158}, year = {2002} } @article{Kelley:2010fk, abstract = {ABSTRACT : We introduce Quake, a program to detect and correct errors in DNA sequencing reads. Using a maximum likelihood approach incorporating quality values and nucleotide specific miscall rates, Quake achieves the highest accuracy on realistically simulated reads. We further demonstrate substantial improvements in de novo assembly and SNP detection after using Quake. Quake can be used for any size project, including more than one billion human reads, and is freely available as open source software from http://www.cbcb.umd.edu/software/quake.}, author = {Kelley, David R and Schatz, Michael C and Salzberg, Steven L}, doi = {10.1186/gb-2010-11-11-r116}, file = {:home/gus/Documents/Mendeley Desktop/Kelley, Schatz, Salzberg\_2010\_Quake quality-aware detection and correction of sequencing errors.pdf:pdf}, journal = {Genome Biol}, number = {11}, pages = {R116}, pmid = {21114842}, title = {{Quake: quality-aware detection and correction of sequencing errors}}, volume = {11}, year = {2010} } @article{Qi2008, abstract = {The yeast synthetic lethal genetic interaction network contains rich information about underlying pathways and protein complexes as well as new genetic interactions yet to be discovered. We have developed a graph diffusion kernel as a unified framework for inferring complex/pathway membership analogous to "friends" and genetic interactions analogous to "enemies" from the genetic interaction network. When applied to the Saccharomyces cerevisiae synthetic lethal genetic interaction network, we can achieve a precision around 50\% with 20\% to 50\% recall in the genome-wide prediction of new genetic interactions, supported by experimental validation. The kernels show significant improvement over previous best methods for predicting genetic interactions and protein co-complex membership from genetic interaction data.}, author = {Qi, Yan and Suhail, Yasir and Lin, Yu-yi and Boeke, Jef D and Bader, Joel S}, doi = {10.1101/gr.077693.108}, file = {:home/gus/Documents/Mendeley Desktop/Qi et al.\_2008\_Finding friends and enemies in an enemies-only network a graph diffusion kernel for predicting novel genetic interactions and co-complex membership from yeast genetic interactions.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Fungal,Gene Expression Regulation,Genes,Genetic,Genomics,Genomics: methods,Models,Protein Interaction Mapping,Protein Interaction Mapping: methods,Reproducibility of Results,Saccharomyces cerevisiae,Saccharomyces cerevisiae Proteins,Saccharomyces cerevisiae Proteins: genetics,Saccharomyces cerevisiae Proteins: metabolism,Saccharomyces cerevisiae: genetics,Saccharomyces cerevisiae: metabolism,Statistical}, month = dec, number = {12}, pages = {1991--2004}, pmid = {18832443}, title = {{Finding friends and enemies in an enemies-only network: a graph diffusion kernel for predicting novel genetic interactions and co-complex membership from yeast genetic interactions.}}, url = {http://genome.cshlp.org/cgi/content/abstract/18/12/1991}, volume = {18}, year = {2008} } @misc{TheMendeleySupportTeam2011, abstract = {A quick introduction to Mendeley. Learn how Mendeley creates your personal digital library, how to organize and annotate documents, how to collaborate and share with colleagues, and how to generate citations and bibliographies.}, address = {London}, author = {{The Mendeley Support Team}}, booktitle = {Mendeley Desktop}, file = {:home/gus/Documents/Mendeley Desktop/The Mendeley Support Team\_2011\_Getting Started with Mendeley.pdf:pdf}, keywords = {Mendeley,how-to,user manual}, pages = {1--16}, publisher = {Mendeley Ltd.}, title = {{Getting Started with Mendeley}}, url = {http://www.mendeley.com}, year = {2011} } @article{Chaisson2008, abstract = {In the last year, high-throughput sequencing technologies have progressed from proof-of-concept to production quality. While these methods produce high-quality reads, they have yet to produce reads comparable in length to Sanger-based sequencing. Current fragment assembly algorithms have been implemented and optimized for mate-paired Sanger-based reads, and thus do not perform well on short reads produced by short read technologies. We present a new Eulerian assembler that generates nearly optimal short read assemblies of bacterial genomes and describe an approach to assemble reads in the case of the popular hybrid protocol when short and long Sanger-based reads are combined.}, author = {Chaisson, Mark J and Pevzner, Pavel A}, doi = {10.1101/gr.7088808}, file = {:home/gus/Documents/Mendeley Desktop/Chaisson, Pevzner\_2008\_Short read fragment assembly of bacterial genomes.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Bacterial,Bacterial: genetics,Contig Mapping,Contig Mapping: methods,DNA,DNA: methods,Genome,Genomics,Genomics: methods,Research Design,Sequence Analysis}, month = feb, number = {2}, pages = {324--30}, pmid = {18083777}, title = {{Short read fragment assembly of bacterial genomes.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2203630\&tool=pmcentrez\&rendertype=abstract}, volume = {18}, year = {2008} } @article{Scally2012, author = {Scally, Aylwyn and Dutheil, Julien Y. and Hillier, LaDeana W. and Jordan, Gregory E. and Goodhead, Ian and Herrero, Javier and Hobolth, Asger and Lappalainen, Tuuli and Mailund, Thomas and Marques-Bonet, Tomas and McCarthy, Shane and Montgomery, Stephen H. and Schwalie, Petra C. and Tang, Y. Amy and Ward, Michelle C. and Xue, Yali and Yngvadottir, Bryndis and Alkan, Can and Andersen, Lars N. and Ayub, Qasim and Ball, Edward V. and Beal, Kathryn and Bradley, Brenda J. and Chen, Yuan and Clee, Chris M. and Fitzgerald, Stephen and Graves, Tina A. and Gu, Yong and Heath, Paul and Heger, Andreas and Karakoc, Emre and Kolb-Kokocinski, Anja and Laird, Gavin K. and Lunter, Gerton and Meader, Stephen and Mort, Matthew and Mullikin, James C. and Munch, Kasper and O’Connor, Timothy D. and Phillips, Andrew D. and Prado-Martinez, Javier and Rogers, Anthony S. and Sajjadian, Saba and Schmidt, Dominic and Shaw, Katy and Simpson, Jared T. and Stenson, Peter D. and Turner, Daniel J. and Vigilant, Linda and Vilella, Albert J. and Whitener, Weldon and Zhu, Baoli and Cooper, David N. and de Jong, Pieter and Dermitzakis, Emmanouil T. and Eichler, Evan E. and Flicek, Paul and Goldman, Nick and Mundy, Nicholas I. and Ning, Zemin and Odom, Duncan T. and Ponting, Chris P. and Quail, Michael A. and Ryder, Oliver A. and Searle, Stephen M. and Warren, Wesley C. and Wilson, Richard K. and Schierup, Mikkel H. and Rogers, Jane and Tyler-Smith, Chris and Durbin, Richard}, doi = {10.1038/nature10842}, file = {:home/gus/Documents/Mendeley Desktop/Scally et al.\_2012\_Insights into hominid evolution from the gorilla genome sequence.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Scally et al.\_2012\_Insights into hominid evolution from the gorilla genome sequence(3).pdf:pdf}, issn = {0028-0836}, journal = {Nature}, month = mar, number = {7388}, pages = {169--175}, publisher = {Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.}, shorttitle = {Nature}, title = {{Insights into hominid evolution from the gorilla genome sequence}}, url = {http://dx.doi.org/10.1038/nature10842}, volume = {483}, year = {2012} } @article{Richter2008, abstract = {The new research field of metagenomics is providing exciting insights into various, previously unclassified ecological systems. Next-generation sequencing technologies are producing a rapid increase of environmental data in public databases. There is great need for specialized software solutions and statistical methods for dealing with complex metagenome data sets.}, author = {Richter, Daniel C and Ott, Felix and Auch, Alexander F and Schmid, Ramona and Huson, Daniel H}, doi = {10.1371/journal.pone.0003373}, editor = {Field, Dawn}, file = {:home/gus/Documents/Mendeley Desktop/Richter et al.\_2008\_MetaSim a sequencing simulator for genomics and metagenomics.pdf:pdf}, issn = {1932-6203}, journal = {PloS one}, keywords = {Databases, Genetic,Genomics,Models, Theoretical,User-Computer Interface}, month = jan, number = {10}, pages = {e3373}, pmid = {18841204}, publisher = {Public Library of Science}, title = {{MetaSim: a sequencing simulator for genomics and metagenomics.}}, url = {http://dx.plos.org/10.1371/journal.pone.0003373}, volume = {3}, year = {2008} } @article{Peterlongo2011, abstract = {Background: The analysis of next-generation sequencing data from large genomes is a timely research topic. Sequencers are producing billions of short sequence fragments from newly sequenced organisms. Computational methods for reconstructing sequences (whole-genome assemblers) are typically employed to process such data. However, one of the main drawback of these methods is the high memory requirement. Results: We present Mapsembler, an iterative targeted assembler which processes large datasets of reads on commodity hardware. Mapsembler checks for the presence of given regions of interest in the reads and reconstructs their neighborhood, either as a plain sequence (consensus) or as a graph (full sequence structure). We introduce new algorithms to retrieve homologues of a sequence from reads and construct an extension graph. Conclusions: Mapsembler is the rst software that enables de novo discovery around a region of interest of gene homologues, SNPs, exon skipping as well as other structural events, directly from raw sequencing reads. Compared to traditional assembly software, memory requirement and execution time of Mapsembler are considerably lower, as data indexing is localized. Mapsembler can be used at http://mapsembler.genouest.org}, author = {Peterlongo, Pierre and Chikhi, Rayan}, file = {:home/gus/Documents/Mendeley Desktop/Peterlongo, Chikhi\_2011\_Mapsembler, targeted assembly of larges genomes on a desktop computer.pdf:pdf}, keywords = {NGS,algorithms,bioinformatics,genome,light memory usage,targeted assembly}, month = mar, title = {{Mapsembler, targeted assembly of larges genomes on a desktop computer}}, url = {http://hal.inria.fr/inria-00577218/ http://hal.inria.fr/docs/00/57/72/18/PDF/RR-7565.pdf}, year = {2011} } @article{michael2004hazard, author = {Michael, M.M.}, file = {:home/gus/Documents/Mendeley Desktop/Michael\_2004\_Hazard pointers Safe memory reclamation for lock-free objects.pdf:pdf}, journal = {Parallel and Distributed Systems, IEEE Transactions on}, number = {6}, pages = {491--504}, publisher = {IEEE}, title = {{Hazard pointers: Safe memory reclamation for lock-free objects}}, url = {http://ieeexplore.ieee.org/xpls/abs\_all.jsp?arnumber=1291819}, volume = {15}, year = {2004} } @article{Yang2011a, abstract = {High-throughput short read sequencing is revolutionizing genomics and systems biology research by enabling cost-effective deep coverage sequencing of genomes and transcriptomes. Error detection and correction are crucial to many short read sequencing applications including de novo genome sequencing, genome resequencing, and digital gene expression analysis. Short read error detection is typically carried out by counting the observed frequencies of kmers in reads and validating those with frequencies exceeding a threshold. In case of genomes with high repeat content, an erroneous kmer may be frequently observed if it has few nucleotide differences with valid kmers with multiple occurrences in the genome. Error detection and correction were mostly applied to genomes with low repeat content and this remains a challenging problem for genomes with high repeat content.}, author = {Yang, Xiao and Aluru, Srinivas and Dorman, Karin S}, doi = {10.1186/1471-2105-12-S1-S52}, file = {:home/gus/Documents/Mendeley Desktop//Yang, Aluru, Dorman\_2011\_Repeat-aware modeling and correction of short read errors.pdf:pdf}, issn = {1471-2105}, journal = {BMC bioinformatics}, keywords = {Algorithms,Computational Biology,Computational Biology: methods,Genomics,Genomics: methods,High-Throughput Nucleotide Sequencing,High-Throughput Nucleotide Sequencing: methods,Likelihood Functions,Models,Software,Statistical}, month = jan, pages = {S52}, pmid = {21342585}, title = {{Repeat-aware modeling and correction of short read errors.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3044310\&tool=pmcentrez\&rendertype=abstract}, volume = {12 Suppl 1}, year = {2011} } @article{Roberts12122004, abstract = {Motivation: Comparison of nucleic acid and protein sequences is a fundamental tool of modern bioinformatics. A dominant method of such string matching is the ‘seed-and-extend’ approach, in which occurrences of short subsequences called ‘seeds’ are used to search for potentially longer matches in a large database of sequences. Each such potential match is then checked to see if it extends beyond the seed. To be effective, the seed-and-extend approach needs to catalogue seeds from virtually every substring in the database of search strings. Projects such as mammalian genome assemblies and large-scale protein matching, however, have such large sequence databases that the resulting list of seeds cannot be stored in RAM on a single computer. This significantly slows the matching process.Results: We present a simple and elegant method in which only a small fraction of seeds, called ‘minimizers’, needs to be stored. Using minimizers can speed up string-matching computations by a large factor while missing only a small fraction of the matches found using all seeds.}, author = {Roberts, Michael and Hayes, Wayne and Hunt, Brian R and Mount, Stephen M and Yorke, James A}, doi = {10.1093/bioinformatics/bth408}, file = {:home/gus/Documents/Mendeley Desktop/Roberts et al.\_2004\_Reducing storage requirements for biological sequence comparison(2).pdf:pdf}, issn = {1367-4803}, journal = {Bioinformatics}, keywords = {Algorithms,Computer-Assisted,Databases,Genetic,Information Storage and Retrieval,Information Storage and Retrieval: methods,Numerical Analysis,Sequence Alignment,Sequence Alignment: methods,Sequence Analysis,Sequence Analysis: methods}, month = dec, number = {18}, pages = {3363--3369}, pmid = {15256412}, title = {{Reducing storage requirements for biological sequence comparison}}, url = {http://bioinformatics.oxfordjournals.org/content/20/18/3363.short}, volume = {20}, year = {2004} } @article{Zhao2011, author = {Zhao, Z and Yin, J and Li, Y}, file = {:home/gus/Documents/Mendeley Desktop/Zhao, Yin, Li\_2011\_An efficient hybrid approach to correcting errors in short reads.pdf:pdf}, journal = {Modeling Decision for Artificial \ldots}, title = {{An efficient hybrid approach to correcting errors in short reads}}, url = {http://www.springerlink.com/index/P53757J416772662.pdf}, year = {2011} } @article{Scally2012, author = {Scally, Aylwyn and Dutheil, Julien Y. and Hillier, LaDeana W. and Jordan, Gregory E. and Goodhead, Ian and Herrero, Javier and Hobolth, Asger and Lappalainen, Tuuli and Mailund, Thomas and Marques-Bonet, Tomas and McCarthy, Shane and Montgomery, Stephen H. and Schwalie, Petra C. and Tang, Y. Amy and Ward, Michelle C. and Xue, Yali and Yngvadottir, Bryndis and Alkan, Can and Andersen, Lars N. and Ayub, Qasim and Ball, Edward V. and Beal, Kathryn and Bradley, Brenda J. and Chen, Yuan and Clee, Chris M. and Fitzgerald, Stephen and Graves, Tina A. and Gu, Yong and Heath, Paul and Heger, Andreas and Karakoc, Emre and Kolb-Kokocinski, Anja and Laird, Gavin K. and Lunter, Gerton and Meader, Stephen and Mort, Matthew and Mullikin, James C. and Munch, Kasper and O’Connor, Timothy D. and Phillips, Andrew D. and Prado-Martinez, Javier and Rogers, Anthony S. and Sajjadian, Saba and Schmidt, Dominic and Shaw, Katy and Simpson, Jared T. and Stenson, Peter D. and Turner, Daniel J. and Vigilant, Linda and Vilella, Albert J. and Whitener, Weldon and Zhu, Baoli and Cooper, David N. and de Jong, Pieter and Dermitzakis, Emmanouil T. and Eichler, Evan E. and Flicek, Paul and Goldman, Nick and Mundy, Nicholas I. and Ning, Zemin and Odom, Duncan T. and Ponting, Chris P. and Quail, Michael A. and Ryder, Oliver A. and Searle, Stephen M. and Warren, Wesley C. and Wilson, Richard K. and Schierup, Mikkel H. and Rogers, Jane and Tyler-Smith, Chris and Durbin, Richard}, doi = {10.1038/nature10842}, file = {:home/gus/Documents/Mendeley Desktop/Scally et al.\_2012\_Insights into hominid evolution from the gorilla genome sequence.pdf:pdf}, issn = {0028-0836}, journal = {Nature}, month = mar, number = {7388}, pages = {169--175}, publisher = {Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.}, shorttitle = {Nature}, title = {{Insights into hominid evolution from the gorilla genome sequence}}, url = {http://dx.doi.org/10.1038/nature10842}, volume = {483}, year = {2012} } @article{Pevzner:2001uq, abstract = {For the last 20 years, fragment assembly in DNA sequencing followed the "overlap-layout-consensus" paradigm that is used in all currently available assembly tools. Although this approach proved useful in assembling clones, it faces difficulties in genomic shotgun assembly. We abandon the classical "overlap-layout-consensus" approach in favor of a new euler algorithm that, for the first time, resolves the 20-year-old "repeat problem" in fragment assembly. Our main result is the reduction of the fragment assembly to a variation of the classical Eulerian path problem that allows one to generate accurate solutions of large-scale sequencing problems. euler, in contrast to the celera assembler, does not mask such repeats but uses them instead as a powerful fragment assembly tool.}, author = {Pevzner, P A and Tang, H and Waterman, M S}, doi = {10.1073/pnas.171285098}, file = {:home/gus/Documents/Mendeley Desktop/Pevzner, Tang, Waterman\_2001\_An Eulerian path approach to DNA fragment assembly.pdf:pdf}, journal = {Proc Natl Acad Sci U S A}, month = aug, number = {17}, pages = {9748--9753}, pmid = {11504945}, title = {{An Eulerian path approach to DNA fragment assembly}}, volume = {98}, year = {2001} } @article{nagarajan2009parametric, author = {Nagarajan, N. and Pop, M.}, file = {:home/gus/Documents/Mendeley Desktop/Nagarajan, Pop\_2009\_Parametric complexity of sequence assembly theory and applications to next generation sequencing.pdf:pdf}, journal = {Journal of computational biology}, number = {7}, pages = {897--908}, publisher = {Mary Ann Liebert, Inc. 140 Huguenot Street, 3rd Floor New Rochelle, NY 10801 USA}, title = {{Parametric complexity of sequence assembly: theory and applications to next generation sequencing}}, url = {http://www.liebertonline.com/doi/abs/10.1089/cmb.2009.0005}, volume = {16}, year = {2009} } @inproceedings{Fomitchev2004, address = {New York, New York, USA}, annote = {http://drdobbs.com/parallel/208801371}, author = {Fomitchev, Mikhail and Ruppert, Eric}, booktitle = {Proceedings of the twenty-third annual ACM symposium on Principles of distributed computing - PODC '04}, doi = {10.1145/1011767.1011776}, file = {:home/gus/Documents/Mendeley Desktop/Fomitchev, Ruppert\_2004\_Lock-free linked lists and skip lists.pdf:pdf}, isbn = {1581138024}, keywords = {amortized analysis,analysis,distributed,efficient,fault-tolerant,linked list,lock-free,skip list}, month = jul, pages = {50}, publisher = {ACM Press}, title = {{Lock-free linked lists and skip lists}}, url = {http://dl.acm.org/citation.cfm?id=1011767.1011776}, year = {2004} } @article{Trapnell2009, abstract = {A new protocol for sequencing the messenger RNA in a cell, known as RNA-Seq, generates millions of short sequence fragments in a single run. These fragments, or 'reads', can be used to measure levels of gene expression and to identify novel splice variants of genes. However, current software for aligning RNA-Seq data to a genome relies on known splice junctions and cannot identify novel ones. TopHat is an efficient read-mapping algorithm designed to align reads from an RNA-Seq experiment to a reference genome without relying on known splice sites.}, author = {Trapnell, Cole and Pachter, Lior and Salzberg, Steven L}, doi = {10.1093/bioinformatics/btp120}, file = {:home/gus/Documents/Mendeley Desktop/Trapnell, Pachter, Salzberg\_2009\_TopHat discovering splice junctions with RNA-Seq(2).pdf:pdf;:home/gus/Documents/Mendeley Desktop/Trapnell, Pachter, Salzberg\_2009\_TopHat discovering splice junctions with RNA-Seq.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,Gene Expression Profiling,Gene Expression Profiling: methods,Genetic,Messenger,Models,RNA,RNA Splicing,RNA Splicing: genetics,Sequence Alignment,Sequence Analysis,Software}, month = may, number = {9}, pages = {1105--11}, pmid = {19289445}, title = {{TopHat: discovering splice junctions with RNA-Seq.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/25/9/1105}, volume = {25}, year = {2009} } @article{Gnerre:2011zr, abstract = {Massively parallel DNA sequencing technologies are revolutionizing genomics by making it possible to generate billions of relatively short (\~{}100-base) sequence reads at very low cost. Whereas such data can be readily used for a wide range of biomedical applications, it has proven difficult to use them to generate high-quality de novo genome assemblies of large, repeat-rich vertebrate genomes. To date, the genome assemblies generated from such data have fallen far short of those obtained with the older (but much more expensive) capillary-based sequencing approach. Here, we report the development of an algorithm for genome assembly, ALLPATHS-LG, and its application to massively parallel DNA sequence data from the human and mouse genomes, generated on the Illumina platform. The resulting draft genome assemblies have good accuracy, short-range contiguity, long-range connectivity, and coverage of the genome. In particular, the base accuracy is high (≥99.95\%) and the scaffold sizes (N50 size = 11.5 Mb for human and 7.2 Mb for mouse) approach those obtained with capillary-based sequencing. The combination of improved sequencing technology and improved computational methods should now make it possible to increase dramatically the de novo sequencing of large genomes. The ALLPATHS-LG program is available at http://www.broadinstitute.org/science/programs/genome-biology/crd.}, annote = { From Duplicate 2 ( High-quality draft assemblies of mammalian genomes from massively parallel sequence data - Gnerre, Sante; Maccallum, Iain; Przybylski, Dariusz; Ribeiro, Filipe J; Burton, Joshua N; Walker, Bruce J; Sharpe, Ted; Hall, Giles; Shea, Terrance P; Sykes, Sean; Berlin, Aaron M; Aird, Daniel; Costello, Maura; Daza, Riza; Williams, Louise; Nicol, Robert; Gnirke, Andreas; Nusbaum, Chad; Lander, Eric S; Jaffe, David B ) }, author = {Gnerre, Sante and Maccallum, Iain and Przybylski, Dariusz and Ribeiro, Filipe J and Burton, Joshua N and Walker, Bruce J and Sharpe, Ted and Hall, Giles and Shea, Terrance P and Sykes, Sean and Berlin, Aaron M and Aird, Daniel and Costello, Maura and Daza, Riza and Williams, Louise and Nicol, Robert and Gnirke, Andreas and Nusbaum, Chad and Lander, Eric S and Jaffe, David B}, doi = {10.1073/pnas.1017351108}, file = {:home/gus/Documents/Mendeley Desktop/Gnerre et al.\_2011\_High-quality draft assemblies of mammalian genomes from massively parallel sequence data.pdf:pdf;::}, issn = {1091-6490}, journal = {Proc Natl Acad Sci U S A}, keywords = {Algorithms,Animals,DNA,DNA: methods,Genome,Genome: genetics,Genomics,Genomics: methods,Humans,Internet,Mice,Reproducibility of Results,Sequence Analysis,Software}, month = jan, number = {4}, pages = {1513--1518}, pmid = {21187386}, title = {{High-quality draft assemblies of mammalian genomes from massively parallel sequence data}}, url = {http://www.pnas.org/cgi/content/abstract/108/4/1513}, volume = {108}, year = {2011} } @article{zhao2011psaec, author = {Zhao, Z. and Yin, J. and Zhan, Y. and Xiong, W. and Li, Y. and Liu, F.