biovizBase/DESCRIPTION0000644000175200017520000000422714136065665015420 0ustar00biocbuildbiocbuildPackage: biovizBase Version: 1.42.0 Title: Basic graphic utilities for visualization of genomic data. Description: The biovizBase package is designed to provide a set of utilities, color schemes and conventions for genomic data. It serves as the base for various high-level packages for biological data visualization. This saves development effort and encourages consistency. Authors@R: c(person("Tengfei", "Yin", role=c("aut"), email="yintengfei@gmail.com"), person("Michael", "Lawrence", role=c("aut", "ths", "cre"), email="michafla@gene.com"), person("Dianne", "Cook", role=c("aut", "ths")), person("Johannes", "Rainer", role="ctb")) Depends: R (>= 3.5.0), methods Imports: grDevices, stats, scales, Hmisc, RColorBrewer, dichromat, BiocGenerics, S4Vectors (>= 0.23.19), IRanges (>= 1.99.28), GenomeInfoDb (>= 1.5.14), GenomicRanges (>= 1.23.21), SummarizedExperiment, Biostrings (>= 2.33.11), Rsamtools (>= 1.17.28), GenomicAlignments (>= 1.1.16), GenomicFeatures (>= 1.21.19), AnnotationDbi, VariantAnnotation (>= 1.11.4), ensembldb (>= 1.99.13), AnnotationFilter (>= 0.99.8), rlang Suggests: BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, BSgenome, rtracklayer, EnsDb.Hsapiens.v75, RUnit License: Artistic-2.0 LazyLoad: Yes LazyData: Yes Collate: utils.R color.R AllGenerics.R crunch-method.R mold-method.R addStepping-method.R getFragLength-method.R shrinkageFun-method.R maxGap-method.R spliceSummary-method.R ideogram.R pileup.R coverage.R labs.R original.R transform.R facets-method.R aes.R scale.R zzz.R biovizBase-package.R biocViews: Infrastructure, Visualization, Preprocessing git_url: https://git.bioconductor.org/packages/biovizBase git_branch: RELEASE_3_14 git_last_commit: f1627b2 git_last_commit_date: 2021-10-26 Date/Publication: 2021-10-26 NeedsCompilation: yes Packaged: 2021-10-26 20:57:25 UTC; biocbuild Author: Tengfei Yin [aut], Michael Lawrence [aut, ths, cre], Dianne Cook [aut, ths], Johannes Rainer [ctb] Maintainer: Michael Lawrence biovizBase/NAMESPACE0000644000175200017520000000713314136047676015132 0ustar00biocbuildbiocbuilduseDynLib(biovizBase, .registration=TRUE) ## ====================================================================== ## Import ## ====================================================================== import(methods) import(BiocGenerics) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### base packages ### importFrom(grDevices, colorRampPalette) importFrom(graphics, par, plot, rect, text) importFrom(stats, approx, as.formula, asOneSidedFormula, setNames) importFrom(utils, menu) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Non-bioconductor packages ### importFrom(RColorBrewer, brewer.pal) importFrom(scales, dichromat_pal, dscale, expand_range, rescale) importFrom(Hmisc, bezier) importFrom(dichromat, colorschemes) importFrom(rlang, quo_text) ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Bioconductor packages ### import(S4Vectors) import(IRanges) import(GenomeInfoDb) import(GenomicRanges) import(SummarizedExperiment) ## Biostrings importFrom(Biostrings, AA_ALPHABET, DNA_ALPHABET, RNA_ALPHABET, IUPAC_CODE_MAP, AMINO_ACID_CODE) importMethodsFrom(Biostrings, getSeq, letterFrequency, letterFrequencyInSlidingView) ## Rsamtools importClassesFrom(Rsamtools, BamFile) importFrom(Rsamtools, index, scanBamFlag, PileupFiles, ApplyPileupsParam) importMethodsFrom(Rsamtools, ScanBamParam, applyPileups, scanBam) ## GenomicAlignments importFrom(GenomicAlignments, cigar, readGAlignments) importClassesFrom(GenomicAlignments, GAlignments) ## GenomicFeatures importClassesFrom(GenomicFeatures, TxDb) importMethodsFrom(GenomicFeatures, transcripts, cdsBy, cdsByOverlaps, exonsBy, exonsByOverlaps, isActiveSeq, "isActiveSeq<-", transcripts, transcriptsByOverlaps) ## AnnotationDbi importFrom(AnnotationDbi, unlist2, select, mappedRkeys, revmap, toTable) ## VariantAnnotation importClassesFrom(VariantAnnotation, VRanges) ## AnnotationFilter importClassesFrom(AnnotationFilter, AnnotationFilter, GRangesFilter, TxIdFilter) importFrom(AnnotationFilter, AnnotationFilter, GRangesFilter, TxIdFilter, AnnotationFilterList, GenenameFilter) ## ensembldb importMethodsFrom(ensembldb, listColumns, exons, transcripts) ## ====================================================================== ## export ## ====================================================================== ## color export(getBioColor, plotColorLegend, genBrewerBlindPalInfo, genDichromatPalInfo, genBlindPalInfo, colorBlindSafePal, blind.pal.info, brewer.pal.blind.info, dichromat.pal.blind.info, estimateCoverage) ## transform export(transformToCircle, transformToRectInCircle, transformToBarInCircle, transformToSegInCircle, transformToLinkInCircle, transformDfToGr, transformGRangesForEvenSpace) exportMethods(transformToGenome,transformToDf) ## utils exportMethods(addStepping, shrinkageFun, maxGap, splitByFacets, getGaps, getXScale, getYLab, getXLab, crunch, mold) export(isIdeogram, isSimpleIdeogram, getIdeogram, containLetters, pileupAsGRanges, pileupGRangesAsVariantTable, GCcontent, showColor, isJunctionRead, isMatchedWithModel, flatGrl, getIdeoGR, getScale, getFormalNames, subsetArgsByFormals, parseArgsForAes, parseArgsForNonAes, strip_formula_dots, is_coord_truncate_gaps, is_coord_genome) ## exportPattern("^[^\\.]") biovizBase/NEWS0000644000175200017520000000113614136047676014407 0ustar00biocbuildbiocbuildCHANGES IN VERSION 1.19.1 ------------------------- NEW FEATURES o crunch method supports now EnsDb objects and related filter objects. CHANGES IN VERSION 1.3.8 ------------------------ NEW FEATURES o transform utils o adding label/scale utils Bug fixing o fix warning o fix bugs in circular view CHANGES IN VERSION 1.1.16 ------------------------ NEW FEATURES o addSteping add extra arugments group.selfish to control stepping method o add estimateCoverage method for fast estimate coverage SIGNIFICANT USER-LEVEL CHANGES o addStepings rename to addStepping biovizBase/R/0000755000175200017520000000000014136047676014110 5ustar00biocbuildbiocbuildbiovizBase/R/AllGenerics.R0000644000175200017520000000061114136047676016421 0ustar00biocbuildbiocbuildsetGeneric("addStepping",function(obj,...) standardGeneric("addStepping")) setGeneric("getFragLength", function(obj, ...) standardGeneric("getFragLength")) setGeneric("shrinkageFun", function(obj,...) standardGeneric("shrinkageFun")) setGeneric("maxGap", function(obj, ...) standardGeneric("maxGap")) setGeneric("spliceSummary", function(obj, model, ...) standardGeneric("spliceSummary")) biovizBase/R/addStepping-method.R0000644000175200017520000000240114136047676017750 0ustar00biocbuildbiocbuildsetMethod("addStepping",c("GenomicRanges"),function(obj, group.name, extend.size = 0, fix = "center", group.selfish = TRUE){ if(!missing(group.name)){ if(! (group.name %in% colnames(values(obj)))) stop("group.name must be one of the elementMetadta column") }else{ group.name <- NULL } ## levels only make sense on different seqnames ## so split them first obj.lst <- split(obj,as.character(seqnames(obj))) lv <- endoapply(obj.lst,function(x){ if(!is.null(group.name)){ if(!group.selfish){ x.n <- split(x, values(x)[,group.name]) irs <- unlist(range(ranges(x.n))) irs.new <- resize(irs, fix = fix, width = width(irs) + extend.size) irs.new <- sort(irs.new) .lvs <- disjointBins(irs.new) values(x)$stepping <- .lvs[as.character(values(x)[,group.name])] x }else{ values(x)$stepping <- as.numeric(as.factor(values(x)[,group.name])) x } }else{ irs <- ranges(x) values(x)$stepping <- as.numeric(disjointBins(resize(irs, fix = "center", width = width(irs) + extend.size))) x }}) res <- unlist(lv) res }) biovizBase/R/aes.R0000644000175200017520000000100614136047676015000 0ustar00biocbuildbiocbuildparseArgsForAes <- function(args){ res <- if ("mapping" %in% names(args)) { args[["mapping"]] } else { Find(function(x) { is(x, "uneval") }, args) } if (is.null(res)) res <- structure(list(), class="uneval") idx <- ggplot2_is_calculated_aes(res) res[idx] <- ggplot2_strip_dots(res[idx]) res } parseArgsForNonAes <- function(args){ Filter(function(x) !is(eval(x, parent.frame()), "uneval"), args) } biovizBase/R/biovizBase-package.R0000644000175200017520000000376014136047676017727 0ustar00biocbuildbiocbuild##' biovizBase is a package which provides utilities and color scheme ##' for higher level graphic package which aim to visualize biological ##' data especially genetic data. ##' ##' This package provides default color scheme for nucleotide, strand, ##' amino acid, try to pass colorblind checking as possible as we can. ##' And also provide giemsa stain result color scheme used to show ##' cytoband. This package also provides utilites to manipulate and ##' summarize raw data to get them ready to be visualized. ##' @name biovizBase-package ##' @aliases biovizBase ##' @docType package NULL ##' Gene symbols with position ##' ##' This data set provides genen symbols in human with position ##' and starnd information, stored as GRanges object. ##' @name genesymbol ##' @docType data ##' @usage data(genesymbol) ##' @format GRanges: length of 16914 ##' @keywords datasets ##' @examples ##' data(genesymbol) ##' head(genesymbol) NULL ##' Hg19 ideogram without cytoband information ##' ##' This data set provides hg19 genome information wihout cytoband ##' information. ##' @name hg19Ideogram ##' @docType data ##' @usage data(hg19Ideogram) ##' @format GRanges: length of 24 ##' @keywords datasets ##' @examples ##' data(hg19Ideogram) ##' hg19Ideogram NULL ##' Hg19 ideogram with cytoband information ##' ##' This data set provides hg19 genome information with cytoband ##' information. ##' @name hg19IdeogramCyto ##' @docType data ##' @usage data(hg19IdeogramCyto) ##' @format GRanges: length of 862 ##' @keywords datasets ##' @examples ##' data(hg19IdeogramCyto) ##' hg19IdeogramCyto NULL ##' Subset of RNA editing sites in hg19 ##' ##' This data set provides a subset(500 sites only) of hg19 RNA editing sites, and ##' originally from DARNED \url{http://darned.ucc.ie/} for the hg19 ##' assembly. ##' @name darned_hg19_subset500 ##' @docType data ##' @usage data(darned_hg19_subset500) ##' @format GRanges: length of 500 ##' @keywords datasets ##' @examples ##' data(darned_hg19_subset500) ##' darned_hg19_subset500 NULL biovizBase/R/color.R0000644000175200017520000002270414136047676015356 0ustar00biocbuildbiocbuild.DNABasesNColor <- function(){ c(A = "#ABD9E9", T = "#2C7BB6", G = "#D7191C", C = "#FDAE61", N = "#FFFFBF") } .DNABasesColor <- function(){ c(A = "#ABD9E9", T = "#2C7BB6", G = "#D7191C", C = "#FDAE61") } .DNAAlphabetColor <- function(pal = c("BluetoDarkOrange.18", "DarkRedtoBlue.18")){ pal <- match.arg(pal) cols <- dscale(DNA_ALPHABET, dichromat_pal(pal)) names(cols) <- DNA_ALPHABET cols } .RNABasesNColor <- function(){ c(A = "#ABD9E9", U = "#2C7BB6", G = "#D7191C", C = "#FDAE61", N = "#FFFFBF") } .RNABasesColor <- function(){ c(A = "#ABD9E9", U = "#2C7BB6", G = "#D7191C", C = "#FDAE61") } ## blind.pal.info .RNAAlphabetColor <- function(){ ## pal <- match.arg(pal) ## cols <- dscale(RNA_ALPHABET, dichromat_pal(pal)) N <- length(RNA_ALPHABET) cols <- colorBlindSafePal("Categorical.12")(N, repeatable = TRUE) names(cols) <- RNA_ALPHABET cols } .IUPACCodeMapColor <- function(){ N <- length(IUPAC_CODE_MAP) ## cols <- dscale(IUPAC_CODE_MAP, dichromat_pal(pal)) cols <- colorBlindSafePal("Categorical.12")(N, repeatable = TRUE) names(cols) <- names(IUPAC_CODE_MAP) cols } .strandColor <- function(){ c("+" = "#1B9E77", "-" = "#7570B3", "*" = "#D95F02") } ## preset gpos1:100 and other widely used color .cytobandColor <- function(){ .getCytobandColor(c("gneg", "gvar", "stalk", "acen", paste0("gpos", 1:100))) } ## got these codes and hints from Florian Hahne, from Gviz .getCytobandColor <- function(type){ type <- as.character(type) ocols <- c(gneg = "grey100", gpos100 = "grey0", gvar = "grey100", stalk = "brown3", acen = "brown4") cols <- c(ocols[c("gneg", "stalk", "acen")], gpos=unname(ocols["gpos100"]), gvar=unname(ocols["gpos100"])) gpcols <- unique(grep("gpos", type, value=TRUE)) crmp <- colorRampPalette(c(cols["gneg"], cols["gpos"]))(100) posCols <- setNames(crmp[as.integer(gsub("gpos", "", gpcols))], gpcols) return(c(cols, posCols)) } .AminoAcidCodeColor <- function(){ N <- length(AMINO_ACID_CODE) cols <- colorBlindSafePal("Categorical.12")(N, repeatable = TRUE) names(cols) <- names(AMINO_ACID_CODE) cols } .AAAlphabetColor <- function(){ N <- length(AA_ALPHABET) cols <- colorBlindSafePal("Categorical.12")(N, repeatable = TRUE) names(cols) <- AA_ALPHABET cols } getBioColor <- function(type = c("DNA_BASES_N", "DNA_BASES", "DNA_ALPHABET", "RNA_BASES_N", "RNA_BASES", "RNA_ALPHABET", "IUPAC_CODE_MAP", "AMINO_ACID_CODE", "AA_ALPHABET", "STRAND", "CYTOBAND"), source = c("option", "default")){ type <- match.arg(type) source <- match.arg(source) if(source == "default"){ cols <- switch(type, DNA_BASES_N = .DNABasesNColor(), DNA_BASES = .DNABasesColor(), DNA_ALPHABET = .DNAAlphabetColor(), RNA_BASES_N = .RNABasesNColor(), RNA_BASES = .RNABasesColor(), RNA_ALPHABET = .RNAAlphabetColor(), IUPAC_CODE_MAP = .IUPACCodeMapColor(), AMINO_ACID_CODE = .AminoAcidCodeColor(), AA_ALPHABET = .AAAlphabetColor(), STRAND = .strandColor(), CYTOBAND = .cytobandColor()) } if(source == "option"){ colname <- switch(type, DNA_BASES_N = "DNABasesNColor", DNA_BASES = "DNABasesColor", DNA_ALPHABET = "DNAAlphabetColor", RNA_BASES_N = "RNABasesNColor", RNA_BASES = "RNABasesColor", RNA_ALPHABET = "RNAAlphabetColor", IUPAC_CODE_MAP = "IUPACCodeMapColor", AMINO_ACID_CODE = "AminoAcidCodeColor", AA_ALPHABET = "AAAlphabetColor", STRAND = "strandColor", CYTOBAND = "cytobandColor") cols <- getOption("biovizBase")[[colname]] ## res <- cols[base] } cols } plotColorLegend <- function(colors, labels, title){ if(missing(labels)) labels <- names(colors) n <- length(colors) plot(c(0, 1), c(1, -n), type = "n", xlab="", ylab="", axes = FALSE) if(!missing(title)) text(0.5, 1, title) rect(0.5, -(1:n), 1, -(1:n)+0.5+0.25, col = colors) text(0, -(1:n) + 0.5, labels) } ## this should include as many as I cann colorBlindSafePal <- function(palette){ namelist <- rownames(blind.pal.info) if(missing(palette)){ return(blind.pal.info) } if(is.numeric(palette) && (palette < nrow(blind.pal.info))) name <- rownames(blind.pal.info)[palette] else{ if(is.character(palette) && (palette %in% namelist)) name <- palette else stop("Invalid palette name, please check colorBlindSafePal().") } pkg <- blind.pal.info[name,"pkg"] maxcolors <- as.numeric(blind.pal.info[name,"maxcolors"]) getPalColor <- function(n, pal, pkg){ cols <- switch(pkg, RColorBrewer = { brewer.pal(n, pal) }, dichromat = { colorschemes[[pal]][seq(n)] }) } function(n, repeatable = FALSE){ if (n < 3) { warning("minimal value for n is 3, returning requested palette with 3 different levels\n") cols <- getPalColor(3, name, pkg) } if (n > maxcolors) { if(!repeatable){ warning(paste("n too large, allowed maximum for palette", name, "is", maxcolors, "\nReturning the palette you asked for with that many colors\n")) cols <- getPalColor(maxcolors, name, pkg) }else{ ## repeatable colors rpt <- n %/% maxcolors res <- n %% maxcolors full.cols <- getPalColor(maxcolors, name, pkg) cols <- c(rep(full.cols, rpt), full.cols[-maxcolors][1:res]) } }else{ cols <- getPalColor(n, name, pkg) } cols } } genBrewerBlindPalInfo <- function(){ res <- RColorBrewer::brewer.pal.info idx.seq <- which(rownames(res) %in% c("Blues","BuPu","GnBu","Greens", "Greys","Oranges","OrRd","PuBu","PuBuGn", "PuRd","Purples","Reds","YlGn","YlGnBu", "YlOrBr","YlOrRd")) idx.div <- which(rownames(res) %in% c("PiYG","PRGn","PuOr","RdBu","RdYlBu")) idx.qual <- which(rownames(res) %in% c("Dark2","Paired","Set2")) res <- res[c(idx.seq, idx.div, idx.qual),] res[rownames(res) %in% c("Dark2", "Set2"), 1] <- 3 res[rownames(res) %in% c("Paired"), 1] <- 4 res[, c("maxcolors", "category"), drop=FALSE] } ## return current pallete which is color-blind safe, if missing n, ## return list of supported pal, if not, use index to return a set ## color. should have qual/div/seq .colorschemes.num <-function(){ lst <- gregexpr("[0-9]",names(colorschemes)) unlist(lapply(1:length(lst), function(i){ pos <- lst[[i]] if(length(pos) == 1) pos <- c(pos, pos) as.numeric(substr(names(colorschemes)[i], pos[1], pos[2])) }))} ## make a similar color pal.info like brewer.pal.info genDichromatPalInfo <- function(){ dichromat.pal.info <- data.frame(maxcolors = .colorschemes.num(), category = "div", stringsAsFactors = FALSE) rownames(dichromat.pal.info) <- names(colorschemes) idx.seq <- rownames(dichromat.pal.info) %in% c("LightBluetoDarkBlue.10", "LightBluetoDarkBlue.7", "SteppedSequential.5") idx.qual <- rownames(dichromat.pal.info) %in% "Categorical.12" dichromat.pal.info[idx.seq, 2] <- "seq" dichromat.pal.info[idx.qual, 2] <- "qual" dichromat.pal.info <- dichromat.pal.info[order(dichromat.pal.info[,2]),] dichromat.pal.info } genBlindPalInfo <- function(){ blind.pal.info <- rbind(brewer.pal.blind.info, dichromat.pal.blind.info) id <- seq(nrow(blind.pal.info)) pkg <- c(rep("RColorBrewer", nrow(brewer.pal.blind.info)), rep("dichromat", nrow(dichromat.pal.blind.info))) blind.pal.info$pkg <- pkg idx <- order(blind.pal.info$category, blind.pal.info$maxcolors) blind.pal.info <- blind.pal.info[idx,] blind.pal.info$pal.id <- id blind.pal.info } brewer.pal.blind.info <- genBrewerBlindPalInfo() dichromat.pal.blind.info <- genDichromatPalInfo() blind.pal.info <- genBlindPalInfo() ## show color show_col2 <- function(colours) { n <- length(colours) ncol <- ceiling(sqrt(n)) nrow <- ceiling(n / ncol) colors <- c(colours, rep(NA, nrow * ncol - length(colours))) colors <- matrix(colors, ncol = ncol, byrow = TRUE) colours <- c(colours, rep(NA, nrow * ncol - length(colours))) nms <- matrix(names(colours), ncol = ncol, byrow = TRUE) old <- par(pty = "s", mar = c(0, 0, 0, 0)) on.exit(par(old)) size <- max(dim(colors)) plot(c(0, size), c(0, -size), type = "n", xlab="", ylab="", axes = FALSE) rect(col(colors) - 1, -row(colors) + 1, col(colors), -row(colors), col = colors) text(col(colors) - 0.5, -row(colors) + 0.5, nms) } showColor <- function(colors, label = c("color", "name")){ label <- match.arg(label) colfun <- switch(label, color = scales::show_col, name = show_col2) colfun(colors) } biovizBase/R/coverage.R0000644000175200017520000000504014136047676016025 0ustar00biocbuildbiocbuild### ========================================================================= ### Coverage utilities ### ------------------------------------------------------------------------- ### - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ### Estimation of coverage ### setGeneric("estimateCoverage", function(x, ...) standardGeneric("estimateCoverage")) setMethod("estimateCoverage", "BamFile", function(x, maxBinSize = 2^14) { ## bai_path <- paste(index(x), ".bai", sep = "") bai_path <- index(x) bai <- file(bai_path, "rb") on.exit(close(bai)) bytes <- readBin(bai, "raw", n = file.info(bai_path)[,"size"]) bam_si <- seqinfo(x) bin_offsets <- .Call(scan_bam_bin_offsets, bytes) names(bin_offsets) <- seqlevels(bam_si) ## CONSTANTS UBSIZE <- 2^16 # hopefully is not going to change CBSIZE <- 19100 # determined empirically BINSIZES <- 2 ^ seq(29, 14, -3) TOTALSIZE <- 2 ^ 29 NBIN <- sum(TOTALSIZE / BINSIZES) METABIN <- NBIN + 1 makeBinRanges <- function() { unlist(List(lapply(BINSIZES[BINSIZES <= maxBinSize], function(x) { chunks <- breakInChunks(TOTALSIZE, chunksize=x) IRanges(start(chunks), end(chunks)) }))) } bin_ranges <- makeBinRanges() bin_offsets <- lapply(bin_offsets, function(x) { x[,x[1,] != METABIN] # drop the samtools metadata bin }) off_scores <- lapply(seqlevels(bam_si), function(sn) { off <- t(bin_offsets[[sn]]) colnames(off) <- c("bin", "start.coffset", "end.coffset", "start.uoffset", "end.uoffset") coffdiff <- off[,"end.coffset"] - off[,"start.coffset"] off_diff <- ifelse(coffdiff > 0, UBSIZE - off[,"start.uoffset"] + UBSIZE * pmax(0, round(coffdiff / CBSIZE - 1)) + off[,"end.uoffset"], off[,"end.uoffset"] - off[,"start.uoffset"]) ## sum bins with multiple chunks off_diff <- rowsum(as.numeric(off_diff), off[,"bin"]) score <- numeric(NBIN) score[as.integer(rownames(off_diff)) + 1L] <- as.vector(off_diff) score[rep(BINSIZES, TOTALSIZE / BINSIZES) <= maxBinSize] }) ## for performance, important to construct GRanges outside of loop sn_bin <- rep(seqlevels(bam_si), each = length(bin_ranges)) bin_ranges <- restrict(rep(bin_ranges, length(bam_si)), end = seqlengths(bam_si)[sn_bin], keep.all.ranges = TRUE) gr <- GRanges(sn_bin, bin_ranges, score = unlist(off_scores), seqlengths = seqlengths(bam_si)) gr[width(gr) > 0] }) biovizBase/R/crunch-method.R0000644000175200017520000004264014136047676017001 0ustar00biocbuildbiocbuildsetGeneric("crunch", function(obj, ...) standardGeneric("crunch")) setMethod("crunch", "TxDb", function(obj, which, columns = c("tx_id", "tx_name","gene_id"), type = c("all", "reduce"), truncate.gaps = FALSE, truncate.fun = NULL, ratio = 0.0025){ type <- match.arg(type) if(is.list(which)){ message("Parsing exons based on which(list) arguments") temp <- exons(obj, columns = columns, filter = which) which <- range(temp) } seqnms <- as.character(unique(seqnames(which))) if(seqnms %in% seqlevels(obj)){ seqlevels(obj, pruning.mode="coarse") <- seqnms }else{ stop(seqnms, " is not matched with seqlevels of your object, please rename your 'which' arguments ") } ## seqlevels(obj, pruning.mode="coarse") <- seqnms on.exit(restoreSeqlevels(obj)) # needed only because TxDb are reference # objects (unlike R objects in general that # have a copy-on-change semantics) ## system.time(cdss <- cdsBy(obj, "tx")) #2.552s message("Parsing transcripts...") ## tx <- transcripts(obj, columns = columns) ## subsetByOverlaps(tx, which) tx <- transcriptsByOverlaps(obj, which, columns = columns) if(!length(tx)){ message("No transcripts found at this region.") return(GRanges()) }else{ message("Parsing exons...") ## system.time(exons <- exonsBy(obj, "tx")) #takes 3.5s exons <- exonsByOverlaps(obj, which, columns = c("exon_id", "tx_id")) # 1.6 txids <- unlist(exons$tx_id) idx <- togroup(PartitioningByWidth(exons$tx_id)) exons <- exons[idx] exons <- exons[,1] exons$tx_id <- txids exons <- split(exons, exons$tx_id) message("Parsing cds...") cdss <- cdsByOverlaps(obj, which, columns = c("exon_id", "tx_id")) txids <- unlist(cdss$tx_id) idx <- togroup(PartitioningByWidth(cdss$tx_id)) cdss <- cdss[idx] cdss <- cdss[,1] cdss$tx_id <- txids cdss <- split(cdss, cdss$tx_id) message("Parsing utrs...") txids <- as.character(values(tx)$tx_id) ## new method operate on GRangesList levels, and it is much faster to aggregate gids <- values(tx)$gene_id gids <- unlist(lapply(gids, function(x) do.call(paste0, list(as.list(x), collapse = ",")))) tx_nm <- values(tx)$tx_name ## match table mt <- data.frame(txids, gids, tx_nm) rownames(mt) <- txids colnames(mt) <- c("tx_id", "gene_id", "tx_name") ## exons message("------exons...") gr.exons <- unlist(exons) .nms <- as.character(gr.exons$tx_id) .gid.nms <- mt[.nms, "gene_id"] .tx.nms <- mt[.nms, "tx_name"] values(gr.exons) <- NULL values(gr.exons) <- data.frame(tx_id = .nms, tx_name = .tx.nms, gene_id = .gid.nms, type = "exon") values(gr.exons)$type <- as.character(values(gr.exons)$type) names(gr.exons) <- NULL ## cds message("------cdss...") gr.cdss <- unlist(cdss) .nms <- as.character(gr.cdss$tx_id) .gid.nms <- mt[.nms, "gene_id"] .tx.nms <- mt[.nms, "tx_name"] if(length(gr.cdss)){ values(gr.cdss) <- NULL values(gr.cdss) <- data.frame(tx_id = .nms, tx_name = .tx.nms, gene_id = .gid.nms, type = "cds") values(gr.cdss)$type <- as.character(values(gr.cdss)$type) names(gr.cdss) <- NULL }else{ gr.cdss <- GRanges() } ## intron message("------introns...") irl.introns <- gaps(ranges(exons)) ir.introns <- unlist(irl.introns) if(length(ir.introns)){ .nms <- names(ir.introns) .gid.nms <- mt[.nms, "gene_id"] .tx.nms <- mt[.nms, "tx_name"] gr.introns <- GRanges(seqnms, ir.introns, tx_id = .nms, tx_name = .tx.nms, gene_id = .gid.nms, type = "gap") names(gr.introns) <- NULL values(gr.introns)$type <- as.character(values(gr.introns)$type) }else{ gr.introns <- GRanges() } ## utrs message("------utr...") if(length(exons) && length(cdss)){ txnms <- intersect(names(exons), names(cdss)) irl.utrs <- setdiff(ranges(exons[txnms]), ranges(cdss[txnms])) ir.utrs <- unlist(irl.utrs) if(length(ir.utrs)){ .nms <- names(ir.utrs) .gid.nms <- mt[.nms, "gene_id"] .tx.nms <- mt[.nms, "tx_name"] gr.utrs <- GRanges(seqnms, ir.utrs, tx_id = .nms, tx_name = .tx.nms, gene_id = .gid.nms, type = "utr") names(gr.utrs) <- NULL values(gr.utrs)$type <- as.character(values(gr.utrs)$type) }else{ gr.utrs <- GRanges() } }else{ gr.utrs <- GRanges() } ## combine res <- c(gr.exons, gr.cdss, gr.introns, gr.utrs) return(reduceNtruncate(res, type=type, truncate.gaps=truncate.gaps, truncate.fun=truncate.fun, ratio=ratio)) } }) setMethod("crunch", "GAlignments", function(obj, which, truncate.gaps = FALSE, truncate.fun = NULL, ratio = 0.0025){ if(!missing(which)) obj <- subsetByOverlaps(obj, which) if(!length(obj)) stop("No entry in the GAlignments data") if(is.null(names(obj))) stop("Missing qname, please make use.names = TRUE, when reading GAlignments") grg <- grglist(obj) grg.u <- stack(grg, ".grl.name") message("extracting information...") values(grg.u)$junction <- rep(ifelse(elementNROWS(grg)>1, TRUE, FALSE), times = elementNROWS(grg)) names(grg.u) <- NULL res <- grg.u if(truncate.gaps){ if(is.null(truncate.fun)){ if("gap" %in% unique(values(res)$type)) idx <- values(res)$type %in% c("utr", "cds") res.s <- reduce(res[idx], ignore.strand = TRUE) truncate.fun <- shrinkageFun(gaps(res.s, min(start(res.s)), max(end(res.s))), maxGap(gaps(res.s, min(start(res.s)), max(end(res.s))), ratio = ratio)) } res <- truncate.fun(res) } res }) setMethod("crunch", "BamFile", function(obj, which, ..., type = c("gapped.pair", "raw", "all"), truncate.gaps = FALSE, truncate.fun = NULL, ratio = 0.0025){ type <- match.arg(type) ## require(Rsamtools) if(type == "gapped.pair"){ message("Read GAlignments from BamFile...") ga <- readGAlignments(obj, param = ScanBamParam(which = which), use.names = TRUE, ...) res <- crunch(ga) } if(type == "raw"){ message("Read Raw from BamFile by calling scanBam...") res <- scanBamGRanges(obj, which, ...) } if(type == "all"){ message("Read Raw from BamFile by calling scanBam...") res.mb <- scanBamGRanges(obj, which, flag = scanBamFlag(isFirstMateRead = TRUE)) message("Read GAlignments from BamFile...") ga <- readGAlignments(obj, param = ScanBamParam(which = which), use.names = TRUE, ...) res.gp <- crunch(ga) message("Combine...") nms <- values(res.mb)$qname ## fow now just, using isize isize <- values(res.mb)$issize names(isize) <- nms values(res.gp)$isize <- isize[values(res.gp)$qname] res <- res.gp } if(truncate.gaps){ if(is.null(truncate.fun)){ if("gap" %in% unique(values(res)$type)) idx <- values(res)$type %in% c("utr", "cds") res.s <- reduce(res[idx], ignore.strand = TRUE) truncate.fun <- shrinkageFun(gaps(res.s, min(start(res.s)), max(end(res.s))), maxGap(gaps(res.s, min(start(res.s)), max(end(res.s))), ratio = ratio)) } res <- truncate.fun(res) } res }) scanBamGRanges <- function(file, which, what = c("rname", "strand", "pos", "qwidth"), ...){ ## check .names <- c("rname", "strand", "pos", "qwidth") if(!all(.names %in% what)){ what <- unique(c(what, .names)) } dfnm <- setdiff(what, .names) param <- ScanBamParam(which = which, what = what,...) message("scanBam...") bam <- scanBam(file, param = param) message("Coerce list to GRanges") .names <- c("rname", "strand", "pos", "qwidth") res <- lapply(1:length(bam), function(i){ bm <- bam[[i]] df <- as(bm, "DataFrame")[,dfnm] if(length(bm$rname)) GRanges(bm$rname, IRanges(start = bm$pos, width = bm$qwidth), strand = bm$strand, df) else GRanges() }) bam.gr <- do.call("c", res) } ####============================================================ ## crunch method from biovizBase ## ## which can be a GRanges object or an object extending BasicFilter, or a ## list of such filter objects. ####------------------------------------------------------------ setMethod("crunch", "EnsDb", function(obj, which, columns = c("tx_id", "gene_name", "gene_id"), type = c("all", "reduce"), truncate.gaps = FALSE, truncate.fun = NULL, ratio = 0.0025){ type <- match.arg(type) ## If which is a GRanges convert that to a GRangesFilter, otherwise just ## pass on the "which" parameter as argument "filter" to the ensembldb ## methods. if(is(which, "GRanges")) { if(length(which) == 0) { message("No transcripts found at this region.") return(GRanges()) } if(length(which) > 1) stop("'which' has to be a single GRanges object.") if(!all(is.na(genome(which)))){ if(!all(genome(which) %in% genome(obj))) stop("Genome versions do not fit! Argument 'which' has ", paste(genome(which), collapse=","), " argument 'obj' ", paste(genome(obj), collapse=","), "!") } ## Check if we've got the seqnames. if(!all(seqnames(which) %in% seqlevels(obj))) stop(paste(seqlevels(which), collapse=", "), " do(es) not match any seqlevel in argument 'obj'!") exFilter <- GRangesFilter(which, type = "any") } else exFilter <- which ## Check input argument 'columns': notAvailable <- !