biovizBase/DESCRIPTION0000644000126300012640000000236012253761745015755 0ustar00biocbuildphs_compbioPackage: biovizBase Version: 1.10.7 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. Author: Tengfei Yin, Michael Lawrence, Dianne Cook Maintainer: Tengfei Yin Depends: R (>= 2.10), methods Imports: methods, grDevices, stats, scales, Hmisc, RColorBrewer, dichromat, BiocGenerics, IRanges, GenomicRanges (>= 1.13.3), Biostrings, Rsamtools (>= 1.13.1), GenomicFeatures Suggests: BSgenome.Hsapiens.UCSC.hg19, TxDb.Hsapiens.UCSC.hg19.knownGene, BSgenome, rtracklayer biocViews: Infrastructure, Visualization, Bioinformatics, Preprocessing License: Artistic-2.0 LazyLoad: Yes Collate: utils.R color.R AllGenerics.R crunch-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 Packaged: 2013-12-17 05:40:53 UTC; biocbuild biovizBase/NAMESPACE0000644000126300012640000000752612227067715015474 0ustar00biocbuildphs_compbiouseDynLib(biovizBase, .registration=TRUE) ## ====================================================================== ## Import ## ====================================================================== ## methods import(methods) importFrom(stats, setNames) ## BiocGenerics import(BiocGenerics) importFrom(grDevices, colorRampPalette) ## importFrom(BiocGenerics, cbind, rbind) ## RColorBrewer import(RColorBrewer) import(dichromat) ## scales import(scales) ## Hmisc importFrom(Hmisc, bezier) ## IRanges importFrom(IRanges, IRanges, disjointBins, seqapply, breakInChunks, findOverlaps, subsetByOverlaps, "elementMetadata", "elementMetadata<-", metadata, "metadata<-", start, width, end, resize, "values", "values<-", ranges, "ranges<-", isTRUEorFALSE, coverage, slice, elementLengths,endoapply, ## viewWhichMins, viewWhichMaxs, ## viewMins, viewMaxs, viewSums, viewMeans, ## runValue, runLength, reduce, punion, pgap, gaps) importMethodsFrom(IRanges, split, sort, as.factor, unlist, restrict, as.data.frame, length, "[","[<-","[[", "[[<-","$", "%in%", show) importClassesFrom(IRanges) ## ## GenomicRanges importFrom(GenomicRanges, keepSeqlevels, renameSeqlevels, "seqnames<-","strand<-", "seqlevels<-", seqinfo, "seqinfo<-", seqlevels, GRanges, GRangesList, Seqinfo, seqlengths, "seqlengths<-") importMethodsFrom(GenomicRanges, ranges, "ranges<-", start, end, width, "start<-", "end<-", "width<-", seqnames, strand, show, "elementMetadata<-", elementMetadata, as.data.frame) importClassesFrom(GenomicRanges, GRanges, GenomicRanges) ## Biostrings importFrom(Biostrings, AA_ALPHABET, DNA_ALPHABET, DNA_BASES, IUPAC_CODE_MAP, RNA_ALPHABET, AMINO_ACID_CODE, RNA_BASES) ## Rsamtools importClassesFrom(Rsamtools, BamFile) importFrom(Rsamtools, index, scanBamFlag, PileupFiles, PileupParam) importMethodsFrom(Rsamtools, path, ScanBamParam, applyPileups, scanBam, readGAlignmentsFromBam) ## GenomicFeatures importClassesFrom(GenomicFeatures,TranscriptDb) importFrom(GenomicFeatures, transcripts) importMethodsFrom(GenomicFeatures, isActiveSeq, "isActiveSeq<-", exonsByOverlaps, transcriptsBy, exonsBy, cdsBy) ## ====================================================================== ## 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) 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/NEWS0000644000126300012640000000071712227067715014747 0ustar00biocbuildphs_compbioCHANGES 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/0000755000126300012640000000000012253714400014431 5ustar00biocbuildphs_compbiobiovizBase/R/AllGenerics.R0000644000126300012640000000061112227067711016751 0ustar00biocbuildphs_compbiosetGeneric("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.R0000644000126300012640000000242712227067711020310 0ustar00biocbuildphs_compbiosetMethod("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, ignore.strand = TRUE))) 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.R0000644000126300012640000000151012227067711015330 0ustar00biocbuildphs_compbioparseArgsForAes <- function(args){ ## aesthetics <- plyr:::compact(args[.all_aesthetics]) ## aesthetics <- aesthetics[!ggplot2_is.constant(aesthetics)] ## aes_names <- names(aesthetics) ## aesthetics <- rename_aes(aesthetics) ## class(aesthetics) <- "uneval" aes.lst <- unlist(lapply(args, function(x){ class(eval(x, parent.frame())) == "uneval" })) if(length(aes.lst)){ idx <- base::which(aes.lst) if(length(idx)){ res <- args[[idx]] ## res <- eval(args[[idx]]) }else{ res <- list() } }else{ res <- list() } ## res <- c(res, aesthetics) idx <- ggplot2_is_calculated_aes(res) res[idx] <- ggplot2_strip_dots(res[idx]) res } parseArgsForNonAes <- function(args){ lst <- unlist(lapply(args, function(x) class(eval(x, parent.frame())) != "uneval")) args[lst] } biovizBase/R/biovizBase-package.R0000644000126300012640000000376012227067711020257 0ustar00biocbuildphs_compbio##' 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.R0000644000126300012640000002263212227067711015706 0ustar00biocbuildphs_compbio.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 } ## 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.R0000644000126300012640000000477612227067711016374 0ustar00biocbuildphs_compbio### ========================================================================= ### 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 <- 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(seqapply(BINSIZES[BINSIZES <= maxBinSize], function(x) { chunks <- breakInChunks(TOTALSIZE, 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.R0000644000126300012640000002522212253714400017317 0ustar00biocbuildphs_compbiosetGeneric("crunch", function(obj, ...) standardGeneric("crunch")) setMethod("crunch", "TranscriptDb", 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, vals = which, columns = columns) which <- range(temp) } seqnms <- as.character(unique(seqnames(which))) if(seqnms %in% seqlevels(obj)){ seqlevels(obj, force = TRUE) <- seqnms }else{ stop(seqnms, " is not matched with seqlevels of your object, please rename your 'which' arguments ") } ## seqlevels(obj, force = TRUE) <- seqnms on.exit(seqlevels0(obj)) ## 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$tx_id) idx <- togroup(exons$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$tx_id) idx <- togroup(cdss$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)$type) }else{ gr.introns <- GRanges() } ## utrs message("------utr...") if(length(exons) && length(cdss)){ suppressWarnings(irl.utrs <- setdiff(ranges(exons), ranges(cdss))) ir.utrs <- unlist(irl.utrs) if(length(ir.utrs)){ .nms <- names(ir.utrs) .gid.nms <- mt[.nms, "gene_id"] .tx.nms <- mt[.nms, "tx_name"] gr.utrs <- GRanges(seqnms, ir.utrs, tx_id = .nms, tx_name = .tx.nms, gene_id = .gid.nms, type = "utr") names(gr.utrs) <- NULL values(gr.utrs)$type <- as.character(values(gr.utrs)$type) }else{ gr.utrs <- GRanges() } }else{ gr.utrs <- GRanges() } ## combine message("aggregating...") res <- c(gr.exons, gr.cdss, gr.introns, gr.utrs) if(!length(res)) res <- GRanges() res$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)$type %in% c("utr", "cds") res.s <- reduce(res[idx], ignore.strand = TRUE) truncate.fun <- shrinkageFun(gaps(res.s, min(start(res.s)), max(end(res.s))), maxGap(gaps(res.s, min(start(res.s)), max(end(res.s))), ratio = ratio)) } res <- truncate.fun(res) } message("Done") res } }) setMethod("crunch", "GAlignments", function(obj, which, truncate.gaps = FALSE, truncate.fun = NULL, ratio = 0.0025){ if(!missing(which)) obj <- subsetByOverlaps(obj, which) if(!length(obj)) stop("No entry in the GAlignments data") if(is.null(names(obj))) stop("Missing qname, please make use.names = TRUE, when reading GAlignments") grg <- grglist(obj) grg.u <- stack(grg, ".grl.name") message("extracting information...") values(grg.u)$junction <- rep(ifelse(elementLengths(grg)>1, TRUE, FALSE), times = elementLengths(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 <- readGAlignmentsFromBam(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 <- readGAlignmentsFromBam(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$strand, df) else GRanges() }) bam.gr <- do.call("c", res) } biovizBase/R/facets-method.R0000644000126300012640000000561012227067711017310 0ustar00biocbuildphs_compbionewDataAfterFacetByGr <- function(gr, which, id.name){ gr <- sort(gr) which <- sort(which) ## suppose which is a GRanges res <- lapply(seq_len(length(which)),function(i){ res <- subsetByOverlaps(gr, which[i]) values(res)$.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 } setOldClass("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[elementLengths(res)>0] res }) setMethod("splitByFacets", c("GRanges", "GRanges"), function(object, facets){ if(length(facets)){ object <- newDataAfterFacetByGr(object, facets) grl <- split(object, values(object)$.bioviz.facetid) }else{ stop("facets is an empty GenomicRanges object") } grl <- grl[elementLengths(grl)>0] grl }) setMethod("splitByFacets", c("GRanges", "missing"), function(object, facets){ res <- split(object, seqnames(object)) res <- res[elementLengths(res)>0] res }) setMethod("splitByFacets", c("GRanges", "NULL"), function(object, facets){ res <- split(object, seqnames(object)) res <- res[elementLengths(res)>0] res }) isFacetByOnlySeq <- function(facets){ allvars <- all.vars(as.formula(facets)) allvars <- allvars[!allvars %in% c(".", "seqnames")] if(!length(allvars)) TRUE else FALSE } ## that's for linear or default! .checkFacetsRestrict <- function(facets, object){ facets <- strip_formula_dots(facets) allvars <- all.vars(as.formula(facets)) if(length(allvars) == 1){ if(allvars[1] != "seqnames") stop("Column of facets formula can only be seqnames, such as . ~ seqnames, in default restrict mode, you can only change row varaibles") } if(length(allvars) > 1){ if(allvars[2] != "seqnames" & allvars[2] != "."){ stop("Column of facets formula can only be seqnames or '.', such as . ~ seqnames, in default restrict mode, you can only change row varaibles") } if(allvars[1] != "."){ if(!allvars[1] %in% c(colnames(values(object)), "strand")) stop(allvars[1]," doesn't exists in data columns") } } } biovizBase/R/getFragLength-method.R0000644000126300012640000000362612227067711020571 0ustar00biocbuildphs_compbiosetMethod("getFragLength", "character", function(obj, model, which, type = "remove.gaps", maxGap = 0L){ require(Rsamtools) if(missing(which)) which <- range(reduce(model)) if(tools::file_ext(obj) == "bam") res <- scanBam(obj, param = ScanBamParam(which = which, flag = scanBamFlag(isProperPair = TRUE, isFirstMateRead = TRUE))) if(!length(res[[1]]$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.R0000644000126300012640000000312412245756764016367 0ustar00biocbuildphs_compbio##----------------------------------------------------------------## ## ideogram ##----------------------------------------------------------------## getIdeogram <- function(genome,subchr = NULL,cytobands=TRUE){ ## to remove the "heavy dependency" we put require here. require(rtracklayer) if(!