}, file = {:home/gus/Documents/Mendeley Desktop/Zhao et al.\_2011\_PSAEC An Improved Algorithm for Short Read Error Correction Using Partial Suffix Arrays.pdf:pdf}, journal = {Frontiers in Algorithmics and Algorithmic Aspects in Information and Management}, pages = {220--232}, publisher = {Springer}, title = {{PSAEC: An Improved Algorithm for Short Read Error Correction Using Partial Suffix Arrays}}, url = {http://www.springerlink.com/index/9L77826718445828.pdf}, year = {2011} } @article{Richter2008, abstract = {The new research field of metagenomics is providing exciting insights into various, previously unclassified ecological systems. Next-generation sequencing technologies are producing a rapid increase of environmental data in public databases. There is great need for specialized software solutions and statistical methods for dealing with complex metagenome data sets.}, author = {Richter, Daniel C and Ott, Felix and Auch, Alexander F and Schmid, Ramona and Huson, Daniel H}, doi = {10.1371/journal.pone.0003373}, editor = {Field, Dawn}, file = {:home/gus/Documents/Mendeley Desktop/Richter et al.\_2008\_MetaSim a sequencing simulator for genomics and metagenomics.pdf:pdf}, issn = {1932-6203}, journal = {PloS one}, keywords = {Databases,Genetic,Genomics,Models,Theoretical,User-Computer Interface}, month = jan, number = {10}, pages = {e3373}, pmid = {18841204}, publisher = {Public Library of Science}, title = {{MetaSim: a sequencing simulator for genomics and metagenomics.}}, url = {http://dx.plos.org/10.1371/journal.pone.0003373}, volume = {3}, year = {2008} } @article{Farach1997, author = {Farach, M.}, file = {:home/gus/Documents/Mendeley Desktop/Farach\_1997\_Optimal suffix tree construction with large alphabets.pdf:pdf}, isbn = {0-8186-8197-7}, keywords = {combinatorial pattern matching,data structure,integer alphabet,integer alphabets,large alphabets,pattern matching,sorting,suffix tree}, month = oct, pages = {137}, title = {{Optimal suffix tree construction with large alphabets}}, url = {http://dl.acm.org/citation.cfm?id=795663.796326}, year = {1997} } @article{yang2010reptile, author = {Yang, X. and Dorman, K.S. and Aluru, S.}, file = {:home/gus/Documents/Mendeley Desktop/Yang, Dorman, Aluru\_2010\_Reptile representative tiling for short read error correction.pdf:pdf}, journal = {Bioinformatics}, number = {20}, pages = {2526}, publisher = {Oxford Univ Press}, title = {{Reptile: representative tiling for short read error correction}}, url = {http://bioinformatics.oxfordjournals.org/content/26/20/2526.short}, volume = {26}, year = {2010} } @article{Chaisson2008, abstract = {In the last year, high-throughput sequencing technologies have progressed from proof-of-concept to production quality. While these methods produce high-quality reads, they have yet to produce reads comparable in length to Sanger-based sequencing. Current fragment assembly algorithms have been implemented and optimized for mate-paired Sanger-based reads, and thus do not perform well on short reads produced by short read technologies. We present a new Eulerian assembler that generates nearly optimal short read assemblies of bacterial genomes and describe an approach to assemble reads in the case of the popular hybrid protocol when short and long Sanger-based reads are combined.}, author = {Chaisson, Mark J and Pevzner, Pavel A}, doi = {10.1101/gr.7088808}, file = {:home/gus/Documents/Mendeley Desktop/Chaisson, Pevzner\_2008\_Short read fragment assembly of bacterial genomes.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Bacterial,Bacterial: genetics,Contig Mapping,Contig Mapping: methods,DNA,DNA: methods,Genome,Genomics,Genomics: methods,Research Design,Sequence Analysis}, month = feb, number = {2}, pages = {324--30}, pmid = {18083777}, title = {{Short read fragment assembly of bacterial genomes.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2203630\&tool=pmcentrez\&rendertype=abstract}, volume = {18}, year = {2008} } @inproceedings{sundell2003fast, author = {Sundell, H. and Tsigas, P.}, booktitle = {Parallel and Distributed Processing Symposium, 2003. Proceedings. International}, file = {:home/gus/Documents/Mendeley Desktop/Sundell, Tsigas\_2003\_Fast and lock-free concurrent priority queues for multi-thread systems.pdf:pdf}, pages = {11--pp}, publisher = {IEEE}, title = {{Fast and lock-free concurrent priority queues for multi-thread systems}}, url = {http://ieeexplore.ieee.org/xpls/abs\_all.jsp?arnumber=1213189}, year = {2003} } @article{Nakamura2011, abstract = {We identified the sequence-specific starting positions of consecutive miscalls in the mapping of reads obtained from the Illumina Genome Analyser (GA). Detailed analysis of the miscall pattern indicated that the underlying mechanism involves sequence-specific interference of the base elongation process during sequencing. The two major sequence patterns that trigger this sequence-specific error (SSE) are: (i) inverted repeats and (ii) GGC sequences. We speculate that these sequences favor dephasing by inhibiting single-base elongation, by: (i) folding single-stranded DNA and (ii) altering enzyme preference. This phenomenon is a major cause of sequence coverage variability and of the unfavorable bias observed for population-targeted methods such as RNA-seq and ChIP-seq. Moreover, SSE is a potential cause of false single-nucleotide polymorphism (SNP) calls and also significantly hinders de novo assembly. This article highlights the importance of recognizing SSE and its underlying mechanisms in the hope of enhancing the potential usefulness of the Illumina sequencers.}, author = {Nakamura, Kensuke and Oshima, Taku and Morimoto, Takuya and Ikeda, Shun and Yoshikawa, Hirofumi and Shiwa, Yuh and Ishikawa, Shu and Linak, Margaret C and Hirai, Aki and Takahashi, Hiroki and Altaf-Ul-Amin, Md and Ogasawara, Naotake and Kanaya, Shigehiko}, doi = {10.1093/nar/gkr344}, file = {:home/gus/Documents/Mendeley Desktop/Nakamura et al.\_2011\_Sequence-specific error profile of Illumina sequencers.pdf:pdf}, issn = {1362-4962}, journal = {Nucleic acids research}, month = may, number = {13}, pages = {e90--}, pmid = {21576222}, title = {{Sequence-specific error profile of Illumina sequencers.}}, url = {http://nar.oxfordjournals.org/cgi/content/abstract/39/13/e90}, volume = {39}, year = {2011} } @article{Yang2011, abstract = {High-throughput short read sequencing is revolutionizing genomics and systems biology research by enabling cost-effective deep coverage sequencing of genomes and transcriptomes. Error detection and correction are crucial to many short read sequencing applications including de novo genome sequencing, genome resequencing, and digital gene expression analysis. Short read error detection is typically carried out by counting the observed frequencies of kmers in reads and validating those with frequencies exceeding a threshold. In case of genomes with high repeat content, an erroneous kmer may be frequently observed if it has few nucleotide differences with valid kmers with multiple occurrences in the genome. Error detection and correction were mostly applied to genomes with low repeat content and this remains a challenging problem for genomes with high repeat content.}, author = {Yang, Xiao and Aluru, Srinivas and Dorman, Karin S}, doi = {10.1186/1471-2105-12-S1-S52}, file = {:home/gus/Documents/Mendeley Desktop//Yang, Aluru, Dorman\_2011\_Repeat-aware modeling and correction of short read errors.pdf:pdf}, issn = {1471-2105}, journal = {BMC bioinformatics}, keywords = {Algorithms,Computational Biology,Computational Biology: methods,Genomics,Genomics: methods,High-Throughput Nucleotide Sequencing,High-Throughput Nucleotide Sequencing: methods,Likelihood Functions,Models,Software,Statistical}, month = jan, number = {Suppl 1}, pages = {S52}, pmid = {21342585}, title = {{Repeat-aware modeling and correction of short read errors.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3044310\&tool=pmcentrez\&rendertype=abstract http://www.biomedcentral.com/1471-2105/12/S1/S52}, volume = {12 Suppl 1}, year = {2011} } @article{Yang2011, abstract = {High-throughput short read sequencing is revolutionizing genomics and systems biology research by enabling cost-effective deep coverage sequencing of genomes and transcriptomes. Error detection and correction are crucial to many short read sequencing applications including de novo genome sequencing, genome resequencing, and digital gene expression analysis. Short read error detection is typically carried out by counting the observed frequencies of kmers in reads and validating those with frequencies exceeding a threshold. In case of genomes with high repeat content, an erroneous kmer may be frequently observed if it has few nucleotide differences with valid kmers with multiple occurrences in the genome. Error detection and correction were mostly applied to genomes with low repeat content and this remains a challenging problem for genomes with high repeat content.}, author = {Yang, Xiao and Aluru, Srinivas and Dorman, Karin S}, doi = {10.1186/1471-2105-12-S1-S52}, file = {:home/gus/Documents/Mendeley Desktop//Yang, Aluru, Dorman\_2011\_Repeat-aware modeling and correction of short read errors.pdf:pdf}, issn = {1471-2105}, journal = {BMC bioinformatics}, keywords = {Algorithms,Computational Biology,Computational Biology: methods,Genomics,Genomics: methods,High-Throughput Nucleotide Sequencing,High-Throughput Nucleotide Sequencing: methods,Likelihood Functions,Models,Software,Statistical}, month = jan, number = {Suppl 1}, pages = {S52}, pmid = {21342585}, title = {{Repeat-aware modeling and correction of short read errors.}}, url = {http://www.biomedcentral.com/1471-2105/12/S1/S52}, volume = {12 Suppl 1}, year = {2011} } @article{Ferragina2000, author = {Ferragina, P. and Manzini, G.}, file = {:home/gus/Documents/Mendeley Desktop/Ferragina, Manzini\_2000\_Opportunistic data structures with applications.pdf:pdf}, isbn = {0-7695-0850-2}, keywords = {Glimpse tool,computational complexity,data compression,data indexing,data set,data structures,database indexing,database theory,entropy,opportunistic data structures,query performance,search,sublinear query time complexity,sublinear space complexity,succinct suffix array,suffix array data structures,suffix tree data structures}, month = nov, pages = {390}, title = {{Opportunistic data structures with applications}}, url = {http://dl.acm.org/citation.cfm?id=795666.796543 http://www.di.unipi.it/~ferragin/Libraries/fmindexV2/index.html}, year = {2000} } @article{Langmead2009, abstract = {Bowtie is an ultrafast, memory-efficient alignment program for aligning short DNA sequence reads to large genomes. For the human genome, Burrows-Wheeler indexing allows Bowtie to align more than 25 million reads per CPU hour with a memory footprint of approximately 1.3 gigabytes. Bowtie extends previous Burrows-Wheeler techniques with a novel quality-aware backtracking algorithm that permits mismatches. Multiple processor cores can be used simultaneously to achieve even greater alignment speeds. Bowtie is open source (http://bowtie.cbcb.umd.edu).}, author = {Langmead, Ben and Trapnell, Cole and Pop, Mihai and Salzberg, Steven L}, doi = {10.1186/gb-2009-10-3-r25}, file = {:home/gus/Documents/Mendeley Desktop/Langmead et al.\_2009\_Ultrafast and memory-efficient alignment of short DNA sequences to the human genome.pdf:pdf}, issn = {1465-6914}, journal = {Genome biology}, keywords = {Algorithms,Base Sequence,Genome,Human,Human: genetics,Humans,Sequence Alignment,Sequence Alignment: methods}, month = jan, number = {3}, pages = {R25}, pmid = {19261174}, title = {{Ultrafast and memory-efficient alignment of short DNA sequences to the human genome.}}, url = {http://genomebiology.com/2009/10/3/R25}, volume = {10}, year = {2009} } @article{Venter2001, author = {Venter, JC and Adams, MD and Myers, EW}, file = {:home/gus/Documents/Mendeley Desktop/Venter, Adams, Myers\_2001\_The sequence of the human genome.pdf:pdf}, journal = {Science's \ldots}, title = {{The sequence of the human genome}}, url = {http://stke.sciencemag.org/cgi/content/abstract/sci;291/5507/1304}, year = {2001} } @article{Butler:2008kx, abstract = {New DNA sequencing technologies deliver data at dramatically lower costs but demand new analytical methods to take full advantage of the very short reads that they produce. We provide an initial, theoretical solution to the challenge of de novo assembly from whole-genome shotgun "microreads." For 11 genomes of sizes up to 39 Mb, we generated high-quality assemblies from 80x coverage by paired 30-base simulated reads modeled after real Illumina-Solexa reads. The bacterial genomes of Campylobacter jejuni and Escherichia coli assemble optimally, yielding single perfect contigs, and larger genomes yield assemblies that are highly connected and accurate. Assemblies are presented in a graph form that retains intrinsic ambiguities such as those arising from polymorphism, thereby providing information that has been absent from previous genome assemblies. For both C. jejuni and E. coli, this assembly graph is a single edge encompassing the entire genome. Larger genomes produce more complicated graphs, but the vast majority of the bases in their assemblies are present in long edges that are nearly always perfect. We describe a general method for genome assembly that can be applied to all types of DNA sequence data, not only short read data, but also conventional sequence reads.}, author = {Butler, Jonathan and MacCallum, Iain and Kleber, Michael and Shlyakhter, Ilya a and Belmonte, Matthew K and Lander, Eric S and Nusbaum, Chad and Jaffe, David B}, doi = {10.1101/gr.7337908}, file = {:home/gus/Documents/Mendeley Desktop/Butler et al.\_2008\_ALLPATHS de novo assembly of whole-genome shotgun microreads.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Bacterial,Bacterial: genetics,Campylobacter jejuni,Campylobacter jejuni: genetics,Computational Biology,Computational Biology: methods,Computer Simulation,DNA,DNA: methods,DNA: standards,Escherichia coli,Escherichia coli: genetics,Genome,Reproducibility of Results,Sequence Analysis}, month = may, number = {5}, pages = {810--20}, pmid = {18340039}, title = {{ALLPATHS: de novo assembly of whole-genome shotgun microreads.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2336810\&tool=pmcentrez\&rendertype=abstract}, volume = {18}, year = {2008} } @article{medvedev2007computability, author = {Medvedev, P. and Georgiou, K. and Myers, G. and Brudno, M.}, file = {:home/gus/Documents/Mendeley Desktop/Medvedev et al.\_2007\_Computability of models for sequence assembly.pdf:pdf}, journal = {Algorithms in Bioinformatics}, pages = {289--301}, publisher = {Springer}, title = {{Computability of models for sequence assembly}}, url = {http://www.springerlink.com/index/H711368771048H21.pdf}, year = {2007} } @article{Manber1990, annote = { From Duplicate 1 ( Suffix arrays: a new method for on-line string searches - Manber, Udi; Myers, Gene ) }, author = {Manber, Udi and Myers, Gene}, file = {:home/gus/Documents/Mendeley Desktop/Manber, Myers\_1990\_Suffix arrays a new method for on-line string searches(2).pdf:pdf;:home/gus/Documents/Mendeley Desktop/Manber, Myers\_1990\_Suffix arrays a new method for on-line string searches.pdf:pdf}, isbn = {0-89871-251-3}, journal = {Proceedings of the first annual ACM-SIAM \ldots}, month = jan, pages = {319--327}, title = {{Suffix arrays: a new method for on-line string searches}}, url = {http://portal.acm.org/citation.cfm?id=320218 http://dl.acm.org/citation.cfm?id=320176.320218}, year = {1990} } @article{herlihy2002repeat, author = {Herlihy, M. and Luchangco, V. and Moir, M.}, file = {:home/gus/Documents/Mendeley Desktop/Herlihy, Luchangco, Moir\_2002\_The repeat offender problem A mechanism for supporting dynamic-sized lock-free data structures.pdf:pdf}, publisher = {Sun Microsystems, Inc.}, title = {{The repeat offender problem: A mechanism for supporting dynamic-sized lock-free data structures}}, url = {http://portal.acm.org/citation.cfm?id=1698158}, year = {2002} } @article{Zerbino2009a, abstract = {Despite the short length of their reads, micro-read sequencing technologies have shown their usefulness for de novo sequencing. However, especially in eukaryotic genomes, complex repeat patterns are an obstacle to large assemblies.}, author = {Zerbino, Daniel R DR and McEwen, GK Gayle K and Margulies, Elliott H and Birney, Ewan}, doi = {10.1371/journal.pone.0008407}, file = {:home/gus/Documents/Mendeley Desktop/Zerbino, McEwen\_2009\_Pebble and rock band heuristic resolution of repeats and scaffolding in the velvet short-read de novo assembler.pdf:pdf}, issn = {1932-6203}, journal = {PloS one}, keywords = {Algorithms,Animals,Artificial,Bacterial,Bacterial: genetics,Chromosomes,Computer Simulation,DNA,DNA: instrumentation,DNA: methods,Ferrets,Ferrets: genetics,Nucleic Acid,Nucleic Acid: genetics,Pseudomonas syringae,Pseudomonas syringae: genetics,Repetitive Sequences,Sequence Analysis}, month = jan, number = {12}, pages = {e8407}, pmid = {20027311}, title = {{Pebble and rock band: heuristic resolution of repeats and scaffolding in the velvet short-read de novo assembler}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2793427\&tool=pmcentrez\&rendertype=abstract http://dx.plos.org/10.1371/journal.pone.0008407}, volume = {4}, year = {2009} } @article{Simpson2009, abstract = {Widespread adoption of massively parallel deoxyribonucleic acid (DNA) sequencing instruments has prompted the recent development of de novo short read assembly algorithms. A common shortcoming of the available tools is their inability to efficiently assemble vast amounts of data generated from large-scale sequencing projects, such as the sequencing of individual human genomes to catalog natural genetic variation. To address this limitation, we developed ABySS (Assembly By Short Sequences), a parallelized sequence assembler. As a demonstration of the capability of our software, we assembled 3.5 billion paired-end reads from the genome of an African male publicly released by Illumina, Inc. Approximately 2.76 million contigs > or =100 base pairs (bp) in length were created with an N50 size of 1499 bp, representing 68\% of the reference human genome. Analysis of these contigs identified polymorphic and novel sequences not present in the human reference assembly, which were validated by alignment to alternate human assemblies and to other primate genomes.}, author = {Simpson, Jared T and Wong, Kim and Jackman, Shaun D and Schein, Jacqueline E and Jones, Steven J M and Birol, Inan\c{c}}, doi = {10.1101/gr.089532.108}, file = {:home/gus/Documents/Mendeley Desktop/Simpson et al.\_2009\_ABySS a parallel assembler for short read sequence data.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Animals,Computational Biology,Computational Biology: methods,Contig Mapping,Escherichia coli K12,Escherichia coli K12: genetics,Genetic Variation,Genome, Human,Humans,Polymorphism, Genetic,Reproducibility of Results,Sequence Analysis, DNA,Sequence Analysis, DNA: methods,Software}, month = jun, number = {6}, pages = {1117--23}, pmid = {19251739}, title = {{ABySS: a parallel assembler for short read sequence data.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2694472\&tool=pmcentrez\&rendertype=abstract}, volume = {19}, year = {2009} } @article{Maccallum:2009vn, abstract = {We demonstrate that genome sequences approaching finished quality can be generated from short paired reads. Using 36 base (fragment) and 26 base (jumping) reads from five microbial genomes of varied GC composition and sizes up to 40 Mb, ALLPATHS2 generated assemblies with long, accurate contigs and scaffolds. Velvet and EULER-SR were less accurate. For example, for Escherichia coli, the fraction of 10-kb stretches that were perfect was 99.8\% (ALLPATHS2), 68.7\% (Velvet), and 42.1\% (EULER-SR).}, author = {Maccallum, Iain and Przybylski, Dariusz and Gnerre, Sante and Burton, Joshua and Shlyakhter, Ilya and Gnirke, Andreas and Malek, Joel and McKernan, Kevin and Ranade, Swati and Shea, Terrance P and Williams, Louise and Young, Sarah and Nusbaum, Chad and Jaffe, David B}, doi = {10.1186/gb-2009-10-10-r103}, file = {:home/gus/Documents/Mendeley Desktop//Maccallum et al.\_2009\_ALLPATHS 2 small genomes assembled accurately and with high continuity from short paired reads.pdf:pdf}, issn = {1465-6914}, journal = {Genome biology}, keywords = {Bacteria,Bacteria: genetics,Base Pairing,Base Pairing: genetics,Fungi,Fungi: genetics,Genome,Genome: genetics,Genomics,Genomics: methods,Reproducibility of Results,Software}, month = jan, number = {10}, pages = {R103}, pmid = {19796385}, title = {{ALLPATHS 2: small genomes assembled accurately and with high continuity from short paired reads.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2784318\&tool=pmcentrez\&rendertype=abstract}, volume = {10}, year = {2009} } @article{Chor2009, abstract = {The empirical frequencies of DNA k-mers in whole genome sequences provide an interesting perspective on genomic complexity, and the availability of large segments of genomic sequence from many organisms means that analysis of k-mers with non-trivial lengths is now possible.}, author = {Chor, Benny and Horn, David and Goldman, Nick and Levy, Yaron and Massingham, Tim}, doi = {10.1186/gb-2009-10-10-r108}, file = {:home/gus/Documents/Mendeley Desktop/Chor et al.\_2009\_Genomic DNA k-mer spectra models and modalities.pdf:pdf}, issn = {1465-6914}, journal = {Genome biology}, keywords = {Animals,Base Composition,Base Composition: genetics,Chickens,Chickens: genetics,Computer Simulation,CpG Islands,CpG Islands: genetics,DNA,DNA: genetics,Genome,Genome: genetics,Humans,Markov Chains,Models, Genetic,Zebrafish,Zebrafish: genetics}, month = jan, number = {10}, pages = {R108}, pmid = {19814784}, title = {{Genomic DNA k-mer spectra: models and modalities.}}, url = {http://genomebiology.com/2009/10/10/R108}, volume = {10}, year = {2009} } @techreport{Drepper2007, author = {Drepper, Ulrich}, file = {:home/gus/Documents/Mendeley Desktop/Drepper\_2007\_What Every Programmer Should Know About Memory.pdf:pdf}, keywords = {Cache,Memory,lock free}, title = {{What Every Programmer Should Know About Memory}}, year = {2007} } @article{Lander1988, abstract = {Results from physical mapping projects have recently been reported for the genomes of Escherichia coli, Saccharomyces cerevisiae, and Caenorhabditis elegans, and similar projects are currently being planned for other organisms. In such projects, the physical map is assembled by first "fingerprinting" a large number of clones chosen at random from a recombinant library and then inferring overlaps between clones with sufficiently similar fingerprints. Although the basic approach is the same, there are many possible choices for the fingerprint used to characterize the clones and the rules for declaring overlap. In this paper, we derive simple formulas showing how the progress of a physical mapping project is affected by the nature of the fingerprinting scheme. Using these formulas, we discuss the analytic considerations involved in selecting an appropriate fingerprinting scheme for a particular project.