(columns %in% listColumns(obj)) if(any(notAvailable)){ if(all(notAvailable)) stop("None of the columns specified by arguments 'columns' are available!", " Allowed values are:", paste(listColumns(obj), collapse=", "), ".") ## Reducing to those which are allowed... warning("Columns ", paste(columns[notAvailable], collapse=", "), " are not", " available in the database and have been removed.") columns <- columns[!notAvailable] } ## Approach: ## 1) Get all exons in that region and retrieve also the ## tx_coding_seq_start. We're fetching the data just once and ## calculating everything we need from that, i.e. cds, utr and introns. message("Fetching data...", appendLF=FALSE) requiredCols <- c("tx_cds_seq_start", "tx_cds_seq_end", "exon_id", "tx_id") ## Forcing tx_id on the columns: columns <- unique(c(columns, "tx_id")) ## In order to solve also the "overlapping" condition I have first to fetch ## the transcripts in the region and their exons. That way we get, for a ## GRangesFilter or GRanges all transcripts that have an exon or an intron ## at the specified region. txInRegion <- transcripts(obj, filter = exFilter) if(length(txInRegion) == 0){ message("No transcripts found at this region.") return(GRanges()) } regExons <- exons(obj, filter = TxIdFilter(unique(txInRegion$tx_id)), columns = unique(c(requiredCols, columns))) ## Simple sanitizing: check if what we got is on the same chromosome! if(length(unique(as.character(seqnames(regExons)))) > 1) stop("Got features from different chromosomes! Please adjust argument", " 'which' in order to fetch only features from a single chromosome.") message("OK") if(length(regExons) > 0){ message("Parsing exons...", appendLF=FALSE) ## Get an DataFrame that we can use as mcols for the GRanges: mDf <- unique(mcols(regExons)[, columns]) ## Actually, with this I have all I need. ## 2) Define introns. regExonsList <- split(regExons, regExons$tx_id) message("OK\nDefining introns...", appendLF=FALSE) ints <- gaps(ranges(regExonsList)) ints <- unlist(ints) if(length(ints) > 0){ regIntrons <- GRanges(seqnames=unique(seqnames(regExons)), ranges=ints, strand="*", mDf[match(names(ints), mDf$tx_id), ]) regIntrons$type <- "gap" }else{ regIntrons <- GRanges() } message("OK\nDefining UTRs...", appendLF=FALSE) ## 3) Define UTRs. codingTx <- regExons[!is.na(regExons$tx_cds_seq_end)] if(length(codingTx) > 0){ ## Define the whole CDS region per tx codingReg <- GRanges(seqnames=seqnames(codingTx), ranges=IRanges(codingTx$tx_cds_seq_start, codingTx$tx_cds_seq_end), strand=strand(codingTx), tx_id=codingTx$tx_id) codingTx <- split(codingTx, codingTx$tx_id) ## Subset to one CDS region per tx and split codingReg <- codingReg[match(names(codingTx), codingReg$tx_id)] codingReg <- split(codingReg, codingReg$tx_id) regUTRs <- unlist(setdiff(codingTx, codingReg)) mcols(regUTRs) <- mDf[match(names(regUTRs), mDf$tx_id), ] regUTRs$type <- rep("utr", length(regUTRs)) message("OK\nDefining CDS...", appendLF=FALSE) ## 4) Define CDS regCDSs <- unlist(intersect(codingTx, codingReg)) mcols(regCDSs) <- mDf[match(names(regCDSs), mDf$tx_id), ] regCDSs$type <- "cds" }else{ regUTRs <- GRanges() regCDSs <- GRanges() } message("OK\n", appendLF=FALSE) regExons <- regExons[, columns] regExons$type <- "exon" ensRes <- c(regExons, regIntrons, regUTRs, regCDSs) }else{ warning("Did not find any transcript at the specified region!") return(GRanges()) } return(reduceNtruncate(ensRes, type=type, truncate.gaps=truncate.gaps, truncate.fun=truncate.fun, ratio=ratio)) }) ## Just some simple helper function to avoid repeating code for TxDb and EnsDb. reduceNtruncate <- function(res, type=c("all", "reduce"), truncate.gaps=FALSE, truncate.fun=NULL, ratio = 0.0025){ message("aggregating...") if(!length(res)) res <- GRanges() res$type <- factor(res$type) if(type == "reduce"){ if(length(res)){ cds.s <- reduce(res[values(res)$type == "cds"]) values(cds.s)$type <- factor("cds") exon.s <- reduce(res[values(res)$type == "exon"]) values(exon.s)$type <- factor("exon") utr.s <- setdiff(exon.s, cds.s) values(utr.s)$type <- factor("utr") gap.s <- gaps(cds.s, start = min(start(cds.s)), end = max(end(cds.s))) values(gap.s)$type <- factor("gap") res <- c(cds.s, utr.s, gap.s) ## change it to * strand(res) <- "*" } } if(truncate.gaps){ message("truncating ...") if(is.null(truncate.fun)){ if("gap" %in% unique(values(res)$type)) idx <- values(res)$type %in% c("utr", "cds") res.s <- reduce(res[idx], ignore.strand = TRUE) truncate.fun <- shrinkageFun(gaps(res.s, min(start(res.s)), max(end(res.s))), maxGap(gaps(res.s, min(start(res.s)), max(end(res.s))), ratio = ratio)) } res <- truncate.fun(res) } message("Done") return(res) } biovizBase/R/facets-method.R0000644000175200017520000000555114136047676016764 0ustar00biocbuildbiocbuildnewDataAfterFacetByGr <- function(gr, which, id.name){ gr <- sort(gr) which <- sort(which) ## suppose which is a GRanges res <- lapply(seq_len(length(which)),function(i){ res <- subsetByOverlaps(gr, which[i]) values(res)$.bioviz.facetid <- i res }) do.call(c, res) } strip_formula_dots <- function(formula){ allvars <- all.vars(as.formula(formula)) idx <- ggplot2_is_calculated_aes(allvars) if(sum(idx)) formula[[which(idx)+1]] <- as.name(unlist(ggplot2_strip_dots(allvars[idx]))) formula } setGeneric("splitByFacets", function(object, facets, ...) standardGeneric("splitByFacets")) setMethod("splitByFacets", c("GRanges", "formula"), function(object, facets){ .checkFacetsRestrict(facets, object) facets <- strip_formula_dots(facets) allvars <- all.vars(as.formula(facets)) if(length(allvars) > 1){ if(allvars[1] == "."){ res <- split(object, seqnames(object)) }else{ if(allvars[1] != "strand") fts <- interaction(as.character(values(object)[,allvars[1]]),as.character(seqnames(object))) else fts <- interaction(as.character(strand(object)),as.character(seqnames(object))) res <- split(object, fts) }} if(length(allvars) == 1) res <- split(object, seqnames(object)) res <- res[elementNROWS(res)>0] res }) setMethod("splitByFacets", c("GRanges", "GRanges"), function(object, facets){ if(length(facets)){ object <- newDataAfterFacetByGr(object, facets) grl <- split(object, values(object)$.bioviz.facetid) }else{ stop("facets is an empty GenomicRanges object") } grl <- grl[elementNROWS(grl)>0] grl }) setMethod("splitByFacets", c("GRanges", "missing"), function(object, facets){ res <- split(object, seqnames(object)) res <- res[elementNROWS(res)>0] res }) setMethod("splitByFacets", c("GRanges", "NULL"), function(object, facets){ res <- split(object, seqnames(object)) res <- res[elementNROWS(res)>0] res }) isFacetByOnlySeq <- function(facets){ allvars <- all.vars(as.formula(facets)) allvars <- allvars[!allvars %in% c(".", "seqnames")] if(!length(allvars)) TRUE else FALSE } ## that's for linear or default! .checkFacetsRestrict <- function(facets, object){ facets <- strip_formula_dots(facets) allvars <- all.vars(as.formula(facets)) if(length(allvars) == 1){ if(allvars[1] != "seqnames") stop("Column of facets formula can only be seqnames, such as . ~ seqnames, in default restrict mode, you can only change row varaibles") } if(length(allvars) > 1){ if(allvars[2] != "seqnames" & allvars[2] != "."){ stop("Column of facets formula can only be seqnames or '.', such as . ~ seqnames, in default restrict mode, you can only change row varaibles") } if(allvars[1] != "."){ if(!allvars[1] %in% c(colnames(values(object)), "strand")) stop(allvars[1]," doesn't exists in data columns") } } } biovizBase/R/getFragLength-method.R0000644000175200017520000000362614136047676020241 0ustar00biocbuildbiocbuildsetMethod("getFragLength", "character", function(obj, model, which, type = "remove.gaps", maxGap = 0L){ require(Rsamtools) if(missing(which)) which <- range(reduce(model)) if(tools::file_ext(obj) == "bam") res <- scanBam(obj, param = ScanBamParam(which = which, flag = scanBamFlag(isProperPair = TRUE, isFirstMateRead = TRUE))) if(!length(res[[1]]$pos)) stop("no paired end reads found in the the data") res <- res[[1]] m1 <- GRanges(res$rname, IRanges(res$pos, width = res$qwidth), mapid = 1:length(res$pos), isize = res$isize) ## suppose they have the same width m2 <- GRanges(res$rname, IRanges(res$mpos, width = res$qwidth), mapid = 1:length(res$pos), isize = res$isize) m <- c(m1, m2) res <- getFragLength(m, model, type = type, maxGap = 0L) res }) setMethod("getFragLength", "GenomicRanges", function(obj, model, maxGap = 0L, type = "remove.gaps"){ model <- reduce(model) if(type == "remove.gaps"){ grl <- split(obj, values(obj)$mapid) gr.res <- unlist(range(grl)) names(gr.res) <- names(grl) mapid <- names(gr.res) idx <- match(mapid, values(obj)$mapid) values(gr.res)$isize <- values(obj)$isize[idx] g.gap <- gaps(c(ranges(obj), ranges(model))) cut.fun <- shrinkageFun(g.gap, maxGap) obj.cut <- cut.fun(obj) grl <- split(obj.cut, values(obj.cut)$mapid) grl.r <- range(grl) .fragLength <- unlist(width(grl.r)) values(gr.res)$.fragLength <- .fragLength[names(gr.res)] gr.res } list(gr = gr.res, cut.fun = cut.fun, gr.cut = unlist(grl.r), ## model.cut = cut.fun(model), ## model = model, reads = obj, ## gaps = g.gap, fragLength = .fragLength) }) biovizBase/R/ideogram.R0000644000175200017520000000400314136047676016017 0ustar00biocbuildbiocbuild##----------------------------------------------------------------## ## ideogram ##----------------------------------------------------------------## getIdeogram <- function(genome,subchr = NULL,cytobands=TRUE){ .gnm <- genome lst <- lapply(.gnm, function(genome){ print(genome) ## to remove the "heavy dependency" we put require here. require(rtracklayer) if(!(exists("session")&&extends(class(session),"BrowserSession"))) session <- rtracklayer::browserSession() if(missing(genome)){ choices <- rtracklayer::ucscGenomes()[,1] res <- menu(choices,title="Please specify genome") genome <- as.character(choices[res]) } if(cytobands){ message("Loading ideogram...") tryres <- try(query <- rtracklayer::ucscTableQuery(session,"cytoBand",genome)) if(!inherits(tryres, "try-error")){ rtracklayer::tableName(query) <- "cytoBand" df <- rtracklayer::getTable(query) gr <- GRanges(seqnames=df$chrom, IRanges(start=df$chromStart,end=df$chromEnd)) values(gr) <- df[,c("name","gieStain")] message("Loading ranges...") gr.r <- rtracklayer::GRangesForUCSCGenome(genome) suppressWarnings(seqlengths(gr) <- seqlengths(gr.r)[names(seqlengths(gr))]) gr <- trim(gr) }else{ message("cytoBand informatin is not available, only get ranges.") message("Loading ranges...") gr <- rtracklayer::GRangesForUCSCGenome(genome) message("Done") } }else{ message("Loading...") gr <- rtracklayer::GRangesForUCSCGenome(genome) message("Done") } if(length(subchr)) gr <- gr[seqnames(gr) == subchr] gr <- sort(gr) gr }) names(lst) <- .gnm if(length(lst) == 1) res <- lst[[1]] else res <- lst res } isIdeogram <- function(obj){ is(obj, "GRanges") && all(c("gieStain", "name") %in% colnames(values(obj))) } isSimpleIdeogram <- function(obj){ is(obj, "GRanges") && all(elementNROWS(split(obj, as.character(seqnames(obj)))) == 1) } biovizBase/R/labs.R0000644000175200017520000000261314136047676015156 0ustar00biocbuildbiocbuild## going to be moved to biovizBase setGeneric("getYLab", function(obj,...) standardGeneric("getYLab")) setMethod("getYLab", "TxDb", function(obj){ md <- metadata(obj) ds <- md[md[,1] == "Data source",2] lb <- character() if(ds == "UCSC"){ lb <- md[md[,1] == "UCSC Table",2] } if(ds == "BioMart"){ lb <- md[md[,1] == "BioMart Database",2] } lb }) ## going to be moved to biovizBase setGeneric("getXLab", function(obj,...) standardGeneric("getXLab")) setMethod("getXLab", "GRanges", function(obj){ chrs <- unique(as.character(seqnames(obj))) gms <- genome(obj) gm <- gms[chrs] if(length(chrs) > 1){ xlab <- "Position" }else{ xlab <- paste(ifelse(is.na(gm), chrs, paste0(gm, "::", chrs))) xlab <- paste("Position on", xlab) } xlab }) setMethod("getXLab", "GRangesList", function(obj){ chrs <- unique(as.character(seqnames(unlist(obj)))) gms <- genome(obj) gm <- gms[chrs] if(length(chrs) > 1){ xlab <- "Position" }else{ xlab <- paste(ifelse(is.na(gm), chrs, paste0(gm, "::", chrs))) xlab <- paste("Position on", xlab) } xlab }) setMethod("getXLab", "GAlignments", function(obj){ chrs <- unique(as.character(seqnames(obj))) gms <- genome(obj) gm <- gms[chrs] if(length(chrs) > 1){ xlab <- "Position" }else{ xlab <- paste(ifelse(is.na(gm), chrs, paste0(gm, "::", chrs))) xlab <- paste("Position on", xlab) } xlab }) biovizBase/R/maxGap-method.R0000644000175200017520000000015314136047676016725 0ustar00biocbuildbiocbuildsetMethod("maxGap", "GenomicRanges", function(obj, ratio = 0.0025){ ratio * width(range(ranges(obj))) }) biovizBase/R/mold-method.R0000644000175200017520000001117714136047676016453 0ustar00biocbuildbiocbuildsetGeneric("mold", function(data, ...) standardGeneric("mold")) setMethod("mold", c("eSet"), function(data){ object <- data pdata <- phenoData(object) df <- as(object, "data.frame") df$sampleNames <- row.names(df) df.m <- melt(df, id.vars = c(varLabels(pdata), "sampleNames")) df.m }) setMethod("mold", c("GRanges"), function(data){ names(data) <- NULL df <- as.data.frame(data) df$midpoint <- (df$start+df$end)/2 df }) setMethod("mold", c("GRangesList"), function(data, indName = "grl_name"){ gr <- biovizBase:::flatGrl(data, indName) df <- mold(gr) df }) setMethod("mold", c("IRanges"), function(data){ df <- as.data.frame(data) df$midpoint <- (df$start+df$end)/2 df }) setMethod("mold", c("Seqinfo"), function(data){ df <- .transformSeqinfo(data) df <- mold(df) df <- cbind(df, as.data.frame(data)) df }) setMethod("mold", c("matrix"), function(data){ x <- seq_len(ncol(data)) y <- seq_len(nrow(data)) cnms <- colnames(data) rnms <- rownames(data) df <- expand.grid(x = x, y = y) df$value <- as.vector(t(data)) df$row <- df$y df$col <- df$x df$colnames <- cnms[df$x] df$rownames <- rnms[df$y] df }) setMethod("mold", c("ExpressionSet"), function(data){ df <- mold(exprs(data)) pd <- pData(data) idx <- seq_len(ncol(exprs(data))) res <- cbind(df, pd[df$x, ]) res }) setMethod("mold", c("RangedSummarizedExperiment"), function(data, assay.id = 1){ ays <- assays(data) stopifnot(length(assay.id) == 1 || length(assay.id) <= length(ays)) if(length(ays) > 1) message("Assay index: ", assay.id, " used") cd <- as.data.frame(colData(data)) rd <- as.data.frame(rowRanges(data)) df <- mold(ays[[assay.id]]) cd.e <- cd[df$x, ] rd.e <- rd[df$y, ] res <- cbind(df, cd.e, rd.e) res }) ## Remove this method once the transition from SummarizedExperiment to ## RangedSummarizedExperiment is complete. [H. Pages - May 12, 2015] setMethod("mold", c("SummarizedExperiment"), function(data, assay.id = 1){ ays <- assays(data) stopifnot(length(assay.id) == 1 || length(assay.id) <= length(ays)) if(length(ays) > 1) message("Assay index: ", assay.id, " used") cd <- as.data.frame(colData(data)) rd <- as.data.frame(rowRanges(data)) df <- mold(ays[[assay.id]]) cd.e <- cd[df$x, ] rd.e <- rd[df$y, ] res <- cbind(df, cd.e, rd.e) res }) ## setMethod("mold", c("VCF"), function(data, ## type = c("geno", "info", "fixed"), ## assay.id = 1){ ## type <- match.arg(type) ## hdr <- metadata(object)[["header"]] ## nms <- rownames(geno(hdr)) ## res <- switch(type, ## geno = { ## nms <- rownames(geno(hdr)) ## if(is.numeric(assay.id)){ ## nm <- nms[assay.id] ## }else if(is.character(assay.id) && assay.id %in% nms){ ## nm <- assay.id ## }else{ ## stop("wrong assay.id specified, only numeric value which indicates ## index of data set under each type or name for that data set.") ## } ## res <- geno(object)[[nm]] ## }, ## info = { ## }, ## fixed = { ## }) ## }) setMethod("mold", c("Views"), function(data){ df.r <- as.data.frame(ranges(data)) nms <- names(data) if(!is.null(nms)) names(data) <- NULL mx <- suppressWarnings(as.matrix(data)) df <- mold(mx) df$start <- rep(df.r$start, each = ncol(mx)) df$end <- rep(df.r$end, each = ncol(mx)) df$width <- rep(df.r$width, each = ncol(mx)) df$midpoint <- (df$start + df$end)/2 if(!is.null(nms)) df$rowname <- rep(nms, each = ncol(mx)) df$row <- factor(df$y) df$col <- factor(df$x) df }) ## setMethod("mold", c("BamFile"), function(data){ ## }) ## setMethod("mold", c("GAlignments"), function(data){ ## }) ## setMethod("mold", c("TxDb"), function(data){ ## }) setMethod("mold", c("Rle"), function(data){ df <- as.data.frame(data) df$x <- as.numeric(rownames(df)) df$y <- 1 df$row <- factor(df$y) df$col <- factor(df$x) df }) setMethod("mold", c("RleList"), function(data){ data <- xRleList nms <- names(data) if(is.null(nms)) nms <- seq_len(length(data)) lst <- lapply(1:length(data), function(i){ x <- data[[i]] df <- mold(x) df$group <- nms[i] df }) res <- do.call(rbind, lst) res }) setMethod("mold", "VRanges", function(data){ res <- as.data.frame(data, row.names=NULL) res$midpoint <- (res$start + res$end)/2 res }) biovizBase/R/original.R0000644000175200017520000000220014136047676016031 0ustar00biocbuildbiocbuild## to reduce burden to import too much packages ## I redfined/move functions in some other packages to here .all_aesthetics <- c("adj", "alpha", "angle", "bg", "cex", "col", "color", "colour", "fg", "fill", "group", "hjust", "label", "linetype", "lower", "lty", "lwd", "max", "middle", "min", "order", "pch", "radius", "sample", "shape" , "size", "srt", "upper", "vjust", "weight", "width", "x" , "xend", "xmax", "xmin", "xintercept", "y", "yend", "ymax", "ymin", "yintercept", "z") ggplot2_is.constant <- function(x){ sapply(x, function(x) "I" %in% all.names(asOneSidedFormula(x))) } ## for ggplot2 ggplot2_is_calculated_aes <- function(aesthetics){ match <- "\\.\\.([a-zA-z._]+)\\.\\." stats <- rep(FALSE, length(aesthetics)) grepl(match, sapply(aesthetics, quo_text)) } ggplot2_strip_dots <- function(aesthetics){ match <- "\\.\\.([a-zA-z._]+)\\.\\." strings <- lapply(aesthetics, quo_text) strings <- lapply(strings, gsub, pattern = match, replacement = "\\1") lapply(strings, function(x) parse(text = x)[[1]]) } biovizBase/R/pileup.R0000644000175200017520000001165114136047676015535 0ustar00biocbuildbiocbuild##' This function summarize reads from bam files for nucleotides on ##' single base unit in a given region, this allows the downstream ##' mismatch summary analysis. ##' ##' It's a wrapper around \code{applyPileup} function in Rsamtools ##' package, more detailed control could be found under manual of ##' ApplyPileupsParam function in Rsamtools. \code{pileupAsGRanges} function ##' return a GRanges object which including summary of nucleotides, ##' depth, bam file path. This object could be read directly into ##' \code{pileupGRangesAsVariantTable} function for mismatch ##' summary. ##' @title Summarize reads for certain region ##' @param bams A character which specify the bam file path. ##' @param regions A GRanges object specifying the region to be ##' summarized. This passed to \code{which} arguments in ##' \code{ApplyPileupsParam}. ##' @param DNABases Nucleotide type you want to summarize in the result ##' and in specified order. It must be one or more of A,C,G,T,N. ##' @param ... Extra parameters passed to \code{ApplyPileupsParam}. ##' @return A GRanges object, each row is one single base unit. and ##' elementMetadata contains summary about this position about all ##' nucleotides specified by DNABases. and \code{depth} for total ##' reads, \code{bam} for file path. ##' @author Michael Lawrence, Tengfei Yin pileupAsGRanges <- function(bams, regions, DNABases = c("A", "C", "G", "T", "N"), ...) { pileupFiles <- PileupFiles(bams) applyPileupsParam <- ApplyPileupsParam(which = regions, ...) ## what if it's multiple bam files bamNames <- names(bams) if (is.null(bamNames)) bamNames <- bams pileupFun <- function(x) { grl <- lapply(seq_len(length(bamNames)), function(i) { seq <- x$seq[DNABases,i,] sn <- unique(names(x$seqnames)) GRanges(seqnames = Rle(names(x$seqnames), x$seqnames), ranges = IRanges(x$pos, width = rep(1L, length(x$pos))), strand = Rle("+", length(x$pos)), t(seq), depth = colSums(seq), bam = Rle(bamNames[i], length(x$pos))) }) do.call(c, grl[!is.null(grl)]) } gr <- do.call(c, applyPileups(pileupFiles, pileupFun, param = applyPileupsParam)) seqinfo(gr) <- seqinfo(regions) gr } ##' Compare to reference genome and compute mismatch summary for ##' certain region of reads. ##' ##' User need to make sure to pass the right reference genome to this ##' function to get the right summary. This function drop the position ##' has no reads and only keep the region with coverage in the ##' summary. The result could be used to show stacked barchart for ##' mismatch summary. ##' @title Mismatch summary ##' @param gr A GRanges object, with nucleotides summary, each base ##' take one column in elementMetadata or user can simply passed the ##' returned result from \code{pileupAsGRanges} function to this ##' function. ##' @param genome BSgenome object, need to be the reference genome. ##' @param DNABases Nucleotide types contained in passed GRanges ##' object. Default is A/C/G/T/N, it tries to match the column names ##' in elementMetadata to those default nucleotides. And treat the ##' matched column as base names. ##' @return A GRanges object. Containing the following elementMetadata ##' \describe{ ##' \itemize{ ##' \item {[ref] Nucleotide in reference genome.} ##' \item {[read] Nucleotide contained in the reads at particular position, ##' if multiple nucleotide, either matched or unmatched are found, they will be ##' summarized in different rows.} ##' \item {[count] Count for read column.} ##' \item{[match] Logical value, whether matched to reference genome or not} ##' \item{[bam] Character indicate bam file path.} ##' } ##' } ##' @author Michael Lawrence, Tengfei Yin pileupGRangesAsVariantTable <- function(gr, genome, DNABases = c("A", "C", "G", "T", "N")) { require(BSgenome) colnms <- colnames(values(gr)) DNAbases <- colnms[colnms %in% DNABases] gr <- rectifySeqlevelsStyle(gr, genome) refBases <- getSeq(genome, gr, as.character = TRUE) counts <- as.matrix(as.data.frame(values(gr)[,DNABases])) refCounts <- counts[cbind(seq(nrow(counts)), match(refBases, DNABases))] variantsForBase <- function(base) { baseCounts <- counts[,base, drop=TRUE] keep <- baseCounts > 0 if(sum(keep)){ count <- baseCounts[keep] gr <- GRanges(seqnames(gr)[keep], ranges(gr)[keep], strand(gr)[keep], ref = refBases[keep], read = base, count = baseCounts[keep], values(gr)[keep, setdiff(colnames(values(gr)), DNABases)]) values(gr)$match <- values(gr)$ref == values(gr)$read gr }else{ NULL } } lst <- lapply(colnames(counts), variantsForBase) idx <- !sapply(lst, is.null) res <- do.call("c", lst[idx]) ## why this is slow if(length(res)) return(res[order(as.numeric(start(res)))]) else GRanges() } biovizBase/R/scale.R0000644000175200017520000000312114136047676015317 0ustar00biocbuildbiocbuild## utils for creating proper scale breaks and labels for certain coordinate setGeneric("getXScale", function(obj, ...) standardGeneric("getXScale")) setMethod("getXScale", "GRanges", function(obj, type = c("default", "all", "left", "right")){ type <- match.arg(type) if(is_coord_truncate_gaps(obj)){ message("using coord:truncate_gaps to parse x scale") res <- switch(type, left = { list(breaks = start(obj), labels = start(values(obj)$.ori)) }, right = { list(breaks = end(obj), labels = end(values(obj)$.ori)) }, all = { list(breaks = c(start(obj), end(obj)), labels = c(start(values(obj)$.ori), end(values(obj)$.ori))) }, default = { breaks = c(min(start(obj)), max(end(obj))) labels = c(min(start(values(obj)$.ori)), max(end(values(obj)$.ori))) list(breaks = breaks, labels = labels) }) }else if(is_coord_genome(obj)){ message("using coord:genome to parse x scale") res <- switch(type, default = { list(breaks = metadata(obj)$breaks, labels = metadata(obj)$labels) }) }else{ stop("coord other than truncate_gaps are not suported for getXScale yet") } res }) biovizBase/R/shrinkageFun-method.R0000644000175200017520000000202414136047676020133 0ustar00biocbuildbiocbuildsetMethod("shrinkageFun", "GenomicRanges", function(obj, max.gap = 1L){ obj <- obj[order(as.numeric(end(obj)))] shrinkage <- pmax(0, width(obj) - max.gap) shrinksum <- c(0L, cumsum(shrinkage)) function(x) { res <- shift(x, -shrinksum[findInterval(start(x), end(obj)) + 1L]) metadata(res)$coord <- "truncate_gaps" metadata(res)$max.gap <- max.gap metadata(res)$gaps <- obj values(res)$.ori <- x res } }) setMethod("shrinkageFun", "IRanges", function(obj, max.gap = 1L){ obj <- obj[order(as.numeric(end(obj)))] shrinkage <- pmax(0, width(obj) - max.gap) shrinksum <- c(0L, cumsum(shrinkage)) function(x) { res <- shift(x, -shrinksum[findInterval(start(x), end(obj)) + 1L]) metadata(res)$coord <- "truncate_gaps" metadata(res)$max.gap <- max.gap metadata(res)$gaps <- obj values(res)$.ori <- x res } }) is_coord_truncate_gaps<- function(obj){ if(!is.null(metadata(obj)$coord)) res <- metadata(obj)$coord == "truncate_gaps" else res <- FALSE res } biovizBase/R/spliceSummary-method.R0000644000175200017520000003731314136047676020355 0ustar00biocbuildbiocbuildsetMethod("spliceSummary", c("GenomicRanges", "GRangesList"), function(obj, model, weighted = TRUE){ lst <- lapply(model, function(md){ logi <- isMatchedWithModel(md, obj) if(!length(logi)) logi <- rep(FALSE, length(obj)) logi }) res <- do.call(rbind, lst) if(weighted){ res.s <- apply(res, 2, sum) idx.all <- res.s > 1 res.n <- as.numeric(res) res.m <- matrix(res.n, nrow = nrow(res)) res.m[,idx.all] <- res.m[,idx.all]/res.s[idx.all] freq <- apply(res.m, 1, sum) }else{ freq <- apply(res, 1, sum) } names(freq) <- names(model) freq }) setMethod("spliceSummary", c("character", "GRangesList"), function(obj, model, weighted = TRUE){ if(tools::file_ext(obj) == "bam"){ ## bf <- BamFile(obj) require(Rsamtools) }else{ stop("Only support file with .bam extention name now") } ## if(missing(which)) which <- range(reduce(unlist(model))) ga <- readGAlignments(obj, param = ScanBamParam(which = which), use.names = TRUE) ## reduce model ## assumption here is that: contains unoverlaped exons. ## must contain exon id exons <- reduce(unlist(model), ignore.strand = TRUE); ## first leave only junction read idx <- sapply(cigar(ga), isJunctionRead) ga.junction <- ga[idx] gr.junction <- as(ga.junction, "GRanges") spliceSummary(gr.junction, model = model, weighted = weighted) }) isJunctionRead <- function(cigar){ grepl("N", cigar) } ## model is a GRanges containing exons, sgr is a single gr object isMatchedWithModel <- function(model, gr){ ## require on the same chromosome now if(length(unique(as.character(seqnames(model)))) > 1) stop("only support single chromosome summary now") if(unique(as.character(seqnames(model))) != unique(as.character(seqnames(gr)))) stop("Cannot be mapped due to different space") model <- sort(model) ## do we consider strand information? countOverlaps(ranges(gr), ranges(model)) == 2 } setMethod("spliceSummary", c("GenomicRanges", "GenomicRanges"), function(obj, model, model_id = NULL){ ov <- findOverlaps(ranges(obj), ranges(model)) mm <- as.matrix(ov) res <- split(mm[,2], mm[,1]) idx <- unlist(lapply(split(mm[,2], mm[,1]),length)) > 1 res <- lapply(res[idx], function(x){ if(!is.null(model_id)) x <- values(model)[,model_id][x] paste(head(x, 1), tail(x, 1), sep = "-") }) nms <- names(table(unlist(res))) res <- as.numeric(table(unlist(res))) names(res) <- nms res }) setMethod("spliceSummary", c("character", "GenomicRanges"), function(obj, model, model_id = NULL){ if(tools::file_ext(obj) == "bam"){ require(Rsamtools) }else{ stop("Only support file with .bam extention name now") } ## if(missing(which)) which <- range(model) ga <- readGAlignments(obj, param = ScanBamParam(which = which), use.names = TRUE) ## first leave only junction read grl <- grglist(ga) idx <- elementNROWS(grl) > 1 ga.junction <- ga[idx] gr.junction <- as(ga.junction, "GRanges") spliceSummary(gr.junction, model = model, model_id = model_id) }) ## functions downbelow from workshop by Michael Lawrence ## will be implmented by into his package, so I will replace this function later ## splicefun <- function(files, txdb, which, id, xlim, txdb.chr.pre = character(), weight = 1){ ## elementGaps <- function(x) { ## x_flat <- unlist(x, use.names = FALSE) ## egaps <- gaps(ranges(x)) ## first_segment <- start(PartitioningByWidth(x)) ## sn <- seqnames(x_flat)[first_segment][togroup(egaps)] ## strand <- strand(x_flat)[first_segment][togroup(egaps)] ## relist(GRanges(sn, unlist(egaps, use.names = FALSE), ## strand, seqlengths = seqlengths(x)), ## egaps) ## } ## pairReadRanges <- function(reads) { ## pairs <- split(unlist(reads, use.names=FALSE), ## factor(names(reads)[togroup(reads)], ## unique(names(reads)))) ## metadata(pairs) <- metadata(reads) ## xs <- values(reads)$XS ## has_xs <- !is.na(xs) ## pair_xs <- setNames(rep.int(NA, length(pairs)), ## names(pairs)) ## pair_xs[names(reads)[has_xs]] <- xs[has_xs] ## values(pairs)$XS <- unname(pair_xs) ## pairs ## } ## strandFromXS <- function(pairs) { ## xs <- values(pairs)$XS ## strand <- ifelse(!is.na(xs) & xs != "?", xs, "*") ## strand(pairs) <- relist(Rle(strand, elementNROWS(pairs)), ## pairs) ## pairs ## } ## gr2key <- function(x) { ## paste(seqnames(x), start(x), end(x), strand(x), ## sep = ":") ## } ## key2gr <- function(x, ...) { ## key_mat <- matrix(unlist(strsplit(x, ":", fixed=TRUE)), ## nrow = 4) ## GRanges(key_mat[1,], ## IRanges(as.integer(key_mat[2,]), ## as.integer(key_mat[3,])), ## key_mat[4,], ...) ## } ## findIsoformOverlaps <- function(pairs) { ## splices <- values(pairs)$splices ## hits <- findOverlaps(pairs, tx) ## hit_pairs <- ranges(pairs)[queryHits(hits)] ## hit_splices <- ranges(splices)[queryHits(hits)] ## hit_tx <- ranges(tx)[subjectHits(hits)] ## read_within <- ## elementNROWS(setdiff(hit_pairs, hit_tx)) == 0L ## tx_within <- ## elementNROWS(intersect(hit_tx, hit_splices)) == 0L ## compatible <- read_within & tx_within ## compat_hits <- hits[compatible] ## reads_unique <- tabulate(queryHits(compat_hits), ## queryLength(compat_hits)) == 1L ## unique <- logical(length(hits)) ## unique[compatible] <- reads_unique[queryHits(compat_hits)] ## strand_specific <- ## all(strand(pairs) != "*")[queryHits(hits)] ## values(hits) <- DataFrame(strand_specific, ## compatible, ## unique) ## list(hits = hits, ## compatible = compatible, ## strand_specific = strand_specific) ## } ## countIsoformHits <- function(hits, compatible, strand_specific) { ## countByTx <- function(x) { ## tabulate(subjectHits(hits)[x], subjectLength(hits)) ## } ## compatible_strand <- ## countByTx(with(values(hits), ## compatible & strand_specific)) ## counts <- DataFrame(compatible_strand, ## lapply(values(hits)[-1], countByTx)) ## counts ## } ## summarizeSplices <- function(reads) { ## splices <- values(reads)$splices ## splices_flat <- unlist(splices, use.names = FALSE) ## if(length(splices_flat)){ ## splice_table <- table(gr2key(splices_flat)) ## splice_summary <- ## key2gr(names(splice_table), ## score = as.integer(splice_table), ## novel = !names(splice_table) %in% tx_keys, ## seqlengths = seqlengths(splices)) ## }else{ ## splice_summary <- GRanges() ## } ## splice_summary ## } ## getUniqueReads <- function(reads, hits) { ## sel <- values(hits)$unique & ## subjectHits(hits) %in% c(1, 4) ## reads[unique(queryHits(hits)[sel])] ## } ## message("Parsing gene structure from txdb...") ## if(!missing(id)){ ## aldoa_gr <- exons(txdb, columns = c("tx_id", "gene_id"), ## filter = list(gene_id = id)) ## aldoa_gr <- keepSeqlevels(aldoa_gr, unique(as.character(seqnames(aldoa_gr)))) ## ## FIXME later ## nms <- as.character(names(seqlengths(aldoa_gr))) ## nms.new <- paste(txdb.chr.pre, nms, sep = "") ## names(nms.new) <- nms ## aldoa_gr <- renameSeqlevels(aldoa_gr, nms.new) ## aldoa_range <- range(aldoa_gr) ## wh <- aldoa_range ## aldoa_vals <- values(aldoa_gr) ## tx <- multisplit(aldoa_gr, aldoa_vals$tx_id) ## tx_to_val <- match(names(tx), unlist(aldoa_vals$tx_id)) ## values(tx)$gene_id <- ## rep(unlist(aldoa_vals$gene_id), ## elementNROWS(aldoa_vals$tx_id))[tx_to_val] ## values(tx)$tx_id <- names(tx) ## }else if(!missing(which) & is(which, "GRanges")){ ## isActiveSeq(txdb)[seqlevels(txdb)] <- FALSE ## seqnms <- as.character(unique(seqnames(which))) ## seqnms <- gsub(txdb.chr.pre, "", seqnms) ## isActiveSeq(txdb)[seqnms] <- TRUE ## ## aldoa_gr <- exons(txdb, columns = c("tx_id", "gene_id")) ## ## aldoa_gr <- keepSeqlevels(aldoa_gr, unique(as.character(seqnames(aldoa_gr)))) ## ## nms <- as.character(names(seqlengths(aldoa_gr))) ## ## nms.new <- paste(txdb.chr.pre, nms, sep = "") ## ## names(nms.new) <- nms ## ## aldoa_gr <- renameSeqlevels(aldoa_gr, nms.new) ## ## aldoa_gr <- subsetByOverlaps(aldoa_gr, which) ## ## aldoa_range <- range(aldoa_gr) ## aldoa_range <- which ## exons_grl <- exonsBy(txdb) ## gr.l <- stack(exons_grl, ".sample") ## gr.l <- keepSeqlevels(gr.l, unique(as.character(seqnames(gr.l)))) ## nms <- as.character(names(seqlengths(gr.l))) ## nms.new <- paste(txdb.chr.pre, nms, sep = "") ## names(nms.new) <- nms ## gr.l <- renameSeqlevels(gr.l, nms.new) ## exons_grl <- split(gr.l, values(gr.l)$.sample) ## ans <- subsetByOverlaps(exons_grl, which) ## values(ans)$tx_id <- names(ans) ## tx_gr <- transcripts(txdb, columns = c("tx_id", "gene_id")) ## values(ans)$gene_id <- ## drop(values(tx_gr)$gene_id)[match(names(ans), ## values(tx_gr)$tx_id)] ## tx <- ans ## ## wh <- aldoa_range ## ## aldoa_vals <- values(aldoa_gr) ## ## tx <- multisplit(aldoa_gr, aldoa_vals$tx_id) ## ## tx_to_val <- match(names(tx), unlist(aldoa_vals$tx_id)) ## ## values(tx)$gene_id <- ## ## rep(unlist(aldoa_vals$gene_id), ## ## elementNROWS(aldoa_vals$tx_id))[tx_to_val] ## ## values(tx)$tx_id <- names(tx) ## } ## message("Parsing bam files") ## bamFiles <- Rsamtools::BamFileList(files) ## message("Analysing...") ## introns <- elementGaps(tx) ## introns_flat <- unlist(introns, use.names = FALSE) ## tx_keys <- gr2key(introns_flat) ## readReadRanges <- function(bam) { ## param <- ScanBamParam(tag = "XS", which = aldoa_range) ## ga <- readGAlignments(path(bam), ## use.names = TRUE, ## param = param) ## reads <- grglist(ga) ## metadata(reads)$bamfile <- bam ## splices <- elementGaps(reads) ## values(splices)$XS <- values(reads)$XS ## pairs <- pairReadRanges(reads) ## pairs <- strandFromXS(pairs) ## splices <- pairReadRanges(splices) ## splices <- strandFromXS(splices) ## values(pairs)$splices <- splices ## pairs ## } ## N <- length(bamFiles) ## nms <- names(bamFiles) ## lst_hits <- lst_counts <- lst_splices <- lst_rr <- list() ## message("parsing hits/counts/splcies") ## for(i in 1:N){ ## bf <- bamFiles[[i]] ## rr <- readReadRanges(bf) ## lst_rr <- c(lst_rr, rr) ## hits.lst <- findIsoformOverlaps(rr) ## lst_hits <- c(lst_hits, hits.lst$hits) ## lst_counts <- c(lst_counts, countIsoformHits(hits.lst$hits, hits.lst$compatible, hits.lst$strand_specific)) ## lst_splices <- c(lst_splices, summarizeSplices(rr)) ## } ## names(lst_hits) <- nms ## names(lst_counts) <- nms ## names(lst_splices) <- nms ## names(lst_rr) <- nms ## ## normal <- readReadRanges(bamFiles) ## ## tumor <- readReadRanges(bamFiles$tumor) ## ## normal_hits <- findIsoformOverlaps(normal) ## ## normal_counts <- countIsoformHits(normal_hits) ## ## normal_splices <- summarizeSplices(normal) ## ## tumor_hits <- findIsoformOverlaps(tumor) ## ## tumor_counts <- countIsoformHits(tumor_hits) ## ## tumor_splices <- summarizeSplices(tumor) ## ################################################### ## ### code chunk number 39: combine-samples ## ################################################### ## assays <- do.call(mapply, c(list(cbind), lst_counts, list(SIMPLIFY = FALSE))) ## ## assays <- mapply(cbind, normal_counts, SIMPLIFY = FALSE) ## ## assays <- mapply(cbind, normal_counts, tumor_counts, ## ## SIMPLIFY = FALSE) ## colData <- DataFrame(tumorStatus = names(bamFiles)) ## rownames(colData) <- colData$tumorStatus ## se <- SummarizedExperiment(assays, tx, colData) ## ################################################### ## ### code chunk number 40: order-se ## ################################################### ## uc <- assay(se, "unique") ## uc_ord <- order(rowSums(uc), decreasing = TRUE) ## uc_top <- uc[head(uc_ord, 2),] ## ## fisher.test(uc_top)$estimate ## ################################################### ## ### code chunk number 41: get-unique-reads ## ################################################### ## lst_uniq <- lapply(1:N, function(i){ ## getUniqueReads(lst_rr[[i]], lst_hits[[i]]) ## }) ## names(lst_uniq) <- nms ## ## normal_uniq <- getUniqueReads(normal, normal_hits) ## ## tumor_uniq <- getUniqueReads(tumor, tumor_hits) ## both_uniq <- do.call(mstack, lapply(lst_uniq, unlist)) ## ################################################### ## ### code chunk number 42: combine-splices ## ################################################### ## lst_uniq_splices <- lapply(lst_uniq, summarizeSplices) ## names(lst_uniq_splices) <- nms ## uniq_splices <- do.call(mstack, lst_uniq_splices) ## all_splices <- do.call(mstack, lst_splices) ## novel_splices <- all_splices[values(all_splices)$novel] ## ## novel_splices <- all_splices[values(all_splices)$novel & ## ## values(all_splices)$score == 9] ## ## novel_splices <- all_splices[values(all_splices)$novel & ## ## values(all_splices)$score == 9] ## ## uniq_novel_splices <- c(uniq_splices, novel_splices) ## ## uniq_novel_splices <- c(uniq_splices, all_splices) ## uniq_novel_splices <- c(uniq_splices, novel_splices) ## both_uniq <- keepSeqlevels(both_uniq, unique(as.character(seqnames(both_uniq)))) ## .wt <- max(width(uniq_novel_splices))/max(coverage(both_uniq)) * weight ## .wt <- as.numeric(.wt) ## aes.res <- do.call(aes,list(size = substitute(score), ## height = substitute(width/.wt, list(.wt = .wt)), ## color = substitute(novel))) ## message("Constructing splicing graphics....") ## p.novel <- do.call(geom_arch, c(list(data = uniq_novel_splices, ## ylab = "coverage", ## rect.height = 0), list(aes.res))) ## p.s <- ggplot() + p.novel + do.call(stat_coverage, list(data = both_uniq, facets = name~.)) ## message("Constructing gene model....") ## if(length(txdb.chr.pre)) ## wh <- GRanges(gsub(txdb.chr.pre, "", as.character(seqnames(wh))), ## ranges(wh)) ## ## browser() ## tx_un <- stack(tx, ".sample") ## tx_cur <- keepSeqlevels(tx_un, unique(as.character(seqnames(tx_un)))) ## tx_cur <- tx_cur[, setdiff(colnames(values(tx_cur)), c("tx_id", "gene_id"))] ## tx_cur <- split(tx_cur, values(tx_cur)$.sample) ## tx_track <- do.call(autoplot, list(object = tx_cur, geom = "alignment", ylab = "")) ## ## tx_track <- autoplot(tx_16, geom = "alignment", ylab = "") ## ## tx_track <- do.call(autoplot, list(object = txdb, which = wh)) ## if(missing(xlim)) ## xlim <- c(start(wh), end(wh)) ## tracks(p.s, tx_track, xlim = xlim, heights = c(3, 1)) ## } biovizBase/R/transform.R0000644000175200017520000005712214136047676016255 0ustar00biocbuildbiocbuild## rules ## 1. add coord into metadata ## 2. never revise oringal ## 3. treak with labels setGeneric("transformToGenome", function(data, ...) standardGeneric("transformToGenome")) setMethod("transformToGenome", "GRanges", function(data, space.skip = 0.1, chr.weight = NULL){ seqs.l <- seqlengths(data) if(all(!is.na(seqs.l))){ chr.l <- seqs.l seqs.suml <- sum(as.numeric(seqs.l)) }else{ ## if no seqlengths are found, use data range chr.l <- max(end(split(data, seqnames(data)))) seqs.suml <- sum(as.numeric(chr.l)) } chr.l0 <- chr.l N <- length(chr.l) .start <- start(data) .end <- end(data) ## proportion specified for certain chromosomes if(!is.null(chr.weight)){ if(any(!is.numeric(chr.weight))) stop("chr.weight must be a vector of numeric values.") if(sum(chr.weight) > 1) stop("sum of chr.weight must be equal or less than 1.") if(length(chr.weight) <= N){ if(!all(names(chr.weight) %in% names(chr.l))) stop("chr.weight names must be a subset of seqinfo chromosome names") if(length(chr.weight) < N){ .chrs <- setdiff(names(chr.l), names(chr.weight)) .w <- chr.l[.chrs]/sum(as.numeric(chr.l[.chrs])) * (1 - sum(chr.weight)) names(.w) <- .chrs chr.weight <- c(chr.weight, .w) } }else{ stop("length of chr.weight cannot exceed length of seqinfo") } chr.l <- seqs.suml * chr.weight .start <- .start/chr.l0[as.character(seqnames(data))] * chr.l[as.character(seqnames(data))] .end <- .end/chr.l0[as.character(seqnames(data))] * chr.l[as.character(seqnames(data))] } chr.l.back <- chr.l space.skip <- space.skip * seqs.suml skps <- space.skip * ((1:length(seqs.l))-1) names(skps) <- names(seqlengths(data)) nms <- names(chr.l) chr.l <- cumsum(as.numeric(chr.l)) chr.l2 <- c(0, chr.l[-length(chr.l)]) .breaks <- chr.l2 + chr.l.back/2 + skps names(.breaks) <- nms names(chr.l2) <- nms sts.new <- .start + skps[as.character(seqnames(data))] + chr.l2[as.character(seqnames(data))] ed.new <- .end + skps[as.character(seqnames(data))] + chr.l2[as.character(seqnames(data))] max.chr <- rev(names(chr.l2))[1] x.max <- chr.l.back[max.chr] + skps[max.chr] + chr.l2[max.chr] + space.skip names(x.max) <- "genome" metadata(data)$breaks <- .breaks metadata(data)$labels <- names(.breaks) values(data)$.start <- round(sts.new) values(data)$.end <- round(ed.new) metadata(data)$space.skip <- space.skip metadata(data)$coord <- "genome" metadata(data)$x.max <- x.max data }) setMethod("transformToGenome", "GRangesList", function(data, space.skip = 0.1, chr.weight = NULL){ obj <- stack(data, ".group") obj <- transformToGenome(obj, space.skip = space.skip, chr.weight = NULL) obj }) is_coord_genome <- function(data){ if(!is.null(metadata(data)$coord)){ res <- metadata(data)$coord == "genome" }else{ res <- FALSE } res } rescaleGr <- function(gr, maxSize = 1e8){ if(!is_coord_genome(gr)) stop("must pass a GRanges of coord genome") x.max <- metadata(gr)$x.max if(x.max > maxSize){ values(gr)$.rescale.idx <- 1:length(gr) gr <- gr[order(values(gr)$.start),] .breaks <- metadata(gr)$breaks metadata(gr)$rescale <- TRUE .v <- rescale(c(1, .breaks, values(gr)$.start, values(gr)$.end), to = c(1, maxSize)) .breaks <- .v[2:(1 + length(.breaks))] .v <- .v[-(1:(1+length(.breaks)))] N <- length(.v) res <- GRanges(seqnames(gr), IRanges(start = .v[1:(N/2)], end = .v[(N/2+1):N])) values(res) <- values(gr) ## res <- sort(res) metadata(res) <- metadata(gr) metadata(res)$breaks <- .breaks res <- res[order(values(res)$.rescale.idx)] }else{ res <- GRanges(seqnames(gr), IRanges(start = values(gr)$.start, end = values(gr)$.end)) values(res) <- values(gr) metadata(res) <- metadata(gr) } res } ## then need a transformation to circlular view ## data is a GRanges dataect transformToCircle <- function(data, x = NULL, y = NULL, ylim = NULL, radius = 10, trackWidth =10, direction = c("clockwise", "anticlockwise"), mul = 0.05){ if(!".midpoint" %in% colnames(values(data))) values(data)$.midpoint <- (values(data)$.start + values(data)$.end)/2 if(!length(y)){ values(data)$.circle.equal.y <- 1 y <- as.character(".circle.equal.y") ## stop("y is missing") }else if(!is.character(y) && !is.numeric(y)){ stop("y must be character or numeric") } if(!length(x)){ x <- ".midpoint" }else{ if(x == "midpoint" & (!"midpoint" %in% colnames(values(data)))) x <- ".midpoint" } if(length(ylim)){ idx <- values(data)[,y] <= max(ylim) & values(data)[,y] >= min(ylim) data <- data[idx] } temp.x <- values(data)[,x] if(is.character(y)) temp.y <- values(data)[,y] if(is.numeric(y)){ temp.y <- y } if(length(ylim)) temp.y.r <- expand_range(ylim, mul = mul) else temp.y.r <- expand_range(range(temp.y), mul = mul) temp.y <- (temp.y - min(temp.y.r))/diff(temp.y.r) * trackWidth + radius ## always from 1 to max direction <- match.arg(direction) if(direction == "clockwise") dir <- 1 else dir <- -1 ## need to use max of "ideo" if(is_coord_genome(data)){ x.max <- metadata(data)$x.max }else{ x.max <- max(end(data)) } angle.unit <- pi* 2/ x.max x.new <- temp.y * sin(angle.unit * (temp.x - 1) * dir) y.new <- temp.y * cos(angle.unit * (temp.x - 1)* dir) values(data)$.circle.x <- x.new values(data)$.circle.y <- y.new values(data)$.circle.angle <- angle.unit * (temp.x-1) * dir data } ## interpolate segment or rectangle ## rectangle only use stepping as y transformToRectInCircle <- function(data, y = NULL, space.skip = 0.1, trackWidth = 10, radius = 10, direction = c("clockwise", "anticlockwise"), n = 100, mul = 0.05, chr.weight = NULL){ if(is_coord_genome(data)) x.max <- values(data)$x.max else x.max <- max(end(data)) x.unit <- x.max/n direction <- match.arg(direction) data.back <- data ## need to consider the space if(length(y)){ temp.y <- as.character(values(data)[,as.character(y)]) if(is.character(temp.y)){ temp.y <- as.numeric(as.factor((temp.y))) } if(!all(check.integer(temp.y))) stop("geom(bar) require specified 'y', must be integer which indicates the levels") values(data)$stepping <- temp.y }else{ values(data)$stepping <- disjointBins(data, ignore.strand = TRUE) } names(data) <- NULL df <- as.data.frame(data) lst <- lapply(1:nrow(df), function(i){ if(df[i,"width"] > 1){ .n <- round(df[i, "width"]/x.unit) if(.n< 5) .n <- 5 inter.fun <- function(x, y) approx(x, y, n = .n) res.x <- as.integer(inter.fun(c(df[i,"start"], df[i,"end"]), c(0, 0))$x) }else{ res.x <- c(df[i, "start"], df[i, "start"]) } res <- data.frame(.biovizBase.new.x = c(res.x, rev(res.x))) N <- nrow(res) res$.biovizBase.group <- i res$.biovizBase.level <- c(rep(df[i, "stepping"] - 0.4, N/2), rep(df[i, "stepping"] + 0.4, N/2)) res <- suppressWarnings(cbind(res, df[i,])) res$.int.id <- seq_len(nrow(res)) res }) res <- do.call("rbind", lst) .y <- ".biovizBase.level" res.gr <- GRanges(res$seqnames, IRanges(start = res$.biovizBase.new.x, width = 1), strand = res$strand) values(res.gr) <- subset(res, select = -c(start, end, width, strand,seqnames)) seqlengths(res.gr) <- seqlengths(data) res <- transformToGenome(res.gr, space.skip = space.skip, chr.weight = chr.weight) res <- transformToCircle(res, y = .y, radius = radius, trackWidth = trackWidth, direction = direction, mul = mul) res } transformToBarInCircle <- function(data, y = NULL, space.skip = 0.1, trackWidth = 10, radius = 10, direction = c("clockwise", "anticlockwise"), n = 100, mul = 0.05, chr.weight = NULL){ if(is_coord_genome(data)) x.max <- values(data)$x.max else x.max <- max(end(data)) x.unit <- x.max/n direction <- match.arg(direction) data.back <- data ## need to consider the space if(length(y)){ values(data)$stepping <- values(data)[, as.character(y)] }else{ if("score" %in% colnames(values(data))){ message("use 'score' for default y, or you can specify it in aes()") values(data)$stepping <- values(data)$score }else{ stop("please provide aes(y = ), or use 'score' as column") } } names(data) <- NULL df <- as.data.frame(data) lst <- lapply(1:nrow(df), function(i){ if(df[i,"width"] > 1){ .n <- round(df[i, "width"]/x.unit) if(.n< 5) .n <- 5 inter.fun <- function(x, y) approx(x, y, n = .n) res.x <- as.integer(inter.fun(c(df[i,"start"], df[i,"end"]), c(0, 0))$x) }else{ res.x <- c(df[i, "start"], df[i, "start"]) } res <- data.frame(.biovizBase.new.x = c(res.x, rev(res.x))) N <- nrow(res) res$.biovizBase.group <- i res$.biovizBase.new <- c(rep(0, N/2), rep(df[i, "stepping"], N/2)) res <- suppressWarnings(cbind(res, df[i,])) res$.int.id <- seq_len(nrow(res)) res }) res <- do.call("rbind", lst) .y <- ".biovizBase.new" res.gr <- GRanges(res$seqnames, IRanges(start = res$.biovizBase.new.x, width = 1), strand = res$strand) values(res.gr) <- subset(res, select = -c(start, end, width, strand,seqnames)) seqlengths(res.gr) <- seqlengths(data) res <- transformToGenome(res.gr, space.skip = space.skip, chr.weight = chr.weight) res <- transformToCircle(res, y = .y, radius = radius, trackWidth = trackWidth, direction = direction, mul = mul) res } ## ok, segment allow user to use a flexible y transformToSegInCircle <- function(data, y = NULL, space.skip = 0.1, trackWidth = 10, radius = 10, direction = c("clockwise", "anticlockwise"), n = 100, chr.weight = NULL){ if(is_coord_genome(data)) x.max <- values(data)$x.max else x.max <- max(end(data)) x.unit <- x.max/n direction <- match.arg(direction) ## do the linear interpolatoin first if(!length(y)){ values(data)$stepping <- disjointBins(ranges(data)) } names(data) <- NULL df <- as.data.frame(data) lst <- lapply(1:nrow(df), function(i){ if(df[i,"width"] > 1){ .n <- round(df[i, "width"]/x.unit) if(.n< 5) .n <- 5 inter.fun <- function(x, y) approx(x, y, n = .n) res.x <- as.integer(inter.fun(c(df[i,"start"], df[i,"end"]), c(0, 0))$x) }else{ res.x <- c(df[i, "start"], df[i, "start"]) } res <- data.frame(.biovizBase.new.x = res.x) res$.biovizBase.group <- i if(!length(y)){ res$.biovizBase.level <- df[i, "stepping"] } N <- nrow(res) df.extra <- do.call("rbind", lapply(1:N, function(k) df[i,])) res <- cbind(res, df.extra) }) res <- do.call("rbind", lst) if(!length(y)) .y <- ".biovizBase.level" else .y <- as.character(y) res.gr <- GRanges(res$seqnames, IRanges(start = res$.biovizBase.new.x, width = 1), strand = res$strand) values(res.gr) <- subset(res, select = -c(start, end, width, strand,seqnames)) seqlengths(res.gr) <- seqlengths(data) res <- transformToGenome(res.gr, space.skip, chr.weight = chr.weight) res <- transformToCircle(res, y = .y, radius = radius, trackWidth =trackWidth, direction = direction) res } transformToSegInCircle2 <- function(data, y = NULL, space.skip = 0.1, trackWidth = 10, radius = 10, direction = c("clockwise", "anticlockwise"), n = 100, mul = 0.05, chr.weight = NULL){ if(is_coord_genome(data)) x.max <- values(data)$x.max else x.max <- max(end(data)) x.unit <- x.max/n direction <- match.arg(direction) data.back <- data ## need to consider the space if(length(y)){ temp.y <- as.character(values(data)[,as.character(y)]) if(is.character(temp.y)){ temp.y <- as.numeric(as.factor((temp.y))) } if(!all(check.integer(temp.y))) stop("geom(bar) require specified 'y', must be integer which indicates the levels") values(data)$stepping <- temp.y }else{ values(data)$stepping <- disjointBins(data, ignore.strand = TRUE) } names(data) <- NULL df <- as.data.frame(data) lst <- lapply(1:nrow(df), function(i){ if(df[i,"width"] > 1){ res.x <- c((df[i, "start"] + df[i, "end"])/2, (df[i, "start"] + df[i, "end"])/2) }else{ res.x <- c(df[i, "start"], df[i, "start"]) } res <- data.frame(.biovizBase.new.x = res.x) N <- nrow(res) res$.biovizBase.group <- i res$.biovizBase.level <- c(df[i, "stepping"] - 0.4, df[i, "stepping"] + 0.4) res <- suppressWarnings(cbind(res, df[i,])) res$.int.id <- seq_len(nrow(res)) res }) res <- do.call("rbind", lst) .y <- ".biovizBase.level" res.gr <- GRanges(res$seqnames, IRanges(start = res$.biovizBase.new.x, width = 1), strand = res$strand) values(res.gr) <- subset(res, select = -c(start, end, width, strand,seqnames)) seqlengths(res.gr) <- seqlengths(data) res <- transformToGenome(res.gr, space.skip = space.skip, chr.weight = chr.weight) res <- transformToCircle(res, y = .y, radius = radius, trackWidth = trackWidth, direction = direction, mul = mul) res } ## for a special GRanges transformToLinkInCircle <- function(data, linked.to, space.skip = 0.1, trackWidth = 10, radius = 10, link.fun = function(x, y, n = 100) bezier(x, y, evaluation = n), direction = c("clockwise", "anticlockwise"), chr.weight = NULL){ direction <- match.arg(direction) if(missing(linked.to)) stop("linked.to must be provided and be a GRanges") ## trace id N <- length(data) values(data)$.biovizBase.idx <- 1:N values(values(data)[, linked.to])$.biovizBase.idx <- 1:N obj <- transformToGenome(data, space.skip, chr.weight = chr.weight) obj <- transformToCircle(obj, y = 0, radius = radius, trackWidth =trackWidth, direction = direction) obj <- obj[order(values(obj)$.biovizBase.idx)] names(obj) <- NULL df <- as.data.frame(obj) linktodata <- values(data)[,linked.to] ## missing y linktodata <- transformToGenome(linktodata, space.skip, chr.weight = chr.weight) ## keep order linktodata <- transformToCircle(linktodata, radius = radius, y = 0, trackWidth =trackWidth, direction = direction) linktodata <- linktodata[order(values(linktodata)$.biovizBase.idx)] linkdf <- as.data.frame(linktodata) extra.df <- subset(df, select = -c(.circle.x, .circle.y)) linkdf2 <- data.frame(from.x = df$.circle.x, from.y = df$.circle.y, to.x = linkdf$.circle.x, to.y = linkdf$.circle.y) linkdf2 <- cbind(linkdf2, extra.df) lst <- lapply(1:nrow(linkdf2), function(i){ ndf <- link.fun(c(linkdf2[i, "from.x"],0,linkdf2[i,"to.x"]), c(linkdf2[i, "from.y"],0,linkdf2[i,"to.y"])) ndf <- as.data.frame(do.call("cbind", ndf)) N <- nrow(ndf) ndf$.biovizBase.group <- i ## need to past other meta data extra.df <- subset(linkdf2[i,], select = -c(from.x, from.y, to.x, to.y)) extra.df2 <- do.call("rbind", lapply(1:N, function(i) extra.df)) ndf <- cbind(ndf, extra.df2) }) res <- do.call("rbind", lst) res } ## ddplyFun <- function(data, .fun, ..., window = 1e5){ ## grl <- split(data, seqnames(data)) ## idx <- elementNROWS(grl) > 0 ## grl <- endoapply(grl[idx], function(gr){ ## ## let's make it more works for multiple seqnames ## bks <- seq(1, max(end(gr)), by = window) ## N <- length(bks) ## seqn <- unique(seqnames(gr)) ## if(length(seq) > 1) ## stop("Multiple seqnames found") ## if(!N%%2){ ## qgr <- GRanges(seqn, IRanges(start = bks[1:(N-1)], ## end = bks[2:N])) ## }else{ ## bks <- c(bks, max(end(gr))) ## N <- length(bks) ## qgr <- GRanges(seqn, IRanges(start = bks[1:(N-1)], ## end = bks[2:N])) ## } ## if(max(end(qgr)) < max(end(gr))){ ## qgr <- c(qgr, GRanges(seqn, IRanges(max(end(qgr))+ 1, ## max(end(gr))))) ## } ## of <- findOverlaps(gr, qgr, select = "first") ## idx <- !is.na(of) ## df <- as.data.frame(gr[idx]) ## df$of <- of[idx] ## resdf <- plyr::ddply(df, .