(exists("session")&&extends(class(session),"BrowserSession"))) session <- browserSession() if(missing(genome)){ choices <- ucscGenomes()[,1] res <- menu(choices,title="Please specify genome") genome <- as.character(choices[res]) } if(cytobands){ message("Loading...") tryres <- try(query <- ucscTableQuery(session,"cytoBand",genome)) if(!inherits(tryres, "try-error")){ tableName(query) <- "cytoBand" df <- getTable(query) gr <- GRanges(seqnames=df$chrom, IRanges(start=df$chromStart,end=df$chromEnd)) values(gr) <- df[,c("name","gieStain")] message("Done") }else{ message("cytoBand informatin is not available, only get ranges.") message("Loading...") gr <- GRangesForUCSCGenome(genome) message("Done") } }else{ message("Loading...") gr <- GRangesForUCSCGenome(genome) message("Done") } if(length(subchr)) gr <- gr[seqnames(gr) == subchr] ## gr <- sortChr(gr) ## sortChr is removed ## gr <- sort(gr) gr } isIdeogram <- function(obj){ is(obj, "GRanges") && (c("gieStain", "name") %in% colnames(values(obj))) } isSimpleIdeogram <- function(obj){ is(obj, "GRanges") && all(elementLengths(split(obj, as.character(seqnames(obj)))) == 1) } biovizBase/R/labs.R0000644000126300012640000000262312227067711015507 0ustar00biocbuildphs_compbio## going to be moved to biovizBase setGeneric("getYLab", function(obj,...) standardGeneric("getYLab")) setMethod("getYLab", "TranscriptDb", 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.R0000644000126300012640000000015312227067711017255 0ustar00biocbuildphs_compbiosetMethod("maxGap", "GenomicRanges", function(obj, ratio = 0.0025){ ratio * width(range(ranges(obj))) }) biovizBase/R/original.R0000644000126300012640000000217612227067711016375 0ustar00biocbuildphs_compbio## 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, deparse)) } ggplot2_strip_dots <- function(aesthetics){ match <- "\\.\\.([a-zA-z._]+)\\.\\." strings <- lapply(aesthetics, deparse) strings <- lapply(strings, gsub, pattern = match, replacement = "\\1") lapply(strings, function(x) parse(text = x)[[1]]) } biovizBase/R/pileup.R0000644000126300012640000001254012227067711016063 0ustar00biocbuildphs_compbio##' 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 ##' PileupParam 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{PileupParam}. ##' @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{PileupParam}. ##' @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) pileupParams <- PileupParam(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,] if(length(seq)){ GRanges(seqnames = rep(names(x$seqnames), each = length(bams[i])), ranges = IRanges(rep(x$pos, each = length(bams[i])), width = 1), strand = "+", t(seq), depth = colSums(seq), bam = bamNames[i]) }else{ N <- width(regions) GRanges(seqnames = rep(as.character(seqnames(regions)),N), ranges = IRanges(start = start(regions):end(regions), width = 1), strand = rep("*", N), A = rep(0, N), C = rep(0, N), G = rep(0, N), T = rep(0, N), N = rep(0, N), depth = rep(0, N), bam = rep(bamNames, N)) }}) do.call(c, grl[!is.null(grl)]) } gr <- do.call(c, applyPileups(pileupFiles, pileupFun, param = pileupParams)) gr ## rc <- strand(gr) == "-" ## if(sum(rc) > 0) ## values(gr)[rc, DNABases] <- ## values(gr)[rc, as.character(complement(DNAStringSet(DNABases)))] ## split(test, values(test)$bam) } ##' 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] 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.R0000644000126300012640000000312112227067711015647 0ustar00biocbuildphs_compbio## 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.R0000644000126300012640000000202412227067711020463 0ustar00biocbuildphs_compbiosetMethod("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.R0000644000126300012640000003734112227067711020706 0ustar00biocbuildphs_compbiosetMethod("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 <- readGAlignmentsFromBam(obj, param = ScanBamParam(which = which), use.name = 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 <- readGAlignmentsFromBam(obj, param = ScanBamParam(which = which), use.name = TRUE) ## first leave only junction read grl <- grglist(ga) idx <- elementLengths(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)$XS ## strand <- ifelse(!is.na(xs) & xs != "?", xs, "*") ## strand(pairs) <- relist(Rle(strand, elementLengths(pairs)), ## pairs) ## pairs ## } ## gr2key <- function(x) { ## paste(seqnames(x), start(x), end(x), strand(x), ## sep = ":") ## } ## key2gr <- function(x, ...) { ## key_mat <- matrix(unlist(strsplit(x, ":", fixed=TRUE)), ## nrow = 4) ## GRanges(key_mat[1,], ## IRanges(as.integer(key_mat[2,]), ## as.integer(key_mat[3,])), ## key_mat[4,], ...) ## } ## findIsoformOverlaps <- function(pairs) { ## splices <- values(pairs)$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 <- ## elementLengths(setdiff(hit_pairs, hit_tx)) == 0L ## tx_within <- ## elementLengths(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, vals = list(gene_id = id), ## columns = c("tx_id", "gene_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), ## elementLengths(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$gene_id), ## ## elementLengths(aldoa_vals$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.R0000644000126300012640000005734512227067711016614 0ustar00biocbuildphs_compbio## 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$.biovizBase.group <- i ## need to past other meta data extra.df <- subset(linkdf2[i,], select = -c(from.x, from.y, to.x, to.y)) extra.df2 <- do.call("rbind", lapply(1:N, function(i) extra.df)) ndf <- cbind(ndf, extra.df2) }) res <- do.call("rbind", lst) res } ## ddplyFun <- function(data, .fun, ..., window = 1e5){ ## grl <- split(data, seqnames(data)) ## idx <- elementLengths(grl) > 0 ## grl <- endoapply(grl[idx], function(gr){ ## ## let's make it more works for multiple seqnames ## bks <- seq(1, max(end(gr)), by = window) ## N <- length(bks) ## seqn <- unique(seqnames(gr)) ## if(length(seq) > 1) ## stop("Multiple seqnames found") ## if(!N%%2){ ## qgr <- GRanges(seqn, IRanges(start = bks[1:(N-1)], ## end = bks[2:N])) ## }else{ ## bks <- c(bks, max(end(gr))) ## N <- length(bks) ## qgr <- GRanges(seqn, IRanges(start = bks[1:(N-1)], ## end = bks[2:N])) ## } ## if(max(end(qgr)) < max(end(gr))){ ## qgr <- c(qgr, GRanges(seqn, IRanges(max(end(qgr))+ 1, ## max(end(gr))))) ## } ## of <- findOverlaps(gr, qgr, select = "first") ## idx <- !is.na(of) ## df <- as.data.frame(gr[idx]) ## df$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)$coord <- "even" gr } validEven <- function(data){ findOverlaps(gr, ignore.self = TRUE) gr2 <- GRanges("chr1", IRanges(c(1, 10), width = 5)) countOverlaps(gr) } transformToEven <- function(data){ st <- start(range(data)) ed <- end(range(data)) wd <- width(range(data)) N <- length(data) wid <- wd/N x.new <- st + wid/2 + (1:N - 1) * wid gr <- GRanges(start = x.new, width = wid) values(gr) <- values(data) ## values(gr)$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.R0000644000126300012640000004206212240272173015722 0ustar00biocbuildphs_compbiocontainLetters <- 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 <- all.vars(as.formula(facets)) allvars.extra <- allvars[!allvars %in% c(".", "seqnames")] 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 <- elementLengths(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(elementLengths(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(gps.sub),,drop = FALSE] strand(gr) <- stds[togroup(gps.sub)] }else{ gr <- GRanges() } gr }) res <- unlist(grl) if(length(res)){ values(res)$type <- "gaps" res <- resize(res, width = width(res) + 2, fix = "center") }else{ res <- 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(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.name = 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,"TranscriptDb")) type <- "all" if(is(obj,"BamFile")) type <- "gapped.pair" } if(is(obj, "TranscriptDb")){ if(!(type %in% .txdb.type)) stop("type for TranscriptDb must be ", .txdb.type) if(is.list(which)){ message("Parsing exons based on which(list) arguments") temp <- exons(obj, vals = which, columns = columns) 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)$type <- factor("gap") res <- c(cds.s, utr.s, gap.s) } } message("Done") } if(is(obj, "GappedAlignments")){ ## require(Rsamtools) ## require(Rsamtools) if(!missing(which)) obj <- subsetByOverlaps(obj, which) if(!length(obj)) stop("No entry in the GappedAlignments data") if(is.null(names(obj))) stop("Missing qname, please make use.name = TRUE, when reading GappedAlignments") grg <- grglist(obj) grg.u <- stack(grg, ".grl.name") message("extracting information...") values(grg.u)$junction <- rep(ifelse(elementLengths(grg)>1, TRUE, FALSE), times = elementLengths(grg)) names(grg.u) <- NULL res <- grg.u } if(is(obj, "BamFile")){ if(!(type %in% .bamfile.type)) stop("type for TranscriptDb must be ", .bamfile.type) ## require(Rsamtools) if(type == "gapped.pair"){ message("Read GappedAlignments from BamFile...") ga <- readBamGappedAlignments(obj, param = ScanBamParam(which = which), use.names = use.name, ...) 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 <- readBamGappedAlignments(obj, param = ScanBamParam(which = which), use.names = use.name, ...) 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 } biovizBase/R/zzz.R0000644000126300012640000000165312227067711015425 0ustar00biocbuildphs_compbio.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/0000755000126300012640000000000012253761745015345 5ustar00biocbuildphs_compbiobiovizBase/build/vignette.rds0000644000126300012640000000035212253761745017704 0ustar00biocbuildphs_compbio‹mQÍ ‚@^úQŸÀw(Dˆ.