}, author = {Lander, E S and Waterman, M S}, file = {:home/gus/Documents/Mendeley Desktop/Lander, Waterman\_1988\_Genomic mapping by fingerprinting random clones a mathematical analysis.pdf:pdf}, issn = {0888-7543}, journal = {Genomics}, keywords = {Animals,Caenorhabditis,Caenorhabditis: genetics,Chromosome Mapping,Cloning,Escherichia coli,Escherichia coli: genetics,Mathematics,Molecular,Nucleotide Mapping,Saccharomyces cerevisiae,Saccharomyces cerevisiae: genetics}, month = apr, number = {3}, pages = {231--9}, pmid = {3294162}, title = {{Genomic mapping by fingerprinting random clones: a mathematical analysis.}}, url = {http://www.ncbi.nlm.nih.gov/pubmed/3294162}, volume = {2}, year = {1988} } @article{Purcell2005, abstract = {We present the first non-blocking hashtable based on open addressing that provides the following benefits: it combines good cache locality, accessing a single cacheline if there are no collisions, with short straight-line code; it needs no storage overhead for pointers and memory allocator schemes, having instead an overhead of two words per bucket; it does not need to periodically reorganise or replicate the table; and it does not need garbage collection, even with arbitrary-sized keys. Open problems include resizing the table and replacing, rather than erasing, entries. The result is a highly-concurrent set algorithm that approaches or outperforms the best externally- chained implementations we tested, with fixed memory costs and no need to select or fine-tune a garbage collector or locking strategy.}, author = {Purcell, Chris and Harris, Tim}, file = {:home/gus/Documents/Mendeley Desktop/Purcell, Harris\_2005\_Non-blocking hatables with open addressing.pdf:pdf}, journal = {University of Cambridge Technical Report}, keywords = {hash table,lock free}, number = {639}, title = {{Non-blocking hatables with open addressing}}, year = {2005} } @article{Zerbino2008, abstract = {We have developed a new set of algorithms, collectively called "Velvet," to manipulate de Bruijn graphs for genomic sequence assembly. A de Bruijn graph is a compact representation based on short words (k-mers) that is ideal for high coverage, very short read (25-50 bp) data sets. Applying Velvet to very short reads and paired-ends information only, one can produce contigs of significant length, up to 50-kb N50 length in simulations of prokaryotic data and 3-kb N50 on simulated mammalian BACs. When applied to real Solexa data sets without read pairs, Velvet generated contigs of approximately 8 kb in a prokaryote and 2 kb in a mammalian BAC, in close agreement with our simulated results without read-pair information. Velvet represents a new approach to assembly that can leverage very short reads in combination with read pairs to produce useful assemblies.}, author = {Zerbino, Daniel R and Birney, Ewan}, doi = {10.1101/gr.074492.107}, file = {:home/gus/Documents/Mendeley Desktop/Zerbino, Birney\_2008\_Velvet algorithms for de novo short read assembly using de Bruijn graphs.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Animals,Artificial,Bacterial,Chromosomes,Computational Biology,Computational Biology: methods,Computer Simulation,DNA,DNA: methods,DNA: standards,Genome,Genomics,Human,Humans,Mammals,Mammals: genetics,Sequence Analysis,Streptococcus,Streptococcus: genetics}, month = may, number = {5}, pages = {821--9}, pmid = {18349386}, title = {{Velvet: algorithms for de novo short read assembly using de Bruijn graphs}}, url = {http://genome.cshlp.org/content/18/5/821.short http://genome.cshlp.org/cgi/content/abstract/18/5/821}, volume = {18}, year = {2008} } @article{Maccallum:2009vn, abstract = {We demonstrate that genome sequences approaching finished quality can be generated from short paired reads. Using 36 base (fragment) and 26 base (jumping) reads from five microbial genomes of varied GC composition and sizes up to 40 Mb, ALLPATHS2 generated assemblies with long, accurate contigs and scaffolds. Velvet and EULER-SR were less accurate. For example, for Escherichia coli, the fraction of 10-kb stretches that were perfect was 99.8\% (ALLPATHS2), 68.7\% (Velvet), and 42.1\% (EULER-SR).}, author = {Maccallum, Iain and Przybylski, Dariusz and Gnerre, Sante and Burton, Joshua and Shlyakhter, Ilya and Gnirke, Andreas and Malek, Joel and McKernan, Kevin and Ranade, Swati and Shea, Terrance P and Williams, Louise and Young, Sarah and Nusbaum, Chad and Jaffe, David B}, doi = {10.1186/gb-2009-10-10-r103}, file = {:home/gus/Documents/Mendeley Desktop//Maccallum et al.\_2009\_ALLPATHS 2 small genomes assembled accurately and with high continuity from short paired reads.pdf:pdf}, issn = {1465-6914}, journal = {Genome biology}, keywords = {Bacteria,Bacteria: genetics,Base Pairing,Base Pairing: genetics,Fungi,Fungi: genetics,Genome,Genome: genetics,Genomics,Genomics: methods,Reproducibility of Results,Software}, month = jan, number = {10}, pages = {R103}, pmid = {19796385}, title = {{ALLPATHS 2: small genomes assembled accurately and with high continuity from short paired reads.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2784318\&tool=pmcentrez\&rendertype=abstract}, volume = {10}, year = {2009} } @article{Melsted2011, abstract = {BACKGROUND:Counting k-mers (substrings of length k in DNA sequence data) is an essential component of many methods in bioinformatics, including for genome and transcriptome assembly, for metagenomic sequencing, and for error correction of sequence reads. Although simple in principle, counting k-mers in large modern sequence data sets can easily overwhelm the memory capacity of standard computers. In current data sets, a large fraction - often more than 50\% - of the storage capacity may be spent on storing k-mers that contain sequencing errors and which are typically observed only a single time in the data. These singleton k-mers are uninformative for many algorithms without some kind of error correction.RESULTS:We present a new method that identifies all the k-mers that occur more than once in a DNA sequence data set. Our method does this using a Bloom filter, a probabilistic data structure that stores all the observed k-mers implicitly in memory with greatly reduced memory requirements. We then make a second sweep through the data to provide exact counts of all nonunique k-mers. For example data sets, we report up to 50\% savings in memory usage compared to current software, with modest costs in computational speed. This approach may reduce memory requirements for any algorithm that starts by counting k-mers in sequence data with errors.CONCLUSIONS:A reference implementation for this methodology, BFCounter, is written in C++ and is GPL licensed. It is available for free download at http://pritch.bsd.uchicago.edu/software.html}, author = {Melsted, Pall and Pritchard, Jonathan K}, doi = {10.1186/1471-2105-12-333}, file = {:home/gus/Documents/Mendeley Desktop/Melsted, Pritchard\_2011\_Efficient counting of k-mers in DNA sequences using a Bloom Filter.pdf:pdf}, issn = {1471-2105}, journal = {BMC Bioinformatics}, number = {1}, pages = {333}, title = {{Efficient counting of k-mers in DNA sequences using a Bloom Filter}}, url = {http://www.biomedcentral.com/1471-2105/12/333}, volume = {12}, year = {2011} } @article{Chaisson2008, abstract = {In the last year, high-throughput sequencing technologies have progressed from proof-of-concept to production quality. While these methods produce high-quality reads, they have yet to produce reads comparable in length to Sanger-based sequencing. Current fragment assembly algorithms have been implemented and optimized for mate-paired Sanger-based reads, and thus do not perform well on short reads produced by short read technologies. We present a new Eulerian assembler that generates nearly optimal short read assemblies of bacterial genomes and describe an approach to assemble reads in the case of the popular hybrid protocol when short and long Sanger-based reads are combined.}, author = {Chaisson, Mark J and Pevzner, Pavel A}, doi = {10.1101/gr.7088808}, file = {:home/gus/Documents/Mendeley Desktop/Chaisson, Pevzner\_2008\_Short read fragment assembly of bacterial genomes.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Bacterial,Bacterial: genetics,Contig Mapping,Contig Mapping: methods,DNA,DNA: methods,Genome,Genomics,Genomics: methods,Research Design,Sequence Analysis}, month = feb, number = {2}, pages = {324--30}, pmid = {18083777}, title = {{Short read fragment assembly of bacterial genomes.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2203630\&tool=pmcentrez\&rendertype=abstract}, volume = {18}, year = {2008} } @article{Li01022010, abstract = {Next-generation massively parallel DNA sequencing technologies provide ultrahigh throughput at a substantially lower unit data cost; however, the data are very short read length sequences, making de novo assembly extremely challenging. Here, we describe a novel method for de novo assembly of large genomes from short read sequences. We successfully assembled both the Asian and African human genome sequences, achieving an N50 contig size of 7.4 and 5.9 kilobases (kb) and scaffold of 446.3 and 61.9 kb, respectively. The development of this de novo short read assembly method creates new opportunities for building reference sequences and carrying out accurate analyses of unexplored genomes in a cost-effective way.}, author = {Li, Ruiqiang and Zhu, Hongmei and Ruan, Jue and Qian, Wubin and Fang, Xiaodong and Shi, Zhongbin and Li, Yingrui and Li, Shengting and Shan, Gao and Kristiansen, Karsten and Li, Songgang and Yang, Huanming and Wang, Jian and Wang, Jun}, doi = {10.1101/gr.097261.109}, file = {:home/gus/Documents/Mendeley Desktop/Li et al.\_2010\_De novo assembly of human genomes with massively parallel short read sequencing.pdf:pdf}, journal = {Genome Research}, number = {2}, pages = {265--272}, title = {{De novo assembly of human genomes with massively parallel short read sequencing}}, url = {http://genome.cshlp.org/content/20/2/265.abstract}, volume = {20}, year = {2010} } @article{Schatz:2010uq, abstract = {Second-generation sequencing technology can now be used to sequence an entire human genome in a matter of days and at low cost. Sequence read lengths, initially very short, have rapidly increased since the technology first appeared, and we now are seeing a growing number of efforts to sequence large genomes de novo from these short reads. In this Perspective, we describe the issues associated with short-read assembly, the different types of data produced by second-gen sequencers, and the latest assembly algorithms designed for these data. We also review the genomes that have been assembled recently from short reads and make recommendations for sequencing strategies that will yield a high-quality assembly.}, author = {Schatz, Michael C and Delcher, Arthur L and Salzberg, Steven L}, doi = {10.1101/gr.101360.109}, file = {:home/gus/Documents/Mendeley Desktop/Schatz, Delcher, Salzberg\_2010\_Assembly of large genomes using second-generation sequencing.pdf:pdf}, issn = {1549-5469}, journal = {Genome research}, keywords = {Algorithms,Base Sequence,DNA,DNA: methods,Genome,Genomics,Genomics: methods,Human,Humans,Sequence Analysis}, month = sep, number = {9}, pages = {1165--73}, pmid = {20508146}, title = {{Assembly of large genomes using second-generation sequencing.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2928494\&tool=pmcentrez\&rendertype=abstract}, volume = {20}, year = {2010} } @article{Maccallum:2009vn, abstract = {We demonstrate that genome sequences approaching finished quality can be generated from short paired reads. Using 36 base (fragment) and 26 base (jumping) reads from five microbial genomes of varied GC composition and sizes up to 40 Mb, ALLPATHS2 generated assemblies with long, accurate contigs and scaffolds. Velvet and EULER-SR were less accurate. For example, for Escherichia coli, the fraction of 10-kb stretches that were perfect was 99.8\% (ALLPATHS2), 68.7\% (Velvet), and 42.1\% (EULER-SR).}, author = {Maccallum, Iain and Przybylski, Dariusz and Gnerre, Sante and Burton, Joshua and Shlyakhter, Ilya and Gnirke, Andreas and Malek, Joel and McKernan, Kevin and Ranade, Swati and Shea, Terrance P and Williams, Louise and Young, Sarah and Nusbaum, Chad and Jaffe, David B}, doi = {10.1186/gb-2009-10-10-r103}, file = {:home/gus/Documents/Mendeley Desktop//Maccallum et al.\_2009\_ALLPATHS 2 small genomes assembled accurately and with high continuity from short paired reads.pdf:pdf}, issn = {1465-6914}, journal = {Genome biology}, keywords = {Bacteria,Bacteria: genetics,Base Pairing,Base Pairing: genetics,Fungi,Fungi: genetics,Genome,Genome: genetics,Genomics,Genomics: methods,Reproducibility of Results,Software}, month = jan, number = {10}, pages = {R103}, pmid = {19796385}, title = {{ALLPATHS 2: small genomes assembled accurately and with high continuity from short paired reads.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2784318\&tool=pmcentrez\&rendertype=abstract}, volume = {10}, year = {2009} } @article{Venter2001, author = {Venter, JC and Adams, MD and Myers, EW}, file = {:home/gus/Documents/Mendeley Desktop/Venter, Adams, Myers\_2001\_The sequence of the human genome.pdf:pdf}, journal = {Science's \ldots}, title = {{The sequence of the human genome}}, url = {http://stke.sciencemag.org/cgi/content/abstract/sci;291/5507/1304}, year = {2001} } @article{Li2009, abstract = {The enormous amount of short reads generated by the new DNA sequencing technologies call for the development of fast and accurate read alignment programs. A first generation of hash table-based methods has been developed, including MAQ, which is accurate, feature rich and fast enough to align short reads from a single individual. However, MAQ does not support gapped alignment for single-end reads, which makes it unsuitable for alignment of longer reads where indels may occur frequently. The speed of MAQ is also a concern when the alignment is scaled up to the resequencing of hundreds of individuals.}, author = {Li, Heng and Durbin, Richard}, doi = {10.1093/bioinformatics/btp324}, file = {:home/gus/Documents/Mendeley Desktop/Li, Durbin\_2009\_Fast and accurate short read alignment with Burrows-Wheeler transform.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,Genomics,Genomics: methods,Sequence Alignment,Sequence Alignment: methods,Sequence Analysis, DNA,Sequence Analysis, DNA: methods,Software}, month = jul, number = {14}, pages = {1754--60}, pmid = {19451168}, title = {{Fast and accurate short read alignment with Burrows-Wheeler transform.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/25/14/1754}, volume = {25}, year = {2009} } @article{Li2011, author = {Li, Yingrui and Zheng, Hancheng and Luo, Ruibang and Wu, Honglong and Zhu, Hongmei and Li, Ruiqiang and Cao, Hongzhi and Wu, Boxin and Huang, Shujia and Shao, Haojing and Ma, Hanzhou and Zhang, Fan and Feng, Shuijian and Zhang, Wei and Du, Hongli and Tian, Geng and Li, Jingxiang and Zhang, Xiuqing and Li, Songgang and Bolund, Lars and Kristiansen, Karsten and de Smith, Adam J and Blakemore, Alexandra I F and Coin, Lachlan J M and Yang, Huanming and Wang, Jian and Wang, Jun}, doi = {10.1038/nbt.1904}, file = {:home/gus/Documents/Mendeley Desktop/Li et al.\_2011\_Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly.pdf:pdf}, issn = {1087-0156}, journal = {Nature Biotechnology}, month = jul, number = {8}, pages = {723--730}, publisher = {Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.}, shorttitle = {Nat Biotech}, title = {{Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly}}, url = {http://dx.doi.org/10.1038/nbt.1904}, volume = {29}, year = {2011} } @article{Kawrykow2012, abstract = {Background Comparative genomics, or the study of the relationships of genome structure and function across different species, offers a powerful tool for studying evolution, annotating genomes, and understanding the causes of various genetic disorders. However, aligning multiple sequences of DNA, an essential intermediate step for most types of analyses, is a difficult computational task. In parallel, citizen science, an approach that takes advantage of the fact that the human brain is exquisitely tuned to solving specific types of problems, is becoming increasingly popular. There, instances of hard computational problems are dispatched to a crowd of non-expert human game players and solutions are sent back to a central server. Methodology/Principal Findings We introduce Phylo, a human-based computing framework applying “crowd sourcing†techniques to solve the Multiple Sequence Alignment (MSA) problem. The key idea of Phylo is to convert the MSA problem into a casual game that can be played by ordinary web users with a minimal prior knowledge of the biological context. We applied this strategy to improve the alignment of the promoters of disease-related genes from up to 44 vertebrate species. Since the launch in November 2010, we received more than 350,000 solutions submitted from more than 12,000 registered users. Our results show that solutions submitted contributed to improving the accuracy of up to 70\% of the alignment blocks considered. Conclusions/Significance We demonstrate that, combined with classical algorithms, crowd computing techniques can be successfully used to help improving the accuracy of MSA. More importantly, we show that an NP-hard computational problem can be embedded in casual game that can be easily played by people without significant scientific training. This suggests that citizen science approaches can be used to exploit the billions of “human-brain peta-flops†of computation that are spent every day playing games. Phylo is available at: http://phylo.cs.mcgill.ca.}, author = {Kawrykow, Alexander and Roumanis, Gary and Kam, Alfred and Kwak, Daniel and Leung, Clarence and Wu, Chu and Zarour, Eleyine and Sarmenta, Luis and Blanchette, Mathieu and Waldisp\"{u}hl, J\'{e}r\^{o}me}, doi = {10.1371/journal.pone.0031362}, editor = {Michalak, Pawel}, file = {:home/gus/Documents/Mendeley Desktop/Kawrykow et al.\_2012\_Phylo A Citizen Science Approach for Improving Multiple Sequence Alignment.pdf:pdf}, issn = {1932-6203}, journal = {PLoS ONE}, keywords = {Biology,Computational Biology,Computer Science,Computer applications,Computing methods,Evolutionary Biology,Genetics,Genetics and Genomics,Genomics,Organismal evolution,Research Article}, month = mar, number = {3}, pages = {e31362}, publisher = {Public Library of Science}, title = {{Phylo: A Citizen Science Approach for Improving Multiple Sequence Alignment}}, url = {http://dx.plos.org/10.1371/journal.pone.0031362}, volume = {7}, year = {2012} } @article{Kurtz2008, abstract = {The challenges of accurate gene prediction and enumeration are further aggravated in large genomes that contain highly repetitive transposable elements (TEs). Yet TEs play a substantial role in genome evolution and are themselves an important subject of study. Repeat annotation, based on counting occurrences of k-mers, has been previously used to distinguish TEs from low-copy genic regions; but currently available software solutions are impractical due to high memory requirements or specialization for specific user-tasks.}, author = {Kurtz, Stefan and Narechania, Apurva and Stein, Joshua C and Ware, Doreen}, doi = {10.1186/1471-2164-9-517}, file = {:home/gus/Documents/Mendeley Desktop/Kurtz et al.\_2008\_A new method to compute K-mer frequencies and its application to annotate large repetitive plant genomes.pdf:pdf}, issn = {1471-2164}, journal = {BMC genomics}, keywords = {Computational Biology,Computational Biology: methods,DNA Transposable Elements,Genome, Plant,Genomics,Genomics: methods,Methods,Oryza sativa,Software,Sorghum,Zea mays}, month = jan, pages = {517}, pmid = {18976482}, title = {{A new method to compute K-mer frequencies and its application to annotate large repetitive plant genomes.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2613927\&tool=pmcentrez\&rendertype=abstract}, volume = {9}, year = {2008} } @inproceedings{Gao2004, author = {Gao, H. and Groote, J.F. F and Hesselink, W.H. H}, booktitle = {18th International Parallel and Distributed Processing Symposium}, doi = {10.1109/IPDPS.2004.1302969}, file = {:home/gus/Documents/Mendeley Desktop/Gao, Groote, Hesselink\_Unknown\_Almost wait-free resizable hashtables.pdf:pdf}, isbn = {0769521320}, number = {C}, pages = {50--58}, publisher = {Ieee}, title = {{Almost wait-free resizable hashtables}}, url = {http://ieeexplore.ieee.org/lpdocs/epic03/wrapper.htm?arnumber=1302969}, volume = {00}, year = {2004} } @article{Chaisson2008, abstract = {In the last year, high-throughput sequencing technologies have progressed from proof-of-concept to production quality. While these methods produce high-quality reads, they have yet to produce reads comparable in length to Sanger-based sequencing. Current fragment assembly algorithms have been implemented and optimized for mate-paired Sanger-based reads, and thus do not perform well on short reads produced by short read technologies. We present a new Eulerian assembler that generates nearly optimal short read assemblies of bacterial genomes and describe an approach to assemble reads in the case of the popular hybrid protocol when short and long Sanger-based reads are combined.}, author = {Chaisson, Mark J and Pevzner, Pavel A}, doi = {10.1101/gr.7088808}, file = {:home/gus/Documents/Mendeley Desktop/Chaisson, Pevzner\_2008\_Short read fragment assembly of bacterial genomes.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Bacterial,Bacterial: genetics,Contig Mapping,Contig Mapping: methods,DNA,DNA: methods,Genome,Genomics,Genomics: methods,Research Design,Sequence Analysis}, month = feb, number = {2}, pages = {324--30}, pmid = {18083777}, title = {{Short read fragment assembly of bacterial genomes.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2203630\&tool=pmcentrez\&rendertype=abstract}, volume = {18}, year = {2008} } @article{Ding2012, author = {Ding, Li and Ley, Timothy J. and Larson, David E. and Miller, Christopher A. and Koboldt, Daniel C. and Welch, John S. and Ritchey, Julie K. and Young, Margaret A. and Lamprecht, Tamara and McLellan, Michael D. and McMichael, Joshua F. and Wallis, John W. and Lu, Charles and Shen, Dong and Harris, Christopher C. and Dooling, David J. and Fulton, Robert S. and Fulton, Lucinda L. and Chen, Ken and Schmidt, Heather and Kalicki-Veizer, Joelle and Magrini, Vincent J. and Cook, Lisa and McGrath, Sean D. and Vickery, Tammi L. and Wendl, Michael C. and Heath, Sharon and Watson, Mark A. and Link, Daniel C. and Tomasson, Michael H. and Shannon, William D. and Payton, Jacqueline E. and Kulkarni, Shashikant and Westervelt, Peter and Walter, Matthew J. and Graubert, Timothy A. and Mardis, Elaine R. and Wilson, Richard K. and DiPersio, John F.}, doi = {10.1038/nature10738}, file = {:home/gus/Documents/Mendeley Desktop/Ding et al.\_2012\_Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing.pdf:pdf}, issn = {0028-0836}, journal = {Nature}, month = jan, number = {7382}, pages = {506--510}, publisher = {Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.