(of), .fun, ...) ## idx <- as.numeric(resdf$of) ## ## idx <- idx[!is.na(idx)] ## res <- qgr[idx] ## values(res) <- as.data.frame(resdf[,2]) ## res ## }) ## res <- unlist(grl[!is.null(grl)]) ## names(res) <- NULL ## sort(res) ## } setGeneric("transformToDf", function(data, ...) standardGeneric("transformToDf")) ## setMethod("transformToDf", c("eSet"), function(model, data){ ## object <- model ## pdata <- phenoData(object) ## df <- as(object, "data.frame") ## df$sampleNames <- row.names(df) ## df.m <- melt(df, id.vars = c(varLabels(pdata), "sampleNames")) ## df.m ## }) setMethod("transformToDf", c("GRanges"), function(data){ vals <- values(data) if(length(vals)){ idx <- !unlist(lapply(vals@listData, function(x) is(x, "List") & !is(x, "DNAStringSet"))) if(sum(!idx)) warning(colnames(vals)[!idx], " column has been dropped for the reason that the corecion of class List is not supported") df <- as.data.frame(data[,idx]) }else{ df <- as.data.frame(data) } df$midpoint <- (df$start+df$end)/2 df }) transformDfToGr <- function(data, seqnames = NULL, start = NULL, end = NULL, width = NULL, strand = NULL, to.seqnames = NULL, to.start = NULL, to.end = NULL, to.width = NULL, to.strand = NULL, linked.to = "to.gr"){ ## this losing seqinfo.... colnms <- colnames(data) if(is.null(seqnames)){ if("seqnames" %in% colnms) seqnames <- "seqnames" else stop("Please sepicify which column represent the seqnames") } seqnames <- data[, seqnames] if(length(c(start, end, width)) <2){ stop("Pleaase sepeicfy two of start/end/width") } if(is.null(end)){ if("end" %in% colnms) end <- data[,"end"] }else{ end <- data[, end] } if(is.null(start)){ if("start" %in% colnms) start <- data[,"start"] }else{ start <- data[, start] } if(is.null(width)){ if("width" %in% colnms) width <- data[,"width"] }else{ width <- data[, width] } gr <- GRanges(as.character(seqnames), IRanges(start = start, width = width, end = end)) if(is.null(strand)){ if("strand" %in% colnms){ strand <- data[, "strand"] strand(gr) <- strand }}else{ strand(gr) <- data[, strand] } values(gr) <- data[,!colnames(data) %in% c(start, end, width, seqnames, strand)] ## linked ranges if(!is.null(to.seqnames)){ message("try to creating a linked GRanges as column to.gr") if(length(c(to.start, to.end, to.width)) > 1){ if(is.null(to.end)){ if("to.end" %in% colnms) to.end <- data[,"to.end"] }else{ to.end <- data[, to.end] } if(is.null(to.start)){ if("to.start" %in% colnms) to.start <- data[,"to.start"] }else{ to.start <- data[, to.start] } if(is.null(width)){ if("to.width" %in% colnms) to.width <- data[,"to.width"] }else{ to.width <- data[, to.width] } to.gr <- GRanges(seqnames = as.character(data[,to.seqnames]), IRanges(start = to.start, end = to.end, width = to.width)) if(!is.null(to.strand)) strand(to.gr) <- data[,to.strand] values(gr)[,linked.to] <- to.gr } } gr } check.integer <- function(x){ sapply(x, function(x) !length(grep("[^[:digit:]]", as.character(x)))) } ## retrun a new GRanges, with new coord transformGRangesForEvenSpace <- function(gr){ st <- start(range(gr)) ed <- end(range(gr)) wd <- width(range(gr)) N <- length(gr) wid <- wd/N x.new <- st + wid/2 + (1:N - 1) * wid values(gr)$x.new <- x.new metadata(gr)$coord <- "even" gr } transformToEven <- function(data){ st <- start(range(data)) ed <- end(range(data)) wd <- width(range(data)) N <- length(data) wid <- wd/N x.new <- st + wid/2 + (1:N - 1) * wid gr <- GRanges(start = x.new, width = wid) values(gr) <- values(data) ## values(gr)$x.new <- x.new values(gr)$.ori <- data metadata(gr)$coord <- "even" data } ## setGeneric("transform") ## setMethod("transform", "GRanges", function(_data, space.skip = 0.1, ## maxSize = 1e9, ## max.gap = 1L, ## method = c("genome", ## "truncate_gap", ## "even")){ ## method <- match.arg(method) ## obj <- switch(method, ## genome = { ## transformToGenome(_data, space.skip = space.skip) ## }, ## truncate_gaps = { ## }, ## even = { ## transformToEven(_data, space.skip = space.skip) ## }) ## } ## autoplot(gr, layout = "circle", geom = "ideo", rect.inter.n = 10, space.skip = 0.2, ## aes(fill = .ori.seqnames)) ## autoplot(gr, coord = "genome") ## autoplot(gr, layout = "circle",space.skip = 0.2, geom = "bar", grid = TRUE) ## gr2 <- transformToGenome(gr, space.skip = 0) ## gr2 ## metadata(gr2)$coord <- NULL ## autoplot(gr2) setGeneric("transformToArch", function(data, ...) standardGeneric("transformToArch")) setMethod("transformToArch", "GRanges", function(data, width = 1){ grl <- split(data, 1:length(data)) grl <- endoapply(grl, function(gr){ sts <- c(start(gr)-width, end(gr)) res <- GRanges(seqnames(gr), IRanges(sts, width = width)) values(res) <- values(gr)[c(1, 1),] seqlengths(res) <- seqlengths(gr) res }) grl }) setMethod("transformToArch", "GRangesList", function(data, width = 1){ coord <- metadata(data)$coord res <- unlist(endoapply(data, function(gr){ gps <- gaps(gr, start = min(start(gr)), end = max(end(gr))) gps <- gps[strand(gps) == "*"] values(gps) <- values(gr[1,]) gps })) metadata(res)$coord <- coord res }) ## ## coord ## library(GenomicRanges) ## gr1 <- GRanges("chr1", IRanges(start = 1:10, width = 5)) ## gr2 <- GRanges("chr1", IRanges(start = 100:110, width = 5)) ## gr3 <- GRanges("chr1", IRanges(start = 200:210, width = 5)) ## grl <- GenomicRangesList(gr1, gr2, gr3) ## setGeneric("transformToOrigin", function(data, ...) standardGeneric("transformToOrigin")) ## setMethod("transformToOrigin", "GRanges", function(data, ...){ ## ori <- metadata(gr)$origin ## if(is.null(ori)) ## ori <- 1 ## values(gr)$.ori <- data ## metadata(gr)$coord <- "even" ## }) ## setMethod("transformToOrigin", "GenomicRangesList", function(data, ...){ ## values(gr)$.ori <- data ## metadata(gr)$coord <- "even" ## }) biovizBase/R/utils.R0000644000175200017520000004647614136047676015414 0ustar00biocbuildbiocbuildcontainLetters <- function(obj, all = FALSE){ obj <- as.character(obj) obj <- tolower(obj) obj <- unlist(strsplit(obj,"")) if(!all){ res <- any(obj%in%letters) }else{ res <- all(obj%in%letters) } res } GCcontent <- function(obj, ..., view.width, as.prob = TRUE){ require(BSgenome) seqs <- getSeq(obj, ..., as.character = FALSE) if(missing(view.width)){ res <- letterFrequency(seqs, letters="CG", as.prob = as.prob) }else{ res <- lapply(seqs, function(x) letterFrequencyInSlidingView(x, view.width, letters="CG", as.prob = as.prob)) if(length(res) == 1) res <- unlist(res) } res } centroidPos <- function(obj){ if(!isIdeogram(obj)) stop("Please pass an ideogram, please check function getIdeogram") obj.s <- split(obj, as.character(seqnames(obj))) lst <- lapply(obj.s,function(x){ arms <- substr(values(x)$name, 1,1) idx <- which(arms == "q")[1] data.frame(x = start(x)[idx], y = 5, seqnames = unique(as.character(seqnames(x)))) }) df <- do.call(rbind, lst) df } ## ## utils to generate pair-end pspanGR <- function(file, region, sameChr = TRUE, isize.cutoff = 170){ ## FIXME: move unmated? bam <- scanBam(file, param=ScanBamParam(which = region), flag = scanBamFlag(hasUnmappedMate = FALSE)) bam <- bam[[1]] bamrd <- GRanges(bam$rname, IRanges(bam$pos, width = bam$qwidth), strand = bam$strand, mseqname = bam$mrnm, mstart = bam$mpos, isize = bam$isize) ## why negative?sometime bamrd <- bamrd[abs(bam$isize) >= isize.cutoff] if(sameChr){ idx <- as.character(seqnames(bamrd)) == values(bamrd)$mseqname bamrd <- bamrd[idx] } if(length(bamrd)){ p1 <- GRanges(seqnames(bamrd), ranges(bamrd)) p2 <- GRanges(values(bamrd)$mseqname, IRanges(values(bamrd)$mstart, width = 75)) pspan <- punion(p1, p2, fill.gap = TRUE) pgaps <- pgap(ranges(p1), ranges(p2)) return(list(pspan = pspan, pgaps = pgaps, p1 = p1, p2 = p2)) }else{ return(NULL) } } genSymbols <- function(org){ ## TODO, add gene id if(!is(org, "OrgDb")){ stop("org must be a OrgDb object") } pkg.name <- paste("package", org$packageName, sep = ":") sym.name <- grep("SYMBOL$", ls(pkg.name), value = TRUE) chr.name <- grep("CHR$", ls(pkg.name), value = TRUE) chrloc.name <- grep("CHRLOC$", ls(pkg.name), value = TRUE) chrlocend.name <- grep("CHRLOCEND$", ls(pkg.name), value = TRUE) en.name <- grep("ENSEMBL$", ls(pkg.name), value = TRUE) ## a little hack sym.obj <- eval(as.name(sym.name)) chr.obj <- eval(as.name(chr.name)) chrloc.obj <- eval(as.name(chrloc.name)) chrlocend.obj <- eval(as.name(chrlocend.name)) en.obj <- eval(as.name(en.name)) symbol_id <- mappedRkeys(sym.obj) message("get genen id...") gene_id <- mget(symbol_id, revmap(sym.obj), ifnotfound=NA) gene_id <- unlist2(gene_id) gene_id <- gene_id[!is.na(gene_id)] message("get chromosome information...") chr <- toTable(chr.obj[gene_id]) chrloc <- toTable(chrloc.obj[gene_id]) chrlocend <- toTable(chrlocend.obj[gene_id]) chrs <- chrloc chrs$end_location <- chrlocend$end_location res <- chrs if(sum(duplicated(gene_id))) stop("Duplicated gene_id")# no duplicate idx <- match(res$gene_id, gene_id) res$symbol <- names(gene_id[idx]) if(sum(with(res, start_location > 0 & end_location < 0))) stop("Wierd pattern found") if(sum(with(res, start_location < 0 & end_location > 0))) stop("Wierd pattern found") message("get strand information...") res$sense <- with(res, start_location>=0&end_location>=0) res.sense <- res[res$sense,] res.antisense <- res[!res$sense,] res$strand <- strand(!res$sense) message("get EMSEMBL ID...") ensembl_id <- unlist(mget(gene_id, en.obj)) idx <- match(res$gene_id, names(ensembl_id)) res$ensembl_id <- ensembl_id[idx] message("generating a GRanges object for genen symbols...") genesymbol <- with(res,GRanges(seqnames = paste("chr",Chromosome,sep = ""), IRanges(abs(start_location), abs(end_location)), strand = strand, symbol = symbol, ensembl_id = ensembl_id)) names(genesymbol) <- values(genesymbol)$symbol message("Done") genesymbol } setGeneric("getGaps", function(obj, ...) standardGeneric("getGaps")) setMethod("getGaps", "GRanges", function(obj, group.name = NULL, facets = NULL){ if(!length(obj)) return(GRanges()) if(!length(facets)) facets <- as.formula(~seqnames) allvars.extra <- colnames(mcols(obj)) if(!is.null(group.name)){ if(!group.name %in% colnames(values(obj))) stop(group.name, " is not in obj") grl <- splitByFacets(obj, facets) grl <- endoapply(grl, function(dt){ res <- split(dt, values(dt)[,group.name]) gps <- gaps(ranges(res)) idx <- elementNROWS(gps) > 0 res.sub <- res[idx,] stds <- unlist(lapply(res.sub, function(x) as.character(strand(x))[1])) gps.sub <- gps[idx,] dfs <- values(unlist(res.sub))[cumsum(elementNROWS(res.sub)),c(allvars.extra, "stepping"), drop = FALSE] ir <- unlist(gps.sub) if(length(ir)){ gr <- GRanges(unique(seqnames(dt)), ir) values(gr) <- dfs[togroup(PartitioningByWidth(gps.sub)),, drop = FALSE] strand(gr) <- stds[togroup(PartitioningByWidth(gps.sub))] }else{ gr <- GRanges() } gr }) res <- unlist(grl) }else{ } if(length(res)){ values(res)$type <- "gaps" res <- resize(res, width = width(res) + 2, fix = "center") }else{ GRanges() } res }) getIdeoGR <- function(gr){ if(!is(gr, "GenomicRanges")) stop("require GenomicRanges") if(all(is.na(seqlengths(gr)))){ warning("geom(ideogram) need valid seqlengths information for accurate mapping, now use reduced information as ideogram... ") res <- range(reduce(gr, ignore = TRUE)) start(res) <- 1 res }else{ res <- as(seqinfo(gr), "GenomicRanges") } res } ## get major/mionr scale, y value, major text? getScale <- function(gr, unit = NULL, n = 100, type = c("M", "B", "sci")){ type <- match.arg(type) if(is.null(unit)){ unit <- sum(as.numeric(width(gr)))/n unit <- 10^floor(log10(unit)) } ## not like normal scale res <- split(gr, seqnames(gr)) grl <- endoapply(res, function(gr){ st <- 1 ed <- end(gr) major.pos <- seq(st, ed, by = 5*unit) minor.pos <- seq(st, ed, by = unit) minor.pos <- setdiff(minor.pos, major.pos) if(type == "M"){ texts <- c(paste(as.character(round(major.pos/1e6, digits = 1)), "M", sep = ""), rep("", length(minor.pos))) } if(type == "B"){ texts <- c(paste(as.character(round(major.pos/1e9, digits = 1)), "B", sep = ""), rep("", length(minor.pos))) } if(type == "sci"){ texts <- c(as.character(format(major.pos, scientific = TRUE, digit = 1)), rep("", length(minor.pos))) } GRanges(seqnames(gr), IRanges(start = c(major.pos, minor.pos), width = 1), type = c(rep("major", length(major.pos)), rep("minor", length(minor.pos))), scale.y = c(rep(3, length(major.pos)), rep(1, length(minor.pos))), text.major = texts) }) res <- unlist(grl) seqlengths(res) <- seqlengths(gr) res } getFormalNames <- function(..., remove.dots = TRUE){ res <- lapply(list(...), function(fun){ if(is.function(fun)){ res <- names(formals(fun)) if(remove.dots) res <- res[ res != "..."] res }else{ stop("arguments passed to getFormalNames must be functions") } }) res <- unlist(res) res <- res[!duplicated(res)] res } subsetArgsByFormals <- function(args, ..., remove.dots = TRUE){ .formals <- getFormalNames(..., remove.dots = remove.dots) res <- args[names(args) %in% .formals] res } flatGrl <- function(object, indName = "grl_name"){ idx <- togroup(PartitioningByWidth(object)) gr <- stack(object, indName) values(gr) <- cbind(values(gr), values(object)[idx,,drop = FALSE]) gr } ## test heterogeneity is_homo <- function(grl){ all(unlist(lapply(grl, function(gr){ length(unique(as.character(seqnames(gr)))) == 1 }))) } genGenesymbolTable <- function(db, keys, keytype = "SYMBOL", columns = c("CHR", "CHRLOC", "CHRLOCEND", "SYMBOL"), unique = TRUE){ res <- select(db, keys = keys, keytype = keytype, columns = columns) chr <- res[, "CHR"] s <- substr(res[, "CHRLOC"], 1, 1) s[s != "-"] <- "+" st <- as.numeric(substr(res[, "CHRLOC"], 2, nchar(res[, "CHRLOC"]))) ed <- as.numeric(substr(res[, "CHRLOCEND"], 2, nchar(res[, "CHRLOCEND"]))) sym <- res[, "SYMBOL"] res.gr <- GRanges(chr, IRanges(start = st, end = ed), strand = s, symbol = sym) if(unique){ res.gr.l <- split(res.gr, sym) syms <- sapply(res.gr.l, function(x) unique(x$symbol)) res.gr.l <- range(res.gr.l) res.gr <- unlist(res.gr.l) names(res.gr) <- syms } res.gr } ## setGeneric("fetch", function(obj, ...) standardGeneric("fetch")) fetch <- function(obj, which, ..., gene.id, truncate.gaps = FALSE, truncate.fun = NULL, ratio = 0.0025, resize.extra = 10, include.level = TRUE, use.names = TRUE, columns = c("tx_id", "tx_name","gene_id"), type = c("all", "single", "exons.reduce", "exons.all", "exons.geneid", "gapped.pair", "raw", "all")){ .txdb.type <- c("all", "single", "exons.reduce", "exons.all", "exons.geneid") .bamfile.type <- c("gapped.pair", "raw", "all") ## type <- match.arg(type) if(length(type) >1){ if(is(obj,"TxDb")) type <- "all" if(is(obj,"BamFile")) type <- "gapped.pair" } if(is(obj, "TxDb")){ if(!(type %in% .txdb.type)) stop("type for TxDb must be ", .txdb.type) if(is.list(which)){ message("Parsing exons based on which(list) arguments") temp <- exons(obj, columns = columns, filter = which) which <- range(temp) } ## 1st set all the sequences to be inactive: isActiveSeq(obj)[seqlevels(obj)] <- FALSE ## Then set only "chr9" to be active: seqnms <- as.character(unique(seqnames(which))) isActiveSeq(obj)[seqnms] <- TRUE ## You can see which are active like this: if(type == "exons.geneid"){ message("return exons within one gene...") ## this require gene id, only exons exons.gene <- exonsBy(obj, by = "gene") if(missing(gene.id)) stop("Please specify the gene id") res <- exons.gene[[as.character(gene.id)]] } if(type == "exons.reduce"){ message("Parsing exons...") exons <- exonsByOverlaps(obj, which, ...) exons <- reduce(exons) values(exons)$type <- "exon" res <- exons } if(type == "exons.all"){ message("Parsing exons...") exons <- exonsByOverlaps(obj, which, ...) values(exons)$type <- "exon" res <- exons } if(type %in% c("all","single")){ message("Parsing exons...") exons <- exonsBy(obj, "tx") message("Parsing cds...") cdss <- cdsBy(obj, "tx") message("Parsing transcripts...") tx <- transcripts(obj, columns = columns) tx <- subsetByOverlaps(tx, which) message("Aggregating...") txids <- values(tx)$tx_id lst <- lapply(txids, function(id){ id <- as.character(id) tx_nm <- values(tx)[values(tx)$tx_id == id, "tx_name"] gene_id <- values(tx)[values(tx)$tx_id == id, "gene_id"] gene_id <- paste(unlist(gene_id), sep = ",") if(!length(gene_id)) gene_id <- NA exons.cur <- exons[[id]] values(exons.cur) <- data.frame(tx_id = id, tx_name = tx_nm, gene_id = gene_id, type = "exon") cds.cur <- cdss[[id]] seqs <- unique(as.character(seqnames(exons.cur))) exon_union <- reduce(exons.cur) ir.g <- IRanges(gaps(ranges(exons.cur))) if(length(ir.g)){ introns.cur <- GRanges(seqs,ir.g) values(introns.cur) <- data.frame(tx_id = id, tx_name = tx_nm, gene_id = gene_id, type = "intron") }else{ introns.cur <- GRanges() } if(!is.null(cds.cur)){ values(cds.cur) <- data.frame(tx_id = id, tx_name = tx_nm, gene_id = gene_id, type = "cds") cds_union <- reduce(cds.cur) utrs <- setdiff(exon_union, cds_union) if(length(utrs)) values(utrs) <- data.frame(tx_id = id, tx_name = tx_nm, gene_id = gene_id, type = "utr") else utrs <- GRanges() ir.g2 <- gaps(reduce(c(ranges(cds_union), ranges(utrs)))) if(length(ir.g2)){ gaps.cur <- GRanges(seqs,ir.g2) values(gaps.cur) <- data.frame(tx_id = id, tx_name = tx_nm, gene_id = gene_id, type = "gap") }else{ gaps.cur <- GRanges() } gr <- c(exons.cur, introns.cur, cds.cur, gaps.cur, utrs) }else{ utrs <- exons.cur values(utrs)$type <- factor("utr") gaps.cur <- introns.cur if(length(gaps.cur)){ values(gaps.cur)$type <- factor("gap") } gr <- c(exons.cur, introns.cur, utrs, gaps.cur) } gr }) res <- do.call("c", lst) isActiveSeq(obj)[seqlevels(obj)] <- TRUE if(length(res)) res <- keepSeqlevels(res, unique(as.character(seqnames(res)))) else res <- GRanges() } if(type == "single"){ if(length(res)){ cds.s <- reduce(res[values(res)$type == "cds"]) values(cds.s)$type <- factor("cds") exon.s <- reduce(res[values(res)$type == "exon"]) values(exon.s)$type <- factor("exon") utr.s <- setdiff(exon.s, cds.s) values(utr.s)$type <- factor("utr") gap.s <- gaps(cds.s, start = min(start(cds.s)), end = max(end(cds.s))) values(gap.s)$type <- factor("gap") res <- c(cds.s, utr.s, gap.s) } } message("Done") } if(is(obj, "GappedAlignments")){ ## require(Rsamtools) ## require(Rsamtools) if(!missing(which)) obj <- subsetByOverlaps(obj, which) if(!length(obj)) stop("No entry in the GappedAlignments data") if(is.null(names(obj))) stop("Missing qname, please make use.names = TRUE, when reading GappedAlignments") grg <- grglist(obj) grg.u <- stack(grg, ".grl.name") message("extracting information...") values(grg.u)$junction <- rep(ifelse(elementNROWS(grg)>1, TRUE, FALSE), times = elementNROWS(grg)) names(grg.u) <- NULL res <- grg.u } if(is(obj, "BamFile")){ if(!(type %in% .bamfile.type)) stop("type for TxDb must be ", .bamfile.type) ## require(Rsamtools) if(type == "gapped.pair"){ message("Read GappedAlignments from BamFile...") ga <- readGAlignments(obj, param = ScanBamParam(which = which), use.names = use.names, ...) res <- fetch(ga) } if(type == "raw"){ message("Read Raw from BamFile by calling scanBam...") res <- scanBamGRanges(obj, which, ...) } if(type == "all"){ message("Read Raw from BamFile by calling scanBam...") res.mb <- scanBamGRanges(obj, which, flag = scanBamFlag(isFirstMateRead = TRUE)) message("Read GappedAlignments from BamFile...") ga <- readGAlignments(obj, param = ScanBamParam(which = which), use.names = use.names, ...) res.gp <- fetch(ga) message("Combine...") nms <- values(res.mb)$qname ## fow now just, using isize isize <- values(res.mb)$issize names(isize) <- nms values(res.gp)$isize <- isize[values(res.gp)$qname] res <- res.gp } } if(truncate.gaps){ if(is.null(truncate.fun)){ if("gap" %in% unique(values(res)$type)) idx <- values(res)$type %in% c("utr", "cds") res.s <- reduce(res[idx], ignore.strand = TRUE) truncate.fun <- shrinkageFun(gaps(res.s, min(start(res.s)), max(end(res.s))), maxGap(gaps(res.s, min(start(res.s)), max(end(res.s))), ratio = ratio)) } res <- truncate.fun(res) } res } rectifySeqlevelsStyle <- function(x, y) { seqlevelsStyle(x) <- seqlevelsStyle(y) x } .transformSeqinfo <- function(obj){ ss <- seqlengths(obj) res <- GRanges(seqnames(obj), IRanges(start = 1, end = ss)) res <- keepSeqlevels(res, names(ss)) seqlengths(res) <- ss res } biovizBase/R/zzz.R0000644000175200017520000000165314136047676015075 0ustar00biocbuildbiocbuild.onLoad <- function(libname, pkgname){ options(biovizBase = list( DNABasesNColor = getBioColor("DNA_BASES_N", source = "default"), DNABasesColor = getBioColor("DNA_BASES", source = "default"), DNAAlphabetColor = getBioColor("DNA_ALPHABET", source = "default"), RNABasesNColor = getBioColor("RNA_BASES_N", source = "default"), RNABasesColor = getBioColor("RNA_BASES", source = "default"), RNAAlphabetColor = getBioColor("RNA_ALPHABET", source = "default"), IUPACCodeMapColor = getBioColor("IUPAC_CODE_MAP", source = "default"), AminoAcidCodeColor = getBioColor("AMINO_ACID_CODE", source = "default"), AAAlphabetColor = getBioColor("AA_ALPHABET", source = "default"), strandColor = getBioColor("STRAND", source = "default"), cytobandColor = getBioColor("CYTOBAND", source = "default") )) } biovizBase/build/0000755000175200017520000000000014136065665015004 5ustar00biocbuildbiocbuildbiovizBase/build/vignette.rds0000644000175200017520000000035314136065665017344 0ustar00biocbuildbiocbuildmQ 0 n3Av$  ċ ^A`uzɝUIǗ4#XġX6a@!.. 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Two other packages are currently built on this package, a static version of graphics is provided by the package \ggbio{}, and an interactive version of graphics is provided by \visnab{}(Currently not released). In this vignette, we will introduce those color schemes and different utilities functions using simple examples and data sets. Utilities includes functions that precess the raw data, validate names, add attributes, and generate summaries such as fragment length, GC content, and mismatch information. \section{Color Schemes} The \biovizBase{} package aims to provide a set of default color schemes for biological data, based on the following principles. \begin{itemize} \item Make biological sense. Data is displayed in a way that is similar to observed results under the microscope. (Example: giemsa stain results) \item Generate aesthetically pleasing colors based on well-defined color sets like \emph{color brewer} \footnote{\url{http://colorbrewer2.org/}}. Produce the appropriate color for \emph{sequential, diverging, and qualitative} color schemes. \item Accommodate colorblind vision by creating color pallets that pass the color blind check on the \emph{Vischeck} website \footnote{\url{http://www.vischeck.com/}} or use palette from package \Rpackage{dichromat} or use color-blind safe color palette checked by \emph{ColorBrewer} website\footnote{\url{http://colorbrewer2.org/}}. There are three types of colorblind checking strategy defined on these website. \begin{description} \item[Deuteranope] a form of red/green color deficit; \item[Protanope] another form of red/green color deficit; \item[Tritanope] a blue/yellow deficit- very rare. \end{description} \end{itemize} Our color scheme try to pass color-blind checking points to make sure all the users can tell the difference between groups of data displayed. To make the implementation easy, we most time just use \Rpackage{dichromat} to check this, \Rpackage{dichromat} collapses red-green color distinctions to approximate the effect of the two common forms of red/green color blindness, protanopia and deuteranopia. Or we could simply implement proved color-blind safe palette from \Rpackage{dichromat} or \Rpackage{RColorBrewer}. All color schemes have a general color generating function and a default color generating function. They are automatically stored in \Rfunction{options} as default when loading the package. Other packages built on \biovizBase{} can use the default color scheme, ensuring consistent color themes across all static and interactive graphics. Users may also change the default color in the \Rfunction{options} to personalize the global color scheme to fit their needs. @ <>= library(biovizBase) ## library(scales) @ %def \subsection{Colorblind Safe Palette} For graphics, it's important to make sure most people can tell the difference between colors on the plots, even for people with deficient or anomalous red-green vision. We will add more and more colorblind safe palette gradually, now we only supported palettes from two packages, \Rpackage{dichromat} or \Rpackage{RColorBrewer}. However, \Rpackage{RColorBrewer} doesn't provide information about colorblind palette. So we need to check manually on \textit{ColorBrewer} website, and add this information with the palette information. For \Rpackage{dichromat} package, it doesn't have a palette information like \Rcode{brewer.pal.info}, which contains three different types, \textbf{qual, div, seq} representing quality, divergent and sequential respectively, and also missing max colors information, so we integrate all these information and generate three palette information. \begin{itemize} \item \Robject{brewer.pal.blind.info} provides only colorblind safe palette subset. \item \Robject{dichromat.pal.blind.info} provides colorblind safe palette with category information and max color allowed. \item \Robject{blind.pal.info} integrate first two, provides a general palette information with extra column like pal.id, which used for function \Rfunction{colorBlindSafePal} as index for arguments \Rfunarg{palette} or maxcolors for allowed number of color. \textit{pkg} providing information about which package it is defined. \end{itemize} @ <>= head(blind.pal.info) @ %def Then we defined a color generating function \Rfunction{colorBlindSafePal}, this function reading in a palette argument which could be a index number or names for palette defined in \Robject{blind.pal.info}. And return a color generating function, a \Rfunarg{repeatable} argument will control, for number over max color numbers required, does it simply repeat it or just providing limited number of colors. @ <>= ## with no arguments, return blind.pal.info head(colorBlindSafePal()) ## mypalFun <- colorBlindSafePal("Set2") ## mypalFun(12, repeatable = FALSE) #only three mypalFun(11, repeatable = TRUE) #repeat @ %def To Collapses red-green color distinctions to approximate the effect of the two common forms of red- green color blindness, protanopia and deuteranopia, we can use function \Rfunction{dichromat} from package \Rpackage{dichromat}, this save us the time to \begin{figure}[h!t!p!b] \centering @ <>= ## for palette "Paried" mypalFun <- colorBlindSafePal(21) par(mfrow = c(1, 3)) showColor(mypalFun(4)) library(dichromat) showColor(dichromat(mypalFun(4), "deutan")) showColor(dichromat(mypalFun(4), "protan")) @ %def \caption{Checking colors with two common type of color blindness. The first one is normal perception, second one for deuteranopia and last one for protanopia. Since we are using selected color palettes in this package, it should be fine with those types of blindness.} \label{fig:dichromat} \end{figure} We only show this as an examples and won't compare all other color schemes in the following sections. Please notice that \begin{itemize} \item If the categorical data contains many levels like amino acid, people cannot easily tell the difference anyway, we did the trick to simply repeat the colors. This might be useful for many other cases like grand linear view for chromosomes, since if the viewed orders of chromosomes is fixed it's OK to use repeated colors since they are not going to be layout as neighbors anyway. \item For schemes like cytobands, we try to follow the biological sense, in this case, we don't really check the color blindness. \end{itemize} \subsection{Cytobands Color} Chemically staining the metaphase chromosomes results in a alternating dark and light banding pattern, which could provide information about abnormalities for chromosomes. Cytogenetic bands could also provide potential predictions of chromosomal structural characteristics, such as repeat structure content, CpG island density, gene density, and GC content. \biovizBase{} package provides utilities to get ideograms from the UCSC genome browser, as a wrapper around some functionality from \Rpackage{rtracklayer}. It gets the table for \emph{cytoBand} and stores the table for certain species as a \Robject{GRanges} object. We found a color setting scheme in package \Rpackage{geneplotter}, and we implemented it in biovisBase. The function .cytobandColor will return a default color set. You could also get it from \Rfunction{options} after you load \biovizBase{} package. And we recommended function \Rfunction{getBioColor} to get the color vector you want, and names of the color is biological categorical data. This function hides interval color genenerators and also the complexity of getting color from options. You could specify whether you want to get colors by default or from options, in this way, you can temporarily edit colors in options and could change or all the graphics. This give graphics a uniform color scheme. @ <>= getOption("biovizBase")$cytobandColor getBioColor("CYTOBAND") ## differece source from default or options. opts <- getOption("biovizBase") opts$DNABasesNColor[1] <- "red" options(biovizBase = opts) ## get from option(default) getBioColor("DNA_BASES_N") ## get default fixed color getBioColor("DNA_BASES_N", source = "default") seqs <- c("A", "C", "T", "G", "G", "G", "C") ## get colors for a sequence. getBioColor("DNA_BASES_N")[seqs] @ %def You can check the color scheme by calling the \Rfunction{plotColorLegend} function. or the \Rfunction{showColor}. \begin{figure}[h!t!p] \centering @ <>= cols <- getBioColor("CYTOBAND") plotColorLegend(cols, title = "cytoband") @ %def \caption{Legend for cytoband color} \label{fig:cytoband} \end{figure} \subsection{Strand Color} In the \Robject{GRanges} object, we have \Robject{strand} which contains three levels, \textbf{+, -, *}. We are using a qualitative color set from \emph{Color Brewer} and check with \Rpackage{dichromat} as Figure\ref{fig:strand} shows, and we can see that this color set passes all three types of colorblind test. Therefore it should be a safe color set to use to color strand. \begin{figure}[h!t!p] \centering @ <>= par(mfrow = c(1, 3)) cols <- getBioColor("STRAND") showColor(cols) showColor(dichromat(cols, "deutan")) showColor(dichromat(cols, "protan")) @ %def \caption{Colorblind vision check for color of strand} \label{fig:strand} \end{figure} \subsection{Nucleotides Color} We start with the five most used nucleotides, \textbf{A,T,C,G,N}, most genome browsers have their own color scheme to represent nucleotides, We chose our color scheme based on the principles introduced above. Since in genetics, \emph{GC-content} usually has special biological significance because GC pair is bound by three hydrogen bonds instead of two like AT pairs. So it has higher thermostability which could result in different significance, like higher annealing temperature in PCR. So we hope to choose warm colors for \textbf{G,C} and cold colors for \textbf{A,T}, and a color in between to represent \textbf{N}. They are chosen from a diverging color set of \emph{color brewer}. So we should be able to easily tell the GC enriched region. Figure \ref{fig:ne} shows the results from \Rpackage{dichromat}, and we can see this color set passes all two types of the colorblind test. It should be a safe color set to use to color the five most used nucleotides. @ <>= getBioColor("DNA_BASES_N") @ %def \begin{figure}[h!t!p] \centering @ <>= par(mfrow = c(1, 3)) cols <- getBioColor("DNA_BASES_N", "default") showColor(cols, "name") cols.deu <- dichromat(cols, "deutan") names(cols.deu) <- names(cols) cols.pro <- dichromat(cols, "protan") names(cols.pro) <- names(cols) showColor(cols.deu, "name") showColor(cols.pro, "name") @ %def \caption{Colorblind vision check for color of nucleotide} \label{fig:ne} \end{figure} \subsection{Amino Acid Color and Other Schemes} We also include some other color schemes created based on existing object in package \Rpackage{Biostrings} and other customized color scheme. Please notice that the object name is not the same as the name in the options. On the left of \textbf{=}, it's name of object, most of them are defined in \Rpackage{Biostrings} and on the right, it's the name in options. \begin{verbatim} DNA_BASES_N = "DNABasesNColor" DNA_BASES = "DNABasesColor" DNA_ALPHABET = "DNAAlphabetColor" RNA_BASES_N = "RNABasesNColor" RNA_BASES = "RNABasesColor" RNA_ALPHABET = "RNAAlphabetColor" IUPAC_CODE_MAP = "IUPACCodeMapColor" AMINO_ACID_CODE = "AminoAcidCodeColor" AA_ALPHABET = "AAAlphabetColor" STRAND = "strandColor" CYTOBAND = "cytobandColor" \end{verbatim} They all could be retrieved by calling function \Rfunction{getBioColor}. \subsection{Future Schemes} Current color schemes are most generated based on known object in \R{}, which has a clear definition and classification. But we do have more interesting events or biological significance need to be color coded. Like most genome browser, they try to color code many events, for instance, color the insertion size which is larger/smaller than the estimated size; for paired RNA-seq data, we may color the paired reads mapped to a different chromosome. We may include more color coded