ºnºÂ€íŠ®JžzòjÖ4rk`fgg¾ùøf÷ìBLb¡›¦–‡aоD7ˆM<à²Á‘7Zc½áþNõ’*– 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/cedilla /.notdef /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/inst/doc/intro.R0000644000126300012640000001670312253761745017255 0ustar00biocbuildphs_compbio### R code from vignette source 'intro.Rnw' ################################################### ### code chunk number 1: options ################################################### options(width=72) ################################################### ### code chunk number 2: color-scheme-option ################################################### library(biovizBase) ## library(scales) ################################################### ### code chunk number 3: color-pal-info ################################################### head(blind.pal.info) ################################################### ### code chunk number 4: colorBlindPal ################################################### ## with no arguments, return blind.pal.info head(colorBlindSafePal()) ## mypalFun <- colorBlindSafePal("Set2") ## mypalFun(12, repeatable = FALSE) #only three mypalFun(11, repeatable = TRUE) #repeat ################################################### ### code chunk number 5: color-dichromat ################################################### ## 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")) ################################################### ### code chunk number 6: cytoband-color ################################################### 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] ################################################### ### code chunk number 7: cytoband-color-legend ################################################### cols <- getBioColor("CYTOBAND") plotColorLegend(cols, title = "cytoband") ################################################### ### code chunk number 8: strand-color ################################################### par(mfrow = c(1, 3)) cols <- getBioColor("STRAND") showColor(cols) showColor(dichromat(cols, "deutan")) showColor(dichromat(cols, "protan")) ################################################### ### code chunk number 9: base-color ################################################### getBioColor("DNA_BASES_N") ################################################### ### code chunk number 10: ne-dichromat ################################################### 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") ################################################### ### code chunk number 11: sample-gr ################################################### 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)) ################################################### ### code chunk number 12: addStepping-gr ################################################### 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) ################################################### ### code chunk number 13: maxGap ################################################### 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) ################################################### ### code chunk number 14: shrink-single ################################################### 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)) ################################################### ### code chunk number 15: shrinkageFun ################################################### 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)) ################################################### ### code chunk number 16: gc-content (eval = FALSE) ################################################### ## library(BSgenome.Hsapiens.UCSC.hg19) ## GCcontent(Hsapiens, GRanges("chr1", IRanges(1e6, 1e6 + 1000))) ## GCcontent(Hsapiens, GRanges("chr1", IRanges(1e6, 1e6 + 1000)), view.width = 300) ################################################### ### code chunk number 17: PileupAsGRanges (eval = FALSE) ################################################### ## 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]) ################################################### ### code chunk number 18: ucsc-genome (eval = FALSE) ################################################### ## library(rtracklayer) ## hg19IdeogramCyto <- getIdeogram("hg19", cytoband = TRUE) ## hg19Ideogram <- getIdeogram("hg19", cytoband = FALSE) ## unknowIdeogram <- getIdeogram() ################################################### ### code chunk number 19: ucsc-genome-db (eval = FALSE) ################################################### ## head(ucscGenomes()$db) ################################################### ### code chunk number 20: default-data ################################################### data(hg19IdeogramCyto) head(hg19IdeogramCyto) data(hg19Ideogram) head(hg19Ideogram) ################################################### ### code chunk number 21: check-ideogram ################################################### isIdeogram(hg19IdeogramCyto) isIdeogram(hg19Ideogram) isSimpleIdeogram(hg19IdeogramCyto) isSimpleIdeogram(hg19Ideogram) ################################################### ### code chunk number 22: genesymbol ################################################### data(genesymbol) head(genesymbol) genesymbol["RBM17"] ################################################### ### code chunk number 23: R-session ################################################### sessionInfo() biovizBase/inst/doc/intro.Rnw0000644000126300012640000010575012227067714017617 0ustar00biocbuildphs_compbio%\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 PileupParam 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} biovizBase/inst/doc/intro.pdf0000644000126300012640000103756712253761745017641 0ustar00biocbuildphs_compbio%PDF-1.4 %ÐÔÅØ 1 0 obj << /S /GoTo /D (section.1) >> endobj 4 0 obj (Introduction) endobj 5 0 obj << /S /GoTo /D (section.2) >> endobj 8 0 obj (Color Schemes) endobj 9 0 obj << /S /GoTo /D (subsection.2.1) >> endobj 12 0 obj (Colorblind Safe Palette) endobj 13 0 obj << /S /GoTo /D (subsection.2.2) >> endobj 16 0 obj (Cytobands Color) endobj 17 0 obj << /S /GoTo /D (subsection.2.3) >> endobj 20 0 obj (Strand Color) endobj 21 0 obj << /S /GoTo /D (subsection.2.4) >> endobj 24 0 obj (Nucleotides Color) endobj 25 0 obj << /S /GoTo /D (subsection.2.5) >> endobj 28 0 obj (Amino 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biovizBase/inst/examples/0000755000126300012640000000000012227067715017036 5ustar00biocbuildphs_compbiobiovizBase/inst/examples/color.R0000644000126300012640000000133112227067715020275 0ustar00biocbuildphs_compbiogetBioColor("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.R0000644000126300012640000000602012227067715020637 0ustar00biocbuildphs_compbiolibrary(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)$symbol save(genesymbol, file = "~/Datas/rdas/genesymbol.rda") save(genesymbol, file = "~/Codes/gitrepos/biovizBase/data/genesymbol.rda") save(hg19IdeogramCyto, file = "~/Codes/gitrepos/biovizBase/data/hg19IdeogramCyto.rda") save(hg19Ideogram, file = "~/Codes/gitrepos/biovizBase/data/hg19Ideogram.rda") id <- unlist2(mget("FOXD4L2", revmap(org.Hs.egSYMBOL))) id <- revmap(org.Hs.egSYMBOL)[["FOXD4L2"]] org.Hs.egCHRLOC[[id]] org.Hs.egCHRLOCEND[[id]] biovizBase/inst/examples/test.R0000644000126300012640000001211712227067715020142 0ustar00biocbuildphs_compbiolibrary(biovizBase) ## ------------------------------------------------------------ ## getBioColor ## ------------------------------------------------------------ opts <- getOption("biovizBase") opts$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) ## library(rtracklayer) library(biovizBase) hg19IdeogramCyto <- getIdeogram("hg19", cytoband = TRUE) hg19Ideogram <- getIdeogram("hg19", cytoband = FALSE) unknowIdeogram <- getIdeogram() head(ucscGenomes()$db) data(hg19IdeogramCyto) head(hg19IdeogramCyto) data(hg19Ideogram) head(hg19Ideogram) ## to be removed library(biovizBase) library(TxDb.Hsapiens.UCSC.hg19.knownGene) data(genesymbol, package = "biovizBase") txdb <- TxDb.Hsapiens.UCSC.hg19.knownGene txdb@organism wh <- genesymbol["BRCA1"] genome(txdb) str(txdb) obj <- txdb ## decrease from 18s to 13s, then to 4.7s system.time(temp <- crunch(txdb, which = genesymbol["BRCA1"], type = "all")) system.time(temp <- crunch(txdb, which = genesymbol["BRCA1"], type = "single")) library("org.Hs.eg.db") hdb <- org.Hs.eg.db k <- keys(hdb, keytype = "SYMBOL") res <- genGenesymbolTable(hdb, keys = c("BRCA1", "BRCA2")) res <- genGenesymbolTable(hdb, keys = c("BRCA1", "BRCA2"), unique = FALSE) biovizBase/inst/extdata/0000755000126300012640000000000012227067714016651 5ustar00biocbuildphs_compbiobiovizBase/inst/extdata/SRR027894subRBM17.bam0000644000126300012640000121454512227067714021735 0ustar00biocbuildphs_compbio‹ÿBCmV[h^Ežü¿‰É_‰ * ""¾H_vgfo±Ä‚O¦ ÑÒJ¼„FB[K!AT„‚k±P+¤Ôx¡7ŸD_¤(æ­ë£xAß‚ |Ñh‘âþgÏ9ÿžœy8û}3³3ßΞǦg†t`jöɱÙ]Ï¿pT«±'vMh2†Ø±ëeŒž[8¨”B…sGŸ=<ÿ⡾%+­¨aUú+e¶9ƒ‰!o´&g¨`t´Þùœá‚QŽ8V9cƒ†4ÌÛg‚"ÃÎ4RsU”@Žƒ­8³òš´­Lf¥/³¹fZ)ݰJ[è`°¹‹¯Ü]Q¯ïƒÎ+盇ÊÛgÞ­¢UÈ+1!FìG}ð U“»:wW–I´Ê{'‡F‹ôQä€FYÌ¢+-Åã6˜+„USj•Fg=6¬ ݼÆÐì<,zÒhRllž ¦LH‡@./$µjð #›gÂU…ysÅFw µk«¼¹¢vÜ›KTŽ¥dDjz¯‚6hóÝmj?]”Ío­«6lô©§˜ÇuÕ™“·6/×Wîyÿ’ KF®q¯´Ë¥.º4ÖI–£v*ïF—*ådÔhÒþï‚ÛV¨T£Xÿ’UÞ±duãò„”®FM± 2b&íl\>}¸jÃôû³¶ÙN>ý½õÆ‹|ê/ËHAäSksZöOâаù²Q‹¼+yÍòþé­Ö·aÀ'Ý\ÐAÌ/]äè/È'ýâëÄøXëgEý‘ÊÂF¬¹ÌÏùB¿xŒÚÉ|Ò/¾nryI>ôäDy1ɇñ7ªD>ÉâE”h*Ôc²A,žÒÿÓÅK,Ò˜lkD驎M`98'oC2]GÌrádÓÃH¦]ÚÛ[ñÔ©â¿XlJ*T‹ƒŠÁYU{‹¢rzâÕeᤔ½“jD²jÌeæ(fÎIµø»½múÝÆw@¤]òf”3/Usr;pRÍ›ÆMÜSÞ?tÊ4^˜½éý¯aÿ×öŒÄ¯˜aåÞ»Fï)W­).œØjà±ÛF«Âæâ[«Áî}¿ŒT+†‡GÔ+SÇî¯W¦?n¸Ú±5ÖÁ˧Zlõâ¹ɡ6[=ðߥN›­^?xduP‹ƒk~KeÛÕàü[Sû/Ô¶­Á î\äÔÈ`íP§ŽàÌŽãÝ»ËÕÖá ÖÞ‚­d}÷ÂpIÂäΟÇË ¨àȧkÝ2öL¬KA ¿vªÂòãÝ2(Â‰×ÆËÁ§¯o+siMG°½[Éúˆ6þèT‰2Ì_ßV. ìxëj¯\Xx´C½2FkÎ#×êv¾:VZ¶Fè¼°•¬OѽUË»¿--[c ¬ÏÕÒ·Æ8u¦³…L)°òS›¬O”OÔ Øüjq´\ÌÀ•)€ÛÓ"@àü›6ŒðûLpò˜3ü}ŸúP€-Œ| À–VØÃ+Kàæ•6;³÷’kž`„ ¡J$øíkfØøR€ ¬ûn¶°:ÑÖ,ÿ5Ô†=<óøf¦„|rY€5ÜX`„oÏ 0ÁÒgÌ0+Y¸|\€-|÷‘;Ø.ÅöÐ=+À|½ ³‚ëBlÖpñcFè š0ÁÌ%føwE€ l?)Àz§ØÁão °‡E)v€ïÖWs¬NN•‹½psóîÿ-íá ]‹ÿBCžB½KŒ,[—T÷öí¾ÿžs*³"#wDìg¨,•„€x? ƒSõ—¬bà¶q²ÔH0bB¡vß[”¡Ôw# É< ˜‡,&ÍÀ€Àc›BHX A Z0€- [ÍZkï™U™¹#óÜS•Uç×_®½öz?~ëʾê¿û^­çùòg®þÔÕßï~÷ÿ[ðê„ï¿ðþ@QõÃØü-M=VM_\]}yuu󧿺úõ¯®®ž×wO«ç<2w¯÷ÑÃ:_›|ýGw«××—__dQ´Žž^Ÿ×·/¯yôðr-Òu²Ù^o³ëøzµe›DܬãïWŸâè›èz˜Üú»{i£à‹š~Ê´Öð+£à»Rø^l¹YƸÚÈ,K²$ÍÒÍÍ&^ýüïýéØ}¤¿óWðcþ'7_\ýW3üü;îuµ÷1ëjèû¡¿úËð1ó×ÕóÝ{½{ØËóëëÓÝ]¾~ùÁä9Àƒ¿ôǾL.éknvð9ü˜‚«eš²ê±9‰À>–¾MÌ —öt3yz‚±Úò4 öNgþÆþ¤”ý•„óas<AW·eÝ—0Ïëêeýrÿ ßî_Yôãúõù` ni­Ìôá5þ_¤6ÂhÎŒ´Ì³A_ômU4'äÓ Þê|vîÇÙ/.@ߺñÇÆ>ÒäÚßÜq(„"Ê\€ oÇ¡®ä³O»ãCc<‹i9‚²†®éO"ÀÏæ>ì¡Ü0–zâÐ  mQ4gi`Üåw¤ßqVþ–#¨Ú¦‡.¼dæžžM$€+ Qy*,GP]UžGï¿´c ã y65òíÐöeFdžö8¼D&^Tþd.@ÐÁ]h‡3œ8»ô@AïtîžïÏh³A[”E@ûpé>³•Éø~#à WB]ÈmÕÀ‹Afw!ßÝ ¢‚¾\´uÝãy¾Ìþ—|Ç’sÿC‚¡ì»ÑñÁÝ«ççA9Þ¿þøüx÷ºBEy? 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Ü6ç‡PioÍÑçó¦úèU_âJ}…[¶Î|8C€}©;y8`ƃàýmòÍF«ƒIö{o’èeuª•W"ê®uwçÞ8œÁ §ˆ‰SW’ÚmŽ´D†Qà€MjW“ÊëtE†©šCÀƒƒæ¤Ž»â‚Pi0–¾Î ‚CpËJn ÐzÂmö•¹&=És¾.r­DÐÔUUÎR„n²¨ Ãç«Që¥N\‡ Wýì ^^!xܤ|óÍÁ¶?>ÉDð W@‹D¿5[Më"Ô¼î羨«¶™¥‚ò•ìMNÈ99’^¶´Å×@ë€uî˼[ ÂÄ#¡7{1*G¿5V+Ï?Ÿ XÕÖVu7Á¹Ê„^P{%¬o‹ór—©´Z—ËË‹ÒùÊ7dŠZ•1,À{'ñ@àgÛ1®m͇5£0bƒ÷HÏ `â¤hî í0“XOò-ã#ñ½ èY( !­}C#Ù+O9·™ ,«ŠQ;x'§Ž¢¤·•”neÌ ‚Ÿ <tËDËà9³>šŸ))§”îGPWCÙ”³Œ(É;!Ÿæ€Ø))…S,ÌbA¯9A Ñû¥m¼ÎSd|tè.