}, shorttitle = {Nature}, title = {{Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing}}, url = {http://dx.doi.org/10.1038/nature10738}, volume = {481}, year = {2012} } @article{Jaffe2003, abstract = {We previously described the whole-genome assembly program Arachne, presenting assemblies of simulated data for small to mid-sized genomes. Here we describe algorithmic adaptations to the program, allowing for assembly of mammalian-size genomes, and also improving the assembly of smaller genomes. Three principal changes were simultaneously made and applied to the assembly of the mouse genome, during a six-month period of development: (1) Supercontigs (scaffolds) were iteratively broken and rejoined using several criteria, yielding a 64-fold increase in length (N50), and apparent elimination of all global misjoins; (2) gaps between contigs in supercontigs were filled (partially or completely) by insertion of reads, as suggested by pairing within the supercontig, increasing the N50 contig length by 50\%; (3) memory usage was reduced fourfold. The outcome of this mouse assembly and its analysis are described in (Mouse Genome Sequencing Consortium 2002).}, author = {Jaffe, David B and Butler, Jonathan and Gnerre, Sante and Mauceli, Evan and Lindblad-Toh, Kerstin and Mesirov, Jill P and Zody, Michael C and Lander, Eric S}, doi = {10.1101/gr.828403}, file = {:home/gus/Documents/Mendeley Desktop/Jaffe et al.\_2003\_Whole-genome sequence assembly for mammalian genomes Arachne 2.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Animals,Computational Biology,Computational Biology: methods,Contig Mapping,Contig Mapping: methods,Genome,Humans,Mice,Software}, month = jan, number = {1}, pages = {91--6}, pmid = {12529310}, title = {{Whole-genome sequence assembly for mammalian genomes: Arachne 2.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=430950\&tool=pmcentrez\&rendertype=abstract}, volume = {13}, year = {2003} } @article{Simpson2010, abstract = {MOTIVATION: Sequence assembly is a difficult problem whose importance has grown again recently as the cost of sequencing has dramatically dropped. Most new sequence assembly software has started by building a de Bruijn graph, avoiding the overlap-based methods used previously because of the computational cost and complexity of these with very large numbers of short reads. Here, we show how to use suffix array-based methods that have formed the basis of recent very fast sequence mapping algorithms to find overlaps and generate assembly string graphs asymptotically faster than previously described algorithms. RESULTS: Standard overlap assembly methods have time complexity O(N(2)), where N is the sum of the lengths of the reads. We use the Ferragina-Manzini index (FM-index) derived from the Burrows-Wheeler transform to find overlaps of length at least tau among a set of reads. As well as an approach that finds all overlaps then implements transitive reduction to produce a string graph, we show how to output directly only the irreducible overlaps, significantly shrinking memory requirements and reducing compute time to O(N), independent of depth. Overlap-based assembly methods naturally handle mixed length read sets, including capillary reads or long reads promised by the third generation sequencing technologies. The algorithms we present here pave the way for overlap-based assembly approaches to be developed that scale to whole vertebrate genome de novo assembly.}, author = {Simpson, Jared T and Durbin, Richard}, doi = {10.1093/bioinformatics/btq217}, file = {:home/gus/Documents/Mendeley Desktop/Simpson, Durbin\_2010\_Efficient construction of an assembly string graph using the FM-index.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,Genomics,Genomics: methods,Sequence Analysis, DNA,Sequence Analysis, DNA: methods,Software}, month = jun, number = {12}, pages = {i367--73}, pmid = {20529929}, title = {{Efficient construction of an assembly string graph using the FM-index.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/26/12/i367}, volume = {26}, year = {2010} } @article{Ladan-Mozes2007, author = {Ladan-Mozes, Edya and Shavit, Nir}, doi = {10.1007/s00446-007-0050-0}, file = {:home/gus/Documents/Mendeley Desktop/Ladan-Mozes, Shavit\_2007\_An optimistic approach to lock-free FIFO queues.pdf:pdf}, issn = {0178-2770}, journal = {Distributed Computing}, month = nov, number = {5}, pages = {323--341}, title = {{An optimistic approach to lock-free FIFO queues}}, url = {http://www.springerlink.com/index/10.1007/s00446-007-0050-0}, volume = {20}, year = {2007} } @article{dalloul2010multi, author = {Dalloul, R.A. and Long, J.A. and Zimin, A.V. and Aslam, L. and Beal, K. and Bouffard, P. and Burt, D.W. and Crasta, O. and Crooijmans, R.P.M.A. and Cooper, K. and Others}, file = {:home/gus/Documents/Mendeley Desktop/Dalloul et al.\_2010\_Multi-platform next-generation sequencing of the domestic turkey (Meleagris gallopavo) genome assembly and analysis.pdf:pdf}, journal = {PLoS biology}, number = {9}, pages = {e1000475}, title = {{Multi-platform next-generation sequencing of the domestic turkey (Meleagris gallopavo): genome assembly and analysis}}, url = {http://dx.plos.org/10.1371/journal.pbio.1000475}, volume = {8}, year = {2010} } @article{Bloom1970, author = {Bloom, Burton H.}, doi = {10.1145/362686.362692}, file = {:home/gus/Documents/Mendeley Desktop/Bloom\_1970\_Spacetime trade-offs in hash coding with allowable errors.pdf:pdf}, issn = {00010782}, journal = {Communications of the ACM}, keywords = {Bloom filter,hash addressing,hash coding,retrieval efficiency,retrieval trade-offs,scatter storage,searching,storage efficiency,storage layout}, mendeley-tags = {Bloom filter}, month = jul, number = {7}, pages = {422--426}, title = {{Space/time trade-offs in hash coding with allowable errors}}, url = {http://dl.acm.org/citation.cfm?id=362686.362692}, volume = {13}, year = {1970} } @inproceedings{michael2002safe, author = {Michael, M.M.}, booktitle = {Proceedings of the twenty-first annual symposium on Principles of distributed computing}, file = {:home/gus/Documents/Mendeley Desktop/Michael\_2002\_Safe memory reclamation for dynamic lock-free objects using atomic reads and writes.pdf:pdf}, pages = {21--30}, publisher = {ACM}, title = {{Safe memory reclamation for dynamic lock-free objects using atomic reads and writes}}, url = {http://portal.acm.org/citation.cfm?id=571829}, year = {2002} } @article{Miller1998, author = {Miller, Peter}, file = {:home/gus/Documents/Mendeley Desktop/Miller\_1998\_Recursive make considered harmful.pdf:pdf}, journal = {AUUGN Journal of AUUG Inc}, number = {1}, pages = {14--25}, title = {{Recursive make considered harmful}}, url = {http://www.unix-ag.uni-kl.de/svn/kbibtex/kbibtex/tags/release-0.1/admin/unsermake/doc/auug97.pdf}, volume = {19}, year = {1998} } @article{Chaisson2008, abstract = {In the last year, high-throughput sequencing technologies have progressed from proof-of-concept to production quality. While these methods produce high-quality reads, they have yet to produce reads comparable in length to Sanger-based sequencing. Current fragment assembly algorithms have been implemented and optimized for mate-paired Sanger-based reads, and thus do not perform well on short reads produced by short read technologies. We present a new Eulerian assembler that generates nearly optimal short read assemblies of bacterial genomes and describe an approach to assemble reads in the case of the popular hybrid protocol when short and long Sanger-based reads are combined.}, author = {Chaisson, Mark J and Pevzner, Pavel A}, doi = {10.1101/gr.7088808}, file = {:home/gus/Documents/Mendeley Desktop/Chaisson, Pevzner\_2008\_Short read fragment assembly of bacterial genomes.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Bacterial,Bacterial: genetics,Contig Mapping,Contig Mapping: methods,DNA,DNA: methods,Genome,Genomics,Genomics: methods,Research Design,Sequence Analysis}, month = feb, number = {2}, pages = {324--30}, pmid = {18083777}, title = {{Short read fragment assembly of bacterial genomes.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2203630\&tool=pmcentrez\&rendertype=abstract}, volume = {18}, year = {2008} } @article{Li2003, abstract = {In shotgun sequencing projects, the genome or BAC length is not always known. We approach estimating genome length by first estimating the repeat structure of the genome or BAC, sometimes of interest in its own right, on the basis of a set of random reads from a genome project. Moreover, we can find the consensus for repeat families before assembly. Our methods are based on the l-tuple content of the reads.}, author = {Li, Xiaoman and Waterman, Michael S}, doi = {10.1101/gr.1251803}, file = {:home/gus/Documents/Mendeley Desktop/Li, Waterman\_2003\_Estimating the repeat structure and length of DNA sequences using L-tuples.pdf:pdf}, issn = {1088-9051}, journal = {Genome research}, keywords = {Algorithms,Artificial,Bacterial,Bacterial: genetics,Base Composition,Chromosome Mapping,Chromosome Mapping: statistics \& numerical data,Chromosomes,Computational Biology,Computational Biology: statistics \& numerical data,Computer Simulation,Computer Simulation: statistics \& numerical data,Consensus Sequence,DNA,Mathematical Computing,Nucleic Acid,Nucleic Acid: genetics,Poisson Distribution,Repetitive Sequences,Software}, month = aug, number = {8}, pages = {1916--22}, pmid = {12902383}, title = {{Estimating the repeat structure and length of DNA sequences using L-tuples.}}, url = {http://genome.cshlp.org/cgi/content/abstract/13/8/1916}, volume = {13}, year = {2003} } @article{Medvedev2011, abstract = {The continuing improvements to high-throughput sequencing (HTS) platforms have begun to unfold a myriad of new applications. As a result, error correction of sequencing reads remains an important problem. Though several tools do an excellent job of correcting datasets where the reads are sampled close to uniformly, the problem of correcting reads coming from drastically non-uniform datasets, such as those from single-cell sequencing, remains open.}, author = {Medvedev, Paul and Scott, Eric and Kakaradov, Boyko and Pevzner, Pavel}, doi = {10.1093/bioinformatics/btr208}, file = {:home/gus/Documents/Mendeley Desktop/Medvedev et al.\_2011\_Error correction of high-throughput sequencing datasets with non-uniform coverage.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, month = jul, number = {13}, pages = {i137--i141}, pmid = {21685062}, title = {{Error correction of high-throughput sequencing datasets with non-uniform coverage.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3117386\&tool=pmcentrez\&rendertype=abstract}, volume = {27}, year = {2011} } @inproceedings{Chazelle:2004:BFE:982792.982797, address = {Philadelphia, PA, USA}, author = {Chazelle, Bernard and Kilian, Joe and Rubinfeld, Ronitt and Tal, Ayellet}, booktitle = {Proceedings of the fifteenth annual ACM-SIAM symposium on Discrete algorithms}, file = {:home/gus/Documents/Mendeley Desktop/Chazelle et al.\_2004\_The Bloomier filter an efficient data structure for static support lookup tables.pdf:pdf}, isbn = {0-89871-558-X}, pages = {30--39}, publisher = {Society for Industrial and Applied Mathematics}, series = {SODA '04}, title = {{The Bloomier filter: an efficient data structure for static support lookup tables}}, url = {http://dl.acm.org/citation.cfm?id=982797 http://dl.acm.org/citation.cfm?id=982792.982797}, year = {2004} } @article{Michael1996, address = {New York, New York, USA}, author = {Michael, Maged M. and Scott, Michael L.}, doi = {10.1145/248052.248106}, file = {:home/gus/Documents/Mendeley Desktop/Michael, Scott\_1996\_Simple, fast, and practical non-blocking and blocking concurrent queue algorithms.pdf:pdf}, isbn = {0897918002}, journal = {Proceedings of the fifteenth annual ACM symposium on Principles of distributed computing - PODC '96}, keywords = {compare and swap,concurrent queue,lock-free,multiprogramming,non-blocking}, pages = {267--275}, publisher = {ACM Press}, title = {{Simple, fast, and practical non-blocking and blocking concurrent queue algorithms}}, url = {http://portal.acm.org/citation.cfm?doid=248052.248106}, year = {1996} } @article{Pugh1990, author = {Pugh, William}, doi = {10.1145/78973.78977}, file = {:home/gus/Documents/Mendeley Desktop//Pugh\_1990\_Skip lists a probabilistic alternative to balanced trees.pdf:pdf}, issn = {00010782}, journal = {Communications of the ACM}, keywords = {data structures,searching,trees}, month = jun, number = {6}, pages = {668--676}, publisher = {ACM}, title = {{Skip lists: a probabilistic alternative to balanced trees}}, url = {http://dl.acm.org/citation.cfm?id=78973.78977 http://dl.acm.org/citation.cfm?id=78977,}, volume = {33}, year = {1990} } @article{Pevzner:2001uq, abstract = {For the last 20 years, fragment assembly in DNA sequencing followed the "overlap-layout-consensus" paradigm that is used in all currently available assembly tools. Although this approach proved useful in assembling clones, it faces difficulties in genomic shotgun assembly. We abandon the classical "overlap-layout-consensus" approach in favor of a new euler algorithm that, for the first time, resolves the 20-year-old "repeat problem" in fragment assembly. Our main result is the reduction of the fragment assembly to a variation of the classical Eulerian path problem that allows one to generate accurate solutions of large-scale sequencing problems. euler, in contrast to the celera assembler, does not mask such repeats but uses them instead as a powerful fragment assembly tool.}, author = {Pevzner, P A and Tang, H and Waterman, M S}, doi = {10.1073/pnas.171285098}, file = {:home/gus/Documents/Mendeley Desktop/Pevzner, Tang, Waterman\_2001\_An Eulerian path approach to DNA fragment assembly.pdf:pdf}, journal = {Proc Natl Acad Sci U S A}, month = aug, number = {17}, pages = {9748--9753}, pmid = {11504945}, title = {{An Eulerian path approach to DNA fragment assembly}}, volume = {98}, year = {2001} } @article{Venter2001, author = {Venter, JC and Adams, MD and Myers, EW}, file = {:home/gus/Documents/Mendeley Desktop/Venter, Adams, Myers\_2001\_The sequence of the human genome.pdf:pdf}, journal = {Science's \ldots}, title = {{The sequence of the human genome}}, url = {http://stke.sciencemag.org/cgi/content/abstract/sci;291/5507/1304}, year = {2001} } @article{Schroder2009, abstract = {MOTIVATION: Second-generation sequencing technologies produce a massive amount of short reads in a single experiment. However, sequencing errors can cause major problems when using this approach for de novo sequencing applications. Moreover, existing error correction methods have been designed and optimized for shotgun sequencing. Therefore, there is an urgent need for the design of fast and accurate computational methods and tools for error correction of large amounts of short read data. RESULTS: We present SHREC, a new algorithm for correcting errors in short-read data that uses a generalized suffix trie on the read data as the underlying data structure. Our results show that the method can identify erroneous reads with sensitivity and specificity of over 99\% and 96\% for simulated data with error rates of up to 3\% as well as for real data. Furthermore, it achieves an error correction accuracy of over 80\% for simulated data and over 88\% for real data. These results are clearly superior to previously published approaches. SHREC is available as an efficient open-source Java implementation that allows processing of 10 million of short reads on a standard workstation.}, author = {Schr\"{o}der, Jan and Schr\"{o}der, Heiko and Puglisi, Simon J and Sinha, Ranjan and Schmidt, Bertil}, doi = {10.1093/bioinformatics/btp379}, file = {:home/gus/Documents/Mendeley Desktop/Schr\"{o}der et al.\_2009\_SHREC a short-read error correction method.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Schr\"{o}der et al.\_2009\_SHREC a short-read error correction method(2).pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,Computational Biology,Computational Biology: methods,DNA,DNA: genetics,DNA: methods,Databases,Error correction,Genome,Genome: genetics,Nucleic Acid,Research Design,Sequence Analysis,Time Factors}, mendeley-tags = {Error correction}, month = sep, number = {17}, pages = {2157--63}, pmid = {19542152}, title = {{SHREC: a short-read error correction method.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/25/17/2157}, volume = {25}, year = {2009} } @article{Richter2008, abstract = {The new research field of metagenomics is providing exciting insights into various, previously unclassified ecological systems. Next-generation sequencing technologies are producing a rapid increase of environmental data in public databases. There is great need for specialized software solutions and statistical methods for dealing with complex metagenome data sets.}, author = {Richter, Daniel C and Ott, Felix and Auch, Alexander F and Schmid, Ramona and Huson, Daniel H}, doi = {10.1371/journal.pone.0003373}, editor = {Field, Dawn}, file = {:home/gus/Documents/Mendeley Desktop/Richter et al.\_2008\_MetaSim a sequencing simulator for genomics and metagenomics.pdf:pdf}, issn = {1932-6203}, journal = {PloS one}, keywords = {Databases, Genetic,Genomics,Models, Theoretical,User-Computer Interface}, month = jan, number = {10}, pages = {e3373}, pmid = {18841204}, publisher = {Public Library of Science}, title = {{MetaSim: a sequencing simulator for genomics and metagenomics.}}, url = {http://dx.plos.org/10.1371/journal.pone.0003373}, volume = {3}, year = {2008} } @article{Brown2012, abstract = {Deep shotgun sequencing and analysis of genomes, transcriptomes, amplified single-cell genomes, and metagenomes enable the sensitive investigation of a wide range of biological phenomena. However, it is increasingly difficult to deal with the volume of data emerging from deep short-read sequencers, in part because of random and systematic sampling variation as well as a high sequencing error rate. These challenges have led to the development of entire new classes of short-read mapping tools, as well as new \{$\backslash$em de novo\} assemblers. Even newer assembly strategies for dealing with transcriptomes, single-cell genomes, and metagenomes have also emerged. Despite these advances, algorithms and compute capacity continue to be challenged by the continued improvements in sequencing technology throughput. We here describe an approach we term digital normalization, a single-pass computational algorithm that discards redundant data and both sampling variation and the number of errors present in deep sequencing data sets. Digital normalization substantially reduces the size of data sets and accordingly decreases the memory and time requirements for \{$\backslash$em de novo\} sequence assembly, all without significantly impacting content of the generated contigs. In doing so, it converts high random coverage to low systematic coverage. Digital normalization is an effective and efficient approach to normalizing coverage, removing errors, and reducing data set size for shotgun sequencing data sets. It is particularly useful for reducing the compute requirements for \{$\backslash$em de novo\} sequence assembly. We demonstrate this for the assembly of microbial genomes, amplified single-cell genomic data, and transcriptomic data. The software is freely available for use and modification.}, archivePrefix = {arXiv}, arxivId = {1203.4802}, author = {Brown, C. Titus and Howe, Adina and Zhang, Qingpeng and Pyrkosz, Alexis B. and Brom, Timothy H.}, eprint = {1203.4802}, file = {:home/gus/Documents/Mendeley Desktop/Brown et al.\_2012\_A single pass approach to reducing sampling variation, removing errors, and scaling \{em de novo\} assembly of shotgun sequences.pdf:pdf}, month = mar, title = {{A single pass approach to reducing sampling variation, removing errors, and scaling \{$\backslash$em de novo\} assembly of shotgun sequences}}, url = {http://arxiv.org/abs/1203.4802}, year = {2012} } @article{Nagaraj2007, abstract = {Expressed sequence tag (EST) sequencing projects are underway for numerous organisms, generating millions of short, single-pass nucleotide sequence reads, accumulating in EST databases. Extensive computational strategies have been developed to organize and analyse both small- and large-scale EST data for gene discovery, transcript and single nucleotide polymorphism analysis as well as functional annotation of putative gene products. We provide an overview of the significance of ESTs in the genomic era, their properties and the applications of ESTs. Methods adopted for each step of EST analysis by various research groups have been compared. Challenges that lie ahead in organizing and analysing the ever increasing EST data have also been identified. The most appropriate software tools for EST pre-processing, clustering and assembly, database matching and functional annotation have been compiled (available online from http://biolinfo.org/EST). We propose a road map for EST analysis to accelerate the effective analyses of EST data sets. An investigation of EST analysis platforms reveals that they all terminate prior to downstream functional annotation including gene ontologies, motif/pattern analysis and pathway mapping.}, author = {Nagaraj, Shivashankar H and Gasser, Robin B and Ranganathan, Shoba}, doi = {10.1093/bib/bbl015}, file = {:home/gus/Documents/Mendeley Desktop/Nagaraj, Gasser, Ranganathan\_2007\_A hitchhiker's guide to expressed sequence tag (EST) analysis.pdf:pdf;:home/gus/Documents/Mendeley Desktop/Nagaraj, Gasser, Ranganathan\_2007\_A hitchhiker's guide to expressed sequence tag (EST) analysis(2).pdf:pdf}, issn = {1467-5463}, journal = {Briefings in bioinformatics}, keywords = {Animals,Complementary,Complementary: chemistry,Consensus Sequence,Consensus Sequence: genetics,DNA,Databases,Expressed Sequence Tags,Genetic,Genetic: standards,Genomics,Genomics: methods,Humans,Nucleic Acid,Nucleic Acid: standards,RNA,Software,Untranslated Regions,Untranslated Regions: chemistry}, mendeley-tags = {RNA}, month = jan, number = 1, pages = {6--21}, pmid = 16772268, title = {{A hitchhiker's guide to expressed sequence tag (EST) analysis.}}, url = {http://bib.oxfordjournals.org/cgi/content/abstract/8/1/6}, volume = 8, year = 2007 } @article{Zimin2009, abstract = {The genome of the domestic cow, Bos taurus, was sequenced using a mixture of hierarchical and whole-genome shotgun sequencing methods.}, author = {Zimin, Aleksey V and Delcher, Arthur L and Florea, Liliana and Kelley, David R and Schatz, Michael C and Puiu, Daniela and Hanrahan, Finnian and Pertea, Geo and {Van Tassell}, Curtis P and Sonstegard, Tad S and Mar\c{c}ais, Guillaume and Roberts, Michael and Subramanian, Poorani and Yorke, James a and Salzberg, Steven L}, doi = {10.1186/gb-2009-10-4-r42}, file = {:home/gus/Documents/Mendeley Desktop/Zimin et al.\_2009\_A whole-genome assembly of the domestic cow, Bos taurus.pdf:pdf}, issn = {1465-6914}, journal = {Genome biology}, keywords = {Animals,Cattle,Cattle: genetics,Chromosome Mapping,Female,Genome,Genome, Human,Genome, Human: genetics,Genome: genetics,Genomics,Humans,Male,Sequence Analysis, DNA,Sequence Analysis, DNA: methods,Sequence Analysis, DNA: statistics \& numerical dat,Synteny,Y Chromosome,Y Chromosome: genetics}, month = jan, number = {4}, pages = {R42}, pmid = {19393038}, title = {{A whole-genome assembly of the domestic cow, Bos taurus.}}, url = {http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2688933\&tool=pmcentrez\&rendertype=abstract}, volume = {10}, year = {2009} } @article{shi2010parallel, author = {Shi, H. and Schmidt, B. and Liu, W. and M\"{u}ller-Wittig, W.}, file = {:home/gus/Documents/Mendeley Desktop/Shi et al.