events in this package in next release. \section{Utilities} \biovizBase{} serves as a basis for the visualization of biological data, especially for genomic data. \Rpackage{IRanges} and \Rpackage{GenomicRanges} are the two most important infrastructure packages to manipulate genomic data. They already have lots of useful and fast utilities for processing genomic data. Some other package such as \Rpackage{rtracklayer}, \Rpackage{Rsamtools}, \Rpackage{ShortRead}, \Rpackage{GenomicFeatures} provide common I/O for certain types of biological data and utilities for processing those raw data. Most of our utilities to be introduced in this section only manipulate the data in a simple and different way to get them ready for visualization. Most cases are only useful for visualization work, like adding brush color attributes to a \Robject{GRanges} object. Some of the other utilities are responsible for summarizing certain types of raw data, getting it ready to be visualized. Some of those utilities may be moved to a separate package later. \subsection{GRanges Related Manipulation} \biovizBase{} mainly focuses on visualizing the genomic data, so we have some utilities for manipulating \Robject{GRanges} object. We are going to introduce these functions in the flow wing sub-sections. Overall, we hope to reduce people's work through these common utilities. % \subsubsection{Chromosome Name Manipulation} % We don't have required canonical chromosome name for % \Robject{seqnames} in \Robject{GRanges}. Most times, we have chromosome % name with prefix \textbf{chr} in lower case. However, we could come % across all kinds of other names with prefix \textbf{Chr}, or % without any prefix at all. This complicates our integration of data % since we need to check with \Robject{seqnames} before we are able to aggregate % them or before we can visualize them. A consistent name scheme is very % important in most graphic packages like \Rpackage{ggplot2}. For % example, you are going to fail if you try to overlay two data in % the same plot which follows a different name schema. Sometimes we % also need to layout our graphics for genomes in a nice ordered way, % which requires some sorting/ordering function to re-order our % \Robject{GRanges} object. % Function \Rfunction{sortChr} works for \Robject{GenomicRanges}, or % characters or factor, sort it based on seqnames. The default is first % showing numeric seqnames in increasing order, then showing mixed % letters names in alphabetical. Function \Rfunction{orderChr} return % an index instead of a \Robject{GenomicRanges} object. The user could also % provide a model which is a vector of seqnames to sort by. % @ % <>= % sort(gr) % head(sortChr(gr, prefix = "chr")) % head(orderChr(gr, prefix = "chr")) % head(sortChr(gr, model = c("chrX", "chr3", "chr1", "chrY", "chr2"))) % sortChr(c("chrX", "chr3", "chr1", "chrY", "chr2")) % orderChr(c("chrX", "chr3", "chr1", "chrY", "chr2")) % sortChr(factor(c("chrX", "chr3", "chr1", "chrY", "chr2"))) % orderChr(factor(c("chrX", "chr3", "chr1", "chrY", "chr2"))) % @ %def \subsubsection{Adding Disjoint Levels} @ <>= library(GenomicRanges) set.seed(1) N <- 500 gr <- GRanges(seqnames = sample(c("chr1", "chr2", "chr3", "chrX", "chrY"), size = N, replace = TRUE), IRanges( start = sample(1:300, size = N, replace = TRUE), width = sample(70:75, size = N,replace = TRUE)), strand = sample(c("+", "-", "*"), size = N, replace = TRUE), value = rnorm(N, 10, 3), score = rnorm(N, 100, 30), group = sample(c("Normal", "Tumor"), size = N, replace = TRUE), pair = sample(letters, size = N, replace = TRUE)) @ %def This is a tricky question. For example, for pair-end RNA-seq data, we may want to put the reads with the same \emph{qname} on the same level, with nothing falling in between. For better visualization of the data, we may hope that adding invisible extensions to the reads will prevent closely neighbored reads from showing up on the same level. \Rfunction{addStepping} function takes a \Robject{GenomicRanges} object and will add an extra column called \textbf{.levels} to the object. This function is essentially a wrapper around a function \Rfunction{disjointBins} but allows a more flexible way to assign levels to each entry. For example, if the arguments \Rfunarg{group.name} is specified to one of the column in elementMetadata, the function will make sure \begin{itemize} \item Grouped intervals are in the same levels( if they are not overlapped each other). \item No entry is following between the grouped intervals. \item If extend.size is provided, it buffers the intervals and then computes the disjoint levels, thus ensuring that two closely positioned intervals will be assigned to different levels, a good practice for visualization. \end{itemize} For now, this function is only useful for visualization purposes. @ <>= head(addStepping(gr)) head(addStepping(gr, group.name = "pair")) gr.close <- GRanges(c("chr1", "chr1"), IRanges(c(10, 20), width = 9)) addStepping(gr.close) addStepping(gr.close, extend.size = 5) @ %def \subsection{Shrink the Gaps} Sometime, in a gene centric view, we hope to truncate or shrink the gaps to better visualize the short reads or annotation data. It's \textbf{DANGEROUS} to shrink the gaps, since it only make sense in visualization. And even in the visualization the x-scale will be discontinued, and labels became somehow meaningless. \textbf{Make sure} you are not using the shrunk version of data when performing the down stream analysis. This is a tricky question too, we hope to provide a flexible way to shrink the gaps. When we have multiple tracks, users would be responsible to shrink all the tracks based on the common gaps, otherwise there will be mis-aligned tracks. \Rfunction{maxGap} computes a suitable estimated gap based on passed \Robject{GenomicRanges} @ <>= gr.temp <- GRanges("chr1", IRanges(start = c(100, 250), end = c(200, 300))) maxGap(gaps(gr.temp, start = min(start(gr.temp)))) maxGap(gaps(gr.temp, start = min(start(gr.temp))), ratio = 0.5) @ %def \Rfunction{shrinkageFun} function will read in a \Robject{GenomicRanges} object which represents the gaps, and returns a function which alters a different \Robject{GenomicRanges} object, to shrink that object based on previously specified gaps shrinking information. You could use this function to treat multiple tracks(e.g. \Robject{GRanges}) to make sure they are shrunk based on the common gaps and the same ratio. Be careful in the following situations. \begin{itemize} \item When use the same shrinkage function to shrink multiple tracks, make sure the gaps passed to \Rfunction{shrinkageFun} function is the common gaps across all tracks, otherwise, it doesn't make sense to cut a overlapped gap within one of the tracks. \item The default max gap is not 0, just for visualization purpose. If for estimation purpose, you might want to make sure you cut all the gaps. \end{itemize} And notice, after shrinking, the x-axis labes only provide approximate position as shown in Figure \ref{fig:shrink-single} and \ref{fig:shrink-two}, because it's clipped. It's just for visualization purpose. @ <>= gr1 <- GRanges("chr1", IRanges(start = c(100, 300, 600), end = c(200, 400, 800))) shrink.fun1 <- shrinkageFun(gaps(gr1), max.gap = maxGap(gaps(gr1), 0.15)) shrink.fun2 <- shrinkageFun(gaps(gr1), max.gap = 0) head(shrink.fun1(gr1)) head(shrink.fun2(gr1)) @ %def \begin{figure}[h!t!p!b] \centering \includegraphics[width = 0.8\textwidth]{intro-shrink-single.pdf} \caption{Shrink single GRanges. The first track is original GRanges, the second one use a ratio which shrink the GRanges a little bit, and default is to remove all gaps shown as the third track } \label{fig:shrink-single} \end{figure} @ <>= gr2 <- GRanges("chr1", IRanges(start = c(100, 350, 550), end = c(220, 500, 900))) gaps.gr <- intersect(gaps(gr1, start = min(start(gr1))), gaps(gr2, start = min(start(gr2)))) shrink.fun <- shrinkageFun(gaps.gr, max.gap = maxGap(gaps.gr)) head(shrink.fun(gr1)) head(shrink.fun(gr2)) @ %def \begin{figure}[h!t!p!b] \centering \includegraphics[width = 0.8\textwidth]{intro-shrinkageFun.pdf} \caption{shrinkageFun demonstration for multiple GRanges, the top two tracks are the original tracks, please note how we clipped common gaps for those two tracks and shown as bottom two tracks.} \label{fig:shrink-two} \end{figure} \subsection{GC content} As mentioned before, GC content is an interesting variable which may be related to various biological questions. So we need a way to compute GC content in a certain region of a reference genome. \Rfunction{GCcontent} function is a wrapper around \Rfunction{getSeq} function in \Rpackage{BSgenome} package and \Rfunction{letterFrequency} in \Rpackage{Biostrings} package. It reads a \Robject{BSgenome} object and returns count/probability for \textbf{GC} content in specified region. @ <>= library(BSgenome.Hsapiens.UCSC.hg19) GCcontent(Hsapiens, GRanges("chr1", IRanges(1e6, 1e6 + 1000))) GCcontent(Hsapiens, GRanges("chr1", IRanges(1e6, 1e6 + 1000)), view.width = 300) @ %def \subsection{Mismatch Summary} Compared to short-read alignment visualization, it's more useful to just show the summary of nucleotides of short reads per base and compare with the reference genome. We need a way to show the mismatched nucleotides, coverage at each position and proportion of mismatched nucleotides, and use the default color to indicate the type of nucleotide. \Rfunction{pileupAsGRanges} function summarizes reads from bam files for nucleotides on single base units in a given region, which allows the downstream mismatch summary analysis. It's a wrapper around \Rfunction{applyPileup} function in Rsamtools package and more detailed control could be found under manual of ApplyPileupsParam function in Rsamtools. \Rfunction{pileupAsGRanges} function returns a GRanges object which includes a summary of nucleotides, depth, and bam file path. This object could be read directly into the \Rfunction{pileupGRangesAsVariantTable} function for a mismatch summary. This function returns a \Robject{GRanges} object with extra \Robject{elementMetadata}, counts for \textbf{A,C,T,G,N} and \textbf{depth} for coverage. \textbf{bam} indicates the bam file path. Each row is single base unit. \Rfunction{pileupGRangesAsVariantTable} performs comparisons to the reference genome(a \Robject{BSgenome} object) and computes the mismatch summary for a certain region of reads. User need to make sure to pass the right reference genome to this function to get the right summary. This function drops the positions that have no reads and only keeps the regions with coverage in the summary. The result could be used to show stacked barchart for the mismatch summary. This function returns a \Robject{GRanges} with the following elementMetadata information. \begin{description} \item[ref] Reference base. \item[read] Sequenced read at that position. Each type of \textbf{A,C,T,G,N} summarize counts at one position, if no counts detected, will not show it. \item[count] Count for each nucleotide. \item[depth] Coverage at that position. \item[match] A logical value, indicate it's matched or not. \item[bam] Indicate bam file path. \end{description} Sample raw data is from SRA(Short Read Archive), Accession: SRR027894 and subset the gene at chr10:6118023-6137427, which within gene RBM17. contains junction reads. @ <>= library(Rsamtools) data(genesymbol) library(BSgenome.Hsapiens.UCSC.hg19) bamfile <- system.file("extdata", "SRR027894subRBM17.bam", package="biovizBase") test <- pileupAsGRanges(bamfile, region = genesymbol["RBM17"]) test.match <- pileupGRangesAsVariantTable(test, Hsapiens) head(test[,-7]) head(test.match[,-5]) @ %def % \subsection{Fragment Length Estimation} % \emph{Fragment length} could be defined in different % ways. Here, the \Rfunction{getFragLength} function simply uses the shrinkage % function (introduced in previous section) to cut all gaps existing in the % provided model and recompute the length for \Robject{GAlignments} % object instead of using its width directly. % @ % <>= % bamfile <- system.file("extdata", "SRR027894subRBM17.bam", package="biovizBase") % library(TxDb.Hsapiens.UCSC.hg19.knownGene) % txdb <- Hsapiens_UCSC_hg19_knownGene_TxDb % exons <- exonsBy(txdb, by = "tx") % model <- subsetByOverlaps(exons, genesymbol["RBM17"]) % ## model <- exonsByOverlaps(txdb, genesymbol[16910]) % frg <- getFragLength(file, model) % @ %def % \subsection{Splicing Summary} % One of the information we could find from the RNA-seq data is the % abundance of different alternative splicing models. There are two ways % to visualizing the slicing summary, one is summary for full model, % which could be represented as \Robject{GRangesList}, for instance, a % \Robject{GRangesList} grouped by transcirpt id, and each element is % \Robject{GRanges} object contains all the exons. Another one is single % model which could be represented as \Robject{GRanges}, for instance, a % \Robject{GRanges} object which just contains all the exons not grouped % by transcript. So we need a way to compute counts support each model % in the full model or splicing junction in the single model. % There are different ways to summarize abundance based on RNA-seq, I % started with a simple approach which just counting reads acrossing the % junction. The algorithm will first filter out reads which are not % junction reads from the raw data, then mapping junction reads to % models. % \begin{itemize} % \item For full model, if one junction reads mapped to one model which % covers two consecutive exons, then this model plus one for % supporting evidence. When \Rfunarg{weighted} turned on to TRUE, if a % junction reads mapped to multiple model, we will simply plus 1/cases % for all the supported model. % \item For single model, we just summarize the splicing of all junction % reads for all the exons. Using notion like \textbf{1-2, 3-4} to % indicate the junction, here the number means the index of given % model, we assume each row in the model is one exon. When % \Rfunarg{model\_id} set to certain column, for example, % 'exon\_id'. Then we use exon\_id for our notion of our summary. % \end{itemize} % The \Rfunction{spliceSummary} is a S4 method which dispatch on the first % arguments, and will return a vector which is total counts for each % model or exon junctions. And names of the vector is transcript name or % notion like \textbf{1-3} to indicate the isoform. % \textbf{Note:} Currently we don't support new model generation, which % means if junction reads cannot mapped to any known model or exons % which passed to argument \Rfunarg{model} of \Rfunction{spliceSummary} % function, we don't give summary about these reads. But in the future, % we would support more flexible summary for this case. % @ % <>= % splice.sum1 <- spliceSummary(bamfile, model) % splice.sum2 <- spliceSummary(bamfile, model, weighted = FALSE) % exonsall <- exons(txdb) % model.single <- subsetByOverlaps(exonsall, genesymbol["RBM17"]) % splice.sum3 <- spliceSummary(bamfile, model.single) % splice.sum4 <- spliceSummary(bamfile, model.single, model_id = "exon_id") % @ %def % \begin{verbatim} % > splice.sum1 % 38191 38192 38193 % 57 57 0 % > splice.sum2 % 38191 38192 38193 % 114 114 0 % > splice.sum3 % 1-2 1-3 % 1 114 % > splice.sum4 % 140875-140876 140875-140887 % 114 1 % \end{verbatim} % \subsection{Aggregating from Raw Data} % Those utilities used inside this package internally, useful % but not exported to users until later, may be dropped or % changed to more general existing method defined in another package, like % package \Rpackage{stream}. \subsection{Get an Ideogram} \Rfunction{getIdeogram} function is a wrapper of some functionality from \Rpackage{rtracklayer} to get certain table like cytoBand. A full table schema can be found \href{http://genome.ucsc.edu/cgi-bin/hgTables}{here} at \emph{UCSC genome browser}. Please click \emph{describe table schema}. This function requires a network connection and will parse the data on the fly. The first argument of \Rfunction{getIdeogram} is \Rfunarg{species}. If \Rcode{missing}, the function will give you a choice hint, so you will not have to remember the name for the database you want, or you can simply get the database name for a different genome using the \Rfunction{ucscGenomes} function in \Rpackage{Rtracklayer}. The second argument \Rfunarg{subchr} is used to subset the result by chromosome name. The third argument cytoband controls if you want to get the gieStain information/band information or not, which is useful for the visualization of the whole genome or single chromosome. You can see some examples in \Rpackage{ggbio}. @ <>= library(rtracklayer) hg19IdeogramCyto <- getIdeogram("hg19", cytoband = TRUE) hg19Ideogram <- getIdeogram("hg19", cytoband = FALSE) unknowIdeogram <- getIdeogram() @ %def \begin{verbatim} Please specify genome 1: hg19 2: hg18 3: hg17 4: hg16 5: felCat4 6: felCat3 7: galGal3 8: galGal2 9: panTro3 10: panTro2 11: panTro1 12: bosTau4 13: bosTau3 14: bosTau2 15: canFam2 16: canFam1 17: loxAfr3 18: fr2 19: fr1 20: cavPor3 21: equCab2 22: equCab1 23: petMar1 24: anoCar2 25: anoCar1 26: calJac3 27: calJac1 28: oryLat2 29: mm9 30: mm8 31: mm7 32: monDom5 33: monDom4 34: monDom1 35: ponAbe2 36: ailMel1 37: susScr2 38: ornAna1 39: oryCun2 40: rn4 41: rn3 42: rheMac2 43: oviAri1 44: gasAcu1 45: tetNig2 46: tetNig1 47: xenTro2 48: xenTro1 49: taeGut1 50: danRer7 51: danRer6 52: danRer5 53: danRer4 54: danRer3 55: ci2 56: ci1 57: braFlo1 58: strPur2 59: strPur1 60: apiMel2 61: apiMel1 62: anoGam1 63: droAna2 64: droAna1 65: droEre1 66: droGri1 67: dm3 68: dm2 69: dm1 70: droMoj2 71: droMoj1 72: droPer1 73: dp3 74: dp2 75: droSec1 76: droSim1 77: droVir2 78: droVir1 79: droYak2 80: droYak1 81: caePb2 82: caePb1 83: cb3 84: cb1 85: ce6 86: ce4 87: ce2 88: caeJap1 89: caeRem3 90: caeRem2 91: priPac1 92: aplCal1 93: sacCer2 94: sacCer1 Selection: \end{verbatim} Here is the example on how to get the genome names. @ <>= head(ucscGenomes()$db) @ %def \begin{verbatim} [1] hg19 hg18 hg17 hg16 felCat4 felCat3 122 Levels: ailMel1 anoCar1 anoCar2 anoGam1 apiMel1 apiMel2 ... \end{verbatim} @ We put the most used hg19 ideogram as our default data set, so you can simply load it and see what they look like. They are all returned by the \Rfunction{getIdeogram} function. The one with cytoband information has two special columns. \begin{description} \item[name] Name of cytogenetic band \item[gieStain] Giemsa stain results \end{description} <>= data(hg19IdeogramCyto) head(hg19IdeogramCyto) data(hg19Ideogram) head(hg19Ideogram) @ %def There are two simple functions to test if the ideogram is valid or not. \Rfunction{isIdeogram} simply tests if the result came from the \Rfunction{getIdeogram} function, making sure it's a \Robject{GenomicRanges} object with an extra column. \Rfunction{isSimpleIdeogram} only tests if it's \Robject{GenomicRanges} and does not require cytoband information. But it double checks to make sure there is only one entry per chromosome. This is useful to show stacked overview for genomes. Please check some examples in \Rpackage{ggbio} to draw stacked overview and single chromosome. @ <>= isIdeogram(hg19IdeogramCyto) isIdeogram(hg19Ideogram) isSimpleIdeogram(hg19IdeogramCyto) isSimpleIdeogram(hg19Ideogram) @ %def \subsection{Other Utilities and Data Sets} We are not going to introduce other utilities in this vignette, please refer to the manual for more details, we have other function to transform a \Robject{GRanges} to a special format only for graphic purpose, such as function \Rfunction{transformGRangesForEvenSpace} and \Rfunction{transformGRangesToDfWithTicks} could be used for grand linear view or linked view as introduced in package \Rpackage{ggbio}. We have introduced data sets like \Robject{hg19IdeogramCyto} and \Robject{hg19Ideogram} in the previous sections. We also have a data set called \Robject{genesymbol}, which is extracted from human annotation package and stored as \Robject{GRanges} object, with extra columns \emph{symbol} and \emph{ensembl\_id}. For fast mapping, we use \emph{symbol} as row names too. This could be used for convenient overlapped subset with other annotation, and has potential use in a auto-complement drop list for gene search bar like most gene browsers have. @ <>= data(genesymbol) head(genesymbol) genesymbol["RBM17"] @ %def \section{Bugs Report and Features Request} Latest code are available on github \url{https://github.com/tengfei/biovizBase} Please file bug/request on issue page, this is preferred way. or email me at yintengfei gmail dot com. It's a new package and under active development. Thanks in advance for any feedback. \section{Acknowledgement} I wish to thank all those who helped me. 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BILFVՊ?Mxc:N!K 񼬰C1~pMڌ-v_ԦyXA#[\F[w}I)"1rEHJŦcz5/k236DԽȷVWX+*8Dho>]0~.sǧxLew;x c9GΌr),7R5{Q~$u#;^*ўbg%7JzZnfD:0e]KLQqx9a֠g!ޑ7~cYwQnu K"t9bσ޺v="ٺ08%JJ4-;bˁI鈇7]Mުt\"m}(%kU~(dhe^{7T0M%jl f&6_pwvj-~:|53m34'/L8=zդH.:33ǻ<)P ,>ҽ=jzc_is^L+o˔Jpr֠7؅ԛS:c9*N7q.sI> endobj 276 0 obj << /Type /ObjStm /N 75 /First 656 /Length 3391 /Filter /FlateDecode >> stream xڵZr۸}W1b;P*;dslg5#K$g9 p)RLLF/$.tgLH˄L8\ɜ\LJ^fzLK X7P3es,e9e3-%X9l<3 +8,0FC0VKl`|Y ̨܍p`c MB|/9g:11#ᗀqN@yr$3!a:C?BWBs r8AȀ'lݩ]>(a79wJ, l9IF: #) Yz[Y[&yA!F\Y5iYt 8w{NXI3Ď_{/ bX\tu ;(Fd~:(Ka[ B?)'W+GX31.Ǵt-JfDű|Ե\3:#*#ixa;UHQAPZI'qh5+; >w6g!r$'4H(MQI}-CSmh MV8NGR\<7'ۤ Zm ٤ !xIcZKREJI1_2X+KktxYP6x('Grkk(Q+UX& 1Cъè D*pc-).< wP* _#JsAKX'JOI4g&B;,ɋҙz!r0\<2 r vNQ.i:j4>暮,kKIRp\)%c^ՎvG yb BW1 *jFv 4 8,i?`'~JR iPDآDRaJzi[5TeZݹ +EJVRbWKRAGQR N:VU.5W/qs\%ialu< :KWhs0vyBzya^]W5JW;2Wc5y\ѳ 𰖋j6гљMTSJU6>ZX 0NJ:=,rۣo8۩3&ah\]Xs:h(ufݢhɩ'=QάSJ7%ˢmk#=THV֦2"4a>,'j}klvq92Sic{ψEC"˓bC i19CJZhgtr;;wFCU(6 al=`#=a{^lCv޲1C\,&˿gvN旗cv V|O;|-pv.b&OK6cs6]A]M [%[N[],k;ߍ<ז9 / !,kr0"XE1|lZ,m6~=Cu0Kr3nՉcSyyޓ9GʞU7,KC Ttc&Ȣ:xg8Zie}a_甲D iV\NeR)'Om{1Zb E]``Q(8 Hy{06ږ$6H|x@BƼ '7FB eDNg xvMm7GLT;{K`)pu*ڪ~~x'@8emڪxpP ђ}h8oE_BΩoU?׫;!UB+DZu|:/*wRWRRj1TbnTx˓=TӲV]kg|2_.ux8^x:$7TzI7WmO*OQȹvo[m{n/;J:{vi]kY o[ԺnUw E-FWAU[aOzc{Kgk:Gx^YHrON٧=!wi]6*VQ)e9֩Ǻ:" xGRĻ?ҡu ^>~ $[JX3&^ޕz5Es,!r~yQT-̪nfeml\+uV\*)^j[Zrʪ9l#M*k9-Ǥ=+yR:5u1R bD*]a1*UjX &OjTUUc@5eZ=\e ܔ)2+OtƐud; .$:]*Q.j؅ז: JilDO^vi-zr׀^@BޓMy&yeXy @ky 3Vy8?w/Vwgwޚw]8wKD-%MίqjhmL_޾\NV#㮩 )ſfV ׷"Td;W8>'خuޚmͶ8A{J"oD1)E]Ud|٭]e֚k0R(EDq bS+:Tp~݆.A@؄B) [vjJcŵ54VL6YZQʦxJcY&Bs"M)n{"5˪)!u[$H6 jZS4N_KĊ.+z0^Q|wi^א їM+t^hY^_`Cf_ endstream endobj 329 0 obj << /Type /XRef /Index [0 330] /Size 330 /W [1 3 1] /Root 327 0 R /Info 328 0 R /ID [<200D85446AF99DE8457A7147B1EDE1EE> <200D85446AF99DE8457A7147B1EDE1EE>] /Length 817 /Filter /FlateDecode >> stream x%KlMQ:W[ZjQGUV~DĀ!)AW"B@$H$bfb$" |Yg߻>ffoU_lr~T)0l&[G!T`b&[C; eVddhAl%m BVKՑ--dh+@%bfک`Y3R`YYL0L &NԐ [D;Ԓ$[H[%kzf%:f9`DhiZ^Fo׾hôbEc[F -( Zs_t^e4wjer6`* VKswmnegnNbe~ {^zdt[Rv#n: ߥ )Gݲcʐ?P>rI"q6嶫;wFNi[6Nz>"t+܎}=slqQ[,ing4!6f]Q j3+xG@@hpHZK=[鋏@hroTRSeHHH]h;X<`b`b`bd^-(rEǿ=n(pܨvDN4(`SvD~d2 CbxSߤA&\ЌB-Tj+U$VU'WUMdCU'UyrORTgUJ@_d>mtNf7@穓rq~{ endstream endobj startxref 229533 %%EOF biovizBase/inst/examples/0000755000175200017520000000000014136047676016502 5ustar00biocbuildbiocbuildbiovizBase/inst/examples/color.R0000644000175200017520000000133114136047676017741 0ustar00biocbuildbiocbuildgetBioColor("DNA_BASES_N") getBioColor("DNA_BASES") getBioColor("DNA_ALPHABET") getBioColor("RNA_BASES_N") getBioColor("RNA_BASES") getBioColor("RNA_ALPHABET") getBioColor("IUPAC_CODE_MAP") getBioColor("AA_ALPHABET") getBioColor("STRAND") getBioColor("CYTOBAND") getBioColor("DNA_BASES_N", source = "default") getBioColor("DNA_BASES", source = "default") getBioColor("DNA_ALPHABET", source = "default") getBioColor("RNA_BASES_N", source = "default") getBioColor("RNA_BASES", source = "default") getBioColor("RNA_ALPHABET", source = "default") getBioColor("IUPAC_CODE_MAP", source = "default") getBioColor("AA_ALPHABET", source = "default") getBioColor("STRAND", source = "default") getBioColor("CYTOBAND", source = "default") biovizBase/inst/examples/data-gen.R0000644000175200017520000001454414136047676020315 0ustar00biocbuildbiocbuildlibrary(biovizBase) library(GenomicRanges) ## with no hg19IdeogramCyto <- getIdeogram("hg19", cytobands = TRUE) seqinfo(hg19Ideogram) hg19Ideogram <- getIdeogram("hg19", cytobands = FALSE) ## then for genesymbol library("org.Hs.eg.db") ls("package:org.Hs.eg.db") available.dbschemas() symbol_id <- mappedRkeys(org.Hs.egSYMBOL) head(symbol_id) length(symbol_id) gene_id <- mget(symbol_id, revmap(org.Hs.egSYMBOL), ifnotfound=NA) gene_id <- unlist2(gene_id) gene_id <- gene_id[!is.na(gene_id)] chr <- toTable(org.Hs.egCHR[gene_id]) chrloc <- toTable(org.Hs.egCHRLOC[gene_id]) chrlocend <- toTable(org.Hs.egCHRLOCEND[gene_id]) identical(chrloc$gene_id, chrlocend$gene_id) chrs <- chrloc head(chrlocend) chrs$end_location <- chrlocend$end_location head(chrs) res <- chrs sum(duplicated(gene_id))# no duplicate idx <- match(res$gene_id, gene_id) res$symbol <- names(gene_id[idx]) sum(with(res, start_location > 0 & end_location < 0))# good sum(with(res, start_location < 0 & end_location > 0))# good ## merge(merge(data.frame(gene_id=gene_id, symbol=names(gene_id)), chrloc), ## chrlocend) ## df <- merge(merge(merge(data.frame(gene_id = gene_id, ## symbol = names(gene_id)), chr), chrloc), chrlocend) ## do I need to subset it? No. ## add extra column to indicate sense or antisense. ## FOXD4L2, res$sense <- with(res, start_location>=0&end_location>=0) head(res) res.sense <- res[res$sense,] sum(with(res.sense, start_location > end_location)) res.antisense <- res[!res$sense,] sum(with(res.antisense, start_location < end_location)) head(res) ## need to make sure you get this right res$strand <- strand(!res$sense) head(res) sum(with(res, start_location == end_location)) ## df2 <- subset(df, start_location>=0&end_location>=0) ## strand <- ifelse(df2$start_location>df2$end_location, "-", "+") ## strand[df2$start_location == df2$end_location] <- "*" ## id <- strand == "-" ## tmp <- df2[id,"start_location"] ## df2[id,"start_location"] <- df2[id,"end_location"] ## df2[id,"end_location"] <- tmp ## df2$strand <- strand ## df2 <- df2[!duplicated(df2),] ## for ensembl ensembl_id <- unlist(mget(gene_id, org.Hs.egENSEMBL)) head(ensembl_id) idx <- match(res$gene_id, names(ensembl_id)) res$ensembl_id <- ensembl_id[idx] head(res) library(GenomicRanges) genesymbol <- with(res,GRanges(seqnames = paste("chr",Chromosome,sep = ""), IRanges(abs(start_location), abs(end_location)), strand = strand, symbol = symbol, ensembl_id = ensembl_id)) names(genesymbol) <- values(genesymbol)$symbol save(genesymbol, file = "~/Datas/rdas/genesymbol.rda") save(genesymbol, file = "~/Codes/gitrepos/biovizBase/data/genesymbol.rda") save(hg19IdeogramCyto, file = "~/Codes/gitrepos/biovizBase/data/hg19IdeogramCyto.rda") save(hg19Ideogram, file = "~/Codes/gitrepos/biovizBase/data/hg19Ideogram.rda") id <- unlist2(mget("FOXD4L2", revmap(org.Hs.egSYMBOL))) id <- revmap(org.Hs.egSYMBOL)[["FOXD4L2"]] org.Hs.egCHRLOC[[id]] org.Hs.egCHRLOCEND[[id]] ## new data generation method, with seqlengths ideogramCyto <- getIdeogram(c("hg19", "hg18", "mm10", "mm9")) ideogram <- getIdeogram(c("hg19", "hg18", "mm10", "mm9"), cytoband = FALSE) ideo <- ideogram ideoCyto <- ideogramCyto save(ideo, file = "../../../../bioc-devel/biovizBase/data/ideo.rda") save(ideoCyto, file = "/Users/tengfei/Code/svnrepos/bioc-devel/biovizBase/data/ideoCyto.rda") hg19 <- ideoCyto$hg19 ideoCyto$hg18 <- keepSeqlevels(ideoCyto$hg18, paste0("chr", c(1:22, "X", "Y"))) ideoCyto$hg19 <- keepSeqlevels(ideoCyto$hg19, paste0("chr", c(1:22, "X", "Y"))) ideoCyto$mm10 <- keepSeqlevels(ideoCyto$mm10, paste0("chr", c(1:19, "X", "Y"))) ideoCyto$mm9 <- keepSeqlevels(ideoCyto$mm9, paste0("chr", c(1:19, "X", "Y"))) ## for circular view crc1 <- system.file("extdata", "crc1-missense.csv", package = "biovizBase") crc1 <- read.csv(crc1) library(GenomicRanges) mut.gr <- with(crc1,GRanges(Chromosome, IRanges(Start_position, End_position), strand = Strand)) values(mut.gr) <- subset(crc1, select = -c(Start_position, End_position, Chromosome)) data("hg19Ideogram", package = "biovizBase") seqs <- seqlengths(hg19Ideogram) ## subset_chr chr.sub <- paste("chr", 1:22, sep = "") ## levels tweak seqlevels(mut.gr) <- c(chr.sub, "chrX") mut.gr <- keepSeqlevels(mut.gr, chr.sub) seqs.sub <- seqs[chr.sub] ## remove wrong position bidx <- end(mut.gr) <= seqs.sub[match(as.character(seqnames(mut.gr)), names(seqs.sub))] mut.gr <- mut.gr[which(bidx)] ## assign_seqlengths seqlengths(mut.gr) <- seqs.sub ## reanme to shorter names new.names <- as.character(1:22) names(new.names) <- paste("chr", new.names, sep = "") new.names mut.gr.new <- renameSeqlevels(mut.gr, new.names) head(mut.gr.new) hg19Ideo <- hg19Ideogram hg19Ideo <- keepSeqlevels(hg19Ideogram, chr.sub) hg19Ideo <- rena rearr <- read.csv(system.file("extdata", "crc-rearrangment.csv", package = "biovizBase")) ## start position gr1 <- with(rearr, GRanges(chr1, IRanges(pos1, width = 1))) ## end position gr2 <- with(rearr, GRanges(chr2, IRanges(pos2, width = 1))) ## add extra column nms <- colnames(rearr) .extra.nms <- setdiff(nms, c("chr1", "chr2", "pos1", "pos2")) values(gr1) <- rearr[,.extra.nms] ## remove out-of-limits data seqs <- as.character(seqnames(gr1)) .mx <- seqlengths(hg19Ideo)[seqs] idx1 <- start(gr1) > .mx seqs <- as.character(seqnames(gr2)) .mx <- seqlengths(hg19Ideo)[seqs] idx2 <- start(gr2) > .mx idx <- !idx1 & !idx2 gr1 <- gr1[idx] seqlengths(gr1) <- seqlengths(hg19Ideo) gr2 <- gr2[idx] seqlengths(gr2) <- seqlengths(hg19Ideo) values(gr1)$to.gr <- gr2 ## rename to gr gr <- gr1 values(gr)$rearrangements <- ifelse(as.character(seqnames(gr)) == as.character(seqnames((values(gr)$to.gr))), "intrachromosomal", "interchromosomal") crc.gr <- gr crc.gr mut.gr <- mut.gr.new hg19sub <- hg19Ideo save(crc.gr, mut.gr, hg19sub, file = "/Users/tengfei/Code/svnrepos/bioc-devel/biovizBase/data/CRC.rda") snp <- read.table("/Users/tengfei/Downloads/plink.assoc.txt", header = TRUE) N <- 2000 set.seed(123) snp <- snp[sample(1:nrow(snp), size = N, replace = FALSE),] rownames(snp) <- NULL head(snp) write.table(snp, file = "/Users/tengfei/Code/svnrepos/bioc-devel/biovizBase/inst/extdata/plink.assoc.sub.txt", row.names = FALSE) ## https://github.com/stephenturner/qqman biovizBase/inst/examples/test.R0000644000175200017520000001220214136047676017601 0ustar00biocbuildbiocbuildlibrary(biovizBase) ## ------------------------------------------------------------ ## getBioColor ## ------------------------------------------------------------ opts <- getOption("biovizBase") opts$DNABasesNColor[1] <- "red" options(biovizBase = opts) ## get from option(default) getBioColor("DNA_BASES_N") ## get default fixed color getBioColor("DNA_BASES_N", source = "default") seqs <- c("A", "C", "T", "G", "G", "G", "C") ## get colors for a sequence. getBioColor("DNA_BASES_N")[seqs] getBioColor("DNA_BASES") getBioColor("DNA_ALPHABET") getBioColor("RNA_BASES_N") getBioColor("RNA_BASES") getBioColor("RNA_ALPHABET") getBioColor("IUPAC_CODE_MAP") getBioColor("AMINO_ACID_CODE") getBioColor("AA_ALPHABET") getBioColor("STRAND") getBioColor("CYTOBAND") ## done ## ------------------------------------------------------------ ## ColorBlindPal ## ------------------------------------------------------------ ## brewer subse of only color blind palette brewer.pal.blind.info genBrewerBlindPalInfo() ## dichromat info dichromat.pal.blind.info genDichromatPalInfo() ## all color blind palette, adding id/pkg. blind.pal.info ## with no parameters, just return blind.pal.info colorBlindSafePal() mypal <- colorBlindSafePal(20) ## or pass character name mypal <- colorBlindSafePal("Set2") mypal12 <- colorBlindSafePal(22) showColor(mypal(12, repeatable = FALSE)) # warning show_col(mypal(11, repeatable = TRUE)) # no warning, and repeat show_col(mypal12(12)) showColor(getBioColor("CYTOBAND"), "name") showColor(getBioColor("DNA_BASES"), "name") plotColorLegend(getBioColor("DNA_BASES")) mypalFun <- colorBlindSafePal(21) par(mfrow = c(1, 3)) showColor(mypalFun(4)) library(dichromat) showColor(dichromat(mypalFun(4), "deutan")) showColor(dichromat(mypalFun(4), "protan")) getOption("biovizBase")$cytobandColor par(mfrow = c(1, 3)) cols <- getBioColor("DNA_BASES_N", "default") showColor(cols, "name") cols.deu <- dichromat(cols, "deutan") names(cols.deu) <- names(cols) cols.pro <- dichromat(cols, "protan") names(cols.pro) <- names(cols) showColor(cols.deu, "name") showColor(cols.pro, "name") library(GenomicRanges) set.seed(1) N <- 500 gr <- GRanges(seqnames = sample(c("chr1", "chr2", "chr3", "chrX", "chrY"), size = N, replace = TRUE), IRanges( start = sample(1:300, size = N, replace = TRUE), width = sample(70:75, size = N,replace = TRUE)), strand = sample(c("+", "-", "*"), size = N, replace = TRUE), value = rnorm(N, 10, 3), score = rnorm(N, 100, 30), group = sample(c("Normal", "Tumor"), size = N, replace = TRUE), pair = sample(letters, size = N, replace = TRUE)) head(addSteppings(gr)) head(addSteppings(gr, group.name = "pair")) gr.close <- GRanges(c("chr1", "chr1"), IRanges(c(10, 20), width = 9)) addSteppings(gr.close) addSteppings(gr.close, extend.size = 5) gr.temp <- GRanges("chr1", IRanges(start = c(100, 250), end = c(200, 300))) maxGap(gaps(gr.temp, start = min(start(gr.temp)))) maxGap(gaps(gr.temp, start = min(start(gr.temp))), ratio = 0.5) gr1 <- GRanges("chr1", IRanges(start = c(100, 300, 600), end = c(200, 400, 800))) shrink.fun1 <- shrinkageFun(gaps(gr1), max.gap = maxGap(gaps(gr1), 0.15)) shrink.fun2 <- shrinkageFun(gaps(gr1), max.gap = 0) library(ggbio) p1 <- qplot(gr1) p2 <- qplot(shrink.fun1(gr1)) p3 <- qplot(shrink.fun2(gr1)) tracks(p1, p2, p3) gr2 <- GRanges("chr1", IRanges(start = c(100, 350, 550), end = c(220, 500, 900))) gaps.gr <- intersect(gaps(gr1, start = min(start(gr1))), gaps(gr2, start = min(start(gr2)))) shrink.fun <- shrinkageFun(gaps.gr, max.gap = maxGap(gaps.gr)) p1 <- qplot(gr1) p2 <- qplot(gr2) p3 <- qplot(shrink.fun(gr1)) p4 <- qplot(shrink.fun(gr2)) tracks(p1, p2, p3, p4) library(Rsamtools) data(genesymbol) library(BSgenome.Hsapiens.UCSC.hg19) bamfile <- system.file("extdata", "SRR027894subRBM17.bam", package="biovizBase") test <- pileupAsGRanges(bamfile, region = genesymbol["RBM17"]) test.match <- pileupGRangesAsVariantTable(test, Hsapiens) ## 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If n is over the \code{maxcolors} column in blind.pal.info, we use \code{maxcolors} instead when \code{repeatable} set to \code{FALSE}, if \code{repeatable} set to \code{TRUE} we repeat the color of all the allowed colors(length equals \code{maxcolors}) in the same order. This has special case in certain graphics which is always displayed side by side and don't worry about the repeated colors being neighbors. \code{genBrewerBlindPalInfo} return \code{brewer.pal.blind.info} data frame containing all color-blind safe palettes from \code{brewer.pal.info} defined in RColorBrewer, but it's not only just subset of it, it also changes some \code{maxcolors} info. \code{genDichromatPalInfo} return \code{dichromat.pal.blind.info} data frame. \code{genBlindPalInfo} return \code{blind.pal.info} data frame. } \examples{ \dontrun{ library(scales) ## brewer subse of only color blind palette brewer.pal.blind.info genBrewerBlindPalInfo() ## dichromat info dichromat.pal.blind.info genDichromatPalInfo() ## all color blind palette, adding id/pkg. blind.pal.info ## with no parameters, just return blind.pal.info colorBlindSafePal() mypal <- colorBlindSafePal(20) ## or pass character name mypal <- colorBlindSafePal("Set2") mypal12 <- colorBlindSafePal(22) show_col(mypal(12, repeatable = FALSE)) # warning show_col(mypal(11, repeatable = TRUE)) # no warning, and repeat show_col(mypal12(12)) } } \author{Tengfei Yin} biovizBase/man/containLetters.Rd0000644000175200017520000000102014136047676017740 0ustar00biocbuildbiocbuild\name{containLetters} \alias{containLetters} \title{Checking if string contains letters or not} \usage{containLetters(obj, all=FALSE) } \description{Test if a string contain any letters} \details{Useful when processing/sorting seqnames} \value{Logical value} \author{tengfei} \arguments{\item{obj}{String} \item{all}{If set to FALSE, return TRUE when any letters appears; if all is set to TRUE, return TRUE only when the string is composed of just letters.} } \examples{containLetters("XYZ123") containLetters("XYZ123", TRUE)} biovizBase/man/crc1.GeRL.Rd0000644000175200017520000000072714136047676016377 0ustar00biocbuildbiocbuild\name{crc1.GeRL} \alias{crc1.GeRL} \alias{crc1.GeRL} \title{crc1.GeRL} \usage{data(crc1.GeRL)} \description{CRC-1 mutation and structural rearrangment} \details{ GenomicRangesList contains somatic mutation, reaarangment etc for a tumor sample, please check the reference for detials. } \docType{data} \keyword{datasets} \references{ Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion} \examples{data(crc1.GeRL) crc1.GeRL } biovizBase/man/crunch-method.Rd0000644000175200017520000000526114136047676017515 0ustar00biocbuildbiocbuild\name{crunch} \alias{crunch} \alias{crunch,TxDb-method} \alias{crunch,EnsDb-method} \alias{crunch,GAlignments-method} \alias{crunch,BamFile-method} \title{Fetching GRanges from various data source} \description{ Fetching Granges from various data source, currently supported objects are TxDb, EnsDb, GAlignments and BamFile. } \usage{ \S4method{crunch}{TxDb}(obj, which, columns = c("tx_id", "tx_name","gene_id"), type = c("all", "reduce"), truncate.gaps = FALSE, truncate.fun = NULL, ratio = 0.0025) \S4method{crunch}{EnsDb}(obj, which, columns = c("tx_id", "gene_name","gene_id"), type = c("all", "reduce"), truncate.gaps = FALSE, truncate.fun = NULL, ratio = 0.0025) \S4method{crunch}{GAlignments}(obj, which, truncate.gaps = FALSE, truncate.fun = NULL, ratio = 0.0025) \S4method{crunch}{BamFile}(obj, which, ..., type = c("gapped.pair", "raw", "all"), truncate.gaps = FALSE, truncate.fun = NULL, ratio = 0.0025) } \arguments{ \item{obj}{ supported objects are \code{TxDb}, \code{GAlignments} and \code{BamFile}. } \item{which}{ GRanges object. For TxDb object, could aslo be a list. For \code{EnsDb}, it can also be a single filter object extending \code{\link[AnnotationFilter]{AnnotationFilter-class}}, an \code{\link[AnnotationFilter]{AnnotationFilterList}} combining several such objects or a filter expression in form of a \code{formula} (see \code{\link[AnnotationFilter]{AnnotationFilter}} for examples). } \item{columns}{ columns to include in the output. } \item{type}{ default 'all' is to show the full model, 'reduce' is to show a single model. } \item{truncate.gaps}{ logical value, default \code{FALSE}. Whether to truncate gaps or not. } \item{truncate.fun}{ shrinkage function. } \item{ratio}{ numeric value, shrinking ratio. } \item{...}{ arguments passed to function \code{readGAlignments}. } } \value{ GRanges object. } \examples{ library(biovizBase) library(TxDb.Hsapiens.UCSC.hg19.knownGene) data(genesymbol, package = "biovizBase") txdb <- TxDb.Hsapiens.UCSC.hg19.knownGene obj <- txdb temp <- crunch(txdb, which = genesymbol["BRCA1"], type = "all") temp <- crunch(txdb, which = genesymbol["BRCA1"], type = "reduce") ## Fetching data from a EnsDb object. library(EnsDb.Hsapiens.v75) edb <- EnsDb.Hsapiens.v75 gr <- genesymbol["BRCA1"] seqlevels(gr) <- sub(seqlevels(gr), pattern="chr", replacement="") temp <- crunch(edb, which = gr) ## Alternatively, use the GenenameFilter from the AnnotationFilter package: temp <- crunch(edb, which = GenenameFilter("BRCA1")) ## Or a filter expression temp <- crunch(edb, which = ~ genename == "BRCA1") } \author{Tengfei Yin} biovizBase/man/darned_hg19_subset500.Rd0000644000175200017520000000074114136047676020652 0ustar00biocbuildbiocbuild\name{darned_hg19_subset500} \alias{darned_hg19_subset500} \alias{darned_hg19_subset500} \title{Subset of RNA editing sites in hg19...} \usage{data(darned_hg19_subset500)} \description{Subset of RNA editing sites in hg19} \details{This data set provides a subset(500 sites only) of hg19 RNA editing sites, and originally from DARNED \url{http://darned.ucc.ie/} for the hg19 assembly.} \docType{data} \keyword{datasets} \examples{data(darned_hg19_subset500) darned_hg19_subset500} biovizBase/man/estimateCoverage-method.Rd0000644000175200017520000000061414136047676021517 0ustar00biocbuildbiocbuild\name{estimateCoverage} \alias{estimateCoverage} \alias{estimateCoverage,BamFile-method} \title{Estimation of Coverage} \description{ Estimation of Coverage } \usage{ \S4method{estimateCoverage}{BamFile}(x, maxBinSize = 2^14) } \arguments{ \item{x}{ A \code{BamFile} object. } \item{maxBinSize}{ Max bin size. } } \value{ A \code{GRanges} object. } \author{Michael Lawrence} biovizBase/man/flatGrl.Rd0000644000175200017520000000145614136047676016352 0ustar00biocbuildbiocbuild\name{flatGrl} \alias{flatGrl} \title{Transform GRangesList to GRanges} \description{ Transform GRangesList to GRanges. } \usage{ flatGrl(object, indName = "grl_name") } \arguments{ \item{object}{ a \code{GRangesList} object. } \item{indName}{ column named by 'indName' that groups the records by their original element in 'object'. } } \value{ A \code{GRanges} object. } \details{ This method is different from default \code{stack}, it integrate elementMetadata of \code{GRangesList} to the final coerced \code{GRanges}. } \examples{ library(GenomicRanges) gr1 <- GRanges("chr1", IRanges(1:10, width = 5)) gr2 <- GRanges("chr2", IRanges(1:10, width = 5)) obj <- GRangesList(gr1, gr2) values(obj) <- data.frame(a = 1:2, b = letters[1:2]) stack(obj) flatGrl(obj) } \author{Tengfei Yin} biovizBase/man/genesymbol.Rd0000644000175200017520000000057614136047676017125 0ustar00biocbuildbiocbuild\name{genesymbol} \alias{genesymbol} \alias{genesymbol} \title{Gene symbols with position...} \usage{data(genesymbol)} \description{Gene symbols with position} \details{This data set provides genen symbols in human with position and starnd information, stored as GRanges object.} \docType{data} \keyword{datasets} \examples{ data(genesymbol) head(genesymbol) genesymbol["RBM17"] } biovizBase/man/getBioColor.Rd0000644000175200017520000001076714136047676017174 0ustar00biocbuildbiocbuild\name{getBioColor} \alias{getBioColor} \title{Color scheme getter for biological data} \description{ This function tries to get default color scheme either from fixed palette or options for specified data set, usually just biological data. } \usage{ getBioColor(type = c("DNA_BASES_N", "DNA_BASES", "DNA_ALPHABET", "RNA_BASES_N", "RNA_BASES", "RNA_ALPHABET", "IUPAC_CODE_MAP", "AMINO_ACID_CODE", "AA_ALPHABET", "STRAND", "CYTOBAND"), source = c("option", "default")) } \arguments{ \item{type}{ Color set based on which you want to get. } \item{source}{ "option" tries to get color scheme from \code{Options}. This allow user to edit the color globally. "default" gets fixed color scheme. } } \value{ A character of vector contains color(rgb), and the names of the vector is originally from the name of different data set. e.g. for DNA_BASES, it's just \code{A,C,T,G}. This allow users to get color for a vector of specified names. Please see the examples below. } \details{ Most data set specified in the type argument are defined in Biostrings package, such as "DNA_BASES", "DNA_ALPHABET", "RNA_BASES", "RNA_ALPHABET", "IUPAC_CODE_MAP", "AMINO_ACID_CODE", "AA_ALPHABET", please check the manual for more details. "DNA_BASES_N" is just "DNA_BASES" with extra "N" used in certain cases, like the result from \code{applyPileup} in Rsamtools package. We start with the five most used nucleotides, \code{A,T,C,G,N}, In genetics, \code{GC-content} usually has special biological significance because GC pair is bound by three hydrogen bonds instead of two like AT pairs. So it has higher thermostability which could result in different significance, like higher annealing temperature in PCR. So we hope to choose warm color for \code{G,C} and cold color for \code{A,T}, and a color in between to represent \code{N}. They are chosen from diverging color set of \code{color brewer}. So we should be able to easily tell the GC enriched region. This set of color also passed vischeck for colorblind people. In \code{GRanges} object, we have \code{strand} which contains three levels, +, -, *. We are using a qualitative color set from \code{Color Brewer}. This color set pass the colorblind test. It should be a safe color set to use to color strand. For most default color scheme if they are under 18, we are trying to use package dichromat to set color for color blind people. But for data set that contains more than 18 objects, it's not possible to assign colorblind-safe color to them anymore. So we need to repeat some color. It should not matter too much, because even normal people cannot tell the difference anymore. Here are the definition for the data sets. \describe{ \item{DNA_BASES}{ Contains \code{A,C,T,G}. } \item{DNA_ALPHABET}{ This alphabet contains all letters from the IUPAC Extended Genetic Alphabet (see "?IUPAC_CODE_MAP") + the gap ("-") and the hard masking ("+") letters. } \item{DNA_BASES_N}{ Contains \code{A,C,T,G,N} } \item{RNA_BASES_N}{ Contains \code{A,C,U,G,N} } \item{RNA_BASES}{ Contains \code{A,C,T,G} } \item{RNA_ALPHABET}{ This alphabet contains all letters from the IUPAC Extended Genetic Alphabet (see ?IUPAC_CODE_MAP) where "T" is replaced by "U" + the gap ("-") and the hard masking ("+") letters. } \item{IUPAC_CODE_MAP}{ The "IUPAC_CODE_MAP" named character vector contains the mapping from the IUPAC nucleotide ambiguity codes to their meaning. } \item{AMINO_ACID_CODE}{ Single-Letter Amino Acid Code (see "?AMINO_ACID_CODE"). } \item{AA_ALPHABET}{ This alphabet contains all letters from the Single-Letter Amino Acid Code (see "?AMINO_ACID_CODE") + the stop ("*"), the gap ("-") and the hard masking ("+") letters } \item{STRAND}{ Contains \code{"+", "-", "*"} } \item{CYTOBAND}{ Contains giemsa stain results:\code{gneg, gpos25, gpos50, gpos75, gpos100, gvar, stalk, acen}. Color defined in package geneplotter. } } } \examples{ opts <- getOption("biovizBase") opts$DNABasesNColor[1] <- "red" options(biovizBase = opts) ## get from option(default) getBioColor("DNA_BASES_N") ## get default fixed color getBioColor("DNA_BASES_N", source = "default") seqs <- c("A", "C", "T", "G", "G", "G", "C") ## get colors for a sequence. getBioColor("DNA_BASES_N")[seqs] } \author{Tengfei Yin} biovizBase/man/getFormalNames.Rd0000644000175200017520000000075014136047676017657 0ustar00biocbuildbiocbuild\name{getFormalNames} \alias{getFormalNames} \title{Get formals from functions} \description{ Get formals from functions, used for dispatching arguments inside. } \usage{ getFormalNames(..., remove.dots = TRUE) } \arguments{ \item{...}{ functions. } \item{remove.dots}{ logical value, indicate remove dots in formals or not, default is \code{TRUE}. } } \value{ A character vector for formal arguments. } \examples{ getFormalNames(plot, sapply) } \author{Tengfei Yin} biovizBase/man/getGaps.Rd0000644000175200017520000000441614136047676016350 0ustar00biocbuildbiocbuild\name{getGaps} \alias{getGaps} \alias{getGaps,GRanges-method} \title{get gaps for a stepping transformed GRanges object} \description{ Get gaps for a stepping transformed GRanges object, for visualization purpose. So a extra "stepping" column is required. Please see details below for motivation. } \usage{ \S4method{getGaps}{GRanges}(obj, group.name = NULL, facets = NULL) } \arguments{ \item{obj}{ A \code{GRanges} object. } \item{group.name}{ group name, such as transcript ID, this is the group method within each panel of facets and gaps will be computed for each group of intervals. } \item{facets}{ formula used for creating graphics, all variables must be present in the data. } } \value{ A \code{GRanges} object representing gaps and for each row, the "stepping" column help later visualization and make sure gaps and intervals they are generated from are showed on the expected place. } \details{ Since faceting is a subset and group process in visualization stage, some statistical computation need to be taken place after that. This leaves some computation like computing gaps hard based on solely \code{GRanges} object. Extra information like facets formula and group method would help to generate gaps which make sure they are aligned on the same level and within the same panel for grouped intervals. facets variables will be added to gaps \code{GRanges} along with group.name. } \examples{ set.seed(1) N <- 100 library(GenomicRanges) gr <- GRanges(seqnames = sample(c("chr1", "chr2", "chr3"), size = N, replace = TRUE), IRanges( start = sample(1:300, size = N, replace = TRUE), width = sample(70:75, size = N,replace = TRUE)), strand = sample(c("+", "-", "*"), size = N, replace = TRUE), value = rnorm(N, 10, 3), score = rnorm(N, 100, 30), sample = sample(c("Normal", "Tumor"), size = N, replace = TRUE), pair = sample(letters, size = N, replace = TRUE)) grl <- splitByFacets(gr, sample ~ seqnames) gr <- unlist(endoapply(grl, addStepping)) gr.gaps <- getGaps(gr, group.name = "stepping", facets = sample ~ seqnames) } \author{Tengfei Yin} biovizBase/man/getIdeoGR.Rd0000644000175200017520000000205614136047676016565 0ustar00biocbuildbiocbuild\name{getIdeoGR} \alias{getIdeoGR} \title{Get ideogram information} \description{ This function tries to parse ideogram information from \code{seqlengths} of a \code{GRanges} object. This information is usually used to plot chromosome background for kaytogram or esitmate proper lengths of chromosomes from data space for showing overview. } \usage{ getIdeoGR(gr) } \arguments{ \item{gr}{ A \code{GRanges} object with or without lengths information. } } \value{ A ideogram \code{GRanges} object, each row indicate one single chromosome, and start with 1 and end with real chromosome length or estimated lengths. } \examples{ library(GenomicRanges) data("hg19IdeogramCyto", package = "biovizBase") hg19IdeogramCyto ## without seqlengths, simply reduce getIdeoGR(hg19IdeogramCyto) ## with seqlengths gr <- GRanges("chr1", IRanges(1,3)) seqlevels(gr) <- c("chr1", "chr2", "chr3") nms <- c(100, 200, 300) names(nms) <- c("chr1", "chr2", "chr3") seqlengths(gr) <- nms gr getIdeoGR(gr) } \author{Tengfei Yin} biovizBase/man/getIdeogram.Rd0000644000175200017520000000210114136047676017172 0ustar00biocbuildbiocbuild\name{getIdeogram} \alias{getIdeogram} \title{Get ideogram.} \usage{getIdeogram(genome, subchr, cytobands=TRUE) } \description{Get ideogram w/o cytoband for certain genome} \details{This function require a network connection, it will parse the data on the fly, function is a wrapper of some functionality from rtracklayer package to get certain table like cytoBand, a full table schema could be found \url{http://genome.ucsc.edu/cgi-bin/hgTables} in UCSC genome browser.This is useful for visualization of the whole genome or single chromosome, you can see some examples in ggbio package.} \value{A GRanges object.} \author{Tengfei Yin} \arguments{\item{genome}{Single specie names, which must be one of the result from \code{ucscGenomes()$db}. If missing, will invoke a menu for users to choose from.} \item{subchr}{A character vector used to subset the result.} \item{cytobands}{If TRUE, return ideogram with gieStain and name column. If FALSE, simply return the genome information for each chromosome.} } \examples{ \dontrun{hg19IdeogramCyto <- getIdeogram("hg19", cytoband = TRUE)} } biovizBase/man/getScale.Rd0000644000175200017520000000143614136047676016504 0ustar00biocbuildbiocbuild\name{getScale} \alias{getScale} \title{Get scale information from a GRanges} \description{ Trying to get scale information from a \code{GRanges} object, used for circular view for geom "scale". } \usage{ getScale(gr, unit = NULL, n = 100, type = c("M", "B", "sci")) } \arguments{ \item{gr}{ a \code{GRanges} object. } \item{unit}{ A numeric value for scale unit. Default \code{NULL} use argument \code{n} to estimate the unit. } \item{n}{ Integer value to indicate how many scale ticks to make. } \item{type}{ unit types to shown. } } \value{ A \code{GRanges} object, with extra column: "type" indicate it's longer major ticks or shorter minor ticks. "scale.y" indicates y height for major and minor ticks. Default ratio is 3:1. } \author{Tengfei Yin} biovizBase/man/hg19Ideogram.Rd0000644000175200017520000000055414136047676017175 0ustar00biocbuildbiocbuild\name{hg19Ideogram} \alias{hg19Ideogram} \alias{hg19Ideogram} \title{Hg19 ideogram without cytoband information...} \usage{data(hg19Ideogram)} \description{Hg19 ideogram without cytoband information} \details{This data set provides hg19 genome information wihout cytoband information.} \docType{data} \keyword{datasets} \examples{data(hg19Ideogram) hg19Ideogram} biovizBase/man/hg19IdeogramCyto.Rd0000644000175200017520000000057414136047676020036 0ustar00biocbuildbiocbuild\name{hg19IdeogramCyto} \alias{hg19IdeogramCyto} \alias{hg19IdeogramCyto} \title{Hg19 ideogram with cytoband information...} \usage{data(hg19IdeogramCyto)} \description{Hg19 ideogram with cytoband information} \details{This data set provides hg19 genome information with cytoband information.} \docType{data} \keyword{datasets} \examples{data(hg19IdeogramCyto) hg19IdeogramCyto} biovizBase/man/ideo.Rd0000644000175200017520000000047214136047676015674 0ustar00biocbuildbiocbuild\name{ideo} \alias{ideo} \title{ideogram without cytoband information} \usage{data(ideo)} \description{ideogram without cytoband information} \details{This data set provides hg19, hg18, mm10, mm9 genome information wihout cytoband information as a lit.} \docType{data} \keyword{datasets} \examples{data(ideo) ideo}biovizBase/man/ideoCyto.Rd0000644000175200017520000000050614136047676016531 0ustar00biocbuildbiocbuild\name{ideoCyto} \alias{ideoCyto} \title{ideogram with cytoband information} \usage{data(ideoCyto)} \description{ideogram with cytoband information} \details{This data set provides hg19, hg18, mm10, mm9 genome information with cytoband information as a lit.} \docType{data} \keyword{datasets} \examples{data(ideoCyto) ideoCyto}biovizBase/man/isIdeogram.Rd0000644000175200017520000000077014136047676017040 0ustar00biocbuildbiocbuild\name{isIdeogram} \alias{isIdeogram} \title{Ideogram checking} \usage{isIdeogram(obj) } \description{Check if an object is ideogram or not} \details{Simply test if it's the result coming from \code{getIdeogram} function or not, make sure it's a \code{GRanges} and with extra column} \value{A logical value to indicate it's a ideogram or not.} \author{Tengfei Yin} \arguments{\item{obj}{object} } \examples{data(hg19IdeogramCyto) data(hg19Ideogram) isIdeogram(hg19IdeogramCyto) isIdeogram(hg19Ideogram)} biovizBase/man/isMatchedWithModel.Rd0000644000175200017520000000276014136047676020474 0ustar00biocbuildbiocbuild\name{isMatchedWithModel} \alias{isMatchedWithModel} \alias{isJunctionRead} \title{Utils for Splicing Summary} \description{ Utilities used for summarizing isoforms } \usage{ isJunctionRead(cigar) isMatchedWithModel(model, gr) } \arguments{ \item{cigar}{ A CIGAR string vector. } \item{model}{ A GRanges object. } \item{gr}{ A GRanges object. } } \value{ Logical vectors. } \details{ \code{isJunctionRead} simply parsing the CIGAR string to see if there is "N" in between and return a logical vector of the same length as cigar parameters, indicate it's junction read or not. \code{isMatchedWithModel} mapping \code{gr} to \code{model}, and counting overlapped cases for each row of model, If \code{gr} contains all the read, this will return a logical vector of the same length as \code{gr}, and indicate if each read is the support for this model. NOTICE: we only assume it's a full model, so each \code{model} here is simply one isoform. So we only treat the gaped reads which only overlapped with two consecutive exons in \code{model} as one support for it. } \examples{ library(GenomicAlignments) bamfile <- system.file("extdata", "SRR027894subRBM17.bam", package="biovizBase") ## get index of junction read which(isJunctionRead(cigar(readGAlignments(bamfile)))) ## model <- GRanges("chr1", IRanges(c(10, 20, 30, 40), width = 5)) gr <- GRanges("chr1", IRanges(c(10, 10, 12, 22, 33), c(31, 40, 22, 32, 44))) isMatchedWithModel(model, gr) } \author{Tengfei Yin} biovizBase/man/isSimpleIdeogram.Rd0000644000175200017520000000105414136047676020206 0ustar00biocbuildbiocbuild\name{isSimpleIdeogram} \alias{isSimpleIdeogram} \title{Simple ideogram checking} \usage{isSimpleIdeogram(obj) } \description{Check if an object is a simple ideogram or not} \details{test if it's GRanges or not, doesn't require cytoband information. But it double check to see if there is only one entry per chromosome} \value{A logical value to indicate it's a simple ideogram or not.} \author{tengfei} \arguments{\item{obj}{object} } \examples{data(hg19IdeogramCyto) data(hg19Ideogram) isSimpleIdeogram(hg19IdeogramCyto) isSimpleIdeogram(hg19Ideogram)} biovizBase/man/labs.Rd0000644000175200017520000000110414136047676015666 0ustar00biocbuildbiocbuild\name{getYLab-method} \alias{getYLab} \alias{getYLab,TxDb-method} \alias{getXLab-method} \alias{getXLab} \alias{getXLab,GRanges-method} \alias{getXLab,GRangesList-method} \alias{getXLab,GAlignments-method} \title{parse x and y label information from a specific object} \description{ parse y label information, object specific. } \usage{ \S4method{getYLab}{TxDb}(obj) \S4method{getXLab}{GRanges}(obj) \S4method{getXLab}{GRangesList}(obj) \S4method{getXLab}{GAlignments}(obj) } \arguments{ \item{obj}{ A \code{TxDb} object. } } \value{ a string. } \author{Tengfei Yin} biovizBase/man/maxGap-method.Rd0000644000175200017520000000175114136047676017450 0ustar00biocbuildbiocbuild\name{maxGap-method} \alias{maxGap} \title{Estimated max gaps} \usage{ \S4method{maxGap}{GenomicRanges}(obj, ratio = 0.0025) } \description{Compute an estimated max gap information, which could be used as max.gap argument in \code{shringkageFun}.