×F¤¢6ŒºAvi˜·Ò®h™wv~þ¡i>ÊCÉÇ5ηt¢¯i¨ †2}åõJþçºTZa›Ë\ðÉ^áI,/íüs Ÿ7±±ìÁ-•‚«d©m†òÃTÿ/ SÍF®yw}EƒT8PõÛ——ÏÉËËÛ/>èO/¿Õæóç¯õû‡7)¾’#}ƒ¯IjߦÇ7îïìë¦ Ûßþݪ<ÊP5•‹ŸÃÃ_ô=üÓÓ‡çgÛ€€ìì—¶}XìÇ›ø9-"“Y†^ËÔ>þþß­â…<׎ô%Ùí6»Ï/Ï›w__>™ÝǯÉÓÓ—G·ûUó°5ÉœËný³©Û:å…íª3h›¶ë ¯áÓ›ñÓ¿¼}2_7´@9 ä§üPG«0Kc3Kú­Rº²mš>…ÀLœ%ŒBKâé[æÒÞ~Õ¾PgTX‰ ®‹ÞÝwó ´Ü†@¤ÈÂŒFɸ&ʨ3hê¾i_ŸÁÓùœ¥ÐôµO+âôÿýÀ2 £´pdÿíÉõ íL¶ñ†Ž(ÒLš~ȯðÁù@¤ 2nM Ö0Ìt“‚T‰]A*]ƒä_N<.§× ß‚qëùÚ-nÑ]±!˜vÍÔÊIÂw“ç/§÷!ví‚y¾@«­ÜIŸ>DuLOfv³"6ê ìPˆP„j”—9uÔDbèŒwÆãæܦ.%ƒwGÌýß /BWÜí0¡E}2Ê5ÚkFá#-Û¿Ÿ ‹*¯»bXİ!\O¶VPµ)t¯Ž³¥w"èë¢(¯ÁLÄ€î±×Â9殑?•'óè¬ü¼?D¨Ã /ŠÌ!´¤Ž:• ã»´Z‚w­DñRÕ-(dß`@M>¿LÂOÔ°PÚßda÷¿ºÆ˜àôÕèq|Kj·Ø‘V«eLÚÍùJâP&ö1š~ÑA ‘3a°ÔF'é~MÞWŰh°ïN¥Ô‘((Ão[ä¨=6“vÜV°·1œØ ¨ƒãll-KûJϹeœ6°Æ„ ySùþ‡Yó¬ÒnÿuÁ  t= ÷wKŸÁn‚ž¦Í-^EJ›ç§æ{eEÁ¹GþR¶É1ù~?‚¡ÆQïjÁT˜«ª€ ÐGÖ3°;å…‹´[å"Uus^@1SYŠ[ƒPI†•Høä)D«Ø/wâ÷š¶Èg¤Æ·½1™ÖLSÌê± #ÅýOŽ  ä~³?oBYGƒ¢®‡Òy·ŽÀ¸ñf¯¥š’nϨÄNØ“ Á‡n¯—¸`²WVºŽESJûI!gVa¿NJܺ`Ïà•(& ŠOaÕ¼1ãìŽð[ðÃß9mùÇ“»}Áv1…ƒiío–÷ q®j„§GßA‘±­ý‡&%r‘\ÕÝ„d:õ¿_Ç଺ûsoC¸ÍµMïr«ŠðÍ”5RSoy%ªÓªÃÁóGý›É¨Q!ÈXApÐUúˆ­G,F‹½©HûL¤i6Mc­D0´}çš².Ï@{ÜööN€Ú“¨gžz”ܦÁé×Y†º+«Ê'Ò®p~ôŽ2§Åð̘ؗÕ};$ˆ8žõ'®DÐwuã·?Ü@”2Õ¹-H PhÇå ¨7 ¹ä~¨Ï7¼,D›-¦NZ’DÚXÓ¦î~ct—Õ¹mZ‰ ¨‡|èç©l3µ„Iu nº½ƒÔ´7%ÉX&Ä!ÁЖµ›§š;çØt*.ß%» šIûK}>K´A_à­µ…Cðî*a¼Oš!±Kýh'r6Y ô‰YwÊB_‚Ÿæ"†*˜°‰Ûõù‡ ûƒïZ¼ÿ †¼Ä>ŒY O϶h$ìÏÂj¿À¤ H(ÇdÇþD¤Lƒ  su·ú’Žu+ì‡u<ò„¶-ÂyÌÀ6¢×ƒ€&(–¨€\vLN‚³®å ú-½€*»-ÂÂlœĔitáŠ_êÝv®µ±_Ú! CÛàeÖg~}CÊì!Ã<ªëw{òù¡†`‡©q>®2ÎE úhABÍKžó &?Z4úÌW] ésŸC¹ÍÊŸIœ$}H^bú¸µÑrªŒ° E>4¾Ø·¤18 ù yÖ‰ä#J‚º¬ë¢["eÑ|ÔàîG¾¸£íSøC„,–mÕuý¢w.i±Mn‰ å»õÔ~Éb´CSÌ{¶t¢lëÖÙû•vcE´~¡ ª¼+Ûn‘ 𻲥­ºbë.^¢l7‚Kl¢•äLÊ>¨ª<죙õ TešIé¤x·ßýLóCÔxd ¢·] „ÈWPÁ¥³Â¦‰ñ2%«äã›ÜG è+`ƒy>Vð3Ø:kF·UØ•]ä%aŽ5ÂCªË¾ÉÛ+|`.ýT;â£V`Áä˜Q¼Hí)ô&c÷û'uƒ|°äÊP0iefË<‚Fx°ö#ާˆ3ðf½vÖGÓÓìUh+OX™¨ìÎ:¯4u]Õ¬>pa*Ò€I4Jª=’«d¿JÊìß›³A“ûyª9*¸= ¹kTè<ÙÚϨ{“Òì*M""&PIþÞœÙhÁßbgoGÆ‚!…9Mv‰èÝfŠ Y™Ñ„ÐÝÕ^åP6ÌóÛ÷>’Ô.)üH…Öû‰o˜½ÎêlcŸ\Õ~QàŒÖ:(¯?ÿîkbp¢+U4&Á­rT6£e¸Íu†4ãeKÖ: EÓs¦õM3îQ.µã~k^Ï:ÿë•Y]ð“ý Í4…õüöóÇçwð/¯o¾\ÇÅSd¦¦ÒX®‹˜*lŒ³TŸýžýåÙ<›·£›è¿øNå'TvD®Ð2!}ðÿð.’Ã׋ÿBCbiovizBase/inst/extdata/SRR027894subRBM17.bam.bai0000644000126300012640000000730012227067714022453 0ustar00biocbuildphs_compbioBAITwç¿çeJ’eÜ,wbiovizBase/inst/extdata/crc-rearrangment.csv0000644000126300012640000035366512227067714022642 0ustar00biocbuildphs_compbio"individual","chr1","str1","pos1","chr2","pos2","class","span","tumreads","normreads","gene1","gene2","site1","site2","fusion","quality","score","BPresult","validation_result" "CRC-4",18,1,56258628,18,58362793,"long_range","2104165",491,2,"MC4R","ZCCHC2","IGR: 69Kb before MC4R(-)","Intron of ZCCHC2(+): 222bp before exon 4","-",1,491,-1,"not_subjected_to_validation" "CRC-4",18,1,44496014,18,57443167,"long_range","12947165",265,0,"KIAA0427","CDH20","Intron of KIAA0427(+): 4Kb after exon 8","IGR: 134Kb before CDH20(+)","-",0.9944118,263.5191,1,"not_subjected_to_validation" "CRC-4",18,0,45023683,18,58380361,"long_range","13356670",238,0,"DYM","ZCCHC2","Intron of DYM(-): 14Kb after exon 13","Intron of ZCCHC2(+): 854bp before exon 9","Protein fusion: in frame (ZCCHC2-DYM)",1,238,1,"somatic" "CRC-4",8,0,52186319,8,52186587,"deletion","268",94,0,"PXDNL","PXDNL","IGR: 208Kb before PXDNL(-)","IGR: 208Kb before PXDNL(-)","-",1,94,-1,"not_subjected_to_validation" "CRC-4",8,0,37328910,20,9561906,"inter_chr","NaN",56,0,"ZNF703","PAK7","IGR: 344Kb before ZNF703(+)","Intron of PAK7(-): 11Kb after exon 4","-",0.9740215,54.54521,1,"somatic" "CRC-4",8,0,35575394,20,36595752,"inter_chr","NaN",53,0,"UNC5D","RALGAPB","Intron of UNC5D(+): 3Kb after exon 4","Intron of RALGAPB(+): 839bp after exon 15","Antisense fusion",1,53,1,"not_subjected_to_validation" "CRC-4",20,1,11072897,20,18064337,"long_range","6991442",51,0,"JAG1","PET117","IGR: 470Kb after JAG1(-)","Promoter of PET117(+): 2Kb from tx start","-",1,51,1,"somatic" "CRC-4",20,1,18085103,20,37021184,"long_range","18936090",49,0,"CSRP2BP","DHX35","Intron of CSRP2BP(+): 3Kb before exon 4","IGR: 3Kb before DHX35(+)","-",0.9895204,48.4865,1,"somatic" "CRC-4",8,1,35357822,8,40866668,"long_range","5508863",47,0,"UNC5D","ZMAT4","Intron of UNC5D(+): 145Kb after exon 1","5'-UTR of ZMAT4(-): 64Kb before coding start","-",1,47,1,"not_detected" "CRC-4",20,0,11078572,20,16865475,"long_range","5786913",47,0,"JAG1","OTOR","IGR: 476Kb after JAG1(-)","IGR: 188Kb before OTOR(+)","-",1,47,1,"somatic" "CRC-4",8,0,40564418,8,41258684,"inversion","694247",42,0,"ZMAT4","SFRP1","Intron of ZMAT4(-): 6Kb before exon 6","Intron of SFRP1(-): 17Kb before exon 3","-",1,42,1,"somatic" "CRC-4",8,0,38794152,20,15734259,"inter_chr","NaN",42,0,"TACC1","MACROD2","Intron of TACC1(+): 2Kb before exon 3","Intron of MACROD2(+): 57Kb before exon 9","Antisense fusion",0.9962541,41.84267,1,"somatic" "CRC-4",8,0,32575936,20,19499614,"inter_chr","NaN",41,0,"NRG1","SLC24A3","Intron of NRG1(+): 3Kb after exon 2","Intron of SLC24A3(+): 9Kb before exon 4","Antisense fusion",1,41,1,"somatic" "CRC-4",20,0,9579492,20,11068460,"long_range","1488970",41,0,"PAK7","JAG1","5'-UTR of PAK7(-): 7Kb before coding start","IGR: 466Kb after JAG1(-)","-",1,41,1,"somatic" "CRC-4",8,1,29956507,8,40870381,"long_range","10913876",40,0,"LOC286135","ZMAT4","IGR: 58Kb before LOC286135(+)","5'-UTR of ZMAT4(-): 68Kb before coding start","-",1,40,1,"somatic" "CRC-4",8,1,40568862,8,41210874,"inversion","642014",39,0,"ZMAT4","SFRP1","Intron of ZMAT4(-): 11Kb before exon 6","IGR: 28Kb before SFRP1(-)","-",1,39,1,"somatic" "CRC-4",8,0,41184494,8,41861964,"deletion","677469",37,0,"SFRP1","ANK1","IGR: 54Kb before SFRP1(-)","Intron of ANK1(-): 11Kb after exon 1","-",1,37,1,"somatic" "CRC-4",8,1,33309871,20,17303124,"inter_chr","NaN",34,0,"FUT10","PCSK2","IGR: 38Kb before FUT10(-)","Intron of PCSK2(+): 5Kb after exon 5","-",1,34,1,"somatic" "CRC-4",8,1,25088587,20,18210598,"inter_chr","NaN",33,0,"DOCK5","ZNF133","IGR: 10Kb before DOCK5(+)","IGR: 7Kb before ZNF133(+)","-",1,33,1,"somatic" "CRC-4",8,1,30408156,20,11069502,"inter_chr","NaN",33,0,"RBPMS","JAG1","Intron of RBPMS(+): 44Kb before exon 2","IGR: 467Kb after JAG1(-)","-",1,33,1,"somatic" "CRC-4",20,1,15506293,20,18142088,"long_range","2635801",33,0,"MACROD2","CSRP2BP","Intron of MACROD2(+): 78Kb after exon 8","IGR: 25Kb after CSRP2BP(+)","-",1,33,1,"somatic" "CRC-4",20,1,18162173,20,21266868,"long_range","3104690",33,0,"ZNF133","XRN2","IGR: 55Kb before ZNF133(+)","Intron of XRN2(+): 819bp before exon 14","-",1,33,1,"not_subjected_to_validation" "CRC-4",8,1,30530516,8,37326190,"long_range","6795643",32,0,"RBPMS","ZNF703","Intron of RBPMS(+): 4Kb after exon 7","IGR: 346Kb before ZNF703(+)","-",1,32,1,"somatic" "CRC-4",20,0,11072781,20,19498233,"long_range","8425437",31,0,"JAG1","SLC24A3","IGR: 470Kb after JAG1(-)","Intron of SLC24A3(+): 10Kb before exon 4","-",1,31,1,"somatic" "CRC-4",20,1,17295462,20,18952001,"long_range","1656554",31,0,"PCSK2","SLC24A3","Intron of PCSK2(+): 2Kb before exon 5","IGR: 189Kb before SLC24A3(+)","-",1,31,1,"somatic" "CRC-4",20,0,19302660,20,25291885,"long_range","5989234",30,0,"SLC24A3","ABHD12","Intron of SLC24A3(+): 93Kb after exon 2","Intron of ABHD12(-): 24Kb before exon 2","Protein fusion: out of frame (SLC24A3-ABHD12)",1,30,1,"somatic" "CRC-4",8,1,36058467,8,40512207,"long_range","4453734",30,0,"UNC5D","ZMAT4","IGR: 287Kb after UNC5D(+)","Intron of ZMAT4(-): 3Kb before exon 7","-",0.9791505,29.37452,1,"somatic" "CRC-4",8,1,28227333,20,21270719,"inter_chr","NaN",29,0,"PNOC","XRN2","IGR: 3Kb before PNOC(+)","Intron of XRN2(+): 1Kb after exon 15","-",1,29,1,"somatic" "CRC-4",8,0,29865798,20,18083453,"inter_chr","NaN",29,0,"LOC286135","CSRP2BP","IGR: 33Kb before LOC286135(+)","Intron of CSRP2BP(+): 4Kb after exon 3","-",1,29,1,"somatic" "CRC-4",8,0,33311546,20,11068323,"inter_chr","NaN",28,0,"FUT10","JAG1","IGR: 36Kb before FUT10(-)","IGR: 466Kb after JAG1(-)","-",1,28,1,"somatic" "CRC-4",4,0,22195633,16,76386760,"inter_chr","NaN",27,0,"GBA3","VAT1L","IGR: 108Kb before GBA3(+)","Intron of VAT1L(+): 6Kb after exon 1","-",1,27,1,"not_subjected_to_validation" "CRC-4",7,0,153554789,7,153709348,"deletion","154543",27,0,"DPP6","DPP6","Intron of DPP6(+): 174Kb after exon 1","Intron of DPP6(+): 65Kb before exon 2","Deletion within intron",1,27,1,"somatic" "CRC-4",8,0,24974004,8,33314079,"long_range","8340061",27,0,"NEFL","FUT10","IGR: 110Kb before NEFL(-)","IGR: 34Kb before FUT10(-)","-",1,27,1,"not_subjected_to_validation" "CRC-4",8,0,28228387,8,29283557,"long_range","1055155",27,0,"PNOC","DUSP4","Promoter of PNOC(+): 2Kb from tx start","IGR: 34Kb before DUSP4(-)","-",1,27,1,"somatic" "CRC-4",8,1,32575153,20,9577156,"inter_chr","NaN",27,0,"NRG1","PAK7","Intron of NRG1(+): 2Kb after exon 2","5'-UTR of PAK7(-): 4Kb before coding start","Transcript fusion (PAK7-NRG1)",1,27,1,"somatic" "CRC-4",5,1,103343225,5,112990395,"long_range","9647173",26,0,"NUDT12","YTHDC2","IGR: 431Kb before NUDT12(-)","IGR: 32Kb after YTHDC2(+)","-",1,26,1,"not_subjected_to_validation" "CRC-4",20,0,11400256,20,21285670,"long_range","9885419",26,0,"BTBD3","XRN2","IGR: 419Kb before BTBD3(+)","Intron of XRN2(+): 364bp after exon 23","-",1,26,1,"somatic" "CRC-7",11,0,110630149,11,110631875,"deletion","1714",26,0,"C11orf53","C11orf53","Promoter of C11orf53(+): 2Kb from tx start","Promoter of C11orf53(+): 50bp from tx start","Deletion within transcript",1,26,1,"somatic" "CRC-4",8,1,33311815,20,17847854,"inter_chr","NaN",26,0,"FUT10","SNX5","IGR: 36Kb before FUT10(-)","IGR: 22Kb before SNX5(-)","-",0.9995995,25.98959,1,"not_subjected_to_validation" "CRC-4",8,0,25090475,8,30527338,"long_range","5436860",25,0,"DOCK5","RBPMS","IGR: 8Kb before DOCK5(+)","Intron of RBPMS(+): 687bp after exon 7","-",1,25,1,"somatic" "CRC-4",8,0,36160000,20,9372180,"inter_chr","NaN",25,0,"UNC5D","PLCB4","IGR: 388Kb after UNC5D(+)","Intron of PLCB4(+): 418bp before exon 29","-",1,25,1,"somatic" "CRC-8",10,0,89642033,10,89732483,"deletion","90440",25,0,"PTEN","PTEN","Intron of PTEN(+): 2Kb before exon 2","IGR: 14Kb after PTEN(+)","-",1,25,1,"not_subjected_to_validation" "CRC-4",4,1,60044609,4,60059497,"tandem_dup","14897",24,0,"LPHN3","LPHN3","IGR: 2Mb before LPHN3(+)","IGR: 2Mb before LPHN3(+)","-",1,24,1,"not_subjected_to_validation" "CRC-4",8,0,30014989,8,32555657,"long_range","2540652",24,0,"TMEM66","NRG1","IGR: 25Kb before TMEM66(-)","Intron of NRG1(+): 17Kb before exon 2","-",1,24,1,"somatic" "CRC-4",8,0,34922223,8,38798886,"long_range","3876645",24,0,"UNC5D","TACC1","IGR: 290Kb before UNC5D(+)","Intron of TACC1(+): 2Kb after exon 3","-",1,24,1,"somatic" "CRC-4",20,1,36536910,20,36621390,"inversion","84486",24,0,"RALGAPB","RALGAPB","5'-UTR of RALGAPB(+): 14Kb before coding start","Intron of RALGAPB(+): 890bp after exon 23","-",1,24,1,"not_subjected_to_validation" "CRC-7",1,1,76130753,1,76154188,"tandem_dup","23444",24,0,"MSH4","ASB17","Intron of MSH4(+): 2Kb after exon 