\_2010\_A parallel algorithm for error correction in high-throughput short-read data on CUDA-enabled graphics hardware.pdf:pdf}, journal = {Journal of Computational Biology}, number = {4}, pages = {603--615}, publisher = {Mary Ann Liebert, Inc. 140 Huguenot Street, 3rd Floor New Rochelle, NY 10801 USA}, title = {{A parallel algorithm for error correction in high-throughput short-read data on CUDA-enabled graphics hardware}}, url = {http://www.liebertonline.com/doi/abs/10.1089/cmb.2009.0062}, volume = {17}, year = {2010} } @article{Gibbs2012, author = {Gibbs, Richard A and Rogers, Jeffrey}, doi = {10.1038/483164a}, file = {:home/gus/Documents/Mendeley Desktop/Gibbs, Rogers\_2012\_Genomics Gorilla gorilla gorilla.pdf:pdf}, issn = {1476-4687}, journal = {Nature}, month = mar, number = {7388}, pages = {164--5}, pmid = {22398552}, publisher = {Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.}, shorttitle = {Nature}, title = {{Genomics: Gorilla gorilla gorilla.}}, url = {http://dx.doi.org/10.1038/483164a}, volume = {483}, year = {2012} } @article{Ruffalo2011, abstract = {Motivation: The advent of next-generation sequencing (NGS) techniques presents many novel opportunities for many applications in life sciences. The vast number of short reads produced by these techniques, however, pose significant computational challenges. The first step in many types of genomic analysis is the mapping of short reads to a reference genome, and several groups have developed dedicated algorithms and software packages to perform this function. As the developers of these packages optimize their algorithms with respect to various considerations, the relative merits of different software packages remain unclear. However, for scientists who generate and use NGS data for their specific research projects, an important consideration is choosing the software that is most suitable for their application. Results: With a view to comparing existing short read alignment software, we develop a simulation and evaluation suite, SEAL, which simulates NGS runs for different configurations of various factors, including sequencing error, indels and coverage. We also develop criteria to compare the performances of software with disparate output structure (e.g. some packages return a single alignment while some return multiple possible alignments). Using these criteria, we comprehensively evaluate the performances of Bowtie, BWA, mr- and mrsFAST, Novoalign, SHRiMP and SOAPv2, with regard to accuracy and runtime. Conclusion: We expect that the results presented here will be useful to investigators in choosing the alignment software that is most suitable for their specific research aims. Our results also provide insights into the factors that should be considered to use alignment results effectively. SEAL can also be used to evaluate the performance of algorithms that use deep sequencing data for various purposes (e.g. identification of genomic variants). Availability: SEAL is available as open source at http://compbio.case.edu/seal/. Contact: matthew.ruffalo@case.edu Supplementary information: Supplementary data are available at Bioinformatics online.}, author = {Ruffalo, M. and LaFramboise, T. and Koyuturk, M.}, doi = {10.1093/bioinformatics/btr477}, file = {:home/gus/Documents/Mendeley Desktop/Ruffalo, LaFramboise, Koyuturk\_2011\_Comparative analysis of algorithms for next-generation sequencing read alignment.pdf:pdf}, issn = {1367-4803}, journal = {Bioinformatics}, month = aug, number = {20}, pages = {2790--2796}, title = {{Comparative analysis of algorithms for next-generation sequencing read alignment}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/27/20/2790}, volume = {27}, year = {2011} } @article{Panda2010, annote = {10.1038/nature08696}, author = {Li, Ruiqiang and Fan, Wei and Tian, Geng and Zhu, Hongmei and He, Lin and Cai, Jing and Huang, Quanfei and Cai, Qingle and Li, Bo and Bai, Yinqi and Zhang, Zhihe and Zhang, Yaping and Wang, Wen and Li, Jun and Wei, Fuwen and Li, Heng and Jian, Min and Li, Jianwen and Zhang, Zhaolei and Nielsen, Rasmus and Li, Dawei and Gu, Wanjun and Yang, Zhentao and Xuan, Zhaoling and Ryder, Oliver A and Leung, Frederick Chi-Ching and Zhou, Yan and Cao, Jianjun and Sun, Xiao and Fu, Yonggui and Fang, Xiaodong and Guo, Xiaosen and Wang, Bo and Hou, Rong and Shen, Fujun and Mu, Bo and Ni, Peixiang and Lin, Runmao and Qian, Wubin and Wang, Guodong and Yu, Chang and Nie, Wenhui and Wang, Jinhuan and Wu, Zhigang and Liang, Huiqing and Min, Jiumeng and Wu, Qi and Cheng, Shifeng and Ruan, Jue and Wang, Mingwei and Shi, Zhongbin and Wen, Ming and Liu, Binghang and Ren, Xiaoli and Zheng, Huisong and Dong, Dong and Cook, Kathleen and Shan, Gao and Zhang, Hao and Kosiol, Carolin and Xie, Xueying and Lu, Zuhong and Zheng, Hancheng and Li, Yingrui and Steiner, Cynthia C and Lam, Tommy Tsan-Yuk and Lin, Siyuan and Zhang, Qinghui and Li, Guoqing and Tian, Jing and Gong, Timing and Liu, Hongde and Zhang, Dejin and Fang, Lin and Ye, Chen and Zhang, Juanbin and Hu, Wenbo and Xu, Anlong and Ren, Yuanyuan and Zhang, Guojie and Bruford, Michael W and Li, Qibin and Ma, Lijia and Guo, Yiran and An, Na and Hu, Yujie and Zheng, Yang and Shi, Yongyong and Li, Zhiqiang and Liu, Qing and Chen, Yanling and Zhao, Jing and Qu, Ning and Zhao, Shancen and Tian, Feng and Wang, Xiaoling and Wang, Haiyin and Xu, Lizhi and Liu, Xiao and Vinar, Tomas and Wang, Yajun and Lam, Tak-Wah and Yiu, Siu-Ming and Liu, Shiping and Zhang, Hemin and Li, Desheng and Huang, Yan and Wang, Xia and Yang, Guohua and Jiang, Zhi and Wang, Junyi and Qin, Nan and Li, Li and Li, Jingxiang and Bolund, Lars and Kristiansen, Karsten and Wong, Gane Ka-Shu and Olson, Maynard and Zhang, Xiuqing and Li, Songgang and Yang, Huanming and Wang, Jian and Wang, Jun}, doi = {http://dx.doi.org/10.1038/nature08696}, issn = {0028-0836}, journal = {Nature}, number = {7279}, pages = {311--317}, publisher = {Macmillan Publishers Limited. All rights reserved}, title = {{The sequence and de novo assembly of the giant panda genome}}, volume = {463}, year = {2010} } @article{Liu2012, abstract = {SUMMARY: SOAP3 is the first short read alignment tool that leverages the multi-processors in a graphic processing unit (GPU) to achieve a drastic improvement in speed. We adapted the compressed full-text index (BWT) used by SOAP2 in view of the advantages and disadvantages of GPU. When tested with millions of Illumina Hiseq 2000 length-100bp reads, SOAP3 takes less than 30 seconds to align a million read pairs onto the human reference genome and is at least 7.5 and 20 times faster than BWA and Bowtie, respectively. For aligning reads with up to 4 mismatches, SOAP3 aligns slightly more reads than BWA and Bowtie; this is because SOAP3, unlike BWA and Bowtie, is not heuristic-based and always reports all answers. AVAILABILITY: SOAP3 is available at: http://www.cs.hku.hk/2bwt-tools/soap3; and http://soap.genomics.org.cn/soap3.html. CONTACT: liruiqiang@gmail.com, twlam@cs.hku.hk.}, author = {Liu, Chi-Man and Wong, Thomas and Wu, Edward and Luo, Ruibang and Yiu, Siu-Ming and Li, Yingrui and Wang, B and Yu, C and Chu, X and Zhao, K and Li, Ruiqiang and Lam, Tak-Wah}, doi = {10.1093/bioinformatics/bts061}, file = {:home/gus/Documents/Mendeley Desktop/Liu et al.\_2012\_SOAP3 Ultra-fast GPU-based parallel alignment tool for short reads.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, month = jan, number = {6}, pages = {878--879}, pmid = {22285832}, title = {{SOAP3: Ultra-fast GPU-based parallel alignment tool for short reads.}}, url = {http://bioinformatics.oxfordjournals.org/cgi/content/abstract/28/6/878}, volume = {28}, year = {2012} } @article{David2011, abstract = {We report on a major update (version 2) of the original SHort Read Mapping Program (SHRiMP). SHRiMP2 primarily targets mapping sensitivity, and is able to achieve high accuracy at a very reasonable speed. SHRiMP2 supports both letter space and color space (AB/SOLiD) reads, enables for direct alignment of paired reads and uses parallel computation to fully utilize multi-core architectures. AVAILABILITY: SHRiMP2 executables and source code are freely available at: http://compbio.cs.toronto.edu/shrimp/.}, author = {David, Matei and Dzamba, Misko and Lister, Dan and Ilie, Lucian and Brudno, Michael}, doi = {10.1093/bioinformatics/btr046}, file = {:home/gus/Documents/Mendeley Desktop/David et al.\_2011\_SHRiMP2 sensitive yet practical SHort Read Mapping.pdf:pdf}, issn = {1367-4811}, journal = {Bioinformatics (Oxford, England)}, keywords = {Algorithms,Chromosome Mapping,DNA,Genetic,Genomics,Genomics: methods,Polymorphism,Sequence Alignment,Sequence Analysis,Software}, month = apr, number = {7}, pages = {1011--2}, pmid = {21278192}, title = {{SHRiMP2: sensitive yet practical SHort Read Mapping.}}, url = {http://www.ncbi.nlm.nih.gov/pubmed/21278192}, volume = {27}, year = {2011} } @article{Waterston2002, abstract = {The sequence of the mouse genome is a key informational tool for understanding the contents of the human genome and a key experimental tool for biomedical research. Here, we report the results of an international collaboration to produce a high-quality draft sequence of the mouse genome. We also present an initial comparative analysis of the mouse and human genomes, describing some of the insights that can be gleaned from the two sequences. We discuss topics including the analysis of the evolutionary forces shaping the size, structure and sequence of the genomes; the conservation of large-scale synteny across most of the genomes; the much lower extent of sequence orthology covering less than half of the genomes; the proportions of the genomes under selection; the number of protein-coding genes; the expansion of gene families related to reproduction and immunity; the evolution of proteins; and the identification of intraspecies polymorphism.}, author = {Waterston, Robert H and Lindblad-Toh, Kerstin and Birney, Ewan and Rogers, Jane and Abril, Josep F and Agarwal, Pankaj and Agarwala, Richa and Ainscough, Rachel and Alexandersson, Marina and An, Peter and Antonarakis, Stylianos E and Attwood, John and Baertsch, Robert and Bailey, Jonathon and Barlow, Karen and Beck, Stephan and Berry, Eric and Birren, Bruce and Bloom, Toby and Bork, Peer and Botcherby, Marc and Bray, Nicolas and Brent, Michael R and Brown, Daniel G and Brown, Stephen D and Bult, Carol and Burton, John and Butler, Jonathan and Campbell, Robert D and Carninci, Piero and Cawley, Simon and Chiaromonte, Francesca and Chinwalla, Asif T and Church, Deanna M and Clamp, Michele and Clee, Christopher and Collins, Francis S and Cook, Lisa L and Copley, Richard R and Coulson, Alan and Couronne, Olivier and Cuff, James and Curwen, Val and Cutts, Tim and Daly, Mark and David, Robert and Davies, Joy and Delehaunty, Kimberly D and Deri, Justin and Dermitzakis, Emmanouil T and Dewey, Colin and Dickens, Nicholas J and Diekhans, Mark and Dodge, Sheila and Dubchak, Inna and Dunn, Diane M and Eddy, Sean R and Elnitski, Laura and Emes, Richard D and Eswara, Pallavi and Eyras, Eduardo and Felsenfeld, Adam and Fewell, Ginger A and Flicek, Paul and Foley, Karen and Frankel, Wayne N and Fulton, Lucinda A and Fulton, Robert S and Furey, Terrence S and Gage, Diane and Gibbs, Richard A and Glusman, Gustavo and Gnerre, Sante and Goldman, Nick and Goodstadt, Leo and Grafham, Darren and Graves, Tina A and Green, Eric D and Gregory, Simon and Guig\'{o}, Roderic and Guyer, Mark and Hardison, Ross C and Haussler, David and Hayashizaki, Yoshihide and Hillier, LaDeana W and Hinrichs, Angela and Hlavina, Wratko and Holzer, Timothy and Hsu, Fan and Hua, Axin and Hubbard, Tim and Hunt, Adrienne and Jackson, Ian and Jaffe, David B and Johnson, L Steven and Jones, Matthew and Jones, Thomas A and Joy, Ann and Kamal, Michael and Karlsson, Elinor K and Karolchik, Donna and Kasprzyk, Arkadiusz and Kawai, Jun and Keibler, Evan and Kells, Cristyn and Kent, W James and Kirby, Andrew and Kolbe, Diana L and Korf, Ian and Kucherlapati, Raju S and Kulbokas, Edward J and Kulp, David and Landers, Tom and Leger, J P and Leonard, Steven and Letunic, Ivica and Levine, Rosie and Li, Jia and Li, Ming and Lloyd, Christine and Lucas, Susan and Ma, Bin and Maglott, Donna R and Mardis, Elaine R and Matthews, Lucy and Mauceli, Evan and Mayer, John H and McCarthy, Megan and McCombie, W Richard and McLaren, Stuart and McLay, Kirsten and McPherson, John D and Meldrim, Jim and Meredith, Beverley and Mesirov, Jill P and Miller, Webb and Miner, Tracie L and Mongin, Emmanuel and Montgomery, Kate T and Morgan, Michael and Mott, Richard and Mullikin, James C and Muzny, Donna M and Nash, William E and Nelson, Joanne O and Nhan, Michael N and Nicol, Robert and Ning, Zemin and Nusbaum, Chad and O'Connor, Michael J and Okazaki, Yasushi and Oliver, Karen and Overton-Larty, Emma and Pachter, Lior and Parra, Gen\'{\i}s and Pepin, Kymberlie H and Peterson, Jane and Pevzner, Pavel and Plumb, Robert and Pohl, Craig S and Poliakov, Alex and Ponce, Tracy C and Ponting, Chris P and Potter, Simon and Quail, Michael and Reymond, Alexandre and Roe, Bruce A and Roskin, Krishna M and Rubin, Edward M and Rust, Alistair G and Santos, Ralph and Sapojnikov, Victor and Schultz, Brian and Schultz, J\"{o}rg and Schwartz, Matthias S and Schwartz, Scott and Scott, Carol and Seaman, Steven and Searle, Steve and Sharpe, Ted and Sheridan, Andrew and Shownkeen, Ratna and Sims, Sarah and Singer, Jonathan B and Slater, Guy and Smit, Arian and Smith, Douglas R and Spencer, Brian and Stabenau, Arne and Stange-Thomann, Nicole and Sugnet, Charles and Suyama, Mikita and Tesler, Glenn and Thompson, Johanna and Torrents, David and Trevaskis, Evanne and Tromp, John and Ucla, Catherine and Ureta-Vidal, Abel and Vinson, Jade P and {Von Niederhausern}, Andrew C and Wade, Claire M and Wall, Melanie and Weber, Ryan J and Weiss, Robert B and Wendl, Michael C and West, Anthony P and Wetterstrand, Kris and Wheeler, Raymond and Whelan, Simon and Wierzbowski, Jamey and Willey, David and Williams, Sophie and Wilson, Richard K and Winter, Eitan and Worley, Kim C and Wyman, Dudley and Yang, Shan and Yang, Shiaw-Pyng and Zdobnov, Evgeny M and Zody, Michael C and Lander, Eric S}, doi = {10.1038/nature01262}, file = {:home/gus/Documents/Mendeley Desktop/Waterston et al.\_2002\_Initial sequencing and comparative analysis of the mouse genome.pdf:pdf}, issn = {0028-0836}, journal = {Nature}, keywords = {Animal,Animals,Base Composition,Chromosomes, Mammalian,Chromosomes, Mammalian: genetics,Conserved Sequence,Conserved Sequence: genetics,CpG Islands,CpG Islands: genetics,DNA,Evolution, Molecular,Gene Expression Regulation,Genes,Genes: genetics,Genetic,Genetic Variation,Genetic Variation: genetics,Genome,Genome, Human,Genomics,Human,Humans,Knockout,Mammalian,Mammalian: genetics,Mice,Mice, Knockout,Mice, Transgenic,Mice: classification,Mice: genetics,Models, Animal,Molecular,Multigene Family,Multigene Family: genetics,Mutagenesis,Neoplasms,Neoplasms: genetics,Nucleic Acid,Nucleic Acid: genetics,Physical Chromosome Mapping,Proteome,Proteome: genetics,Pseudogenes,Pseudogenes: genetics,Quantitative Trait Loci,Quantitative Trait Loci: genetics,RNA, Untranslated,RNA, Untranslated: genetics,Repetitive Sequences, Nucleic Acid,Repetitive Sequences, Nucleic Acid: genetics,Selection, Genetic,Sequence Analysis, DNA,Sex Chromosomes,Sex Chromosomes: genetics,Species Specificity,Synteny,Transgenic,Untranslated,Untranslated: genetics}, month = dec, number = {6915}, pages = {520--62}, pmid = {12466850}, publisher = {Macmillian Magazines Ltd.}, shorttitle = {Nature}, title = {{Initial sequencing and comparative analysis of the mouse genome.}}, url = {http://dx.doi.org/10.1038/nature01262}, volume = {420}, year = {2002} } @article{Mackenzie2001, abstract = {Rhodobacter sphaeroides 2.4.1 is an alpha-3 purple nonsulfur eubacterium with an extensive metabolic repertoire. Under anaerobic conditions, it is able to grow by photosynthesis, respiration and fermentation. Photosynthesis may be photoheterotrophic using organic compounds as both a carbon and a reducing source, or photoautotrophic using carbon dioxide as the sole carbon source and hydrogen as the source of reducing power. In addition, R. sphaeroides can grow both chemoheterotrophically and chemoautotrophically. The structural components of this metabolically diverse organism and their modes of integrated regulation are encoded by a genome of approximately 4.5 Mb in size. The genome comprises two chromosomes CI and CII (2.9 and 0.9 Mb, respectively) and five other replicons. Sequencing of the genome has been carried out by two groups, the Joint Genome Institute, which carried out shotgun-sequencing of the entire genome and The University of Texas-Houston Medical School, which carried out a targeted sequencing strategy of CII. Here we describe our current understanding of the genome when data from both of these groups are combined. Previous work had suggested that the two chromosomes are equal partners sharing responsibilities for fundamental cellular processes. This view has been reinforced by our preliminary analysis of the virtually completed genome sequence. We also have some evidence to suggest that two of the plasmids, pRS241a and pRS241b encode chromosomal type functions and their role may be more than that of accessory elements, perhaps representing replicons in a transition state.}, author = {Mackenzie, C and Choudhary, M and Larimer, F W and Predki, P F and Stilwagen, S and Armitage, J P and Barber, R D and Donohue, T J and Hosler, J P and Newman, J E and Shapleigh, J P and Sockett, R E and Zeilstra-Ryalls, J and Kaplan, S}, doi = {10.1023/A:1013831823701}, file = {:home/gus/Documents/Mendeley Desktop/Mackenzie et al.\_2001\_The home stretch, a first analysis of the nearly completed genome of Rhodobacter sphaeroides 2.4.1.pdf:pdf}, issn = {1573-5079}, journal = {Photosynthesis research}, language = {en}, month = jan, number = {1}, pages = {19--41}, pmid = {16228360}, title = {{The home stretch, a first analysis of the nearly completed genome of Rhodobacter sphaeroides 2.4.1.}}, url = {http://link.springer.com/article/10.1023/A\%3A1013831823701}, volume = {70}, year = {2001} } @article{Bentley2008, abstract = {DNA sequence information underpins genetic research, enabling discoveries of important biological or medical benefit. Sequencing projects have traditionally used long (400-800 base pair) reads, but the existence of reference sequences for the human and many other genomes makes it possible to develop new, fast approaches to re-sequencing, whereby shorter reads are compared to a reference to identify intraspecies genetic variation. Here we report an approach that generates several billion bases of accurate nucleotide sequence per experiment at low cost. Single molecules of DNA are attached to a flat surface, amplified in situ and used as templates for synthetic sequencing with fluorescent reversible terminator deoxyribonucleotides. Images of the surface are analysed to generate high-quality sequence. We demonstrate application of this approach to human genome sequencing on flow-sorted X chromosomes and then scale the approach to determine the genome sequence of a male Yoruba from Ibadan, Nigeria. We build an accurate consensus sequence from >30x average depth of paired 35-base reads. We characterize four million single-nucleotide polymorphisms and four hundred thousand structural variants, many of which were previously unknown. Our approach is effective for accurate, rapid and economical whole-genome re-sequencing and many other biomedical applications.}, author = {Bentley, DR David R and Balasubramanian, Shankar and Swerdlow, Harold P and Smith, Geoffrey P and Milton, John and Brown, Clive G and Hall, Kevin P and Evers, Dirk J and Barnes, Colin L and Bignell, Helen R and Boutell, Jonathan M and Bryant, Jason and Carter, Richard J and {Keira Cheetham}, R and Cox, Anthony J and Ellis, Darren J and Flatbush, Michael R and Gormley, Niall A and Humphray, Sean J and Irving, Leslie J and Karbelashvili, Mirian S and Kirk, Scott M and Li, Heng and Liu, Xiaohai and Maisinger, Klaus S and Murray, Lisa J and Obradovic, Bojan and Ost, Tobias and Parkinson, Michael L and Pratt, Mark R and Rasolonjatovo, Isabelle M J and Reed, Mark T and Rigatti, Roberto and Rodighiero, Chiara and Ross, Mark T and Sabot, Andrea and Sankar, Subramanian V and Scally, Aylwyn and Schroth, Gary P and Smith, Melanie A Mark E and Smith, Vincent P and Spiridou, Anastassia and Torrance, Peta E and Tzonev, Svilen S and Vermaas, Eric H and Walter, Klaudia and Wu, Xiaolin and Zhang, Lu and Alam, Mohammed D and Anastasi, Carole and Aniebo, Ify C and Bailey, David M D and Bancarz, Iain R and Banerjee, Saibal and Barbour, Selena G and Baybayan, Primo A and Benoit, Vincent A and Benson, Kevin F and Bevis, Claire and Black, Phillip J and Boodhun, Asha and Brennan, Joe S and Bridgham, John A and Brown, Rob C and Brown, Andrew A and Buermann, Dale H and Bundu, Abass A and Burrows, James C and Carter, Nigel P and Castillo, Nestor and {Chiara E Catenazzi}, Maria and Chang, Simon and {Neil Cooley}, R and Crake, Natasha R and Dada, Olubunmi O and Diakoumakos, Konstantinos D and Dominguez-Fernandez, Belen and Earnshaw, David J and Egbujor, Ugonna C and Elmore, David W and Etchin, Sergey S and Ewan, Mark R and Fedurco, Milan and Fraser, Louise J and {Fuentes Fajardo}, Karin V and {Scott Furey}, W and George, David and Gietzen, Kimberley J and Goddard, Colin P and Golda, George S and Granieri, Philip A and Green, David E and Gustafson, David L and Hansen, Nancy F and Harnish, Kevin and Haudenschild, Christian D and Heyer, Narinder I and Hims, Matthew M and Ho, Johnny T and Horgan, Adrian M and Hoschler, Katya and Hurwitz, Steve and Ivanov, Denis V and Johnson, Maria Q and James, Terena and {Huw Jones}, T A and Kang, Gyoung-Dong and Kerelska, Tzvetana H and Kersey, Alan D and Khrebtukova, Irina and Kindwall, Alex P and Kingsbury, Zoya and Kokko-Gonzales, Paula I and Kumar, Anil and Laurent, Marc A and Lawley, Cynthia T and Lee, Sarah E and Lee, Xavier and Liao, Arnold K and Loch, Jennifer A and Lok, Mitch and Luo, Shujun and Mammen, Radhika M and Martin, John W and McCauley, Patrick G and McNitt, Paul and Mehta, Parul and Moon, Keith W and Mullens, Joe W and Newington, Taksina and Ning, Zemin and {Ling Ng}, Bee and Novo, Sonia M and O'Neill, Michael J and Osborne, Mark A and Osnowski, Andrew and Ostadan, Omead and Paraschos, Lambros L and Pickering, Lea and Pike, Alger C Andrew C and {Chris Pinkard}, D and Pliskin, Daniel P and Podhasky, Joe and Quijano, Victor J and Raczy, Come and Rae, Vicki H and Rawlings, Stephen R and {Chiva Rodriguez}, Ana and Roe, Phyllida M and Rogers, John Jane and {Rogert Bacigalupo}, Maria C and Romanov, Nikolai and Romieu, Anthony and Roth, Rithy K and Rourke, Natalie J and Ruediger, Silke T and Rusman, Eli and Sanches-Kuiper, Raquel M and Schenker, Martin R and Seoane, Josefina M and Shaw, Richard J and Shiver, Mitch K and Short, Steven W and Sizto, Ning L and Sluis, Johannes P and {Ernest Sohna Sohna}, Jean and Spence, Eric J and Stevens, Kim and Sutton, Neil and Szajkowski, Lukasz and Tregidgo, Carolyn L and Turcatti, Gerardo and Vandevondele, Stephanie and Verhovsky, Yuli and Virk, Selene M and Wakelin, Suzanne and Walcott, Gregory C and Wang, Jingwen and Worsley, Graham J and Yan, Juying and Yau, Ling and Zuerlein, Mike and Mullikin, James C and Hurles, Matthew E and McCooke, Nick J and West, John S and Oaks, Frank L and Lundberg, Peter L and Klenerman, David and Durbin, Richard and Smith, Anthony J}, doi = {10.1038/nature07517}, file = {:home/gus/Documents/Mendeley Desktop/Bentley et al.