} \details{This function tries to estimate an appropriate max gap to be used for creating a shrinkage function.} \value{A numeric value} \author{Tengfei Yin} \docType{methods} \alias{maxGap,GenomicRanges-method} \seealso{\code{\link{shrinkageFun}}} \arguments{\item{obj}{GenomicRanges object} \item{ratio}{Multiple by the range of the provided gaps as the max gap.} } \examples{require(GenomicRanges) gr1 <- GRanges("chr1", IRanges(start = c(100, 300, 600), end = c(200, 400, 800))) gr2 <- GRanges("chr1", IRanges(start = c(100, 350, 550), end = c(220, 500, 900))) gaps.gr <- intersect(gaps(gr1, start = min(start(gr1))), gaps(gr2, start = min(start(gr2)))) shrink.fun <- shrinkageFun(gaps.gr, max.gap = maxGap(gaps.gr)) shrink.fun(gr1) shrink.fun(gr2)} biovizBase/man/mold-method.Rd0000644000175200017520000000277514136047676017175 0ustar00biocbuildbiocbuild\name{mold} \alias{mold} \alias{mold,IRanges-method} \alias{mold,GRanges-method} \alias{mold,GRangesList-method} \alias{mold,Seqinfo-method} \alias{mold,matrix-method} \alias{mold,eSet-method} \alias{mold,ExpressionSet-method} \alias{mold,RangedSummarizedExperiment-method} \alias{mold,SummarizedExperiment-method} \alias{mold,Views-method} \alias{mold,Rle-method} \alias{mold,RleList-method} \alias{mold,VRanges-method} \title{mold data into data.frame} \description{ mold data into data.frame usued for visualization, so it's sometimes not as simple as coersion, for example, we add midpoint varialbe for mapping. } \usage{ \S4method{mold}{IRanges}(data) \S4method{mold}{GRanges}(data) \S4method{mold}{GRangesList}(data,indName = "grl_name") \S4method{mold}{Seqinfo}(data) \S4method{mold}{matrix}(data) \S4method{mold}{eSet}(data) \S4method{mold}{ExpressionSet}(data) \S4method{mold}{RangedSummarizedExperiment}(data, assay.id = 1) \S4method{mold}{Views}(data) \S4method{mold}{Rle}(data) \S4method{mold}{RleList}(data) \S4method{mold}{VRanges}(data) } \arguments{ \item{data}{ data to be mold into data.frame with additional column that helped mapping.For example we add 'midpoint' variable to a ranged converted \link{data.frame}. } \item{indName}{ when collapsing a \link{GRangesList}, list names are aggregated into extra column named by this parameter. } \item{assay.id}{ define the assay id you want to convert into a \link{data.frame}. } } \value{ a data.frame object. } \author{Tengfei Yin} biovizBase/man/pileupAsGRanges.Rd0000644000175200017520000000332614136047676020006 0ustar00biocbuildbiocbuild\name{pileupAsGRanges} \alias{pileupAsGRanges} \title{Summarize reads for certain region} \usage{pileupAsGRanges(bams, regions, DNABases=c("A", "C", "G", "T", "N"), ...) } \description{This function summarize reads from bam files for nucleotides on single base unit in a given region, this allows the downstream mismatch summary analysis.} \details{It's a wrapper around \code{applyPileup} function in Rsamtools package, more detailed control could be found under manual of ApplyPileupsParam function in Rsamtools. \code{pileupAsGRanges} function return a GRanges object which including summary of nucleotides, depth, bam file path. This object could be read directly into \code{pileupGRangesAsVariantTable} function for mismatch summary.} \value{A GRanges object, each row is one single base unit. and elementMetadata contains summary about this position about all nucleotides specified by DNABases. and \code{depth} for total reads, \code{bam} for file path.} \author{Michael Lawrence, Tengfei Yin} \arguments{\item{bams}{A character which specify the bam file path.} \item{regions}{A GRanges object specifying the region to be summarized. This passed to \code{which} arguments in \code{ApplyPileupsParam}.} \item{DNABases}{Nucleotide type you want to summarize in the result and in specified order. It must be one or more of A,C,G,T,N.} \item{...}{Extra parameters passed to \code{ApplyPileupsParam}.} } \examples{ \dontrun{ library(Rsamtools) data(genesymbol) library(BSgenome.Hsapiens.UCSC.hg19) bamfile <- system.file("extdata", "SRR027894subRBM17.bam", package="biovizBase") test <- pileupAsGRanges(bamfile, region = genesymbol["RBM17"]) test.match <- pileupGRangesAsVariantTable(test, Hsapiens) head(test[,-7]) head(test.match[,-5]) } } biovizBase/man/pileupGRangesAsVariantTable.Rd0000644000175200017520000000356014136047676022303 0ustar00biocbuildbiocbuild\name{pileupGRangesAsVariantTable} \alias{pileupGRangesAsVariantTable} \title{Mismatch summary} \usage{pileupGRangesAsVariantTable(gr, genome, DNABases=c("A", "C", "G", "T", "N")) } \description{Compare to reference genome and compute mismatch summary for certain region of reads.} \details{User need to make sure to pass the right reference genome to this function to get the right summary. This function drop the position has no reads and only keep the region with coverage in the summary. The result could be used to show stacked barchart for mismatch summary.} \value{A GRanges object. Containing the following elementMetadata \itemize{ \item {ref}{Nucleotide in reference genome.} \item {read}{Nucleotide contained in the reads at particular position, if multiple nucleotide, either matched or unmatched are found, they will be summarized in different rows.} \item {count}{Count for read column.} \item{match}{Logical value, whether matched to reference genome or not} \item{bam}{Character indicate bam file path.} }} \author{Michael Lawrence, Tengfei Yin} \arguments{\item{gr}{A GRanges object, with nucleotides summary, each base take one column in elementMetadata or user can simply passed the returned result from \code{pileupAsGRanges} function to this function.} \item{genome}{BSgenome object, need to be the reference genome.} \item{DNABases}{Nucleotide types contained in passed GRanges object. Default is A/C/G/T/N, it tries to match the column names in elementMetadata to those default nucleotides. And treat the matched column as base names.} } \examples{ \dontrun{ library(Rsamtools) data(genesymbol) library(BSgenome.Hsapiens.UCSC.hg19) bamfile <- system.file("extdata", "SRR027894subRBM17.bam", package="biovizBase") test <- pileupAsGRanges(bamfile, region = genesymbol["RBM17"]) test.match <- pileupGRangesAsVariantTable(test, Hsapiens) head(test[,-7]) head(test.match[,-5]) } } biovizBase/man/plotColorLegend.Rd0000644000175200017520000000115314136047676020045 0ustar00biocbuildbiocbuild\name{plotColorLegend} \alias{plotColorLegend} \title{Show colors} \usage{plotColorLegend(colors, labels, title) } \description{Plot color legend, simple way to check your default color scheme} \details{Show color sheme as a legend style, labels} \value{A graphic device showing color legend.} \author{Tengfei Yin} \arguments{\item{colors}{A character vector of colors} \item{labels}{Labels to put aside colors, if \code{missing}, use names of the colors character vector.} \item{title}{Title for the color legend.} } \examples{cols <- getOption("biovizBase")$baseColor plotColorLegend(cols, title = "strand legend")} biovizBase/man/scale.Rd0000644000175200017520000000224514136047676016043 0ustar00biocbuildbiocbuild\name{getXScale} \alias{getXScale} \alias{getXScale,GRanges-method} \title{get x scale breaks and labels} \description{ get x scale breaks and labels for GRanges with different coordintes(currently only "truncate_gaps" and "genome" supported). } \usage{ \S4method{getXScale}{GRanges}(obj, type = c("default", "all", "left", "right")) } \arguments{ \item{obj}{ a \code{GRanges} object. "coord" in metadata shows proper coordinates transformation for this object. } \item{type}{ types of labels for transformed data. } } \value{ list of breaks and labels. } \examples{ library(GenomicRanges) gr1 <- GRanges("chr1", IRanges(start = c(100, 300, 600), end = c(200, 400, 800))) shrink.fun1 <- shrinkageFun(gaps(gr1), max.gap = maxGap(gaps(gr1), 0.15)) shrink.fun2 <- shrinkageFun(gaps(gr1), max.gap = 0) s1 <- shrink.fun1(gr1) getXScale(s1) # coord:genome set.seed(1) gr1 <- GRanges("chr1", IRanges(start = as.integer(runif(20, 1, 100)), width = 5)) gr2 <- GRanges("chr2", IRanges(start = as.integer(runif(20, 1, 100)), width = 5)) gr <- c(gr1, gr2) gr.t <- transformToGenome(gr, space.skip = 1) getXScale(gr.t) } \author{Tengfei Yin} biovizBase/man/showColor.Rd0000644000175200017520000000073514136047676016735 0ustar00biocbuildbiocbuild\name{showColor} \alias{showColor} \title{Show colors} \description{ Show colors with color string or names of color vectors. } \usage{ showColor(colors, label = c("color", "name")) } \arguments{ \item{colors}{ A color character vector. } \item{label}{ "color" label color with simple color string, and "name" label color with names of the vectors. } } \value{ A plot. } \examples{ \dontrun{ showColor(getBioColor("CYTOBAND")) } } \author{Tengfei Yin} biovizBase/man/shrinkageFun-method.Rd0000644000175200017520000000355514136047676020663 0ustar00biocbuildbiocbuild\name{shrinkageFun-method} \alias{shrinkageFun} \alias{is_coord_truncate_gaps} \usage{ ## For IRanges \S4method{shrinkageFun}{IRanges}(obj, max.gap = 1L) ## For GenomicRanges \S4method{shrinkageFun}{GenomicRanges}(obj, max.gap = 1L) is_coord_truncate_gaps(obj) } \title{Shrinkage function} \description{Create a shrinkage function based on specified gaps and shrinkage rate.} \details{ \code{shrinkageFun} function will read in a GenomicRanges object which represent the gaps, and return a function which works for another GenomicRanges object, to shrink that object based on previously specified gaps shrinking information. You could use this function to treat multiple tracks(e.g. GRanges) to make sure they shrunk based on the common gaps and the same ratio. \code{is_coord_truncate_gaps} is used to check if a \code{GRanges} object is in "truncate_gaps" coordiantes or not. } \value{ A shrinkage function which could shrink a GenomicRanges object, this function will add coord "truncate_gaps" and max.gap to metadata, ".ori" for oringal data as extra column } \alias{shrinkageFun,GenomicRanges-method} \alias{shrinkageFun,IRanges-method} \author{Michael Lawrence, Tengfei Yin} \arguments{\item{obj}{GenomicRanges object which represent gaps} \item{max.gap}{Gaps to be kept, it's a fixed value, if this value is bigger than certain gap interval, then that gap is not going to be shrunk.} } \examples{ library(GenomicRanges) gr1 <- GRanges("chr1", IRanges(start = c(100, 300, 600), end = c(200, 400, 800))) shrink.fun1 <- shrinkageFun(gaps(gr1), max.gap = maxGap(gaps(gr1), 0.1)) shrink.fun2 <- shrinkageFun(gaps(gr1, start(gr1), end(gr1)), max.gap = maxGap(gaps(gr1), 0.1)) shrink.fun3 <- shrinkageFun(gaps(gr1), max.gap = 0) s1 <- shrink.fun1(gr1) s2 <- shrink.fun2(gr1) s3 <- shrink.fun3(gr1) metadata(s1)$coord values(s1)$.ori is_coord_truncate_gaps(s1) } biovizBase/man/splitByFacets-method.Rd0000644000175200017520000000420114136047676021000 0ustar00biocbuildbiocbuild\name{splitByFacets} \alias{splitByFacets} \alias{splitByFacets,GRanges,formula-method} \alias{splitByFacets,GRanges,GRanges-method} \alias{splitByFacets,GRanges,NULL-method} \alias{splitByFacets,GRanges,missing-method} \title{split a GRanges by formula} \description{ Split a GRanges by formula into GRangesList. Parse variables in formula and form a interaction factors then split the \code{GRanges} by the factos. } \usage{ \S4method{splitByFacets}{GRanges,formula}(object, facets) \S4method{splitByFacets}{GRanges,GRanges}(object, facets) \S4method{splitByFacets}{GRanges,NULL}(object, facets) \S4method{splitByFacets}{GRanges,missing}(object, facets) } \arguments{ \item{object}{ \code{GRanges} object. } \item{facets}{ formula object, such as . ~ seqnames. Or \code{GRanges} object, or \code{NULL}. } } \value{ A \code{GRangesList}. } \details{ if facets is formula, factors are crreated based on interaction of variables in formula, then split it with this factor. If facets is \code{GRanges} object, it first subset the original data by facets \code{GRanges}, then split by each region in the facets. If facets is \code{NULL}, split just by seqnames. This function is used to perform computation in conjunction with facets argments in higher level graphic function. } \examples{ library(GenomicRanges) N <- 1000 gr <- GRanges(seqnames = sample(c("chr1", "chr2", "chr3"), size = N, replace = TRUE), IRanges( start = sample(1:300, size = N, replace = TRUE), width = sample(70:75, size = N,replace = TRUE)), strand = sample(c("+", "-", "*"), size = N, replace = TRUE), value = rnorm(N, 10, 3), score = rnorm(N, 100, 30), sample = sample(c("Normal", "Tumor"), size = N, replace = TRUE), pair = sample(letters, size = N, replace = TRUE)) facets <- sample ~ seqnames splitByFacets(gr, facets) splitByFacets(gr) gr.sub <- GRanges("chr1", IRanges(c(1, 200, 250), width = c(50, 10, 30))) splitByFacets(gr, gr.sub) } \author{Tengfei Yin} biovizBase/man/strip_formula_dots.Rd0000644000175200017520000000071114136047676020667 0ustar00biocbuildbiocbuild\name{strip_formula_dots} \alias{strip_formula_dots} \title{strip dots around a formula variables} \description{ strip dots around variables in a formula. } \usage{ strip_formula_dots(formula) } \arguments{ \item{formula}{ A formula. such as coverage ~ seqnames, or ..coverage.. ~ seqnames. } } \value{ A formula wihout ".." around for all variables. } \examples{ obj <- ..coverage.. ~ seqnames strip_formula_dots(obj) } \author{Tengfei Yin} biovizBase/man/subsetArgsByFormals.Rd0000644000175200017520000000121614136047676020712 0ustar00biocbuildbiocbuild\name{subsetArgsByFormals} \alias{subsetArgsByFormals} \title{Subset list of arguments by functions} \description{ find arguments matched by formals of passed functions, } \usage{ subsetArgsByFormals(args, ..., remove.dots = TRUE) } \arguments{ \item{args}{ list of arguments with names indicate the formals. } \item{...}{ functions used to parse formals. } \item{remove.dots}{ logical value indicate whether to include dots in formals or not. } } \value{ argumnets that matched with passed function. } \examples{ args <- list(x = 1:3, simplify = TRUE, b = "b") subsetArgsByFormals(args, plot, sapply) } \author{Tengfei Yin} biovizBase/man/transform.Rd0000644000175200017520000001440114136047676016764 0ustar00biocbuildbiocbuild\name{transformToGenome} \alias{transformToGenome} \alias{transformToGenome,GRanges-method} \alias{transformToGenome,GRangesList-method} \alias{transformToArch} \alias{transformToArch,GRanges-method} \alias{transformToCircle} \alias{transformToRectInCircle} \alias{transformToBarInCircle} \alias{transformToSegInCircle} \alias{transformToLinkInCircle} \alias{transformDfToGr} \alias{transformToDf} \alias{transformToDf-method} \alias{transformToDf,GRanges-method} \alias{is_coord_genome} \title{Transform GRanges to different coordinates and layout} \description{ Used for coordiante genome transformation, other transformation in circular view. } \usage{ \S4method{transformToGenome}{GRanges}(data, space.skip = 0.1, chr.weight = NULL) \S4method{transformToGenome}{GRangesList}(data, space.skip = 0.1, chr.weight = NULL) \S4method{transformToArch}{GRanges}(data, width = 1) transformToCircle(data, x = NULL, y = NULL, ylim = NULL, radius = 10, trackWidth =10, direction = c("clockwise", "anticlockwise"), mul = 0.05) transformToRectInCircle(data, y = NULL, space.skip = 0.1, trackWidth = 10, radius = 10, direction = c("clockwise", "anticlockwise"), n = 100, mul = 0.05, chr.weight = NULL) transformToBarInCircle(data, y = NULL, space.skip = 0.1, trackWidth = 10, radius = 10, direction = c("clockwise", "anticlockwise"), n = 100, mul = 0.05, chr.weight = NULL) transformToSegInCircle(data, y = NULL, space.skip = 0.1, trackWidth = 10, radius = 10, direction = c("clockwise", "anticlockwise"), n = 100, chr.weight = NULL) transformToLinkInCircle(data, linked.to, space.skip = 0.1, trackWidth = 10, radius = 10, link.fun = function(x, y, n = 100) bezier(x, y, evaluation = n), direction = c("clockwise", "anticlockwise"), chr.weight = NULL) transformDfToGr(data, seqnames = NULL, start = NULL, end = NULL, width = NULL, strand = NULL, to.seqnames = NULL, to.start = NULL, to.end = NULL, to.width = NULL, to.strand = NULL, linked.to = to.gr) \S4method{transformToDf}{GRanges}(data) is_coord_genome(data) } \arguments{ \item{data}{ a \code{GRanges} object. for function \code{transformDfToGr} it's data.frame. } \item{x}{ character for variable as x axis used for transformation. } \item{y}{ character for variable as y axis used for transformation. } \item{ylim}{ numeric range to control the ylimits on tracks when 'y' information is involved. } \item{space.skip}{ numeric values indicates skipped ratio of whole space, not skipped space is identical between each space. } \item{radius}{ numeric value, indicates radius when transform to a circle. } \item{trackWidth}{ numeric value, for track width. } \item{direction}{ "clockwise" or "counterclockwise", for layout or transform direction to circle. } \item{mul}{ numeric value, passed to \code{expand_range} function, to control margin of y in the track. } \item{n}{ integer value, control interpolated points numbers. } \item{linked.to}{ a column name of \code{GRanges} object, indicate the linked line's end point which represented as a \code{GRanges} too.. } \item{link.fun}{ function used to generate linking lines. } \item{seqnames}{ character or integer values for column name or index indicate variable mapped to seqnames, default \code{NULL} use "seqnames". } \item{start}{ character or integer values for column name or index indicate variable mapped to start, default \code{NULL} use "start". } \item{end}{ character or integer values for column name or index indicate variable mapped to end, default \code{NULL} use "end". } \item{width}{ character or integer values for column name or index indicate variable mapped to width, default \code{NULL} use "width". } \item{strand}{ character or integer values for column name or index indicate variable mapped to strand, default \code{NULL} use "strand". } \item{to.seqnames}{ character or integer values for column name or index indicate variable mapped to linked seqnames, default \code{NULL}, create GRanges without new GRanges attached as column. If this varialbe is not \code{NULL}, this mean you try to parse linked \code{GRanges} object. } \item{to.start}{ character or integer values for column name or index indicate variable mapped to start of linked GRanges, default \code{NULL} use "to.start". } \item{to.end}{ character or integer values for column name or index indicate variable mapped to end of linked GRanges, default \code{NULL} use "to.end". } \item{to.width}{ character or integer values for column name or index indicate variable mapped to width of linked GRanges, default \code{NULL} use "to.width". } \item{to.strand}{ character or integer values for column name or index indicate variable mapped to strand, default \code{NULL} use "to.strand" or just use *. } \item{chr.weight}{ numeric vectors which sum to <1, the names of vectors has to be matched with seqnames in seqinfo, and you can only specify part of the seqnames, other lengths of chromosomes will be assined proportionally to their seqlengths, for example, you could specify chr1 to be 0.5, so the chr1 will take half of the space and other chromosomes squeezed to take left of the space. } } \value{ A \code{GRanges} object, with calculated new variables, including ".circle.x" for transformed x position, ".circle.y" for transformed y position, ".circle.angle" for transformed angle. } \examples{ library(biovizBase) library(GenomicRanges) set.seed(1) gr1 <- GRanges("chr1", IRanges(start = as.integer(runif(20, 1, 2e9)), width = 5)) gr2 <- GRanges("chr2", IRanges(start = as.integer(runif(20, 1, 2e9)), width = 5)) gr <- c(gr1, gr2) gr.t <- transformToGenome(gr, space.skip = 0.1) is_coord_genome(gr.t) transformToCircle(gr.t) transformToRectInCircle(gr) transformToSegInCircle(gr) values(gr1)$to.gr <- gr2 transformToLinkInCircle(gr1, linked.to = "to.gr") } \author{Tengfei Yin} biovizBase/man/transformGRangesForEvenSpace.Rd0000644000175200017520000000163514136047676022501 0ustar00biocbuildbiocbuild\name{transformGRangesForEvenSpace} \alias{transformGRangesForEvenSpace} \title{Transform GRanges with New Coordinates} \description{ For graphics, like linked plot, e.g. generated by \code{qplotRangesLinkedToData} function in package ggbio. we need to generate a new set of coordinates which is used for even spaced statistics track. } \usage{ transformGRangesForEvenSpace(gr) } \arguments{ \item{gr}{ A GRanges object. } } \value{ A GRanges object as passed in, with new column x.new which indicate the static track coordinates, in this way, we could map the new coordinates with the old one. } \details{ Most used internally for special graphics, like \code{qplotRangesLinkedToData} function in package ggbio. } \examples{ library(GenomicRanges) gr <- GRanges("chr1", IRanges(seq(1,100, length.out = 10), width = 5)) library(biovizBase) transformGRangesForEvenSpace(gr) } \author{Tengfei Yin} biovizBase/src/0000755000175200017520000000000014136065665014474 5ustar00biocbuildbiocbuildbiovizBase/src/R_init_biovizBase.c0000644000175200017520000000044214136047676020243 0ustar00biocbuildbiocbuild#include #include "bin_offsets.h" static const R_CallMethodDef callMethods[] = { {"scan_bam_bin_offsets", (DL_FUNC) & scan_bam_bin_offsets, 1}, {NULL, NULL, 0} }; void R_init_biovizBase(DllInfo * info) { R_registerRoutines(info, NULL, callMethods, NULL, NULL); } biovizBase/src/bin_offsets.c0000644000175200017520000000313414136047676017144 0ustar00biocbuildbiocbuild#include #include "bin_offsets.h" static int _scan_bin_chunk_count(Rbyte **b) { *b += 4; // skip the bin id int32_t count = *(int32_t *)(*b); *b += 4 + count * 16; // skip the actual counts return count; } static void _scan_bin_offsets(Rbyte **b, double **m) { int32_t bin = *(int32_t *)(*b); *b += 4; int32_t nchunks = *(int32_t *)(*b); *b += 4; for (int i = 0; i < nchunks; i++, *m += 5) { int64_t start = *(int64_t *)(*b); *b += 8; int64_t end = *(int64_t *)(*b); *b += 8; (*m)[0] = bin; (*m)[1] = start >> 16; (*m)[2] = end >> 16; (*m)[3] = (uint16_t)start; (*m)[4] = (uint16_t)end; } } static SEXP _scan_bin_offsets_seq(Rbyte **b) { int32_t nbin = *(int32_t *)(*b); *b += 4; Rbyte *tmp_bytes = *b; int nchunks = 0; for (int i = 0; i < nbin; i++) { nchunks += _scan_bin_chunk_count(&tmp_bytes); } // need real values, because 32 bits is generally not enough SEXP ans; PROTECT(ans = allocMatrix(REALSXP, 5, nchunks)); double *m = REAL(ans); for (int i = 0; i < nbin; i++) { _scan_bin_offsets(b, &m); } // skip past the interval index *b += 4 + *(int32_t *)(*b) * 8; UNPROTECT(1); return ans; } SEXP scan_bam_bin_offsets(SEXP bytes) { SEXP ans; if (!IS_RAW(bytes)) Rf_error("'bytes' must be a raw vector"); Rbyte *b = RAW(bytes); if (strncmp(b, "BAI\1", 4)) Rf_error("wrong magic number"); b += 4; int32_t nref = *(int32_t *)b; b += 4; PROTECT(ans = NEW_LIST(nref)); for (int i = 0; i < nref; i++) SET_VECTOR_ELT(ans, i, _scan_bin_offsets_seq(&b)); UNPROTECT(1); return ans; } 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/hungarumlaut /ogonek /caron /space] >> endobj 10 0 obj << /Type /Font /Subtype /Type1 /Name /F2 /BaseFont /Helvetica /Encoding 9 0 R >> endobj xref 0 11 0000000000 65535 f 0000000021 00000 n 0000000164 00000 n 0000002115 00000 n 0000002198 00000 n 0000002310 00000 n 0000002343 00000 n 0000000213 00000 n 0000000293 00000 n 0000005038 00000 n 0000005295 00000 n trailer << /Size 11 /Info 1 0 R /Root 2 0 R >> startxref 5392 %%EOF biovizBase/vignettes/intro.Rnw0000644000175200017520000010575614136047676017560 0ustar00biocbuildbiocbuild%\VignetteIndexEntry{An Introduction to biovizBase} %\VignetteDepends{} %\VignetteKeywords{visualization utilities} %\VignettePackage{biovizBase} \documentclass[10pt]{article} % \SweaveOpts{width = 5, height = 4.5} % \usepackage{times} \usepackage{hyperref} \usepackage{verbatim} \textwidth=6.5in \textheight=8.5in %\parskip=.3cm \oddsidemargin=-.1in \evensidemargin=-.1in \headheight=-.3in \newcommand{\Rfunction}[1]{{\texttt{#1}}} \newcommand{\Robject}[1]{{\texttt{#1}}} \newcommand{\Rpackage}[1]{{\textit{#1}}} \newcommand{\Rmethod}[1]{{\texttt{#1}}} \newcommand{\Rfunarg}[1]{{\texttt{#1}}} \newcommand{\Rclass}[1]{{\textit{#1}}} \newcommand{\Rcode}[1]{{\texttt{#1}}} \newcommand{\software}[1]{\textsf{#1}} \newcommand{\R}{\software{R}} \newcommand{\IRanges}{\Rpackage{IRanges}} \newcommand{\biovizBase}{\Rpackage{biovizBase}} \newcommand{\ggbio}{\Rpackage{ggbio}} \newcommand{\visnab}{\Rpackage{visnab}} \title{An Introduction to \biovizBase{}} \author{Tengfei Yin, Michael Lawrence, Dianne Cook} \date{\today} \begin{document} \maketitle \newpage \tableofcontents \newpage <>= options(width=72) @ \section{Introduction} The \biovizBase{} package is designed to provide a set of utilities and color schemes serving as the basis for visualizing biological data, especially genomic data. Two other packages are currently built on this package, a static version of graphics is provided by the package \ggbio{}, and an interactive version of graphics is provided by \visnab{}(Currently not released). In this vignette, we will introduce those color schemes and different utilities functions using simple examples and data sets. Utilities includes functions that precess the raw data, validate names, add attributes, and generate summaries such as fragment length, GC content, and mismatch information. \section{Color Schemes} The \biovizBase{} package aims to provide a set of default color schemes for biological data, based on the following principles. \begin{itemize} \item Make biological sense. Data is displayed in a way that is similar to observed results under the microscope. (Example: giemsa stain results) \item Generate aesthetically pleasing colors based on well-defined color sets like \emph{color brewer} \footnote{\url{http://colorbrewer2.org/}}. Produce the appropriate color for \emph{sequential, diverging, and qualitative} color schemes. \item Accommodate colorblind vision by creating color pallets that pass the color blind check on the \emph{Vischeck} website \footnote{\url{http://www.vischeck.com/}} or use palette from package \Rpackage{dichromat} or use color-blind safe color palette checked by \emph{ColorBrewer} website\footnote{\url{http://colorbrewer2.org/}}. There are three types of colorblind checking strategy defined on these website. \begin{description} \item[Deuteranope] a form of red/green color deficit; \item[Protanope] another form of red/green color deficit; \item[Tritanope] a blue/yellow deficit- very rare. \end{description} \end{itemize} Our color scheme try to pass color-blind checking points to make sure all the users can tell the difference between groups of data displayed. To make the implementation easy, we most time just use \Rpackage{dichromat} to check this, \Rpackage{dichromat} collapses red-green color distinctions to approximate the effect of the two common forms of red/green color blindness, protanopia and deuteranopia. Or we could simply implement proved color-blind safe palette from \Rpackage{dichromat} or \Rpackage{RColorBrewer}. All color schemes have a general color generating function and a default color generating function. They are automatically stored in \Rfunction{options} as default when loading the package. Other packages built on \biovizBase{} can use the default color scheme, ensuring consistent color themes across all static and interactive graphics. Users may also change the default color in the \Rfunction{options} to personalize the global color scheme to fit their needs. @ <>= library(biovizBase) ## library(scales) @ %def \subsection{Colorblind Safe Palette} For graphics, it's important to make sure most people can tell the difference between colors on the plots, even for people with deficient or anomalous red-green vision. We will add more and more colorblind safe palette gradually, now we only supported palettes from two packages, \Rpackage{dichromat} or \Rpackage{RColorBrewer}. However, \Rpackage{RColorBrewer} doesn't provide information about colorblind palette. So we need to check manually on \textit{ColorBrewer} website, and add this information with the palette information. For \Rpackage{dichromat} package, it doesn't have a palette information like \Rcode{brewer.pal.info}, which contains three different types, \textbf{qual, div, seq} representing quality, divergent and sequential respectively, and also missing max colors information, so we integrate all these information and generate three palette information. \begin{itemize} \item \Robject{brewer.pal.blind.info} provides only colorblind safe palette subset. \item \Robject{dichromat.pal.blind.info} provides colorblind safe palette with category information and max color allowed. \item \Robject{blind.pal.info} integrate first two, provides a general palette information with extra column like pal.id, which used for function \Rfunction{colorBlindSafePal} as index for arguments \Rfunarg{palette} or maxcolors for allowed number of color. \textit{pkg} providing information about which package it is defined. \end{itemize} @ <>= head(blind.pal.info) @ %def Then we defined a color generating function \Rfunction{colorBlindSafePal}, this function reading in a palette argument which could be a index number or names for palette defined in \Robject{blind.pal.info}. And return a color generating function, a \Rfunarg{repeatable} argument will control, for number over max color numbers required, does it simply repeat it or just providing limited number of colors. @ <>= ## with no arguments, return blind.pal.info head(colorBlindSafePal()) ## mypalFun <- colorBlindSafePal("Set2") ## mypalFun(12, repeatable = FALSE) #only three mypalFun(11, repeatable = TRUE) #repeat @ %def To Collapses red-green color distinctions to approximate the effect of the two common forms of red- green color blindness, protanopia and deuteranopia, we can use function \Rfunction{dichromat} from package \Rpackage{dichromat}, this save us the time to \begin{figure}[h!t!p!b] \centering @ <>= ## for palette "Paried" mypalFun <- colorBlindSafePal(21) par(mfrow = c(1, 3)) showColor(mypalFun(4)) library(dichromat) showColor(dichromat(mypalFun(4), "deutan")) showColor(dichromat(mypalFun(4), "protan")) @ %def \caption{Checking colors with two common type of color blindness. The first one is normal perception, second one for deuteranopia and last one for protanopia. Since we are using selected color palettes in this package, it should be fine with those types of blindness.