17","IGR: 3Kb before ASB17(-)","-",1,24,1,"not_subjected_to_validation" "CRC-4",8,1,25100854,8,38798630,"long_range","13697776",23,0,"DOCK5","TACC1","Intron of DOCK5(+): 2Kb after exon 1","Intron of TACC1(+): 1Kb after exon 3","-",1,23,0,"somatic" "CRC-4",8,0,40498457,8,41622567,"long_range","1124150",23,0,"ZMAT4","NKX6-3","IGR: 9Kb before ZMAT4(-)","IGR: 412bp before NKX6-3(-)","-",1,23,1,"not_subjected_to_validation" "CRC-4",8,1,37454709,20,11070889,"inter_chr","NaN",23,0,"ZNF703","JAG1","IGR: 218Kb before ZNF703(+)","IGR: 468Kb after JAG1(-)","-",1,23,1,"somatic" "CRC-4",4,0,14254205,4,14874661,"deletion","620468",22,0,"CPEB2","C1QTNF7","IGR: 360Kb before CPEB2(+)","IGR: 76Kb before C1QTNF7(+)","-",1,22,1,"not_subjected_to_validation" "CRC-4",8,1,38628449,8,39830749,"long_range","1202302",22,0,"RNF5P1","IDO1","IGR: 52Kb before RNF5P1(-)","IGR: 60Kb before IDO1(+)","-",1,22,1,"not_subjected_to_validation" "CRC-8",8,1,133850681,8,137902592,"long_range","4051942",22,0,"PHF20L1","FAM135B","IGR: 6Kb before PHF20L1(+)","IGR: 1Mb before FAM135B(-)","-",1,22,1,"not_subjected_to_validation" "CRC-4",8,0,25102333,20,9397869,"inter_chr","NaN",21,0,"DOCK5","PLCB4","Intron of DOCK5(+): 4Kb after exon 1","Intron of PLCB4(+): 554bp after exon 34","Antisense fusion",1,21,1,"not_subjected_to_validation" "CRC-4",20,0,23952551,20,23954112,"deletion","1549",21,0,"GGTLC1","GGTLC1","IGR: 39Kb before GGTLC1(-)","IGR: 40Kb before GGTLC1(-)","-",1,21,1,"not_subjected_to_validation" "CRC-4",20,1,15333991,20,23960108,"long_range","8626130",20,0,"MACROD2","GGTLC1","Intron of MACROD2(+): 26Kb before exon 7","IGR: 46Kb before GGTLC1(-)","-",1,20,1,"somatic" "CRC-8",8,0,131330341,8,131477464,"deletion","147133",20,0,"ASAP1","ASAP1","Intron of ASAP1(-): 12Kb before exon 3","Intron of ASAP1(-): 6Kb after exon 1","Deletion of 1 exon: out of frame",1,20,1,"somatic" "CRC-8",14,0,50989908,14,51021989,"deletion","32075",20,0,"FRMD6","FRMD6","IGR: 36Kb before FRMD6(+)","IGR: 4Kb before FRMD6(+)","-",1,20,1,"somatic" "CRC-3",6,0,27910367,6,106918619,"long_range","79008239",19,0,"HIST1H2AK","ATG5","IGR: 3Kb before HIST1H2AK(-)","IGR: 38Kb after ATG5(-)","-",1,19,1,"somatic" "CRC-4",5,0,103343228,5,109521576,"long_range","6178364",19,0,"NUDT12","TMEM232","IGR: 431Kb before NUDT12(-)","IGR: 262Kb before TMEM232(-)","-",1,19,1,"not_subjected_to_validation" "CRC-4",8,0,30538770,8,32581683,"long_range","2042931",19,0,"RBPMS","NRG1","3'-UTR of RBPMS(+): 3Kb after coding stop","Intron of NRG1(+): 932bp before exon 3","-",1,19,1,"somatic" "CRC-5",16,0,7111605,16,7460628,"deletion","349008",19,0,"A2BP1","A2BP1","Intron of A2BP1(+): 70Kb after exon 4","Intron of A2BP1(+): 48Kb before exon 2","Deletion of 3 exons: in frame",1,19,1,"not_detected" "CRC-9",2,0,12232853,2,12362670,"deletion","129825",19,0,"LPIN1","TRIB2","IGR: 429Kb before LPIN1(+)","IGR: 412Kb before TRIB2(+)","-",1,19,1,"not_subjected_to_validation" "CRC-9",20,1,32008872,20,32031634,"tandem_dup","22774",19,0,"RALY","RALY","IGR: 37Kb before RALY(+)","IGR: 14Kb before RALY(+)","-",1,19,1,"not_subjected_to_validation" "CRC-4",4,0,97533521,4,97617439,"deletion","83951",18,0,"PDHA2","PDHA2","IGR: 553Kb before PDHA2(+)","IGR: 637Kb before PDHA2(+)","-",1,18,1,"not_subjected_to_validation" "CRC-4",8,0,30530225,20,19302099,"inter_chr","NaN",18,0,"RBPMS","SLC24A3","Intron of RBPMS(+): 4Kb after exon 7","Intron of SLC24A3(+): 92Kb after exon 2","Protein fusion: out of frame (RBPMS-SLC24A3)",1,18,0,"somatic" "CRC-4",18,0,3252928,18,3667075,"deletion","414147",18,0,"MYL12B","DLGAP1","5'-UTR of MYL12B(+): 10Kb before coding start","Intron of DLGAP1(-): 52Kb after exon 4","Antisense fusion",1,18,0,"not_subjected_to_validation" "CRC-4",20,1,18951206,20,18954029,"tandem_dup","2802",18,0,"SLC24A3","SLC24A3","IGR: 190Kb before SLC24A3(+)","IGR: 187Kb before SLC24A3(+)","-",1,18,1,"somatic" "CRC-4",20,0,9567639,20,17892276,"long_range","8324620",18,0,"PAK7","SNX5","Intron of PAK7(-): 5Kb after exon 4","Intron of SNX5(-): 5Kb after exon 1","-",1,18,1,"somatic" "CRC-8",7,0,41091150,7,41091631,"deletion","491",18,0,"C7orf10","C7orf10","IGR: 224Kb after C7orf10(+)","IGR: 225Kb after C7orf10(+)","-",1,18,1,"somatic" "CRC-3",2,1,53628330,2,53629451,"inversion","1121",17,0,"ASB3","ASB3","IGR: 122Kb before ASB3(-)","IGR: 121Kb before ASB3(-)","-",1,17,1,"germline" "CRC-4",4,1,15431666,4,22709584,"long_range","7277879",17,0,"CD38","GBA3","Intron of CD38(+): 4Kb before exon 3","IGR: 406Kb before GBA3(+)","-",1,17,1,"not_subjected_to_validation" "CRC-4",4,0,127937758,4,127945196,"deletion","7464",17,0,"INTU","INTU","IGR: 836Kb before INTU(+)","IGR: 828Kb before INTU(+)","-",1,17,1,"not_subjected_to_validation" "CRC-8",1,1,196022172,1,197048910,"long_range","1026733",17,0,"DENND1B","MIR181B1","IGR: 11Kb after DENND1B(-)","IGR: 46Kb before MIR181B1(-)","-",1,17,1,"not_subjected_to_validation" "CRC-4",4,0,22197860,16,76377794,"inter_chr","NaN",17,0,"GBA3","VAT1L","IGR: 106Kb before GBA3(+)","Promoter of VAT1L(+): 2Kb from tx start","-",0.9990934,16.98459,1,"somatic" "CRC-3",3,0,6566468,3,7578764,"long_range","1012293",17,0,"GRM7","GRM7","IGR: 311Kb before GRM7(+)","Intron of GRM7(+): 16Kb before exon 8","-",0.9989916,16.98286,1,"somatic" "CRC-4",8,0,37458596,20,16855593,"inter_chr","NaN",16,0,"ZNF703","OTOR","IGR: 214Kb before ZNF703(+)","IGR: 179Kb before OTOR(+)","-",1,16,1,"somatic" "CRC-4",14,0,57321226,21,20491241,"inter_chr","NaN",16,0,"C14orf37","C21orf131","IGR: 219Kb before C14orf37(-)","IGR: 546Kb before C21orf131(-)","-",1,16,1,"not_subjected_to_validation" "CRC-6",5,1,158747640,11,68093742,"inter_chr","NaN",16,0,"LOC285627","SAPS3","IGR: 60Kb before LOC285627(-)","Intron of SAPS3(+): 57bp before exon 11","-",1,16,1,"not_subjected_to_validation" "CRC-7",16,0,79091579,16,79092712,"deletion","1127",16,0,"MIR548H4","MIR548H4","5'-UTR of MIR548H4(+): 165Kb before coding start","5'-UTR of MIR548H4(+): 164Kb before coding start","Deletion within transcript",1,16,1,"somatic" "CRC-8",5,0,50568570,10,117185887,"inter_chr","NaN",16,0,"ISL1","ATRNL1","IGR: 146Kb before ISL1(+)","Intron of ATRNL1(+): 10Kb after exon 21","-",1,16,1,"not_subjected_to_validation" "CRC-9",7,1,146612439,7,146656035,"inversion","43600",16,0,"CNTNAP2","CNTNAP2","Intron of CNTNAP2(+): 16Kb before exon 9","Intron of CNTNAP2(+): 28Kb after exon 9","-",1,16,1,"not_subjected_to_validation" "CRC-9",12,0,72668271,12,73565822,"deletion","897555",16,0,"LOC552889","KCNC2","IGR: 550Kb before LOC552889(+)","IGR: 154Kb before KCNC2(-)","-",1,16,1,"not_subjected_to_validation" "CRC-4",8,0,35244643,8,41402287,"long_range","6157635",15,0,"UNC5D","GOLGA7","Intron of UNC5D(+): 32Kb after exon 1","IGR: 65Kb before GOLGA7(+)","-",1,15,1,"not_subjected_to_validation" "CRC-4",16,0,76376882,16,76386047,"inversion","9176",15,0,"VAT1L","VAT1L","IGR: 3Kb before VAT1L(+)","Intron of VAT1L(+): 6Kb after exon 1","-",1,15,1,"somatic" "CRC-5",20,1,34039754,20,39702663,"long_range","5662867",15,0,"C20orf152","CHD6","Intron of C20orf152(+): 917bp after exon 7","IGR: 22Kb after CHD6(-)","-",1,15,1,"not_subjected_to_validation" "CRC-8",3,0,106703280,3,107759386,"long_range","1056099",15,0,"ALCAM","LOC100302640","Intron of ALCAM(+): 18Kb before exon 2","IGR: 552Kb before LOC100302640(-)","-",1,15,1,"not_subjected_to_validation" "CRC-8",8,1,143007140,8,146177598,"long_range","3170455",15,0,"NCRNA00051","ZNF252","IGR: 270Kb before NCRNA00051(+)","3'-UTR of ZNF252(-): 21Kb after coding stop","-",1,15,1,"somatic" "CRC-8",18,0,18010463,18,18013227,"inversion","2742",15,0,"GATA6","GATA6","Intron of GATA6(+): 446bp before exon 3","Intron of GATA6(+): 2Kb after exon 3","Antisense fusion",1,15,1,"not_subjected_to_validation" "CRC-8",18,0,28470841,18,30537689,"long_range","2066834",15,0,"KLHL14","DTNA","IGR: 36Kb before KLHL14(-)","5'-UTR of DTNA(+): 52Kb before coding start","-",1,15,1,"not_subjected_to_validation" "CRC-9",2,0,36985044,2,81047932,"long_range","44062885",15,0,"STRN","CTNNA2","Intron of STRN(-): 1Kb after exon 4","IGR: 318Kb after CTNNA2(+)","-",1,15,1,"somatic" "CRC-9",4,1,92306666,4,92378573,"inversion","71912",15,0,"FAM190A","FAM190A","Intron of FAM190A(+): 80Kb after exon 10","Intron of FAM190A(+): 152Kb after exon 10","-",1,15,1,"somatic" "CRC-9",5,0,84227073,5,84347348,"deletion","120272",15,0,"EDIL3","EDIL3","IGR: 953Kb before EDIL3(-)","IGR: 1Mb before EDIL3(-)","-",1,15,1,"not_subjected_to_validation" "CRC-4",2,0,125106624,2,125349147,"deletion","242507",15,0,"CNTNAP5","CNTNAP5","Intron of CNTNAP5(+): 15Kb before exon 13","Intron of CNTNAP5(+): 5Kb after exon 21","Deletion of 9 exons: in frame",0.989925,14.84887,1,"somatic" "CRC-8",11,0,50691941,11,50695426,"deletion","3485",16,0,"LOC646813","LOC646813","IGR: 367Kb before LOC646813(+)","IGR: 371Kb before LOC646813(+)","-",0.8899949,14.23992,0,"not_subjected_to_validation" "CRC-4",4,0,15322903,16,74907715,"inter_chr","NaN",16,0,"BST1","CNTNAP4","Intron of BST1(+): 298bp after exon 4","Intron of CNTNAP4(+): 111bp before exon 2","Protein fusion: out of frame (BST1-CNTNAP4)",0.8765974,14.02556,1,"somatic" "CRC-2",2,0,126884333,2,191185033,"long_range","64300704",14,0,"GYPC","NAB1","IGR: 246Kb before GYPC(+)","IGR: 37Kb before NAB1(+)","-",1,14,1,"somatic" "CRC-4",4,0,15425543,4,21193396,"long_range","5767853",14,0,"CD38","KCNIP4","Intron of CD38(+): 2Kb before exon 2","Intron of KCNIP4(-): 115Kb after exon 1","Antisense fusion",1,14,0,"not_subjected_to_validation" "CRC-4",4,1,22195631,16,70665402,"inter_chr","NaN",14,0,"GBA3","HPR","IGR: 108Kb before GBA3(+)","Intron of HPR(+): 25bp after exon 2","-",1,14,1,"somatic" "CRC-4",8,1,34921160,20,18953496,"inter_chr","NaN",14,0,"UNC5D","SLC24A3","IGR: 291Kb before UNC5D(+)","IGR: 188Kb before SLC24A3(+)","-",1,14,0,"somatic" "CRC-5",20,1,15401746,20,19041446,"long_range","3639702",14,0,"MACROD2","SLC24A3","Intron of MACROD2(+): 27Kb before exon 8","IGR: 100Kb before SLC24A3(+)","-",1,14,1,"not_detected" "CRC-5",20,1,22479048,20,25562740,"long_range","3083696",14,0,"C20orf56","NANP","IGR: 10Kb before C20orf56(-)","IGR: 21Kb before NANP(-)","-",1,14,1,"not_subjected_to_validation" "CRC-5",20,0,22985917,20,35006918,"long_range","12020999",14,0,"THBD","SAMHD1","IGR: 8Kb after THBD(-)","Intron of SAMHD1(-): 2Kb after exon 2","-",1,14,1,"not_detected" "CRC-6",5,0,98134842,11,58106127,"inter_chr","NaN",14,0,"RGMB","ZFP91","Intron of RGMB(+): 571bp after exon 2","Intron of ZFP91(+): 2Kb after exon 1","Protein fusion: in frame (RGMB-ZFP91)",1,14,1,"somatic" "CRC-8",3,0,96025612,3,97703860,"long_range","1678297",14,0,"LOC255025","EPHA6","IGR: 