\_2008\_Accurate whole human genome sequencing using reversible terminator chemistry.pdf:pdf}, issn = {1476-4687}, journal = {Nature}, keywords = {Chromosomes,Consensus Sequence,Consensus Sequence: genetics,DNA,DNA: economics,DNA: methods,Genome,Genomics,Genomics: economics,Genomics: methods,Genotype,Human,Human: genetics,Humans,Male,Nigeria,Polymorphism,Sensitivity and Specificity,Sequence Analysis,Single Nucleotide,Single Nucleotide: genetics,X,X: genetics}, month = nov, number = {7218}, pages = {53--9}, pmid = {18987734}, publisher = {Nature Publishing Group}, title = {{Accurate whole human genome sequencing using reversible terminator chemistry.}}, url = {http://www.nature.com/nature/journal/vaop/ncurrent/full/nature07517.html http://www.mendeley.com/research/accurate-whole-human-genome-sequencing-using-reversible-terminator-chemistry/}, volume = {456}, year = {2008} } Quorum-1.1.1/paper/bmc_article.bst000077500000000000000000001171541301151230400170710ustar00rootroot00000000000000%% % % bmc_article.bst ver: 1.01 % % % %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %% BibTeX BST file for BioMed Central %% %% a style syntax for latex .bib %% %% bibliographies %% %% %% %% <1 September 2003> %% %% %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% % % % The order in the reference list is that by which the % works were originally cited in the text, or that in % the database. % % % This file is based on the style 'unsrt.bst' % ------------------------------------------ % BibTeX standard bibliography style `unsrt' % version 0.99a for BibTeX versions 0.99a % or later, LaTeX version 2.09. % Copyright (C) 1985, all rights reserved. % Copying of this file is authorized only if either % (1) you make absolutely no changes to your copy, including name, or % (2) if you do make changes, you name it something other than % btxbst.doc, plain.bst, unsrt.bst, alpha.bst, and abbrv.bst. % This restriction helps ensure that all standard styles are identical. % The file btxbst.doc has the documentation for this style. % --------------------------------------------------------- %% ENTRY { address archive author booktitle chapter edition editor eid howpublished institution journal key month note number organization pages publisher school series title type url volume year } {} { label } % Global variables - most initialised and used locally. STRINGS { longest.label } STRINGS { cur tag source bibinfo} STRINGS { p q r s t z name names } STRINGS { lr lp lt ls} % local copys fxns with these call no other fxns. INTEGERS { number.label longest.label.width } INTEGERS { multiresult nameptr namesleft numnames global.counter} INTEGERS { i j k l ll li} INTEGERS { output.state before.all mid.sentence after.sentence after.block } FUNCTION {init.state.consts} { #0 'before.all := #1 'mid.sentence := #2 'after.sentence := #3 'after.block := #0 'global.counter := } % Logical operators on integers FUNCTION {not} { { #0 } { #1 } if$ } FUNCTION {and} { 'skip$ { pop$ #0 } if$ } FUNCTION {or} { { pop$ #1 } 'skip$ if$ } FUNCTION {field.or.null} { duplicate$ empty$ { pop$ "" } 'skip$ if$ } FUNCTION {remove.dots} { 'z := "" { z empty$ not } { z #1 #1 substring$ z #2 global.max$ substring$ 'z := duplicate$ "." = 'pop$ { * } if$ } while$ } %% % myreverse % % Takes 1 string % Returns the myreverse string % % not to be confused with REVERSE (opposite of ITERATE) %% FUNCTION {myreverse} { 'lt := "" 'ls := { lt empty$ not } { lt #1 #1 substring$ ls * 'ls := lt #2 global.max$ substring$ 'lt := } while$ ls } %% % search % % Takes 2 strings (txt, pattern) % Retruns 1 if found 0 if not %% FUNCTION {search} { 'lp := % pattern 'lt := % text to search #0 'i := % result lp text.length$ 'll := % length of the search pattern { lt empty$ not } { lt #1 ll substring$ lp = { #1 'li := "" 'lt := } % force exit { lt #2 global.max$ substring$ 'lt := } % pop 1 char if$ } while$ li } %% % general replace % % Takes 3 strings (txt, pattern, replace-str) % replaces all instances of pattern % Retruns a new string %% FUNCTION {replace} { 'lr := % replace string 'lp := % pattern 'lt := % text to search "" 'ls := % result string lp text.length$ 'll := % length of the search pattern { lt empty$ not } { lt #1 ll substring$ lp = { ls lr * 'ls := lt ll #1 + global.max$ substring$ 'lt := } { ls lt #1 #1 substring$ * 'ls := lt #2 global.max$ substring$ 'lt := } if$ } while$ ls } %% % strip.letters % % Takes 1 arg (string) % if string has letters get rid of them % - useful for 2nd -> 2 % Returns string %% FUNCTION {strip.letters} { "" 's := duplicate$ missing$ 'pop$ { 't := { t "" = not } { % ascii '0' = 48, '9' = 57 t #1 #1 substring$ chr.to.int$ 'i := i #47 > i #58 < and { s t #1 #1 substring$ * 's := } 'skip$ if$ t #2 global.max$ substring$ 't := } while$ } if$ s } FUNCTION {output.nonnull} { 's := output.state mid.sentence = { ", " * write$ } { output.state after.block = { add.period$ write$ newline$ "\newblock " write$ } { output.state before.all = %{ "OS=(" * output.state int.to.str$ * ") " * write$ } 'write$ { add.period$ " " * write$ } % after.sentence if$ } if$ mid.sentence 'output.state := } if$ s } FUNCTION {output} { duplicate$ empty$ 'pop$ 'output.nonnull if$ } % raises an error (warning message) if type not present. FUNCTION {output.check} { 't := duplicate$ empty$ { pop$ "empty " t * " in " * cite$ * warning$ } 'output.nonnull if$ } FUNCTION {fin.entry} { add.period$ write$ newline$ } FUNCTION {new.block} { output.state before.all = 'skip$ { after.block 'output.state := } if$ } FUNCTION {new.sentence} { output.state after.block = 'skip$ { output.state before.all = 'skip$ { after.sentence 'output.state := } if$ } if$ } FUNCTION {add.blank} { " " * before.all 'output.state := } FUNCTION {add.bold.colon} { duplicate$ empty$ 'skip$ { "\textbf{:}" * add.blank } if$ } FUNCTION {add.colon} { duplicate$ empty$ 'skip$ { ":" * add.blank } if$ } FUNCTION {bold} { duplicate$ empty$ { pop$ "" } { "\textbf{" swap$ * "}" * } if$ } FUNCTION {emphasize} { duplicate$ empty$ { pop$ "" } { "\emph{" swap$ * "}" * } if$ } FUNCTION {tie.or.space.prefix} { duplicate$ text.length$ #3 < { "~" } { " " } if$ swap$ } FUNCTION {capitalize} { "u" change.case$ "t" change.case$ } FUNCTION {space.word} { " " swap$ * " " * } % if field not entered - push empty string "" FUNCTION {bibinfo.check} { swap$ duplicate$ missing$ { pop$ pop$ "" } { duplicate$ empty$ { swap$ pop$ } { swap$ pop$ } if$ } if$ } FUNCTION {bibinfo.warn} { swap$ duplicate$ missing$ { swap$ "missing " swap$ * " in " * cite$ * warning$ pop$ "" } { duplicate$ empty$ { swap$ "empty " swap$ * " in " * cite$ * warning$ } { swap$ pop$ } if$ } if$ } FUNCTION {format.thesis.type} { type duplicate$ empty$ 'pop$ { swap$ pop$ "t" change.case$ "type" bibinfo.check } if$ } % Here are the language-specific definitions for explicit words. % Each function has a name bbl.xxx where xxx is the English word. % The language selected here is ENGLISH FUNCTION {bbl.and} { "and"} FUNCTION {bbl.etal} { "et~al." } FUNCTION {bbl.editors} { "(Eds)" } %{ "editors" } FUNCTION {bbl.editor} { "(Ed)" } %{ "editor" } FUNCTION {bbl.edby} { "Edited by" } FUNCTION {bbl.edition} { "edition" } %{ "edn." } FUNCTION {bbl.volume} { "Volume" } %{ "vol." } FUNCTION {bbl.of} { "of" } FUNCTION {bbl.number} { "no." } FUNCTION {bbl.nr} { "no." } FUNCTION {bbl.in} { "in" } FUNCTION {bbl.pages} { "" } FUNCTION {bbl.page} { "" } FUNCTION {bbl.chapter} { "chap." } FUNCTION {bbl.techrep} { "Tech. Rep." } FUNCTION {bbl.mthesis} { "Master's thesis" } FUNCTION {bbl.phdthesis} { "PhD thesis" } MACRO {jan} {"Jan."} MACRO {feb} {"Feb."} MACRO {mar} {"Mar."} MACRO {apr} {"Apr."} MACRO {may} {"May"} MACRO {jun} {"Jun."} MACRO {jul} {"Jul."} MACRO {aug} {"Aug."} MACRO {sep} {"Sep."} MACRO {oct} {"Oct."} MACRO {nov} {"Nov."} MACRO {dec} {"Dec."} MACRO {acmcs} {"ACM Computing Surveys"} MACRO {acta} {"Acta Informatica"} MACRO {cacm} {"Communications of the ACM"} MACRO {ibmjrd} {"IBM Journal of Research and Development"} MACRO {ibmsj} {"IBM Systems Journal"} MACRO {ieeese} {"IEEE Transactions on Software Engineering"} MACRO {ieeetc} {"IEEE Transactions on Computers"} MACRO {ieeetcad} {"IEEE Transactions on Computer-Aided Design of Integrated Circuits"} MACRO {ipl} {"Information Processing Letters"} MACRO {jacm} {"Journal of the ACM"} MACRO {jcss} {"Journal of Computer and System Sciences"} MACRO {scp} {"Science of Computer Programming"} MACRO {sicomp} {"SIAM Journal on Computing"} MACRO {tocs} {"ACM Transactions on Computer Systems"} MACRO {tods} {"ACM Transactions on Database Systems"} MACRO {tog} {"ACM Transactions on Graphics"} MACRO {toms} {"ACM Transactions on Mathematical Software"} MACRO {toois} {"ACM Transactions on Office Information Systems"} MACRO {toplas} {"ACM Transactions on Programming Languages and Systems"} MACRO {tcs} {"Theoretical Computer Science"} % Takes 2 args (author field) and string "author" FUNCTION {format.names} { 'bibinfo := duplicate$ empty$ 'skip$ { 's := "" 't := #1 'nameptr := s num.names$ 'numnames := numnames 'namesleft := { namesleft #0 > } { s nameptr "{vv~}{ll}{ f{}}{ jj}" format.name$ remove.dots bibinfo bibinfo.check 't := nameptr #1 > { nameptr #3 #1 + = numnames #5 > and { "others" 't := #1 'namesleft := } 'skip$ if$ namesleft #1 > { ", " * t * } { "," * s nameptr "{ll}" format.name$ duplicate$ "others" = { 't := } { pop$ } if$ t "others" = { " " * bbl.etal * } { " " * t * } if$ } if$ } 't if$ nameptr #1 + 'nameptr := namesleft #1 - 'namesleft := } while$ } if$ } %"{f{~}~}{vv~}{ll}{ jj}" FUNCTION {format.names.ed} { 'bibinfo := duplicate$ empty$ 'skip$ { 's := "" 't := #1 'nameptr := s num.names$ 'numnames := numnames 'namesleft := { namesleft #0 > } { s nameptr "{vv~}{ll}{ f{}}{ jj}" format.name$ remove.dots bibinfo bibinfo.check 't := nameptr #1 > { namesleft #1 > { ", " * t * } { "," * s nameptr "{ll}" format.name$ duplicate$ "others" = { 't := } { pop$ } if$ t "others" = { " " * bbl.etal * } { " " * t * } if$ } if$ } 't if$ nameptr #1 + 'nameptr := namesleft #1 - 'namesleft := } while$ } if$ } FUNCTION {format.authors} { author "author" format.names } FUNCTION {get.bbl.editor} { editor num.names$ #1 > 'bbl.editors 'bbl.editor if$ } FUNCTION {format.editors} { editor "editor" format.names duplicate$ empty$ 'skip$ { " " * get.bbl.editor * %% "," * " " * get.bbl.editor * } if$ } FUNCTION {format.note} { % url empty$ % 'skip$ % { % "\urlprefix\url{[" url * "]}" * output } % if$ note empty$ { "" } { note "l" change.case$ "in press" = { after.sentence 'output.state := " in press" } { after.sentence 'output.state := note #1 #1 substring$ duplicate$ "{" = 'skip$ { output.state mid.sentence = { "l" } { "u" } if$ change.case$ % leave note * As Is * } if$ note #2 global.max$ substring$ * "note" bibinfo.check "[" swap$ * "]" * } if$ } if$ } FUNCTION {bold.format.title} { title "title" bibinfo.check duplicate$ empty$ 'skip$ { bold } if$ } FUNCTION {emph.format.title} { title "title" bibinfo.check duplicate$ empty$ 'skip$ { emphasize } if$ } % Returns "" FUNCTION {output.bibitem} { newline$ "\bibitem{" write$ cite$ write$ "}" write$ newline$ "" before.all 'output.state := } FUNCTION {output.allinfo.comment} { } FUNCTION {n.dashify} { 't := "" { t empty$ not } { t #1 #1 substring$ "-" = { t #1 #2 substring$ "--" = not { "--" * t #2 global.max$ substring$ 't := } { { t #1 #1 substring$ "-" = } { "-" * t #2 global.max$ substring$ 't := } while$ } if$ } { t #1 #1 substring$ * t #2 global.max$ substring$ 't := } if$ } while$ } FUNCTION {word.in} { bbl.in capitalize " " * } FUNCTION {format.date} { before.all 'output.state := "" duplicate$ empty$ year "year" bibinfo.check duplicate$ empty$ { swap$ 'skip$ { "there's a month but no year in " cite$ * warning$ } if$ * } { swap$ 'skip$ { swap$ " " * swap$ } if$ * remove.dots } if$ duplicate$ "" = 'skip$ { " " swap$ * } if$ } % Source = book, conference, journal, manual % have the source avaliable on the stack FUNCTION {format.source} { 'source := source "source" bibinfo.check duplicate$ empty$ 'skip$ { emphasize } if$ } FUNCTION {format.title} { title "title" bibinfo.check duplicate$ empty$ 'skip$ { bold } if$ } FUNCTION {either.or.check} { empty$ 'pop$ { "can't use both " swap$ * " fields in " * cite$ * warning$ } if$ } FUNCTION {format.bvolume} { volume empty$ { "" } { bbl.volume volume tie.or.space.prefix "volume" bibinfo.check * * series "series" bibinfo.check duplicate$ empty$ 'pop$ { swap$ bbl.of space.word * swap$ emphasize * } if$ emphasize "volume and number" number either.or.check } if$ } FUNCTION {format.number.series} { volume empty$ { number empty$ { series field.or.null } { series empty$ { number "number" bibinfo.check } { output.state mid.sentence = { bbl.number } { bbl.number capitalize } if$ number tie.or.space.prefix "number" bibinfo.check * * bbl.in space.word * series "series" bibinfo.check * } if$ } if$ } { "" } if$ } FUNCTION {format.edition} { edition duplicate$ empty$ 'skip$ { output.state mid.sentence = { "l" } { "t" } if$ change.case$ "edition" bibinfo.check " " * bbl.edition * } if$ } FUNCTION {multi.page.check} { 't := #0 'multiresult := { multiresult not t empty$ not and } { t #1 #1 substring$ duplicate$ "-" = swap$ duplicate$ "," = swap$ "+" = or or { #1 'multiresult := } { t #2 global.max$ substring$ 't := } if$ } while$ multiresult } FUNCTION {format.pages} { pages duplicate$ empty$ 'skip$ { duplicate$ multi.page.check { n.dashify } { } if$ "pages" bibinfo.check ":" swap$ * } if$ } FUNCTION {format.journal.pages} { pages duplicate$ empty$ 'pop$ { swap$ duplicate$ empty$ { pop$ pop$ format.pages } { ":" * swap$ n.dashify "pages" bibinfo.check * } if$ } if$ } FUNCTION {format.journal.eid} { eid "eid" bibinfo.check duplicate$ empty$ 'pop$ { swap$ duplicate$ empty$ 'skip$ { ":" * } if$ swap$ * } if$ } % ignore issue (num) if == 1 FUNCTION {format.vol.num.pages} { volume field.or.null duplicate$ empty$ 'skip$ { "volume" bibinfo.check bold } if$ number "number" bibinfo.check duplicate$ empty$ 'skip$ { duplicate$ "1" = {pop$ ""} { swap$ duplicate$ empty$ { "there's a number but no volume in " cite$ * warning$ } 'skip$ if$ swap$ "(" swap$ * ")" * } if$ } if$ * eid empty$ { format.journal.pages } { format.journal.eid } if$ } FUNCTION {format.chapter.pages} { chapter empty$ 'format.pages { type empty$ { bbl.chapter } { type "l" change.case$ "type" bibinfo.check } if$ chapter tie.or.space.prefix "chapter" bibinfo.check * * pages empty$ 'skip$ { ", " * format.pages * } if$ } if$ } %% FUNCTION {format.in.ed.booktitle} %% { booktitle format.source duplicate$ empty$ 'skip$ %% { %% editor "editor" format.names.ed duplicate$ empty$ 'pop$ %% { %% bbl.edby %% " " * swap$ * %% swap$ %% "," * %% " " * swap$ %% * } %% if$ %% word.in swap$ * %% } %% if$ %% } FUNCTION{format.edited.by} { editor "editor" format.names.ed duplicate$ empty$ 'pop$ { bbl.edby " " * swap$ * swap$ ". " * swap$ * } if$ } FUNCTION {format.in.booktitle} { booktitle format.source duplicate$ empty$ 'skip$ { word.in swap$ * } if$ } FUNCTION {format.in.journal} { journal format.source duplicate$ empty$ 'skip$ { word.in swap$ * } if$ } FUNCTION {empty.misc.check} { author empty$ title empty$ howpublished empty$ month empty$ year empty$ note empty$ and and and and and { "all relevant fields are empty in " cite$ * warning$ } 'skip$ if$ } FUNCTION {format.tr.number} { number "number" bibinfo.check type duplicate$ empty$ { pop$ bbl.techrep } 'skip$ if$ "type" bibinfo.check swap$ duplicate$ empty$ { pop$ "t" change.case$ } { tie.or.space.prefix * * } if$ } FUNCTION {format.article.crossref} { key duplicate$ empty$ { pop$ journal duplicate$ empty$ { "need key or journal for " cite$ * " to crossref " * crossref * warning$ } { "journal" bibinfo.check emphasize word.in swap$ * } if$ } { word.in swap$ * " " *} if$ " \cite{" * crossref * "}" * } FUNCTION {format.crossref.editor} { editor #1 "{vv~}{ll}" format.name$ "editor" bibinfo.check editor num.names$ duplicate$ #2 > { pop$ "editor" bibinfo.check " " * bbl.etal * } { #2 < 'skip$ { editor #2 "{ff }{vv }{ll}{ jj}" format.name$ "others" = { "editor" bibinfo.check " " * bbl.etal * } { bbl.and space.word * editor #2 "{vv~}{ll}" format.name$ "editor" bibinfo.check * } if$ } if$ } if$ } FUNCTION {format.book.crossref} { volume duplicate$ empty$ { "empty volume in " cite$ * "'s crossref of " * crossref * warning$ pop$ word.in } { bbl.volume capitalize swap$ tie.or.space.prefix "volume" bibinfo.check * * bbl.of space.word * } if$ editor empty$ editor field.or.null author field.or.null = or { key empty$ { series empty$ { "need editor, key, or series for " cite$ * " to crossref " * crossref * warning$ "" * } { series emphasize * } if$ } { key * } if$ } { format.crossref.editor * } if$ " \cite{" * crossref * "}" * } FUNCTION {format.incoll.inproc.crossref} { editor empty$ editor field.or.null author field.or.null = or { key empty$ { booktitle format.source duplicate$ empty$ { "need editor, key, or booktitle for " cite$ * " to crossref " * crossref * warning$ } { word.in swap$ * } if$ } { word.in key * " " *} if$ } { word.in format.crossref.editor * " " *} if$ " \cite{" * crossref * "}" * } % Takes 1 arg (publisher or organisation} % if present appends address to the front. ie New York: Sachai Ltd % returns the formatted string. FUNCTION {format.org.or.pub} { 't := t empty$ { address empty$ 'skip$ { address "address" bibinfo.check 't := } if$ } { address empty$ 'skip$ { address "address" bibinfo.check ": " * t * 't :=} if$ } if$ t } FUNCTION {format.publisher.address} { publisher "publisher" bibinfo.warn format.org.or.pub } FUNCTION {format.organization.address} { organization "organization" bibinfo.check format.org.or.pub } FUNCTION {article} { output.bibitem author empty$ { format.editors "author or editor" output.check add.colon } { format.authors output.nonnull add.colon crossref missing$ { "author and editor" editor either.or.check } 'skip$ if$ } if$ bold.format.title "title" output.check new.sentence crossref missing$ { journal "journal" bibinfo.check format.source "journal" output.check format.date "year" output.check format.vol.num.pages output } { format.article.crossref output.nonnull format.pages output } if$ format.note output fin.entry } FUNCTION {wholejournal} { output.bibitem author empty$ { format.editors "author or editor" output.check add.colon } { format.authors output.nonnull add.colon crossref missing$ { "author and editor" editor either.or.check } 'skip$ if$ } if$ bold.format.title "title" output.check new.sentence crossref missing$ { journal emphasize word.in swap$ * "journal" output.check format.date "year" output.check format.vol.num.pages output } { format.article.crossref output.nonnull format.pages output } if$ format.note output fin.entry } FUNCTION {book} { output.bibitem author empty$ { format.editors "author and editor" output.check add.colon } { format.authors output.nonnull add.colon crossref missing$ { "author and editor" editor either.or.check } 'skip$ if$ } if$ title format.source "source" output.check crossref missing$ { format.bvolume output new.sentence format.number.series output format.publisher.address output } { new.sentence format.book.crossref output.nonnull } if$ format.edition output format.date "year" output.check format.note output fin.entry } FUNCTION {inbook} { output.bibitem author empty$ { format.editors "author and editor" output.check add.colon } { format.authors output.nonnull add.colon crossref missing$ { "author and editor" editor either.or.check } 'skip$ if$ } if$ title format.source "title" output.check crossref missing$ { format.publisher.address output format.bvolume output new.sentence format.number.series output } { new.sentence format.book.crossref output.nonnull } if$ format.edition output format.date "year" output.check add.blank format.chapter.pages "chapter and/or pages" output.check format.note output fin.entry } % In . Volume X. y edition. Edited by . % Add: Pub; date:pages. FUNCTION {incollection} { output.bibitem format.authors "author" output.check add.colon bold.format.title "title" output.check new.sentence crossref missing$ { format.in.booktitle "booktitle" output.check %format.in.ed.booktitle "booktitle" output.check format.bvolume output format.number.series output format.edition output booktitle empty$ 'skip$ {format.edited.by} if$ format.publisher.address output } { format.incoll.inproc.crossref output.nonnull } if$ format.date "year" output.check before.all 'output.state := %no space,comma,etc.. -> 1991:23 format.pages output format.note output fin.entry } FUNCTION {inproceedings} { output.bibitem format.authors "author" output.check add.colon bold.format.title "title" output.check new.sentence crossref missing$ % In . Volume X. x nd edition. Edited by . { format.in.booktitle "booktitle" output.check format.bvolume output format.edition output format.number.series output booktitle missing$ 'skip$ { booktitle missing$ 'skip$ {format.edited.by} if$ } if$ publisher missing$ { format.organization.address output } { organization "organization" bibinfo.check output format.publisher.address output } if$ } { format.incoll.inproc.crossref output.nonnull } if$ format.date "year" output.check before.all 'output.state := %no space,comma,etc.. format.pages output format.note output fin.entry } FUNCTION {conference} {inproceedings} FUNCTION {mastersthesis} { output.bibitem format.authors "author" output.check add.colon bold.format.title "title" output.check new.sentence bbl.mthesis format.thesis.type format.source output.nonnull school "school" bibinfo.warn output address "address" bibinfo.check output format.date "year" output.check format.note output fin.entry } % old manual style syntax % all optional: (author, title, howpublished, month, year, note) % maybe missing: (organization, address, edition) FUNCTION {misc} { output.bibitem author empty$ { organization missing$ 'skip$ { organization output } if$ } { format.authors output } if$ add.colon bold.format.title output new.sentence howpublished "howpublished" bibinfo.check format.source output new.sentence edition missing$ 'skip$ {edition output} if$ author empty$ 'skip$ { organization missing$ 'skip$ {organization output} if$ } if$ address missing$ 'skip$ {address output} if$ format.date output format.note output fin.entry empty.misc.check } FUNCTION {webpage} { output.bibitem author empty$ { organization missing$ 'skip$ { organization output } if$ } { format.authors output } if$ add.colon bold.format.title " " * output new.sentence howpublished "howpublished" bibinfo.check format.source output new.sentence edition missing$ 'skip$ {edition output} if$ author empty$ 'skip$ { organization missing$ 'skip$ {organization output} if$ } if$ address missing$ 'skip$ {address output} if$ format.date output format.note output fin.entry empty.misc.check } FUNCTION {inpress} { output.bibitem author empty$ { organization missing$ 'skip$ { organization output } if$ } { format.authors output } if$ add.colon bold.format.title output new.sentence journal emphasize output "in press" output fin.entry empty.misc.check } FUNCTION {manual} { output.bibitem author empty$ { organization missing$ 'skip$ { organization output } if$ } { format.authors output } if$ add.colon title output emphasize new.sentence howpublished "howpublished" bibinfo.check format.source output new.sentence edition missing$ 'skip$ {edition output} if$ author empty$ 'skip$ { organization missing$ 'skip$ {organization output} if$ } if$ address missing$ 'skip$ {address output} if$ format.date output format.note output fin.entry empty.misc.check } FUNCTION {booklet}{misc} FUNCTION {phdthesis} { output.bibitem format.authors "author" output.check add.colon bold.format.title "title" output.check new.sentence bbl.phdthesis format.thesis.type format.source output.nonnull school "school" bibinfo.warn output address "address" bibinfo.check output format.date "year" output.check format.note output fin.entry } FUNCTION {proceedings} { output.bibitem editor empty$ { organization "organization" bibinfo.check output } { format.editors output.nonnull } if$ add.colon title format.source "source" output.check format.bvolume output format.number.series output editor empty$ { publisher empty$ 'skip$ { format.publisher.address output } if$ } { publisher empty$ { format.organization.address output } { organization "organization" bibinfo.check output format.publisher.address output } if$ } if$ format.date "year" output.check format.note output fin.entry } FUNCTION {techreport} { output.bibitem format.authors "author" output.check add.colon bold.format.title "title" output.check new.sentence format.tr.number output.nonnull institution "institution" bibinfo.warn output address "address" bibinfo.check output format.date "year" output.check format.note output fin.entry } FUNCTION {unpublished} { output.bibitem format.authors "author" output.check add.colon bold.format.title "title" output.check format.date output format.note "note" output.check fin.entry } FUNCTION {default.type} { misc } %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %%%% %%% %%%%%%% %% %%%%%%%%% %% %%%% %% %%%% % %%%%% % %% %%%%%%%%% %% %%%%% %%%%% %% %%% %% %% %%%%%%%%% %% %%%%%% %%%%%% %%% % %%% %% %%%%%%%%% %% %%%%% %%%%% %%%% %%%% %% %%%%%%%%% %% %%%% %% %%%% %%%%%%%%%%% %% %%%%%%%%% %% %% %%%% %%% %%%%%%%%%%% %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% % % Function for printing out all data in xml format. % { address archive author booktitle chapter edition editor % howpublished institution journal key month note number % organization pages publisher school series title % type url volume year % } % %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% % output.xml % %% FUNCTION {output.xml} { duplicate$ "" = 'pop$ { " " swap$ * write$ newline$ } if$ } %% % markup.xml % % Takes 2 args text & tag {"the text " "tag"} % Returns 1 string {"the text <\tag>"} %% FUNCTION {markup.xml} { "" 'r := % result 't := % tag duplicate$ missing$ 'pop$ { 'r := } if$ r "" = 'skip$ { "<" t * ">" * r * "" * 'r := } if$ r } %% Takes 2 args - tag, string FUNCTION{markup.xml.title} { pop$ % tag duplicate$ missing$ 'pop$ { 's := % string s "\&" "&" replace 's := s "p" markup.xml 's := s "title" markup.xml output.xml } if$ } %% % markup.xml.pages % % Takes 1 arg (pages string) % seperates into and if % there is a - seperator. else no lpage. % % need to remove others %% FUNCTION{markup.xml.pages} { "" 'r := % fpage "" 's := % lpage duplicate$ missing$ 'pop$ { 't := t " " "" replace 't := % remove all spaces. pgs must be - seperated { t empty$ not } { t #1 #1 substring$ "-" = { t #2 global.max$ substring$ 's := "" 't := % break while loop }{ r t #1 #1 substring$ * 'r := t #2 global.max$ substring$ 't := } if$ } while$ } if$ r "fpage" markup.xml output.xml s "lpage" markup.xml output.xml } %% % markup.xml.names % % Takes 2 args % tag, namefield (eg. author "au") % splits fields into and % writes info % returns nothing %% FUNCTION {markup.xml.names} { 't := % tag "" 'r := "" 's := duplicate$ empty$ { pop$ organization missing$ { institution "cnm" markup.xml "au" markup.xml "aug" markup.xml output.xml } { organization "cnm" markup.xml "au" markup.xml "aug" markup.xml output.xml } if$ } { " " write$ newline$ 'names := % names string names num.names$ 'j := % num of names #1 'i := % init counter { i #1 j + < } % while (i <= j) { " " write$ % Initial first names % if first name all in capitals % - assume is initial list of first names. names i "{ff{ }}" format.name$ duplicate$ "u" change.case$ = { names i "{ff{ }}" format.name$ } { names i "{f{}}" format.name$ } if$ % if last name but no first name use cnm; else snm duplicate$ "" = { names i "{ll{ }}" format.name$ % last names space seperated. "cnm" markup.xml write$ } { names i "{ll{ }}" format.name$ % last names space seperated. "snm" markup.xml write$ } if$ "fnm" markup.xml write$ "" write$ newline$ i #1 + 'i := } while$ " " write$ newline$ } if$ } %% % markup.xml.pub % % Takes 4 args (school address publisher tag) % prints concatenation % returns nothing %% FUNCTION {markup.xml.pub} { 't := % Tag "" 'p := % Publisher "" 'q := % Address "" 'r := % School "" 's := % Answer duplicate$ missing$ 'pop$ { 'p := } if$ duplicate$ missing$ 'pop$ { 'q := } if$ duplicate$ missing$ 'pop$ { 'r := } if$ "" r = not % school not empty { r 's := } % return school as publisher { % else "" p = "" q = and % address and pub empty 'skip$ { "" q = { p 's := } % return pub { "" p = { q 's := } % return add { q ": " * p * 's := } % return add : pub if$ } if$ } if$ } if$ s t markup.xml output.xml } %% % xml.phd % % Takes nothing % Returns type (phd/msc) of empty string %% FUNCTION {xml.phd} { "phdthesis" type$ = "mastersthesis" type$ = OR { "phdthesis" type$ = { bbl.phdthesis format.thesis.type } { bbl.mthesis format.thesis.type } if$ } { type } % usually empty if$ } % markup.xml.edition % % edition is a numeric value. ie "2" % if format 2nd 1st etc.. strip letters. % FUNCTION {markup.xml.edition} { pop$ pop$ %clear stack edition strip.letters duplicate$ "" = { pop$ edition } 'skip$ if$ "edition" markup.xml output.xml } %% [bmc@xmlcomment] % this is an environment that returns nothing % so although it will be embedded in the bbl file it % will not display anything %% FUNCTION{begin.bmcxmlcomment}{ newline$ "\newcommand{\BMCxmlcomment}[1]{}" write$ newline$ newline$ "\BMCxmlcomment{" write$ newline$ newline$ "" write$ newline$ } FUNCTION{end.bmcxmlcomment}{ newline$ "" write$ newline$ "} % end of \BMCxmlcomment" write$ newline$ } %% % export.xml % % done for each entry referenced in the BibTeX database %% FUNCTION {export.xml}{ newline$ global.counter #1 + 'global.counter := "" * write$ newline$ % title "\&" "&" replace "title" markup.xml.title title "title" markup.xml.title author "aug" markup.xml.names % org. and inst. here howpublished missing$ { booktitle missing$ { journal missing$ { xml.phd } % Phd/Msc {journal} if$ } {booktitle} if$ } { howpublished } if$ "source" markup.xml output.xml school address publisher "publisher" markup.xml.pub editor "editor" markup.xml output.xml edition "edition" markup.xml.edition series "p" markup.xml "title" markup.xml "series" markup.xml output.xml chapter "p" markup.xml "title" markup.xml "section" markup.xml output.xml % month % ignore year "pubdate" markup.xml output.xml note missing$ { volume "volume" markup.xml output.xml number "issue" markup.xml output.xml pages markup.xml.pages url "url" markup.xml output.xml } { note "l" change.case$ "in press" = { " " write$ newline$ } { volume "volume" markup.xml output.xml number "issue" markup.xml output.xml pages markup.xml.pages url "url" markup.xml output.xml note "note" markup.xml output.xml } if$ } if$ "" write$ newline$ } % xml fields not used % suppliment conference xrefbib issn issb archive key % BioMed_Central_Tex_Template_v1.01 %%%%%%%%%%%%%%%% % % % Main % % % %%%%%%%%%%%%%%%% READ FUNCTION {initialize.longest.label} { "" 'longest.label := #1 'number.label := #0 'longest.label.width := } FUNCTION {longest.label.pass} { number.label int.to.str$ 'label := number.label #1 + 'number.label := label width$ longest.label.width > { label 'longest.label := label width$ 'longest.label.width := } 'skip$ if$ } EXECUTE {initialize.longest.label} ITERATE {longest.label.pass} FUNCTION {begin.bib} { "%% BioMed_Central_Bib_Style_v1.01" write$ newline$ newline$ preamble$ empty$ 'skip$ { preamble$ write$ newline$ } if$ "\begin{thebibliography}{" longest.label * "}" * write$ newline$ "\providecommand{\url}[1]{[#1]}" write$ newline$ "\providecommand{\urlprefix}{}" write$ newline$ } EXECUTE {begin.bib} EXECUTE {init.state.consts} ITERATE {call.type$} FUNCTION {end.bib} { newline$ "\end{thebibliography}" write$ newline$ } EXECUTE {end.bib} EXECUTE {begin.bmcxmlcomment} ITERATE {export.xml} EXECUTE {end.bmcxmlcomment} %% End of customized bst file %% %% End of file `basic.bst'. Quorum-1.1.1/paper/bmc_article.cls000077500000000000000000000107511301151230400170550ustar00rootroot00000000000000%% % % bmc_article.cls ver: 1.03 % % % %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% % %% % A Style Class based on article for %% % formating towards BioMed Central %% % guidelines %% % %% % <1 September 2003> %% % %% % %% % %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% % % See Readme.txt for ToDo list. %% % \NeedsTeXFormat{LaTeX2e}[1995/12/01] \ProvidesClass{bmc_article}[2003/09/01 v1.01 BioMed Central article class] \LoadClassWithOptions{article} \renewcommand\@biblabel[1]{#1.} \def\hi{} \def\pb{\\*[0.42cm]} \AtBeginDocument{} \def\@abstractline{\textwidth} \newcounter{bmc@correspondingauthor} \setcounter{bmc@correspondingauthor}{0} %never changes \newcounter{bmc@emailcounter} \setcounter{bmc@emailcounter}{0} % Corresponding Authors. % adds an asterisk * as a marker. \def\correspondingauthor{$^*$} \def\@corresponding{\footnotesize\correspondingauthor Corresponding author} % Email. % A variable to store names and emails. \gdef\bmc@email{Email: } \newcommand\bmc@curname{} \newcommand\email[1]{\relax \g@addto@macro\bmc@email{#1; }} % has trailing ; \def\@bmc@email{\relax\footnotesize{\bmc@email}} % Address \def\address#1{ \def\@address{\begin{hi}\footnotesize#1\end{hi}}} \def\iid(#1){\hi$^#1$} % Thanks \def\thempfootnote{\normalfont\@arabic\c@mpfootnote} \def\thanks#1{% \stepcounter{footnote}% \hbox{\@textsuperscript{\normalfont\thefootnote}}% \protected@xdef\@thanks{\@thanks% \protect\footnotetext[\the\c@footnote]{#1}}% } % Maketitle \let\old@maketitle\maketitle \renewcommand\maketitle{ \begin{flushleft}\mbox{ \global\let\@date\@empty % @date = null. {\sffamily\begin{minipage}{\textwidth}% \@maketitle {\raggedright% {\noindent\@address}\\ \hbox{} {\noindent\@bmc@email}\\ \hbox{} {\noindent\@corresponding}% }%end \raggedright \end{minipage}% } \renewcommand\thefootnote{\old@thefootnote} % } % \mbox \end{flushleft} } \def\and{, } \def\@maketitle{% \newpage \null \vskip 2em% {\noindent\LARGE \bfseries\@title \par}% \vskip 1.5em% {\large %\lineskip .5em% \noindent\@author \par}% \vskip 1em% \par \vskip 1.5em} % reformats abstract to BMC looks \let\old@abstract\abstract \renewenvironment{abstract} { \ifhmode\begingroup\parskip0pt\par\noindent\endgroup\fi% \begin{sffamily} \vspace{1cm} % use \topsep in list {\noindent\bfseries\large\abstractname\vspace{-0.5em}} {\par\vbox{\hrule width \@abstractline}} }{ \ifhmode\begingroup\parskip0pt\par\noindent\endgroup\fi % \vbox{\hrule width \@abstractline} \vspace{1cm} % \end{sffamily} } %% \@startsection{sec-name}{level}{indent}{pre-skip} %% {post-skip}{style}*[srt title]{title} \renewcommand\section{\@startsection {section}{1}{\z@}% {-0.84cm \@plus -1ex \@minus -.2ex} {.2ex \@plus.2ex} %% {\normalfont\large\bfseries\sffamily}} \renewcommand\subsection{\@startsection{subsection}{2}{\z@}% {-0.84cm \@plus -1ex \@minus -.2ex} {.2ex \@plus.2ex} %% {\normalfont\normalsize\bfseries\sffamily}} \renewcommand\subsubsection{\@startsection{subsubsection}{3}{\z@}% {-0.84cm \@plus -1ex \@minus -.2ex} {.2ex \@plus.2ex} %% {\normalfont\normalsize\sffamily\itshape}} \renewcommand\paragraph{\@startsection{paragraph}{4}{\z@}% {-.2em \@plus1ex \@minus.2ex} {-0.5em} %% {\normalfont\small\bfseries\sffamily}} \renewcommand\subparagraph{\@startsection{subparagraph}{5}{\parindent}% {-.2em \@plus1ex \@minus.2ex} {-0.5em} %% {\normalfont\normalsize\sffamily}} \endinput %% end of bmc_article.cls Quorum-1.1.1/paper/bmc_article.tex000066400000000000000000001167631301151230400171030ustar00rootroot00000000000000%% BioMed_Central_Tex_Template_v1.05 %% % % bmc_article.tex ver: 1.05 % % % %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %% LaTeX template for BioMed Central %% %% journal article submissions %% %% %% %% <27 January 2006> %% %% %% %% %% %% Uses: %% %% cite.sty, url.sty, bmc_article.cls %% %% ifthen.sty. multicol.sty %% %% %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %% For instructions on how to fill out this Tex template %% %% document please refer to Readme.pdf and the instructions for %% %% authors page on the biomed central website %% %% http://www.biomedcentral.com/info/authors/ %% %% %% %% Please do not use \input{...} to include other tex files. %% %% Submit your LaTeX manuscript as one .tex document. %% %% %% %% All additional figures and files should be attached %% %% separately and not embedded in the \TeX\ document itself. %% %% %% %% BioMed Central currently use the MikTex distribution of %% %% TeX for Windows) of TeX and LaTeX. This is available from %% %% http://www.miktex.org %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \NeedsTeXFormat{LaTeX2e}[1995/12/01] \documentclass[10pt]{bmc_article} % Load packages \usepackage{cite} % Make references as [1-4], not [1,2,3,4] \usepackage{url} % Formatting web addresses \usepackage{ifthen} % Conditional \usepackage{multicol} %Columns \usepackage[utf8]{inputenc} %unicode support %\usepackage[applemac]{inputenc} %applemac support if unicode package fails %\usepackage[latin1]{inputenc} %UNIX support if unicode package fails \usepackage{siunitx} \usepackage{etoolbox} \usepackage{booktabs} \usepackage{xspace} \urlstyle{rm} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %% If you wish to display your graphics for %% %% your own use using includegraphic or %% %% includegraphics, then comment out the %% %% following two lines of code. %% %% NB: These line *must* be included when %% %% submitting to BMC. %% %% All figure files must be submitted as %% %% separate graphics through the BMC %% %% submission process, not included in the %% %% submitted article. %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \def\includegraphic{} \def\includegraphics{} \setlength{\topmargin}{0.0cm} \setlength{\textheight}{21.5cm} \setlength{\oddsidemargin}{0cm} \setlength{\textwidth}{16.5cm} \setlength{\columnsep}{0.6cm} \newboolean{publ} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %% You may change the following style settings %% %% Should you wish to format your article %% %% in a publication style for printing out and %% %% sharing with colleagues, but ensure that %% %% before submitting to BMC that the style is %% %% returned to the Review style setting. %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %Review style settings %\newenvironment{bmcformat}{\begin{raggedright}\baselineskip20pt\sloppy\setboolean{publ}{false}}{\end{raggedright}\baselineskip20pt\sloppy} %Publication style settings \newenvironment{bmcformat}{\fussy\setboolean{publ}{true}}{\fussy} % Begin ... \begin{document} \begin{bmcformat} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% Formatting macros %%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \newcommand{\quorum}{QuorUM\xspace} \hyphenation{quor-um} \newcommand{\species}[1]{\textit{#1}} \newcommand{\cov}[1]{\ensuremath #1\textrm{x}\xspace} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %% Enter the title of your article here %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \title{\quorum: an error corrector for Illumina reads} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %% Enter the authors here %% %% %% %% Ensure \and is entered between all but %% %% the last two authors. This will be %% %% replaced by a comma in the final article %% %% %% %% Ensure there are no trailing spaces at %% %% the ends of the lines %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \author{Guillaume Mar\c{c}ais\correspondingauthor$^1$% \email{Guillaume Mar\c{c}ais\correspondingauthor - gmarcais@umd.edu}% \and Aleksey Zimin\correspondingauthor$^1$% \email{Aleksey Zimin\correspondingauthor- alekseyz@ipst.umd.edu}% \ and James A. Yorke$^1$% \email{James Yorke - yorke@umd.edu} } %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %% Enter the authors' addresses here %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \address{% \iid(1)University of Maryland, College Park, MD }% \maketitle %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %% The Abstract begins here %% %% %% %% The Section headings here are those for %% %% a Research article submitted to a %% %% BMC-Series journal. %% %% %% %% If your article is not of this type, %% %% then refer to the Instructions for %% %% authors on http://www.biomedcentral.com %% %% and change the section headings %% %% accordingly. %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \begin{abstract} % Do not use inserted blank lines (ie \\) until main body of text. \paragraph*{Background:} Illumina Sequencing data can provide high coverage of a genome by relatively short (\SI{100}{bp} to \SI{150}{bp}) reads at a low cost. The base error rates in the reads vary greatly along the read sequence. Low quality bases can be trimmed off or error-corrected. Trimming, especially based on the quality scores, can eliminate large amounts of useful sequence in the reads. Error correction is an alternative to trimming that takes advantage of the high coverage of the genome to make the high confidence base corrections in the reads. Error correction allows for more effective use of the sequencing data thus reducing the coverage depth requirements in sequencing projects and increasing the quality of the resulting assemblies. The vast majority of errors in Illumina data are substitutions, where a base call is incorrect, and \quorum focuses on this type of error. The software is available under the GPL open source license at \url{ftp://ftp.genome.umd.edu/pub/quorum}. \paragraph*{Results:} We propose software, called \quorum, for error correcting substitution error in Illumina reads. It provides accurate correction and is suitable for large data sets ($48$ billion bases corrected per hours on $48$ threads). \paragraph*{Conclusions:} For each test of the three genomes, either Quake or \quorum performed best (see Table~\ref{table:left-introduced}). Generally, Quake leaves fewer errors at a cost of discarding more sequence. \quorum outputs more reads that align perfectly to the finished sequence (see Table~\ref{table:perfect-reads}). \end{abstract} \ifthenelse{\boolean{publ}}{\begin{multicols}{2}}{} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %% The Main Body begins here %% %% %% %% The Section headings here are those for %% %% a Research article submitted to a %% %% BMC-Series journal. %% %% %% %% If your article is not of this type, %% %% then refer to the instructions for %% %% authors on: %% %% http://www.biomedcentral.com/info/authors%% %% and change the section headings %% %% accordingly. %% %% %% %% See the Results and Discussion section %% %% for details on how to create sub-sections%% %% %% %% use \cite{...} to cite references %% %% \cite{koon} and %% %% \cite{oreg,khar,zvai,xjon,schn,pond} %% %% \nocite{smith,marg,hunn,advi,koha,mouse}%% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %%%%%%%%%%%%%%%% %% Background %% %% \section*{Background} While second generation sequencing technologies have progressed tremendously and offer ever longer reads with low overall sequencing error rate, correcting errors in reads remains an important pre-processing step in \emph{de novo} genome assembly. In general, error correcting the reads leads to assemblies with longer contiguous sequences and fewer misassemblies~\cite{Salzberg2011}. For Illumina sequencing, the base quality degrades toward the 3' ends of the reads, therefore one can trim the reads either by a fixed amount or based on the quality values reported by the sequencing machine. Although these simple trimming schemes will reduce the number of erroneous bases, it still leaves many errors in the reads and needlessly discards a lot of valid sequence. Aggressive trimming results in fragmented assemblies. On the other hand, trimming can be an integral part of error correction. The distribution of sequencing errors on the reads is complex and for some percentage of the reads, the sequence beyond a certain point contains too many errors to be corrected or, even worse, does not correspond to any sequence in the original genome. It is important to trim those reads to avoid misassemblies~\cite{Salzberg2011}. %% I still think a paragraph explaining why error correction is even %% possible is necessary. % Genomes are sequenced at some depth. % Meaning that every part of the genome should be present in more than one sequencing read. % As sequencing machines make a mistake reading a base, this error can be detected by comparing the read to others covering the same region of the genome. % Put another way, erroneous base should follow a different probability distribution than correct bases. There is a number of published error correctors that use different techniques to detect and correct these erroneous bases~\cite{Yang2012}. Coral~\cite{salmela2011correcting} and Echo~\cite{Kao2011} use multiple alignment of the reads. Then, a statistical model of sequencing is used to correct misaligned bases. HiTec~\cite{Ilie2011b} uses a suffix array to find and correct potentially erroneous bases. Quake~\cite{Kelley:2010fk} uses the distribution of $k$-mers, or the $k$-spectrum, to detect $k$-mers containing erroneous bases. The first three error correctors only attempt to make base substitutions, while the last one, Quake, will also trim reads. % We propose a new error correction procedure and software package, named \quorum (Quality Optimized Reads from the University of Maryland), that provides accurate trimming and error correction. \quorum (Quality Optimized Reads from the University of Maryland) uses both the $k$-spectrum and the quality scores reported by the sequencing machine. In addition, \quorum is flexible: it can correct reads of varying length and reads containing ambiguous base calls (Ns). % TODOcheck number below It is also fast (1 billion $\SI{100}{bases}$ long reads in a day) and can tackle the large data sets produced by today's high throughput sequencing machine. QuorUM only corrects substitution errors, not insertions and deletions. It is well suited for correcting reads sequenced using Illumina technology~\cite{Bentley2008}, where the substitutions errors are the most common. We evaluate the error correction and trimming skill of QuorUM and compare it to other published error correctors (HiTec, Echo, Coral and Quake), on three genomes that have Illumina reads and have genome assemblies of finished quality. We compare the error correctors by aligning the original reads and the error corrected reads to the finished sequence and measure the improvements. % First, we report the number of substitution errors left after error correction and the number of new errors introduced (i.e.\@ false positive rate) (Table~\ref{table:left-introduced}). % This measures how well the software corrects individual substitution errors. % % % Second, we measure the number of chimeric reads before and after error correction (Table~\ref{table:chimeric}). % % Def chimeric has been added. Is this OK? % A read is called chimeric if it does not match the finished genome in one piece but the read can be split into two parts that match the genome in two widely separated places. % This measures the likelihood of the software to over correct by gluing sequences that do not belong together. % % % Third, we report the amount of sequence which is error free reads (i.e.