} \label{fig:dichromat} \end{figure} We only show this as an examples and won't compare all other color schemes in the following sections. Please notice that \begin{itemize} \item If the categorical data contains many levels like amino acid, people cannot easily tell the difference anyway, we did the trick to simply repeat the colors. This might be useful for many other cases like grand linear view for chromosomes, since if the viewed orders of chromosomes is fixed it's OK to use repeated colors since they are not going to be layout as neighbors anyway. \item For schemes like cytobands, we try to follow the biological sense, in this case, we don't really check the color blindness. \end{itemize} \subsection{Cytobands Color} Chemically staining the metaphase chromosomes results in a alternating dark and light banding pattern, which could provide information about abnormalities for chromosomes. Cytogenetic bands could also provide potential predictions of chromosomal structural characteristics, such as repeat structure content, CpG island density, gene density, and GC content. \biovizBase{} package provides utilities to get ideograms from the UCSC genome browser, as a wrapper around some functionality from \Rpackage{rtracklayer}. It gets the table for \emph{cytoBand} and stores the table for certain species as a \Robject{GRanges} object. We found a color setting scheme in package \Rpackage{geneplotter}, and we implemented it in biovisBase. The function .cytobandColor will return a default color set. You could also get it from \Rfunction{options} after you load \biovizBase{} package. And we recommended function \Rfunction{getBioColor} to get the color vector you want, and names of the color is biological categorical data. This function hides interval color genenerators and also the complexity of getting color from options. You could specify whether you want to get colors by default or from options, in this way, you can temporarily edit colors in options and could change or all the graphics. This give graphics a uniform color scheme. @ <>= getOption("biovizBase")$cytobandColor getBioColor("CYTOBAND") ## differece source from default or options. opts <- getOption("biovizBase") opts$DNABasesNColor[1] <- "red" options(biovizBase = opts) ## get from option(default) getBioColor("DNA_BASES_N") ## get default fixed color getBioColor("DNA_BASES_N", source = "default") seqs <- c("A", "C", "T", "G", "G", "G", "C") ## get colors for a sequence. getBioColor("DNA_BASES_N")[seqs] @ %def You can check the color scheme by calling the \Rfunction{plotColorLegend} function. or the \Rfunction{showColor}. \begin{figure}[h!t!p] \centering @ <>= cols <- getBioColor("CYTOBAND") plotColorLegend(cols, title = "cytoband") @ %def \caption{Legend for cytoband color} \label{fig:cytoband} \end{figure} \subsection{Strand Color} In the \Robject{GRanges} object, we have \Robject{strand} which contains three levels, \textbf{+, -, *}. We are using a qualitative color set from \emph{Color Brewer} and check with \Rpackage{dichromat} as Figure\ref{fig:strand} shows, and we can see that this color set passes all three types of colorblind test. Therefore it should be a safe color set to use to color strand. \begin{figure}[h!t!p] \centering @ <>= par(mfrow = c(1, 3)) cols <- getBioColor("STRAND") showColor(cols) showColor(dichromat(cols, "deutan")) showColor(dichromat(cols, "protan")) @ %def \caption{Colorblind vision check for color of strand} \label{fig:strand} \end{figure} \subsection{Nucleotides Color} We start with the five most used nucleotides, \textbf{A,T,C,G,N}, most genome browsers have their own color scheme to represent nucleotides, We chose our color scheme based on the principles introduced above. Since in genetics, \emph{GC-content} usually has special biological significance because GC pair is bound by three hydrogen bonds instead of two like AT pairs. So it has higher thermostability which could result in different significance, like higher annealing temperature in PCR. So we hope to choose warm colors for \textbf{G,C} and cold colors for \textbf{A,T}, and a color in between to represent \textbf{N}. They are chosen from a diverging color set of \emph{color brewer}. So we should be able to easily tell the GC enriched region. Figure \ref{fig:ne} shows the results from \Rpackage{dichromat}, and we can see this color set passes all two types of the colorblind test. It should be a safe color set to use to color the five most used nucleotides. @ <>= getBioColor("DNA_BASES_N") @ %def \begin{figure}[h!t!p] \centering @ <>= par(mfrow = c(1, 3)) cols <- getBioColor("DNA_BASES_N", "default") showColor(cols, "name") cols.deu <- dichromat(cols, "deutan") names(cols.deu) <- names(cols) cols.pro <- dichromat(cols, "protan") names(cols.pro) <- names(cols) showColor(cols.deu, "name") showColor(cols.pro, "name") @ %def \caption{Colorblind vision check for color of nucleotide} \label{fig:ne} \end{figure} \subsection{Amino Acid Color and Other Schemes} We also include some other color schemes created based on existing object in package \Rpackage{Biostrings} and other customized color scheme. Please notice that the object name is not the same as the name in the options. On the left of \textbf{=}, it's name of object, most of them are defined in \Rpackage{Biostrings} and on the right, it's the name in options. \begin{verbatim} DNA_BASES_N = "DNABasesNColor" DNA_BASES = "DNABasesColor" DNA_ALPHABET = "DNAAlphabetColor" RNA_BASES_N = "RNABasesNColor" RNA_BASES = "RNABasesColor" RNA_ALPHABET = "RNAAlphabetColor" IUPAC_CODE_MAP = "IUPACCodeMapColor" AMINO_ACID_CODE = "AminoAcidCodeColor" AA_ALPHABET = "AAAlphabetColor" STRAND = "strandColor" CYTOBAND = "cytobandColor" \end{verbatim} They all could be retrieved by calling function \Rfunction{getBioColor}. \subsection{Future Schemes} Current color schemes are most generated based on known object in \R{}, which has a clear definition and classification. But we do have more interesting events or biological significance need to be color coded. Like most genome browser, they try to color code many events, for instance, color the insertion size which is larger/smaller than the estimated size; for paired RNA-seq data, we may color the paired reads mapped to a different chromosome. We may include more color coded events in this package in next release. \section{Utilities} \biovizBase{} serves as a basis for the visualization of biological data, especially for genomic data. \Rpackage{IRanges} and \Rpackage{GenomicRanges} are the two most important infrastructure packages to manipulate genomic data. They already have lots of useful and fast utilities for processing genomic data. Some other package such as \Rpackage{rtracklayer}, \Rpackage{Rsamtools}, \Rpackage{ShortRead}, \Rpackage{GenomicFeatures} provide common I/O for certain types of biological data and utilities for processing those raw data. Most of our utilities to be introduced in this section only manipulate the data in a simple and different way to get them ready for visualization. Most cases are only useful for visualization work, like adding brush color attributes to a \Robject{GRanges} object. Some of the other utilities are responsible for summarizing certain types of raw data, getting it ready to be visualized. Some of those utilities may be moved to a separate package later. \subsection{GRanges Related Manipulation} \biovizBase{} mainly focuses on visualizing the genomic data, so we have some utilities for manipulating \Robject{GRanges} object. We are going to introduce these functions in the flow wing sub-sections. Overall, we hope to reduce people's work through these common utilities. % \subsubsection{Chromosome Name Manipulation} % We don't have required canonical chromosome name for % \Robject{seqnames} in \Robject{GRanges}. Most times, we have chromosome % name with prefix \textbf{chr} in lower case. However, we could come % across all kinds of other names with prefix \textbf{Chr}, or % without any prefix at all. This complicates our integration of data % since we need to check with \Robject{seqnames} before we are able to aggregate % them or before we can visualize them. A consistent name scheme is very % important in most graphic packages like \Rpackage{ggplot2}. For % example, you are going to fail if you try to overlay two data in % the same plot which follows a different name schema. Sometimes we % also need to layout our graphics for genomes in a nice ordered way, % which requires some sorting/ordering function to re-order our % \Robject{GRanges} object. % Function \Rfunction{sortChr} works for \Robject{GenomicRanges}, or % characters or factor, sort it based on seqnames. The default is first % showing numeric seqnames in increasing order, then showing mixed % letters names in alphabetical. Function \Rfunction{orderChr} return % an index instead of a \Robject{GenomicRanges} object. The user could also % provide a model which is a vector of seqnames to sort by. % @ % <>= % sort(gr) % head(sortChr(gr, prefix = "chr")) % head(orderChr(gr, prefix = "chr")) % head(sortChr(gr, model = c("chrX", "chr3", "chr1", "chrY", "chr2"))) % sortChr(c("chrX", "chr3", "chr1", "chrY", "chr2")) % orderChr(c("chrX", "chr3", "chr1", "chrY", "chr2")) % sortChr(factor(c("chrX", "chr3", "chr1", "chrY", "chr2"))) % orderChr(factor(c("chrX", "chr3", "chr1", "chrY", "chr2"))) % @ %def \subsubsection{Adding Disjoint Levels} @ <>= library(GenomicRanges) set.seed(1) N <- 500 gr <- GRanges(seqnames = sample(c("chr1", "chr2", "chr3", "chrX", "chrY"), size = N, replace = TRUE), IRanges( start = sample(1:300, size = N, replace = TRUE), width = sample(70:75, size = N,replace = TRUE)), strand = sample(c("+", "-", "*"), size = N, replace = TRUE), value = rnorm(N, 10, 3), score = rnorm(N, 100, 30), group = sample(c("Normal", "Tumor"), size = N, replace = TRUE), pair = sample(letters, size = N, replace = TRUE)) @ %def This is a tricky question. For example, for pair-end RNA-seq data, we may want to put the reads with the same \emph{qname} on the same level, with nothing falling in between. For better visualization of the data, we may hope that adding invisible extensions to the reads will prevent closely neighbored reads from showing up on the same level. \Rfunction{addStepping} function takes a \Robject{GenomicRanges} object and will add an extra column called \textbf{.levels} to the object. This function is essentially a wrapper around a function \Rfunction{disjointBins} but allows a more flexible way to assign levels to each entry. For example, if the arguments \Rfunarg{group.name} is specified to one of the column in elementMetadata, the function will make sure \begin{itemize} \item Grouped intervals are in the same levels( if they are not overlapped each other). \item No entry is following between the grouped intervals. \item If extend.size is provided, it buffers the intervals and then computes the disjoint levels, thus ensuring that two closely positioned intervals will be assigned to different levels, a good practice for visualization. \end{itemize} For now, this function is only useful for visualization purposes. @ <>= head(addStepping(gr)) head(addStepping(gr, group.name = "pair")) gr.close <- GRanges(c("chr1", "chr1"), IRanges(c(10, 20), width = 9)) addStepping(gr.close) addStepping(gr.close, extend.size = 5) @ %def \subsection{Shrink the Gaps} Sometime, in a gene centric view, we hope to truncate or shrink the gaps to better visualize the short reads or annotation data. It's \textbf{DANGEROUS} to shrink the gaps, since it only make sense in visualization. And even in the visualization the x-scale will be discontinued, and labels became somehow meaningless. \textbf{Make sure} you are not using the shrunk version of data when performing the down stream analysis. This is a tricky question too, we hope to provide a flexible way to shrink the gaps. When we have multiple tracks, users would be responsible to shrink all the tracks based on the common gaps, otherwise there will be mis-aligned tracks. \Rfunction{maxGap} computes a suitable estimated gap based on passed \Robject{GenomicRanges} @ <>= gr.temp <- GRanges("chr1", IRanges(start = c(100, 250), end = c(200, 300))) maxGap(gaps(gr.temp, start = min(start(gr.temp)))) maxGap(gaps(gr.temp, start = min(start(gr.temp))), ratio = 0.5) @ %def \Rfunction{shrinkageFun} function will read in a \Robject{GenomicRanges} object which represents the gaps, and returns a function which alters a different \Robject{GenomicRanges} object, to shrink that object based on previously specified gaps shrinking information. You could use this function to treat multiple tracks(e.g. \Robject{GRanges}) to make sure they are shrunk based on the common gaps and the same ratio. Be careful in the following situations. \begin{itemize} \item When use the same shrinkage function to shrink multiple tracks, make sure the gaps passed to \Rfunction{shrinkageFun} function is the common gaps across all tracks, otherwise, it doesn't make sense to cut a overlapped gap within one of the tracks. \item The default max gap is not 0, just for visualization purpose. If for estimation purpose, you might want to make sure you cut all the gaps. \end{itemize} And notice, after shrinking, the x-axis labes only provide approximate position as shown in Figure \ref{fig:shrink-single} and \ref{fig:shrink-two}, because it's clipped. It's just for visualization purpose. @ <>= gr1 <- GRanges("chr1", IRanges(start = c(100, 300, 600), end = c(200, 400, 800))) shrink.fun1 <- shrinkageFun(gaps(gr1), max.gap = maxGap(gaps(gr1), 0.15)) shrink.fun2 <- shrinkageFun(gaps(gr1), max.gap = 0) head(shrink.fun1(gr1)) head(shrink.fun2(gr1)) @ %def \begin{figure}[h!t!p!b] \centering \includegraphics[width = 0.8\textwidth]{intro-shrink-single.pdf} \caption{Shrink single GRanges. The first track is original GRanges, the second one use a ratio which shrink the GRanges a little bit, and default is to remove all gaps shown as the third track } \label{fig:shrink-single} \end{figure} @ <>= gr2 <- GRanges("chr1", IRanges(start = c(100, 350, 550), end = c(220, 500, 900))) gaps.gr <- intersect(gaps(gr1, start = min(start(gr1))), gaps(gr2, start = min(start(gr2)))) shrink.fun <- shrinkageFun(gaps.gr, max.gap = maxGap(gaps.gr)) head(shrink.fun(gr1)) head(shrink.fun(gr2)) @ %def \begin{figure}[h!t!p!b] \centering \includegraphics[width = 0.8\textwidth]{intro-shrinkageFun.pdf} \caption{shrinkageFun demonstration for multiple GRanges, the top two tracks are the original tracks, please note how we clipped common gaps for those two tracks and shown as bottom two tracks.} \label{fig:shrink-two} \end{figure} \subsection{GC content} As mentioned before, GC content is an interesting variable which may be related to various biological questions. So we need a way to compute GC content in a certain region of a reference genome. \Rfunction{GCcontent} function is a wrapper around \Rfunction{getSeq} function in \Rpackage{BSgenome} package and \Rfunction{letterFrequency} in \Rpackage{Biostrings} package. It reads a \Robject{BSgenome} object and returns count/probability for \textbf{GC} content in specified region. @ <>= library(BSgenome.Hsapiens.UCSC.hg19) GCcontent(Hsapiens, GRanges("chr1", IRanges(1e6, 1e6 + 1000))) GCcontent(Hsapiens, GRanges("chr1", IRanges(1e6, 1e6 + 1000)), view.width = 300) @ %def \subsection{Mismatch Summary} Compared to short-read alignment visualization, it's more useful to just show the summary of nucleotides of short reads per base and compare with the reference genome. We need a way to show the mismatched nucleotides, coverage at each position and proportion of mismatched nucleotides, and use the default color to indicate the type of nucleotide. \Rfunction{pileupAsGRanges} function summarizes reads from bam files for nucleotides on single base units in a given region, which allows the downstream mismatch summary analysis. It's a wrapper around \Rfunction{applyPileup} function in Rsamtools package and more detailed control could be found under manual of ApplyPileupsParam function in Rsamtools. \Rfunction{pileupAsGRanges} function returns a GRanges object which includes a summary of nucleotides, depth, and bam file path. This object could be read directly into the \Rfunction{pileupGRangesAsVariantTable} function for a mismatch summary. This function returns a \Robject{GRanges} object with extra \Robject{elementMetadata}, counts for \textbf{A,C,T,G,N} and \textbf{depth} for coverage. \textbf{bam} indicates the bam file path. Each row is single base unit. \Rfunction{pileupGRangesAsVariantTable} performs comparisons to the reference genome(a \Robject{BSgenome} object) and computes the mismatch summary for a certain region of reads. User need to make sure to pass the right reference genome to this function to get the right summary. This function drops the positions that have no reads and only keeps the regions with coverage in the summary. The result could be used to show stacked barchart for the mismatch summary. This function returns a \Robject{GRanges} with the following elementMetadata information. \begin{description} \item[ref] Reference base. \item[read] Sequenced read at that position. Each type of \textbf{A,C,T,G,N} summarize counts at one position, if no counts detected, will not show it. \item[count] Count for each nucleotide. \item[depth] Coverage at that position. \item[match] A logical value, indicate it's matched or not. \item[bam] Indicate bam file path. \end{description} Sample raw data is from SRA(Short Read Archive), Accession: SRR027894 and subset the gene at chr10:6118023-6137427, which within gene RBM17. contains junction reads. @ <>= library(Rsamtools) data(genesymbol) library(BSgenome.Hsapiens.UCSC.hg19) bamfile <- system.file("extdata", "SRR027894subRBM17.bam", package="biovizBase") test <- pileupAsGRanges(bamfile, region = genesymbol["RBM17"]) test.match <- pileupGRangesAsVariantTable(test, Hsapiens) head(test[,-7]) head(test.match[,-5]) @ %def % \subsection{Fragment Length Estimation} % \emph{Fragment length} could be defined in different % ways. Here, the \Rfunction{getFragLength} function simply uses the shrinkage % function (introduced in previous section) to cut all gaps existing in the % provided model and recompute the length for \Robject{GAlignments} % object instead of using its width directly. % @ % <>= % bamfile <- system.file("extdata", "SRR027894subRBM17.bam", package="biovizBase") % library(TxDb.Hsapiens.UCSC.hg19.knownGene) % txdb <- Hsapiens_UCSC_hg19_knownGene_TxDb % exons <- exonsBy(txdb, by = "tx") % model <- subsetByOverlaps(exons, genesymbol["RBM17"]) % ## model <- exonsByOverlaps(txdb, genesymbol[16910]) % frg <- getFragLength(file, model) % @ %def % \subsection{Splicing Summary} % One of the information we could find from the RNA-seq data is the % abundance of different alternative splicing models. There are two ways % to visualizing the slicing summary, one is summary for full model, % which could be represented as \Robject{GRangesList}, for instance, a % \Robject{GRangesList} grouped by transcirpt id, and each element is % \Robject{GRanges} object contains all the exons. Another one is single % model which could be represented as \Robject{GRanges}, for instance, a % \Robject{GRanges} object which just contains all the exons not grouped % by transcript. So we need a way to compute counts support each model % in the full model or splicing junction in the single model. % There are different ways to summarize abundance based on RNA-seq, I % started with a simple approach which just counting reads acrossing the % junction. The algorithm will first filter out reads which are not % junction reads from the raw data, then mapping junction reads to % models. % \begin{itemize} % \item For full model, if one junction reads mapped to one model which % covers two consecutive exons, then this model plus one for % supporting evidence. When \Rfunarg{weighted} turned on to TRUE, if a % junction reads mapped to multiple model, we will simply plus 1/cases % for all the supported model. % \item For single model, we just summarize the splicing of all junction % reads for all the exons. Using notion like \textbf{1-2, 3-4} to % indicate the junction, here the number means the index of given % model, we assume each row in the model is one exon. When % \Rfunarg{model\_id} set to certain column, for example, % 'exon\_id'. Then we use exon\_id for our notion of our summary. % \end{itemize} % The \Rfunction{spliceSummary} is a S4 method which dispatch on the first % arguments, and will return a vector which is total counts for each % model or exon junctions. And names of the vector is transcript name or % notion like \textbf{1-3} to indicate the isoform. % \textbf{Note:} Currently we don't support new model generation, which % means if junction reads cannot mapped to any known model or exons % which passed to argument \Rfunarg{model} of \Rfunction{spliceSummary} % function, we don't give summary about these reads. But in the future, % we would support more flexible summary for this case. % @ % <>= % splice.sum1 <- spliceSummary(bamfile, model) % splice.sum2 <- spliceSummary(bamfile, model, weighted = FALSE) % exonsall <- exons(txdb) % model.single <- subsetByOverlaps(exonsall, genesymbol["RBM17"]) % splice.sum3 <- spliceSummary(bamfile, model.single) % splice.sum4 <- spliceSummary(bamfile, model.single, model_id = "exon_id") % @ %def % \begin{verbatim} % > splice.sum1 % 38191 38192 38193 % 57 57 0 % > splice.sum2 % 38191 38192 38193 % 114 114 0 % > splice.sum3 % 1-2 1-3 % 1 114 % > splice.sum4 % 140875-140876 140875-140887 % 114 1 % \end{verbatim} % \subsection{Aggregating from Raw Data} % Those utilities used inside this package internally, useful % but not exported to users until later, may be dropped or % changed to more general existing method defined in another package, like % package \Rpackage{stream}. \subsection{Get an Ideogram} \Rfunction{getIdeogram} function is a wrapper of some functionality from \Rpackage{rtracklayer} to get certain table like cytoBand. A full table schema can be found \href{http://genome.ucsc.edu/cgi-bin/hgTables}{here} at \emph{UCSC genome browser}. Please click \emph{describe table schema}. This function requires a network connection and will parse the data on the fly. The first argument of \Rfunction{getIdeogram} is \Rfunarg{species}. If \Rcode{missing}, the function will give you a choice hint, so you will not have to remember the name for the database you want, or you can simply get the database name for a different genome using the \Rfunction{ucscGenomes} function in \Rpackage{Rtracklayer}. The second argument \Rfunarg{subchr} is used to subset the result by chromosome name. The third argument cytoband controls if you want to get the gieStain information/band information or not, which is useful for the visualization of the whole genome or single chromosome. You can see some examples in \Rpackage{ggbio}. @ <>= library(rtracklayer) hg19IdeogramCyto <- getIdeogram("hg19", cytoband = TRUE) hg19Ideogram <- getIdeogram("hg19", cytoband = FALSE) unknowIdeogram <- getIdeogram() @ %def \begin{verbatim} Please specify genome 1: hg19 2: hg18 3: hg17 4: hg16 5: felCat4 6: felCat3 7: galGal3 8: galGal2 9: panTro3 10: panTro2 11: panTro1 12: bosTau4 13: bosTau3 14: bosTau2 15: canFam2 16: canFam1 17: loxAfr3 18: fr2 19: fr1 20: cavPor3 21: equCab2 22: equCab1 23: petMar1 24: anoCar2 25: anoCar1 26: calJac3 27: calJac1 28: oryLat2 29: mm9 30: mm8 31: mm7 32: monDom5 33: monDom4 34: monDom1 35: ponAbe2 36: ailMel1 37: susScr2 38: ornAna1 39: oryCun2 40: rn4 41: rn3 42: rheMac2 43: oviAri1 44: gasAcu1 45: tetNig2 46: tetNig1 47: xenTro2 48: xenTro1 49: taeGut1 50: danRer7 51: danRer6 52: danRer5 53: danRer4 54: danRer3 55: ci2 56: ci1 57: braFlo1 58: strPur2 59: strPur1 60: apiMel2 61: apiMel1 62: anoGam1 63: droAna2 64: droAna1 65: droEre1 66: droGri1 67: dm3 68: dm2 69: dm1 70: droMoj2 71: droMoj1 72: droPer1 73: dp3 74: dp2 75: droSec1 76: droSim1 77: droVir2 78: droVir1 79: droYak2 80: droYak1 81: caePb2 82: caePb1 83: cb3 84: cb1 85: ce6 86: ce4 87: ce2 88: caeJap1 89: caeRem3 90: caeRem2 91: priPac1 92: aplCal1 93: sacCer2 94: sacCer1 Selection: \end{verbatim} Here is the example on how to get the genome names. @ <>= head(ucscGenomes()$db) @ %def \begin{verbatim} [1] hg19 hg18 hg17 hg16 felCat4 felCat3 122 Levels: ailMel1 anoCar1 anoCar2 anoGam1 apiMel1 apiMel2 ... \end{verbatim} @ We put the most used hg19 ideogram as our default data set, so you can simply load it and see what they look like. They are all returned by the \Rfunction{getIdeogram} function. The one with cytoband information has two special columns. \begin{description} \item[name] Name of cytogenetic band \item[gieStain] Giemsa stain results \end{description} <>= data(hg19IdeogramCyto) head(hg19IdeogramCyto) data(hg19Ideogram) head(hg19Ideogram) @ %def There are two simple functions to test if the ideogram is valid or not. \Rfunction{isIdeogram} simply tests if the result came from the \Rfunction{getIdeogram} function, making sure it's a \Robject{GenomicRanges} object with an extra column. \Rfunction{isSimpleIdeogram} only tests if it's \Robject{GenomicRanges} and does not require cytoband information. But it double checks to make sure there is only one entry per chromosome. This is useful to show stacked overview for genomes. Please check some examples in \Rpackage{ggbio} to draw stacked overview and single chromosome. @ <>= isIdeogram(hg19IdeogramCyto) isIdeogram(hg19Ideogram) isSimpleIdeogram(hg19IdeogramCyto) isSimpleIdeogram(hg19Ideogram) @ %def \subsection{Other Utilities and Data Sets} We are not going to introduce other utilities in this vignette, please refer to the manual for more details, we have other function to transform a \Robject{GRanges} to a special format only for graphic purpose, such as function \Rfunction{transformGRangesForEvenSpace} and \Rfunction{transformGRangesToDfWithTicks} could be used for grand linear view or linked view as introduced in package \Rpackage{ggbio}. We have introduced data sets like \Robject{hg19IdeogramCyto} and \Robject{hg19Ideogram} in the previous sections. We also have a data set called \Robject{genesymbol}, which is extracted from human annotation package and stored as \Robject{GRanges} object, with extra columns \emph{symbol} and \emph{ensembl\_id}. For fast mapping, we use \emph{symbol} as row names too. This could be used for convenient overlapped subset with other annotation, and has potential use in a auto-complement drop list for gene search bar like most gene browsers have. @ <>= data(genesymbol) head(genesymbol) genesymbol["RBM17"] @ %def \section{Bugs Report and Features Request} Latest code are available on github \url{https://github.com/tengfei/biovizBase} Please file bug/request on issue page, this is preferred way. or email me at yintengfei gmail dot com. It's a new package and under active development. Thanks in advance for any feedback. \section{Acknowledgement} I wish to thank all those who helped me. Without them, I could not have started this project. \begin{description} \item[Genentech]{Sponsorship and valuable feed back and help for this project and my other project.} \item[Jennifer Chang]{Feedback on this package} \end{description} \section{Session Information} @ <>= sessionInfo() @ %def \end{document}

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