114Kb before LOC255025(+)","IGR: 312Kb before EPHA6(+)","-",1,14,1,"not_subjected_to_validation" "CRC-8",8,0,40558022,8,41483346,"deletion","925341",14,0,"ZMAT4","GOLGA7","Intron of ZMAT4(-): 88bp before exon 6","Intron of GOLGA7(+): 369bp before exon 5","-",1,14,1,"somatic" "CRC-8",11,1,129730607,15,37876662,"inter_chr","NaN",14,0,"ADAMTS8","GPR176","IGR: 49Kb before ADAMTS8(-)","IGR: 4Kb before GPR176(-)","-",1,14,1,"somatic" "CRC-8",13,1,63986314,14,61689939,"inter_chr","NaN",14,0,"OR7E156P","FLJ43390","IGR: 777Kb before OR7E156P(+)","IGR: 36Kb before FLJ43390(+)","-",1,14,1,"not_subjected_to_validation" "CRC-9",3,0,115588610,3,115631191,"inversion","42573",14,0,"ZBTB20","ZBTB20","5'-UTR of ZBTB20(-): 35Kb before coding start","5'-UTR of ZBTB20(-): 78Kb before coding start","-",1,14,1,"not_subjected_to_validation" "CRC-9",5,1,132992885,5,133040700,"tandem_dup","47811",14,0,"FSTL4","MIR1289-2","IGR: 17Kb after FSTL4(-)","IGR: 250Kb before MIR1289-2(-)","-",1,14,1,"not_subjected_to_validation" "CRC-9",5,1,96131900,5,171355322,"long_range","75223431",14,0,"CAST","FBXW11","Intron of CAST(+): 92bp before exon 26","Intron of FBXW11(-): 11Kb after exon 1","Protein fusion: in frame (FBXW11-CAST)",1,14,1,"somatic" "CRC-3",3,1,3795729,3,5546204,"long_range","1750454",14,0,"LRRN1","EDEM1","IGR: 20Kb before LRRN1(+)","IGR: 342Kb before EDEM1(+)","-",0.9846154,13.78462,1,"somatic" "CRC-3",7,1,110724998,7,110927085,"tandem_dup","202075",13,0,"IMMP2L","IMMP2L","Intron of IMMP2L(-): 190Kb after exon 3","Intron of IMMP2L(-): 12Kb before exon 3","Duplication of 1 exon: out of frame",1,13,1,"somatic" "CRC-4",16,0,46478966,16,46479751,"deletion","785",13,0,"ABCC12","ABCC12","IGR: 195Kb before ABCC12(-)","IGR: 195Kb before ABCC12(-)","-",1,13,0,"not_subjected_to_validation" "CRC-5",16,0,5442014,16,5583562,"deletion","141570",13,0,"FAM86A","A2BP1","IGR: 368Kb before FAM86A(-)","IGR: 426Kb before A2BP1(+)","-",1,13,1,"not_subjected_to_validation" "CRC-6",18,0,44926172,18,46013514,"long_range","1087386",13,0,"DYM","CCDC11","Intron of DYM(-): 18Kb after exon 14","Intron of CCDC11(-): 5Kb after exon 7","Protein fusion: out of frame (CCDC11-DYM)",1,13,1,"somatic" "CRC-6",20,1,15267860,20,15450481,"tandem_dup","182600",13,0,"MACROD2","MACROD2","Intron of MACROD2(+): 92Kb before exon 7","Intron of MACROD2(+): 22Kb after exon 8","Duplication of 2 exons: in frame",1,13,1,"somatic" "CRC-7",11,1,2089659,11,2222935,"tandem_dup","133245",13,0,"IGF2","ASCL2","IGR: 17Kb before IGF2(-)","IGR: 23Kb before ASCL2(-)","-",1,13,1,"somatic" "CRC-9",2,1,44338468,2,163484313,"long_range","119145841",13,0,"SLC3A1","KCNH7","IGR: 18Kb before SLC3A1(+)","IGR: 496Kb before KCNH7(-)","-",1,13,1,"not_subjected_to_validation" "CRC-9",2,0,31750804,2,206306220,"long_range","174555434",13,0,"SRD5A2","NRP2","IGR: 148Kb before SRD5A2(-)","Intron of NRP2(+): 5Kb after exon 7","-",1,13,1,"not_subjected_to_validation" "CRC-9",4,1,68554602,4,68639421,"tandem_dup","84828",13,0,"TMPRSS11F","TMPRSS11F","IGR: 47Kb before TMPRSS11F(-)","Intron of TMPRSS11F(-): 471bp before exon 3","-",1,13,1,"not_subjected_to_validation" "CRC-9",10,0,114220869,10,114760545,"deletion","539677",13,0,"VTI1A","TCF7L2","Intron of VTI1A(+): 6Kb after exon 3","Intron of TCF7L2(+): 29Kb before exon 4","Protein fusion: in frame (VTI1A-TCF7L2)",1,13,1,"somatic" "CRC-9",12,0,44480038,12,44522731,"deletion","42681",13,0,"ARID2","ARID2","Intron of ARID2(+): 11Kb before exon 4","Intron of ARID2(+): 3Kb after exon 11","Deletion of 8 exons: out of frame",1,13,1,"somatic" "CRC-9",17,0,61475164,17,69287777,"long_range","7812618",13,0,"CCDC46","C17orf54","Intron of CCDC46(-): 5Kb after exon 12","3'-UTR of C17orf54(-): 48Kb after coding stop","-",1,13,1,"not_subjected_to_validation" "CRC-1",2,1,166689629,2,166746367,"tandem_dup","56734",13,0,"SCN1A","SCN9A","IGR: 51Kb after SCN1A(-)","IGR: 14Kb before SCN9A(-)","-",1,13,1,"somatic" "CRC-1",7,0,117078022,7,117082897,"deletion","4872",13,0,"CFTR","CFTR","Intron of CFTR(+): 2Kb before exon 24","Intron of CFTR(+): 3Kb after exon 24","Deletion of 1 exon: in frame",1,13,1,"somatic" "CRC-6",5,1,98214924,5,157876135,"long_range","59661144",14,0,"CHD1","EBF1","IGR: 4Kb before CHD1(-)","IGR: 179Kb before EBF1(-)","-",0.9071118,12.69956,1,"not_subjected_to_validation" "CRC-8",1,1,179037750,1,179039954,"tandem_dup","2204",14,0,"XPR1","XPR1","Intron of XPR1(+): 1Kb before exon 4","Intron of XPR1(+): 584bp after exon 4","Duplication of 1 exon: out of frame",0.8752137,12.25299,0,"somatic" "CRC-3",1,0,224945390,1,233909251,"long_range","8963858",12,0,"ITPKB","LYST","Intron of ITPKB(-): 42Kb before exon 3","Intron of LYST(-): 2Kb before exon 49","-",1,12,1,"somatic" "CRC-3",1,0,245475793,3,5894391,"inter_chr","NaN",12,0,"VN1R5","EDEM1","IGR: 10Kb before VN1R5(+)","IGR: 690Kb before EDEM1(+)","-",1,12,1,"somatic" "CRC-3",2,0,60636921,2,60639951,"inversion","3003",12,0,"BCL11A","BCL11A","Promoter of BCL11A(-): 3Kb from tx start","IGR: 6Kb after BCL11A(-)","-",1,12,1,"germline" "CRC-3",5,0,178065040,5,178899590,"deletion","834550",12,0,"ZNF354A","RUFY1","IGR: 6Kb before ZNF354A(-)","IGR: 11Kb before RUFY1(+)","-",1,12,0,"somatic" "CRC-4",11,0,93716656,11,94163529,"inversion","446883",12,0,"GPR83","AMOTL1","IGR: 33Kb before GPR83(-)","Intron of AMOTL1(+): 4Kb before exon 2","-",1,12,1,"not_subjected_to_validation" "CRC-5",3,0,156382305,3,156383209,"deletion","922",12,0,"MME","MME","3'-UTR of MME(+): 1Kb after coding stop","3'-UTR of MME(+): 2Kb after coding stop","-",1,12,1,"not_subjected_to_validation" "CRC-5",20,0,18596717,20,19107437,"deletion","510733",12,0,"DTD1","SLC24A3","Intron of DTD1(+): 40Kb after exon 4","IGR: 34Kb before SLC24A3(+)","-",1,12,1,"not_subjected_to_validation" "CRC-6",1,1,191671679,1,191819910,"inversion","148271",12,0,"B3GALT2","B3GALT2","IGR: 257Kb before B3GALT2(-)","IGR: 405Kb before B3GALT2(-)","-",1,12,1,"not_subjected_to_validation" "CRC-6",5,1,122741029,5,159744189,"long_range","37003145",12,0,"CEP120","C5orf54","Exon 17 of CEP120(-)","IGR: 9Kb before C5orf54(-)","-",1,12,1,"not_subjected_to_validation" "CRC-6",5,0,122736211,11,130217878,"inter_chr","NaN",12,0,"CEP120","SNX19","Intron of CEP120(-): 31bp after exon 18","IGR: 33Kb before SNX19(-)","-",1,12,1,"somatic" "CRC-8",2,0,34991039,2,41117665,"long_range","6126626",12,0,"MYADML","SLC8A1","IGR: 1Mb before MYADML(-)","IGR: 925Kb before SLC8A1(-)","-",1,12,1,"not_subjected_to_validation" "CRC-8",8,1,144964027,8,145598351,"inversion","634360",12,0,"SCRIB","CPSF1","Intron of SCRIB(-): 145bp before exon 14","Intron of CPSF1(-): 506bp before exon 3","Antisense fusion",1,12,1,"somatic" "CRC-9",2,1,25211480,2,232333210,"long_range","207121730",12,0,"EFR3B","PDE6D","Intron of EFR3B(+): 356bp before exon 13","Intron of PDE6D(-): 21Kb after exon 1","-",1,12,1,"somatic" "CRC-9",2,0,137894652,2,210182496,"long_range","72287839",12,0,"THSD7B","MAP2","Intron of THSD7B(+): 9Kb after exon 13","5'-UTR of MAP2(+): 44Kb before coding start","Transcript fusion (THSD7B-MAP2)",1,12,1,"not_subjected_to_validation" "CRC-9",3,0,61129192,3,61351047,"deletion","221854",12,0,"FHIT","PTPRG","5'-UTR of FHIT(-): 631Kb before coding start","IGR: 171Kb before PTPRG(+)","-",1,12,1,"somatic" "CRC-9",4,0,127964670,4,128269073,"deletion","304426",12,0,"INTU","INTU","IGR: 809Kb before INTU(+)","IGR: 505Kb before INTU(+)","-",1,12,1,"not_subjected_to_validation" "CRC-9",6,0,63307699,6,63365629,"deletion","57951",12,0,"KHDRBS2","KHDRBS2","IGR: 254Kb after KHDRBS2(-)","IGR: 312Kb after KHDRBS2(-)","-",1,12,1,"not_subjected_to_validation" "CRC-9",6,0,161908772,6,161999363,"deletion","90596",12,0,"PARK2","PARK2","Intron of PARK2(-): 2Kb after exon 5","Intron of PARK2(-): 89Kb before exon 5","Deletion of 1 exon: out of frame",1,12,1,"somatic" "CRC-9",6,0,162499195,6,162627648,"deletion","128469",12,0,"PARK2","PARK2","Intron of PARK2(-): 43Kb after exon 4","Intron of PARK2(-): 24Kb before exon 3","Deletion of 2 exons: in frame",1,12,1,"somatic" "CRC-9",8,1,95836356,8,95919906,"tandem_dup","83528",12,0,"DPY19L4","INTS8","Intron of DPY19L4(+): 1Kb before exon 7","Exon 8 of INTS8(+)","Protein fusion: mid-exon (INTS8-DPY19L4)",1,12,1,"somatic" "CRC-9",8,0,113786799,8,114028116,"deletion","241323",12,0,"CSMD3","CSMD3","Intron of CSMD3(-): 15Kb before exon 15","Intron of CSMD3(-): 1Kb after exon 10","Deletion of 4 exons: out of frame",1,12,1,"somatic" "CRC-9",10,0,9494689,10,9598185,"deletion","103484",12,0,"GATA3","SFTA1P","IGR: 1Mb before GATA3(+)","IGR: 1Mb before SFTA1P(-)","-",1,12,1,"not_subjected_to_validation" "CRC-9",12,0,72073769,12,72667244,"deletion","593472",12,0,"TRHDE","LOC552889","IGR: 1Mb before TRHDE(+)","IGR: 551Kb before LOC552889(+)","-",1,12,1,"not_subjected_to_validation" "CRC-9",17,1,62486069,17,69958675,"long_range","7472603",12,0,"CACNG1","GPRC5C","IGR: 3Kb after CACNG1(+)","IGR: 4Kb after GPRC5C(+)","-",1,12,1,"not_subjected_to_validation" "CRC-9",20,0,14642500,20,14724673,"deletion","82186",12,0,"MACROD2","MACROD2","Intron of MACROD2(+): 29Kb after exon 5","Intron of MACROD2(+): 111Kb after exon 5","Deletion within intron",1,12,1,"somatic" "CRC-9",21,0,15701850,21,16090703,"deletion","388863",12,0,"USP25","USP25","IGR: 323Kb before USP25(+)","Intron of USP25(+): 3Kb before exon 6","-",1,12,1,"not_subjected_to_validation" "CRC-4",11,1,93716665,11,94163527,"inversion","446848",13,0,"GPR83","AMOTL1","IGR: 33Kb before GPR83(-)","Intron of AMOTL1(+): 4Kb before exon 2","-",0.9089541,11.8164,1,"not_subjected_to_validation" "CRC-9",7,1,85831810,7,86628218,"inversion","796432",12,0,"GRM3","DMTF1","IGR: 279Kb before GRM3(+)","5'-UTR of DMTF1(+): 4Kb before coding start","-",0.9846154,11.81538,1,"not_subjected_to_validation" "CRC-3",1,0,240378413,1,245369879,"long_range","4991473",12,0,"PLD5","ZNF124","Intron of PLD5(-): 24Kb before exon 7","IGR: 16Kb before ZNF124(-)","-",0.9641551,11.56986,1,"somatic" "CRC-3",1,1,10754998,1,10897669,"tandem_dup","142673",11,0,"CASZ1","C1orf127","5'-UTR of CASZ1(-): 78Kb before coding start","IGR: 31Kb before C1orf127(-)","-",1,11,1,"somatic" "CRC-3",1,0,245318786,1,245412605,"deletion","93850",11,0,"ZNF669","ZNF124","IGR: 11Kb before ZNF669(-)","IGR: 27Kb before ZNF124(-)","-",1,11,1,"somatic" "CRC-3",1,1,236419236,3,5566303,"inter_chr","NaN",11,0,"LOC339535","EDEM1","IGR: 291Kb before LOC339535(-)","IGR: 362Kb before EDEM1(+)","-",1,11,1,"somatic" "CRC-3",3,0,2897939,3,6212189,"long_range","3314285",11,0,"CNTN4","GRM7","Intron of CNTN4(+): 2Kb before exon 8","IGR: 