\@ reads which aligns perfectly to the finished sequence) (Table~\ref{table:perfect-reads}). % These reads are easy for assemblers to use, and this is a measure of how well the correction and trimming work. % % % Fourth, we report the contig sizes of ``idealized contigs'' created by aligning error corrected reads to the finished sequence (Table~\ref{table:icontigs}). % This procedure, similar to a guided assembly, provides some estimate of the maximum contig size achievable through assembly, without the bias of using a particular assembler. % Finally, we will report the time and memory consumption to carry out the correction. % We use the evaluation toolkit of~\cite{Yang2012} with some modifications (see~\ref{sec:Methods}). %%%%%%%%%%%%%%%%%%%%%%%%%%%% %% Results and Discussion %% %% \section*{Results and Discussion} We evaluated the error correction software by error correcting the reads of three organisms, two bacterial genomes and a mammalian genome, for which a finished sequence is available: \species{Rhodobacter sphareoides} (rhodobacter)~\cite{Mackenzie2001}, \species{Mus musculus} (mouse)~\cite{Waterston2002} and \species{Staphylococcus aureus} (staphylococcus). These genomes present different type of challenges for error correction. The \species{Rhodobacter sphaeroides} bacteria genome (\SI{4.6}{Mb} long) has a high GC content and is consequently difficult to sequence using Illumina technology. The mouse genome, being a mammalian genome, is larger and more complex. For the sake of simplicity, we only use chromosome 16 of the mouse genome which has \SI{98}{Mb} in finished sequence. We were able to successfully run all five error correctors on the bacterial data sets. Echo and HiTEC failed on the larger mouse data. In addition, we implemented two simple programs that only trim the input reads. trim20B trims $20$ bases off the 3' end of the reads, while trimQual5 trims the 3' end of a read at a base where the quality goes below or equal to $5$ and subsequently never goes above $5$. When applicable, we also compare the results to doing no correction at all, mentioned in the result tables as the ``none'' corrector. A corrector can foul some of the reported metrics by very aggressively trimming the reads. At the extreme, a corrector can trim every read to one base and, as a result, obtain only perfect reads. More realistically, there is a trade-off between trimming off the hard to correct regions of the reads and attempting to correct these regions; a trade-off between the amount of sequence in the corrected reads and the quality of the sequence. *As seen in Table~\ref{table:perfect-reads} and~\ref{table:left-introduced}, \quorum achieves a balance between aggressive trimming and accurate correction. Table~\ref{table:perfect-reads} reports the number of reads and the total sequence in perfect corrected reads; i.e.\@ corrected reads which have a full length error free alignment with the finished sequence. \quorum consistently produces the largest number of perfect reads and the largest amount of sequence in perfect reads. Although \quorum trims and discards some reads (see Table~\ref{table:left-introduced}), the amount of perfect sequence is larger than that produced by the correctors that do not trim or discard any reads, such as Echo, HiTEC and Coral. Moreover, \quorum trims less aggressively than Quake while still producing a higher percentage of perfect reads. We call a read \emph{chimeric} when it merges together sequences from two or more distant regions of the genome. Such reads typically cannot be corrected, they have to be trimmed or discarded. The Illumina technology generates few chimeric reads (usually less than $1\%$ of all the reads). When doing very aggressive error correction, one runs the risk of creating new chimeric reads; i.e.\@ sequence from a distant, possibly repeated, region of the genome is used to rewrite significant portion of a read. Table~\ref{table:chimeric} shows that Quake and \quorum decrease significantly the number of chimeric reads. HiTEC actually increases the number of chimeric reads while Echo and Coral make only small decreases in chimeric reads. For Table~\ref{table:left-introduced}, we record the sequencing errors in the reads by comparing the sequence of a reads to its best alignment against the finished sequence. After error correction, we record which errors where corrected or not. Although in practice error correction and trimming are done concurrently, Table~\ref{table:left-introduced} shows the results as if these two operations are done one after the other. The second column shows the proportion of errors that are within the trim region and the third column shows proportion of these errors which are not corrected. The fourth column shows the proportion of errors which are introduced by the correction routine (the False Positive rate). The last column is the proportion of the errors left after trimming and correction over the total number of errors. Quake leaves the fewest errors in the reads ($C_5$) but at the expense of very aggressive trimming (over $40\%$ of the reads on the bacterial genomes, see $C_1$). \quorum discards a lot less sequence ($C_1$) while output reads with few errors ($C_5$). Coral, Echo and HiTEC do not trim and are not very aggressive in the correction ($C_3$), hence the corrected reads still contain many errors. %%%%%%%%%%%%%%%%%%%%%% \section*{Conclusions} Our goal in creating an error corrector is to aid in assembly of whole genome shotgun reads. The results we produce are aimed at a partial evaluation of that goal. Coral, Echo and HiTEC correct errors without trimming the reads, but some reads have so many errors at the 3' end that the reads cannot be corrected effectively. These three correctors leave more errors than either Quake or \quorum (see column $C_5$ of Table~\ref{table:left-introduced}). If an assembly project generates sufficiently deep coverage (e.g.\@ \cov{100}), then Quake's tendency to discard sequence (up to $42\%$ in our study) may not be a handicap. Whether Quake or \quorum assists an assembly program to produce a better assembly may depend upon the particular assembly program, the depth of coverage and the idiosyncrasies of the genome being assembled. %%%%%%%%%%%%%%%%%% \section*{Methods} \label{sec:Methods} \subsection*{Correcting bases} \label{sec:meth-error-correction} % \quorum error corrects reads by replacing low quality $k$-mers in the input reads with high quality $k$-mers. % The quality of a $k$-mer is based first on the quality values reported by the sequencing machine of the bases in the mer and second by its number of occurrences in the reads. % \quorum uses the Jellyfish~\cite{Marcais2011} software to count the number of occurrences of the $k$-mers in the input reads. % First it counts the occurrences of all $k$-mers and second it counts the occurrences $k$-mers in which all bases have a quality value greater than a threshold (by default $5$ above the minimum quality). We call the latter $k$-mers ``high quality''. % Then, every read is examined in turn. % \quorum searches for an \emph{anchor} $k$-mer: a $k$-mer whose number of occurrences is higher than a threshold $a$ ($a = 3$ by default). % Starting from this anchor, \quorum will look at every base, extending toward the 5' and 3' ends, and decide to make a correction based on the $k$-mer ending at that base. % Let $m = xb$ bet the $k$-mer, where $|m| = k$, $x$ is a prefix with $|x| = k - 1$, and $b$ is the base under consideration. % If $m$ has a number of occurrences greater than $a$, then no correction is made. % Otherwise, the 3 possible alternatives $b'$ are considered. % \quorum considers in priority the $k$-mers $m' = xb'$ in the high-quality set. % Only if all $m'$ have count 0 in the high-quality set is the set containing all $k$-mers considered. % \quorum substitutes base $b$ by $b'$ if only one of the alternative has a occurrence count at least 3 times that of $m$. % Moreover, \quorum checks that this substitution is not a dead-end. % I.e.\@ that at least one the of four extensions of $m'$ is present in the input reads, where the extensions of $m'$ are the four possible $k$-suffixes of $m'b''$ and $b''$ is a base. % {\bf Correcting a base in a read.} We designed QuorUM algorithm to produce error corrected reads that are most useful for de novo assembly and mapping. We based our algorithm on the following observations. First, the base quality is the best at the 5' end, and it degrades towards the 3' end of the reads. Second, the read coverage is not uniform, there are biases, for example due to CG content of the sequencing fragments and other reasons. Therefore the low $k$-mer counts are not always indicative of errors in those $k$-mers. We classify $k$-mers in the reads based on their max-min quality as follows. For any $k$-mer $m$, i.e. a given string of $k$ bases, an instance of $m$ (call it $m_i$) is the occurrence of the sequence of $m$ in a read, associated with $k$ quality scores. The max-min quality of $m$ is the maximum over all instances $m_i$ of $m$ of the minimum of the quality scores of $m_i$. If the max-min quality is above a certain threshold $q$, we call the $k$-mer reliable. In other words, a $k$-mer is reliable if there exists at least one instance of $m$ where all bases have a quality score of at least $q$. \quorum error corrects reads by replacing low quality $k$-mers in the input reads with high quality $k$-mers. It uses Jellyfish~\cite{Marcais2011} to create a database of the reliable $k$-mers and all $k$-mers. \quorum first look for an \emph{anchor}: a group of reliable $k$-mers with counts above a threshold close to the 5' end of the reads. The size of the group and the count threshold ($a$) are parameters to \quorum. Starting from this anchor, \quorum will look at every base, extending in turn toward the 5' and 3' ends. Here we consider extension toward the 3' end and leave the reverse to the reader. As \quorum shifts the $k$-mer toward the 3' end one base at a time, it and decides whether to make a correction based on the $k$-mer ending at that base. Let $m = xb$ be the anchor $k$-mer, where the length $|m| = k$, and $x$ is a prefix with length $|x| = k - 1$, and $b$ is the base under consideration. If $m$ has a number of occurrences greater than $a$ in the entire database, then no correction is made; otherwise, the 3 possible alternative bases $b'$ are considered. \quorum determines if any of the three $k$-mers $m' = xb'$ are in the high-quality set. Only if all three $m'$ have count 0 in the high-quality set is the set containing all $k$-mers considered. \quorum substitutes base $b'$ for $b$ if only one of the alternative $xb'$ considered has an occurrence count at least 3 times that of $m$. Moreover, \quorum checks that this substitution is not a dead-end; i.e.\@ at least one the of four extensions of $m'$ is present in the input reads, where the extensions of $m'$ are the four possible $k$-suffixes of $m'b''$ and $b''$ is a base. If there were two base errors in a row, \quorum would be very unlikely to make a change. \subsection*{Trimming} \label{sec:meth-trimming} The maximum number of corrections made in a window of length $10$ is by default capped at $3$. \quorum will trim the read at the beginning of the window if the number of errors is higher. % These options were not used in the work on this paper. Yes or No??? % The first option was not used. The second one was the Rhodobacter data. In addition, \quorum has two extra optional procedure for trimming reads. It takes as input a set of contaminant $k$-mers and it will trim a read wherever it contains such a contaminant mer. Also, in high or low GC genome, the Illumina sequencers tend to erroneously generate long homo-polymer run toward the 3' end of the reads. \quorum can optionally detect and trim off these homo-polymer. \subsection*{Evaluation} The reads for \species{S. aureus} have accessions SRR022868. The finished sequence is version USA300\_TCH1516. The genome is $\SI{2.9}{Mb}$ in length. There are $5\,176\,416$ reads of length $\SI{101}{bases}$, for a coverage of $\cov{180}$. The reads for \species{R. sphaeroides} have accessions SRR081522. The finished sequence is version 2.4.1. The genome is $\SI{4.6}{Mb}$ in length. There are reads of length $\SI{101}{bases}$, for a coverage of $\cov{43}$. The reads for the \species{M. musculus} have accessions SRR067634, SRR067650, SRR067648, SRR067622, SRR067649, SRR067641, SRR067670, SRR067636, SRR067612, SRR067616, SRR067615, SRR067623, SRR067605, SRR067646, SRR067633, SRR067620, SRR067606, SRR067611, SRR067625, SRR067601, SRR067624, SRR067645, SRR067635, SRR067653, SRR067607, SRR067669, SRR067603, SRR067660, SRR067619, SRR067658, SRR067604, SRR067631, SRR067639, SRR067657, SRR067610, SRR067654, SRR067644, SRR067618, SRR067652, SRR067663, SRR067823, SRR067839, SRR067846, SRR067858, and SRR067830. The finished sequence is UCSC's mm10 build. For this evaluation, we use only chromosome 16, $\SI{98.2}{Mb}$ in length. We aligned all the reads to all the chromosomes with the bowtie2 aligner and selected any read pair that has an alignment to chromosome 16 consistent with the library length within $5$ standard deviations. We instructed bowtie2 to consider up to $5$ seeds (switch {\tt -R 5}) and to report the best out of $6$ alignments (switch {\tt -M 5}). Also, we consider partial alignments (switch {\tt --local}). %% 1Somewhat inaccurate. The error correctors will attempt to error %% correct the reads with no alignment. They are just not used in the %% ratios of the first table. % The purpose of the study is to see what fraction of the errors are eliminated. % That requires us to match the original reads against the finished sequence for each of the three genomes in order to determine how many errors the original reads have. % Some reads have enough errors that the aligner could not match them against the finished sequence. % These reads were eliminated from the study and all results ignore the deleted reads. % In particular, the fractions of reads eliminated before the study began were $8.9\%$ for \species{R. sphaeroides}, $15.6\%$ for \species{S.aureus} and $2.5\%$ for \species{M. musculus}. %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% \section*{Authors contributions} G.M. provided the implementation of Quorum and performed the evaluation. A.Z. provided code improvements. All the authors contributed to the development of the algorithm, writing of the manuscript and approved it for publication. %%%%%%%%%%%%%%%%%%%%%%%%%%% \section*{Acknowledgements} \ifthenelse{\boolean{publ}}{\small}{ } The authors were supported by grant ... %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% The Bibliography %% %% %% %% Bmc_article.bst will be used to %% %% create a .BBL file for submission, which includes %% %% XML structured for BMC. %% %% %% %% %% %% Note that the displayed Bibliography will not %% %% necessarily be rendered by Latex exactly as specified %% %% in the online Instructions for Authors. %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% { \ifthenelse{\boolean{publ}}{\footnotesize}{\small} \bibliographystyle{bmc_article} % Style BST file \bibliography{bmc_article} } % Bibliography file (usually '*.bib' ) %%%%%%%%%%% \ifthenelse{\boolean{publ}}{\end{multicols}}{} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %% Figures %% %% %% %% NB: this is for captions and %% %% Titles. All graphics must be %% %% submitted separately and NOT %% %% included in the Tex document %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% Do not use \listoffigures as most will included as separate files % \section*{Figures} % \subsection*{Figure 1 - Sample figure title} % A short description of the figure content % should go here. % \subsection*{Figure 2 - Sample figure title} % Figure legend text. %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %% Tables %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% % \newrobustcmd{\bnum}[1]{\bfseries #1} %% Use of \listoftables is discouraged. %% \newcounter{tablecounter} \newcommand{\tabledesc}[1]{% \refstepcounter{tablecounter}% \subsection*{Table \thetablecounter\ - #1}% } %% Winner number in a table \newcommand{\winner}[1]{\bfseries #1} \newcommand{\tn}[1]{S[detect-weight,table-format=#1]} \section*{Tables} \robustify\bfseries \tabledesc{Perfect output reads and bases as percent of input.} \label{table:perfect-reads} A perfect read is a read (possibly trimmed) that aligns with no error on its full length to the finish sequence. This table reports in the ``Reads'' column the number of perfect error-corrected reads as a proportion of the number of original reads (with an alignment to the finished sequence). The ``Sequence'' column displays the number of bases in perfect error-corrected reads as a proportion of the number of bases in original reads (with an alignment to the finished sequence). These ratios ignore the original reads which do not align at all. Because in the input data, all the reads have the same length ($\approx \SI{100}{bases}$), the two columns are equal for the correctors that do not trim the reads. \bigskip \begin{tabular}{@{}lS[detect-weight,table-format=2.1]S[detect-weight,table-format=2.1]S[detect-weight,table-format=2.1]S[detect-weight,table-format=2.1]S[detect-weight,table-format=2.1]S[detect-weight,table-format=2.1]@{}} \toprule Corrector & \multicolumn{2}{c}{Rhodobacter} & \multicolumn{2}{c}{Staphylococcus} &\multicolumn{2}{c}{Mouse} \\ \cmidrule(rl){2-3} \cmidrule(rl){4-5} \cmidrule(l){6-7} {} & {Reads (\%)} & {Sequence (\%)} & {Reads (\%)} & {Sequence (\%)} & {Reads (\%)} & {Sequence (\%)} \\ \midrule none & 20.9 & 20.9 & 33.1 & 33.1 & 48.3 & 48.3 \\ trim20B & 44.4 & 35.6 & 46.3 & 37.2 & 79.4 & 63.6 \\ trimQual5 & 76.2 & 51.2 & 35.3 & 35.1 & 78.0 & 71.9 \\ coral & 58.2 & 58.2 & 73.5 & 73.5 & 80.9 & 80.9 \\ echo & 56.3 & 56.3 & 65.1 & 65.1 & & \\ hitec & 60.8 & 60.8 & 77.9 & \winner{77.9} & & \\ % quakedk & 61.9 & 48.5 & & & & \\ quake & 80.5 & 58.9 & 68.2 & 57.6 & 88.7 & 81.3 \\ \quorum & \winner{90.2} & \winner{68.2} & \winner{84.8} & 69.8 & \winner{90.9} & \winner{86.9} \\ \bottomrule \end{tabular} % % \tabledesc{Chimeric reads} \label{table:chimeric} % Jim: We have to make sure that our definitions agree with what I put in the main text. Two distinct pieces allows one to be extremely small and it does not say that the whole read is the union of the two pieces. A chimeric read is defined here as a read that does not align in one piece while it has two disjoint subsequences that align to far apart regions of the finished sequence. The table shows the number of chimeric reads after error correction. ``None'' denote the number without any error correction. \bigskip \begin{tabular}{@{}lS[detect-weight,table-format=4]S[detect-weight,table-format=4]S[detect-weight,table-format=6]@{}} \toprule {Corrector} & {Rhodobacter} & {Staphylococcus} & {Mouse} \\ \midrule none & 2086 & 733 & 296772 \\ trim20B & 1655 & 597 & 250382 \\ trimQual5 & 649 & 720 & 148439 \\ coral & 2047 & 1024 & 225052 \\ echo & 1809 & 704 & \\ hitec & 6375 & 1200 & \\ quake & 61 & 651 & \winner{63079} \\ quorum & \winner{46} & \winner{35} & 93158 \\ \bottomrule \end{tabular} % % \tabledesc{Errors in output including introduced errors} \label{table:left-introduced} The ``Bases trimmed'' is the percentage of bases in trimmed reads compared with bases in the original reads. All the bases in a discarded read count as bases trimmed off. The ``Errors not trimmed from reads'' is the percentage of errors in the trimmed reads compared with the errors in the original reads. The ``errors left in trimmed reads'' is the percentage of errors in the corrected reads compared with the errors in the trimmed reads. The ``Errors introduced'' is the number of errors introduced divided by the number of errors in the original reads. These are counted in the previous column ``errors left in trimmed reads''. Finally, the ``Errors in corrected trimmed reads'' is the percentage of errors in corrected reads compared with the errors in the original reads. If $C_i$ is the value in the $i$-th column, then following holds: $C_2 \cdot C_3 = C_5$. For a corrector that does not trim, then $C_1 = 0.0$ (no bases trim) and $C_2 = 100$ (all the original errors are left because of the absence of trimming). A pure trimmer has $C_3 = 100$ (no correction made) and $C_4 = 0$ (no error introduced). \bigskip \begin{tabular}{@{}lS[detect-weight,table-format=2.1]S[detect-weight,table-format=3.1]S[detect-weight,table-format=2.2]S[detect-weight,table-format=2.1]S[detect-weight,table-format=2.1]@{}} \toprule & 1 & 2 & 3 & 4 & 5 \\ \cmidrule{2-6} {} & {\% bases} & {\% errors not} & {\% of errors left} & {\% errors} & {\% errors in corrected} \\ Corrector & {trimmed} & {trimmed from reads} & {in trimmed reads} & {introduced} & {trimmed reads} \\ \midrule {} & \multicolumn{5}{c}{Rhodobacter} \\ \cmidrule{2-6} trim20B & 19.8 & 43.9 & 100 & 0.00 & 43.9 \\ trimQual5 & 36.0 & 11.2 & 100 & 0.00 & 11.2 \\ coral & 0.00 & 100 & 77.7 & 0.766 & 77.7 \\ echo & 0.00 & 100 & 65.1 & 2.11 & 65.1 \\ hitec & 0.00 & 100 & 61.1 & 10.4 & 61.1 \\ % quakedk & 30.6 & 81.5 & 98.2 & 0.365 & 80.1 \\ quake & 40.6 & \winner{2.06} & 16.6 & \winner{0.0473} & 0.342 \\ quorum & 31.2 & 14.7 & \winner{2.13} & 0.0669 & \winner{0.314} \\ \cmidrule{2-6} {} & \multicolumn{5}{c}{Staphylococcus} \\ \cmidrule{2-6} trim20B & 19.8 & 53.8 & 100 & 0.00 & 53.8 \\ trimQual5 & 1.30 & 91.7 & 100 & 0.00 & 91.7 \\ coral & 0.00 & 100 & 52.8 & 1.08 & 52.8 \\ echo & 0.00 & 100 & 38.6 & 0.628 & 38.6 \\ hitec & 0.00 & 100 & 21.3 & 1.57 & 21.3 \\ quake & 42.0 & \winner{13 .7} & 4.98 & 0.115 & 0.682 \\ quorum & 29.8 & 42.1 & \winner{1.14} & \winner{0.0882} & \winner{0.478} \\ \cmidrule{2-6} {} & \multicolumn{5}{c}{Mouse} \\ \cmidrule{2-6} trim20B & 19.8 & 29.0 & 100 & 0.00 & 29.0 \\ trimQual5 & 10.5 & 28.0 & 100 & 0.00 & 28.0 \\ coral & 0.00 & 100 & 69.0 & 12.5 & 69.0 \\ quake & 14.2 & \winner{10.4} & 71.5 & \winner{.494} & \winner{7.40} \\ quorum & 6.75 & 29.4 & \winner{34.7} & .786 & 10.2 \\ \bottomrule \end{tabular} % % % % %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% %% %% %% Additional Files %% %% %% %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% % \section*{Additional Files} % \subsection*{Additional file 1 --- Sample additional file title} % Additional file descriptions text (including details of how to % view the file, if it is in a non-standard format or the file extension). 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endstream endobj 83 0 obj 282231 endobj 84 0 obj << /Type /XObject /Subtype /Image /Width 2480 /Height 3508 /ColorSpace /DeviceGray /BitsPerComponent 8 /Length 8478 /Filter /FlateDecode >> stream xÚìÁ€ÿ«ë €Ùƒ 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(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢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(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢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(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢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(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢Š(¢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