666Kb before GRM7(+)","-",1,11,1,"somatic" "CRC-3",3,1,10830132,5,178740539,"inter_chr","NaN",11,0,"SLC6A11","ADAMTS2","Promoter of SLC6A11(+): 3Kb from tx start","IGR: 36Kb after ADAMTS2(-)","-",1,11,1,"somatic" "CRC-5",9,1,138146288,17,20094334,"inter_chr","NaN",11,0,"C9orf69","CYTSB","3'-UTR of C9orf69(-): 2Kb after coding stop","Intron of CYTSB(+): 3Kb before exon 8","-",1,11,1,"not_subjected_to_validation" "CRC-5",20,0,22795591,20,43578339,"long_range","20782749",11,0,"SSTR4","SPINT3","IGR: 168Kb before SSTR4(+)","Promoter of SPINT3(-): 659bp from tx start","-",1,11,1,"not_subjected_to_validation" "CRC-6",5,0,125637905,11,130222298,"inter_chr","NaN",11,0,"GRAMD3","SNX19","IGR: 86Kb before GRAMD3(+)","IGR: 29Kb before SNX19(-)","-",1,11,0,"somatic" "CRC-6",5,1,103605949,11,95790285,"inter_chr","NaN",11,0,"NUDT12","JRKL","IGR: 694Kb before NUDT12(-)","IGR: 27Kb before JRKL(+)","-",1,11,1,"somatic" "CRC-6",16,0,6526415,16,6960093,"deletion","433693",11,0,"A2BP1","A2BP1","5'-UTR of A2BP1(+): 516Kb before coding start","5'-UTR of A2BP1(+): 82Kb before coding start","Deletion within transcript",1,11,1,"somatic" "CRC-7",12,1,16574504,12,116296166,"long_range","99721656",11,0,"LMO3","NOS1","IGR: 18Kb before LMO3(-)","IGR: 12Kb after NOS1(-)","-",1,11,1,"not_subjected_to_validation" "CRC-8",1,0,190627145,1,193222439,"long_range","2595347",11,0,"RGS21","KCNT2","IGR: 24Kb after RGS21(+)","IGR: 1Mb before KCNT2(-)","-",1,11,1,"somatic" "CRC-8",3,0,194622778,3,194693577,"inversion","70815",11,0,"ATP13A4","ATP13A4","Intron of ATP13A4(-): 8Kb before exon 26","Intron of ATP13A4(-): 4bp after exon 4","-",1,11,1,"somatic" "CRC-8",4,0,141938317,4,143425464,"long_range","1487145",11,0,"TBC1D9","INPP4B","IGR: 41Kb after TBC1D9(-)","Intron of INPP4B(-): 14Kb before exon 10","-",1,11,1,"not_subjected_to_validation" "CRC-8",8,1,123841614,8,142986879,"long_range","19145271",11,0,"ZHX2","NCRNA00051","IGR: 21Kb before ZHX2(+)","IGR: 291Kb before NCRNA00051(+)","-",1,11,1,"somatic" "CRC-8",12,0,57410582,12,80804825,"long_range","23394235",11,0,"LRIG3","CCDC59","IGR: 142Kb before LRIG3(-)","IGR: 465Kb before CCDC59(-)","-",1,11,1,"somatic" "CRC-8",14,0,55086848,14,61689936,"long_range","6603113",11,0,"C14orf33","FLJ43390","IGR: 26Kb before C14orf33(-)","IGR: 36Kb before FLJ43390(+)","-",1,11,1,"not_subjected_to_validation" "CRC-9",1,0,71548858,1,71682807,"deletion","133971",11,0,"NEGR1","NEGR1","IGR: 92Kb before NEGR1(-)","Intron of NEGR1(-): 37Kb before exon 7","-",1,11,1,"not_subjected_to_validation" "CRC-9",2,0,165428888,2,165547687,"deletion","118800",11,0,"SLC38A11","SLC38A11","IGR: 34Kb before SLC38A11(-)","IGR: 27Kb after SLC38A11(-)","-",1,11,1,"not_subjected_to_validation" "CRC-9",2,0,186444249,2,186838068,"deletion","393824",11,0,"ZC3H15","ZC3H15","IGR: 615Kb before ZC3H15(+)","IGR: 221Kb before ZC3H15(+)","-",1,11,1,"not_subjected_to_validation" "CRC-9",2,0,232331040,4,183400097,"inter_chr","NaN",11,0,"PDE6D","MIR1305","Intron of PDE6D(-): 19Kb before exon 2","IGR: 73Kb before MIR1305(+)","-",1,11,1,"somatic" "CRC-9",5,0,96133849,5,97002501,"deletion","868684",11,0,"ERAP1","RIOK2","Intron of ERAP1(-): 4Kb after exon 19","IGR: 474Kb before RIOK2(-)","-",1,11,1,"not_subjected_to_validation" "CRC-9",5,0,102287279,5,102965355,"deletion","678099",11,0,"PAM","NUDT12","Intron of PAM(+): 1Kb before exon 5","IGR: 53Kb before NUDT12(-)","-",1,11,1,"not_subjected_to_validation" "CRC-9",8,1,47092714,18,39670428,"inter_chr","NaN",11,0,"BEYLA","SYT4","IGR: 779Kb before BEYLA(+)","IGR: 569Kb before SYT4(-)","-",1,11,1,"somatic" "CRC-9",12,0,19238750,12,20448808,"long_range","1210071",11,0,"PLEKHA5","PDE3A","Intron of PLEKHA5(+): 59Kb before exon 4","Intron of PDE3A(+): 34Kb after exon 1","Protein fusion: out of frame (PLEKHA5-PDE3A)",1,11,1,"somatic" "CRC-9",12,0,73604863,12,99031034,"long_range","25426209",11,0,"KCNC2","UHRF1BP1L","IGR: 115Kb before KCNC2(-)","Intron of UHRF1BP1L(-): 5Kb before exon 2","-",1,11,1,"not_subjected_to_validation" "CRC-9",13,0,87112264,13,87820140,"deletion","707899",11,0,"SLITRK5","SLITRK5","IGR: 11Kb before SLITRK5(+)","IGR: 697Kb before SLITRK5(+)","-",1,11,1,"not_subjected_to_validation" "CRC-9",17,0,34646392,17,35460956,"deletion","814557",11,0,"LOC90110","MED24","IGR: 16Kb before LOC90110(-)","Intron of MED24(-): 2Kb after exon 3","-",1,11,1,"not_subjected_to_validation" "CRC-1",3,0,172221091,3,172299683,"deletion","78586",11,0,"SLC2A2","TNIK","Intron of SLC2A2(-): 2Kb before exon 2","Intron of TNIK(-): 2Kb after exon 22","Protein fusion: out of frame (TNIK-SLC2A2)",1,11,1,"somatic" "CRC-9",2,0,127990783,2,128009511,"deletion","18708",11,0,"IWS1","MYO7B","Intron of IWS1(-): 7Kb after exon 2","Promoter of MYO7B(+): 347bp from tx start","-",0.999999,10.99999,1,"not_subjected_to_validation" "CRC-4",8,0,37340845,8,38794493,"long_range","1453628",11,0,"ZNF703","TACC1","IGR: 332Kb before ZNF703(+)","Intron of TACC1(+): 2Kb before exon 3","-",0.995868,10.95455,1,"somatic" "CRC-4",16,1,70024265,16,74933305,"long_range","4909040",12,0,"ZNF23","CNTNAP4","IGR: 15Kb before ZNF23(-)","Intron of CNTNAP4(+): 13Kb before exon 3","-",0.9089541,10.90745,0,"somatic" "CRC-7",1,1,31239406,1,31255104,"tandem_dup","15706",11,0,"PUM1","PUM1","Intron of PUM1(-): 1Kb after exon 6","Intron of PUM1(-): 3Kb before exon 4","Duplication of 3 exons: out of frame",0.9406691,10.34736,1,"somatic" "CRC-3",1,1,224945525,1,233870037,"long_range","8924507",10,0,"ITPKB","GNG4","Intron of ITPKB(-): 42Kb before exon 3","5'-UTR of GNG4(-): 56Kb before coding start","Antisense fusion",1,10,1,"somatic" "CRC-3",1,1,235922389,3,4611675,"inter_chr","NaN",10,0,"RYR2","ITPR1","Intron of RYR2(+): 5Kb after exon 63","Intron of ITPR1(+): 33Kb before exon 5","-",1,10,1,"somatic" "CRC-3",1,0,235918361,3,11080171,"inter_chr","NaN",10,0,"RYR2","SLC6A1","Intron of RYR2(+): 928bp after exon 63","IGR: 24Kb after SLC6A1(+)","-",1,10,1,"somatic" "CRC-3",1,0,233862655,5,178278887,"inter_chr","NaN",10,0,"GNG4","ZFP2","5'-UTR of GNG4(-): 49Kb before coding start","5'-UTR of ZFP2(+): 12Kb before coding start","-",1,10,1,"somatic" "CRC-3",3,1,2853112,3,5935342,"long_range","3082253",10,0,"CNTN4","EDEM1","Intron of CNTN4(+): 17Kb after exon 6","IGR: 731Kb before EDEM1(+)","-",1,10,1,"somatic" "CRC-3",3,1,6559791,3,7177138,"tandem_dup","617363",10,0,"GRM7","GRM7","IGR: 318Kb before GRM7(+)","Intron of GRM7(+): 14Kb after exon 2","-",1,10,1,"somatic" "CRC-5",6,0,162801313,6,162908242,"deletion","106907",10,0,"PARK2","PARK2","Intron of PARK2(-): 17Kb before exon 2","Intron of PARK2(-): 124Kb before exon 2","Deletion within intron",1,10,1,"not_detected" "CRC-5",20,1,57674907,20,61252518,"long_range","3577611",10,0,"PHACTR3","MIR124-3","Intron of PHACTR3(+): 61Kb after exon 1","IGR: 28Kb before MIR124-3(+)","-",1,10,0,"not_detected" "CRC-6",5,0,122741036,5,125720100,"long_range","2979101",10,0,"CEP120","GRAMD3","Exon 17 of CEP120(-)","IGR: 4Kb before GRAMD3(+)","-",1,10,1,"not_subjected_to_validation" "CRC-6",5,1,122723838,11,130217949,"inter_chr","NaN",10,0,"CEP120","SNX19","Intron of CEP120(-): 4Kb after exon 19","IGR: 33Kb before SNX19(-)","-",1,10,1,"not_subjected_to_validation" "CRC-6",18,0,46013512,18,53897496,"long_range","7883984",10,0,"CCDC11","NEDD4L","Intron of CCDC11(-): 5Kb after exon 7","Intron of NEDD4L(+): 35Kb after exon 1","-",1,10,0,"not_subjected_to_validation" "CRC-7",3,1,60231614,3,60236308,"tandem_dup","4672",10,0,"FHIT","FHIT","Intron of FHIT(-): 257Kb before exon 6","Intron of FHIT(-): 261Kb after exon 5","Duplication within intron",1,10,1,"somatic" "CRC-7",20,1,24120934,20,26108834,"long_range","1987900",10,0,"GGTLC1","MIR663","IGR: 207Kb before GGTLC1(-)","IGR: 28Kb before MIR663(-)","-",1,10,0,"not_detected" "CRC-8",8,0,133850668,8,137902592,"long_range","4051906",10,0,"PHF20L1","FAM135B","IGR: 6Kb before PHF20L1(+)","IGR: 1Mb before FAM135B(-)","-",1,10,1,"not_subjected_to_validation" "CRC-8",8,0,143005336,8,143114260,"inversion","108882",10,0,"NCRNA00051","NCRNA00051","IGR: 272Kb before NCRNA00051(+)","IGR: 163Kb before NCRNA00051(+)","-",1,10,1,"somatic" "CRC-8",11,0,129730601,15,37876667,"inter_chr","NaN",10,0,"ADAMTS8","GPR176","IGR: 49Kb before ADAMTS8(-)","IGR: 4Kb before GPR176(-)","-",1,10,1,"not_subjected_to_validation" "CRC-8",18,1,18011578,18,18777720,"inversion","766102",10,0,"GATA6","RBBP8","Intron of GATA6(+): 555bp after exon 3","Intron of RBBP8(+): 3Kb before exon 3","-",1,10,1,"not_subjected_to_validation" "CRC-8",18,1,4158942,22,27395925,"inter_chr","NaN",10,0,"DLGAP1","TTC28","IGR: 289Kb after DLGAP1(-)","Intron of TTC28(-): 10Kb after exon 1","-",1,10,1,"somatic" "CRC-9",1,0,195979259,1,196995705,"long_range","1016461",10,0,"DENND1B","PTPRC","Intron of DENND1B(-): 28Kb before exon 3","IGR: 3Kb after PTPRC(+)","-",1,10,1,"not_subjected_to_validation" "CRC-9",1,0,232984550,1,233226558,"deletion","241996",10,0,"IRF2BP2","TOMM20","IGR: 178Kb before IRF2BP2(-)","IGR: 113Kb before TOMM20(-)","-",1,10,1,"somatic" "CRC-9",1,0,215734118,1,216450915,"deletion","716814",10,0,"GPATCH2","RRP15","Intron of GPATCH2(-): 2Kb before exon 8","IGR: 74Kb before RRP15(+)","-",1,10,1,"somatic" "CRC-9",2,0,19009265,2,19106373,"deletion","97108",10,0,"NT5C1B","OSR1","IGR: 402Kb before NT5C1B(-)","IGR: 308Kb before OSR1(-)","-",1,10,1,"not_subjected_to_validation" "CRC-9",2,0,33158068,2,33176908,"deletion","18839",10,0,"LTBP1","LTBP1","Intron of LTBP1(+): 31Kb before exon 4","Intron of LTBP1(+): 12Kb before exon 4","Deletion within intron",1,10,1,"not_subjected_to_validation" "CRC-9",2,0,157905024,2,157905676,"deletion","650",10,0,"ERMN","ERMN","IGR: 22Kb before ERMN(-)","IGR: 22Kb before ERMN(-)","-",1,10,1,"somatic" "CRC-9",3,0,45033734,3,85621106,"long_range","40587406",10,0,"EXOSC7","CADM2","IGR: 5Kb after EXOSC7(+)","Intron of CADM2(+): 237Kb before exon 2","-",1,10,1,"not_detected" "CRC-9",3,1,105150620,3,105177567,"tandem_dup","26912",10,0,"ALCAM","ALCAM","IGR: 1Mb before ALCAM(+)","IGR: 1Mb before ALCAM(+)","-",1,10,1,"not_subjected_to_validation" "CRC-9",5,0,43240320,5,43893389,"deletion","653060",10,0,"MGC42105","NNT","5'-UTR of MGC42105(+): 41Kb before coding start","IGR: 254Kb before NNT(+)","-",1,10,1,"not_subjected_to_validation" "CRC-9",7,0,16007432,7,16046219,"deletion","38790",10,0,"ISPD","ISPD","IGR: 86Kb before ISPD(-)","IGR: 47Kb before ISPD(-)","-",1,10,1,"not_subjected_to_validation" "CRC-9",8,0,2723961,8,3036552,"deletion","312589",10,0,"CSMD1","CSMD1","IGR: 56Kb before CSMD1(-)","Intron of CSMD1(-): 2Kb before exon 34","-",1,10,1,"not_subjected_to_validation" "CRC-9",8,0,133214582,8,133715156,"deletion","500614",10,0,"KCNQ3","LRRC6","Intron of KCNQ3(-): 877bp before exon 14","Intron of LRRC6(-): 793bp before exon 5","Protein fusion: out of frame (LRRC6-KCNQ3)",1,10,1,"somatic" "CRC-9",10,0,114840872,10,114842007,"deletion","1119",10,0,"TCF7L2","TCF7L2","Intron of TCF7L2(+): 2Kb after exon 5","Intron of TCF7L2(+): 3Kb after exon 5","Deletion within intron",1,10,1,"not_subjected_to_validation" "CRC-9",11,0,81425009,11,81426659,"deletion","1637",10,0,"FAM181B","FAM181B","IGR: 696Kb before FAM181B(-)","IGR: 694Kb before FAM181B(-)","-",1,10,1,"not_subjected_to_validation" "CRC-9",17,1,60442943,19,33997302,"inter_chr","NaN",10,0,"GNA13","LOC148145","Intron of GNA13(-): 2Kb before exon 4","IGR: 151Kb before LOC148145(+)","-",1,10,1,"not_subjected_to_validation" "CRC-9",18,0,1600128,18,12880453,"long_range","11280330",10,0,"C18orf2","PTPN2","IGR: 342Kb before C18orf2(-)","IGR: 6Kb after PTPN2(-)","-",1,10,1,"not_subjected_to_validation" "CRC-9",19,0,61070027,19,61116899,"deletion","46932",10,0,"NLRP4","NLRP13","Intron of NLRP4(+): 901bp before exon 6","Intron of NLRP13(-): 447bp before exon 5","Antisense fusion",1,10,1,"not_subjected_to_validation" "CRC-9",20,1,14259421,20,14270650,"tandem_dup","11168",10,0,"MACROD2","MACROD2","Intron of MACROD2(+): 163Kb before exon 4","Intron of MACROD2(+): 152Kb before exon 4","Duplication within intron",1,10,1,"not_detected" "CRC-9",20,0,14747741,20,14813985,"deletion","66297",10,0,"MACROD2","MACROD2","Intron of MACROD2(+): 134Kb after exon 5","Intron of MACROD2(+): 200Kb after exon 5","Deletion within intron",1,10,1,"somatic" "CRC-9",20,0,31565878,20,31620328,"deletion","54447",10,0,"CBFA2T2","CBFA2T2","Intron of CBFA2T2(+): 24Kb after exon 1","Intron of CBFA2T2(+): 38Kb before exon 2","Deletion within intron",1,10,1,"not_subjected_to_validation" "CRC-9",22,0,23415678,22,23765191,"deletion","349534",10,0,"PIWIL3","KIAA1671","IGR: 29Kb before PIWIL3(-)","Exon 3 of KIAA1671(+)","-",1,10,1,"somatic" "CRC-3",7,0,110547181,7,110729058,"deletion","181873",10,0,"IMMP2L","IMMP2L","Intron of IMMP2L(-): 156Kb before exon 4","Intron of IMMP2L(-): 185Kb after exon 3","Deletion within intron",0.9999933,9.999933,1,"somatic" "CRC-8",18,1,28018948,18,30497234,"long_range","2478277",10,0,"MEP1B","DTNA","IGR: 5Kb before MEP1B(+)","5'-UTR of DTNA(+): 93Kb before coding start","-",0.9999819,9.999819,1,"somatic" "CRC-5",20,0,50057495,20,54461259,"long_range","4403757",10,0,"ZFP64","CASS4","IGR: 76Kb before ZFP64(-)","Exon 6 of CASS4(+)","-",0.9933796,9.933796,1,"not_subjected_to_validation" "CRC-3",1,1,5466610,3,7316755,"inter_chr","NaN",10,0,"NPHP4","GRM7","IGR: 379Kb before NPHP4(-)","Intron of GRM7(+): 1Kb after exon 3","-",0.9884099,9.884099,1,"somatic" "CRC-3",3,1,5911194,3,7354302,"long_range","1443104",11,0,"EDEM1","GRM7","IGR: 707Kb before EDEM1(+)","Intron of GRM7(+): 31Kb after exon 4","-",0.8888889,9.777778,1,"somatic" "CRC-3",1,0,49446322,1,49489944,"deletion","43671",9,0,"AGBL4","AGBL4","Intron of AGBL4(-): 38Kb after exon 4","Intron of AGBL4(-): 6Kb before exon 4","Deletion of 1 exon: out of frame",1,9,1,"somatic" "CRC-3",1,0,233632828,3,5932076,"inter_chr","NaN",9,0,"TBCE","EDEM1","Intron of TBCE(+): 1Kb after exon 3","IGR: 728Kb before EDEM1(+)","-",1,9,1,"somatic" "CRC-3",1,1,236254591,3,5170554,"inter_chr","NaN",9,0,"ZP4","ARL8B","IGR: 142Kb before ZP4(-)","Intron of ARL8B(+): 17Kb before exon 2","-",1,9,1,"somatic" "CRC-3",3,0,2702507,3,8331278,"long_range","5628789",9,0,"CNTN4","LMCD1","Intron of CNTN4(+): 50Kb before exon 4","IGR: 187Kb before LMCD1(+)","-",1,9,1,"somatic" "CRC-3",6,0,66391721,6,75299704,"long_range","8907994",9,0,"EYS","COL12A1","5'-UTR of EYS(-): 130Kb before coding start","IGR: 551Kb before COL12A1(-)","-",1,9,1,"somatic" "CRC-3",6,0,127469925,6,128781514,"long_range","1311573",9,0,"RSPO3","PTPRK","IGR: 12Kb before RSPO3(+)","Intron of PTPRK(-): 21Kb before exon 2","-",1,9,1,"somatic" "CRC-5",5,0,59106648,5,59252079,"deletion","145455",9,0,"PDE4D","PDE4D","Intron of PDE4D(-): 118Kb after exon 1","Intron of PDE4D(-): 68Kb after exon 3","Deletion of 2 exons: in frame",1,9,1,"not_detected" "CRC-5",7,0,110153215,7,110199899,"deletion","46684",9,0,"IMMP2L","IMMP2L","Intron of IMMP2L(-): 62Kb before exon 6","Intron of IMMP2L(-): 109Kb before exon 6","Deletion within intron",1,9,1,"not_detected" "CRC-5",16,1,7079502,16,7507957,"tandem_dup","428436",9,0,"A2BP1","A2BP1","Intron of A2BP1(+): 37Kb after exon 4","Intron of A2BP1(+): 202bp before exon 2","Duplication of 3 exons: in frame",1,9,1,"not_detected" "CRC-5",20,1,15945326,20,22700330,"long_range","6754947",9,0,"MACROD2","FOXA2","Intron of MACROD2(+): 25Kb before exon 16","IGR: 191Kb before FOXA2(-)","-",1,9,1,"not_detected" "CRC-5",20,0,20398053,20,35031865,"long_range","14633826",9,0,"RALGAPA2","RBL1","Intron of RALGAPA2(-): 3Kb after exon 37","IGR: 28Kb before RBL1(-)","-",1,9,1,"not_detected" "CRC-5",20,1,39343983,20,56957570,"long_range","17613561",9,0,"ZHX3","TH1L","5'-UTR of ZHX3(-): 77Kb before coding start","IGR: 32Kb before TH1L(+)","-",1,9,1,"not_subjected_to_validation" "CRC-5",20,0,39559402,20,55175640,"long_range","15616225",9,0,"CHD6","BMP7","Intron of CHD6(-): 31bp after exon 8","IGR: 2Kb before BMP7(-)","-",1,9,1,"not_subjected_to_validation" "CRC-5",20,0,41841448,20,47715505,"long_range","5874128",9,0,"GTSF1L","B4GALT5","IGR: 53Kb before GTSF1L(-)","Intron of B4GALT5(-): 9Kb before exon 2","-",1,9,1,"not_detected" "CRC-5",20,1,49366490,20,56931399,"long_range","7564962",9,0,"NFATC2","GNAS","IGR: 75Kb before NFATC2(-)","IGR: 31Kb before GNAS(+)","-",1,9,1,"not_detected" "CRC-5",20,1,16259982,20,59540924,"long_range","43280932",9,0,"KIF16B","CDH4","Intron of KIF16B(-): 5Kb after exon 24","Intron of CDH4(+): 211Kb before exon 3","Protein fusion: out of frame (KIF16B-CDH4)",1,9,1,"not_detected" "CRC-5",21,1,19383878,21,46651469,"long_range","27267590",9,0,"PRSS7","PCNT","IGR: 821Kb before PRSS7(-)","Intron of PCNT(+): 4Kb before exon 28","-",1,9,1,"not_subjected_to_validation" "CRC-6",1,0,191671680,1,191819913,"inversion","148206",9,0,"B3GALT2","B3GALT2","IGR: 257Kb before B3GALT2(-)","IGR: 405Kb before B3GALT2(-)","-",1,9,1,"not_subjected_to_validation" "CRC-6",5,1,96606058,5,123104889,"long_range","26498882",9,0,"RIOK2","CSNK1G3","IGR: 61Kb after RIOK2(-)","IGR: 229Kb before CSNK1G3(+)","-",1,9,1,"not_subjected_to_validation" "CRC-6",5,0,103599978,5,153955365,"long_range","50355387",9,0,"NUDT12","LARP1","IGR: 688Kb before NUDT12(-)","IGR: 117Kb before LARP1(+)","-",1,9,0,"not_detected" "CRC-6",5,0,96226634,11,100153009,"inter_chr","NaN",9,0,"ERAP2","FLJ32810","IGR: 11Kb before ERAP2(+)","Intron of FLJ32810(+): 7Kb after exon 2","-",1,9,1,"not_subjected_to_validation" "CRC-6",5,1,103600037,11,94602050,"inter_chr","NaN",9,0,"NUDT12","SESN3","IGR: 688Kb before NUDT12(-)","Intron of SESN3(-): 2Kb after exon 1","-",1,9,1,"not_subjected_to_validation" "CRC-6",9,0,4573928,9,4674674,"deletion","100778",9,0,"SLC1A1","CDC37L1","Intron of SLC1A1(+): 727bp after exon 11","Intron of CDC37L1(+): 200bp before exon 2","Protein fusion: out of frame (SLC1A1-CDC37L1)",1,9,1,"not_subjected_to_validation" "CRC-7",10,0,29114925,10,29117724,"deletion","2822",9,0,"BAMBI","BAMBI","IGR: 108Kb before BAMBI(+)","IGR: 111Kb before BAMBI(+)","-",1,9,1,"somatic" "CRC-7",20,0,14832573,20,14858129,"deletion","25620",9,0,"MACROD2","MACROD2","Intron of MACROD2(+): 219Kb after exon 5","Intron of MACROD2(+): 245Kb after exon 5","Deletion within intron",1,9,1,"somatic" "CRC-8",2,0,127481808,2,139373651,"long_range","11891874",9,0,"BIN1","NXPH2","IGR: 40Kb before BIN1(-)","IGR: 230Kb before NXPH2(-)","-",1,9,1,"not_subjected_to_validation" "CRC-8",5,1,90339932,5,90582063,"tandem_dup","242061",9,0,"GPR98","ARRDC3","Intron of GPR98(+): 23Kb after exon 85","IGR: 118Kb before ARRDC3(-)","-",1,9,1,"somatic" "CRC-9",2,0,44813610,2,214457289,"long_range","169643690",9,0,"C2orf34","SPAG16","Intron of C2orf34(+): 11Kb before exon 8","Intron of SPAG16(+): 22Kb after exon 11","Antisense fusion",1,9,1,"somatic" "CRC-9",2,0,196593192,2,197088892,"deletion","495698",9,0,"DNAH7","HECW2","Intron of DNAH7(-): 932bp before exon 9","5'-UTR of HECW2(-): 83Kb before coding start","Transcript fusion (HECW2-DNAH7)",1,9,1,"not_subjected_to_validation" "CRC-9",3,0,60627046,3,60999773,"deletion","372729",9,0,"FHIT","FHIT","5'-UTR of FHIT(-): 129Kb before coding start","5'-UTR of FHIT(-): 502Kb before coding start","Deletion within transcript",1,9,1,"somatic" "CRC-9",4,0,107518556,4,107790802,"deletion","272231",9,0,"AIMP1","DKK2","IGR: 61Kb before AIMP1(+)","IGR: 272Kb before DKK2(-)","-",1,9,1,"not_subjected_to_validation" "CRC-9",6,0,33434278,6,33495011,"deletion","60738",9,0,"LYPLA2P1","SYNGAP1","IGR: 6Kb before LYPLA2P1(-)","Promoter of SYNGAP1(+): 807bp from tx start","-",1,9,1,"somatic" "CRC-9",7,0,56225749,7,56314589,"deletion","88865",9,0,"LOC389493","LOC650226","IGR: 76Kb before LOC389493(-)","IGR: 144Kb before LOC650226(-)","-",1,9,1,"not_subjected_to_validation" "CRC-9",8,0,54160701,8,54286671,"deletion","125970",9,0,"OPRK1","OPRK1","IGR: 140Kb before OPRK1(-)","IGR: 14Kb before OPRK1(-)","-",1,9,-1,"not_subjected_to_validation" "CRC-9",8,0,92337046,8,92520696,"deletion","183671",9,0,"SLC26A7","SLC26A7","Intron of SLC26A7(+): 6Kb after exon 2","IGR: 41Kb after SLC26A7(+)","-",1,9,1,"somatic" "CRC-9",9,0,14785533,9,15197581,"deletion","412053",9,0,"FREM1","TTC39B","Intron of FREM1(-): 2Kb after exon 21","Intron of TTC39B(-): 3Kb after exon 4","Protein fusion: out of frame (TTC39B-FREM1)",1,9,1,"somatic" "CRC-9",11,0,57489435,11,58097973,"deletion","608578",9,0,"OR9Q1","LPXN","IGR: 58Kb before OR9Q1(+)","Intron of LPXN(-): 2Kb after exon 1","-",1,9,1,"somatic" "CRC-9",12,0,54451929,12,54453298,"deletion","1366",9,0,"SARNP","SARNP","Intron of SARNP(-): 11Kb before exon 10","Intron of SARNP(-): 13Kb before exon 10","Deletion within intron",1,9,1,"not_subjected_to_validation" "CRC-9",14,1,36680492,14,36783887,"tandem_dup","103358",9,0,"SLC25A21","MIPOL1","Intron of SLC25A21(-): 31Kb after exon 1","5'-UTR of MIPOL1(+): 3Kb before coding start","Antisense fusion",1,9,1,"not_subjected_to_validation" "CRC-9",17,0,39761844,17,39831695,"deletion","69844",9,0,"SLC25A39","GPATCH8","IGR: 4Kb after SLC25A39(-)","Exon 8 of GPATCH8(-)","-",1,9,1,"not_subjected_to_validation" "CRC-9",19,0,12424765,19,13100694,"deletion","675929",9,0,"ZNF709","NACC1","IGR: 8Kb before ZNF709(-)","5'-UTR of NACC1(+): 6Kb before coding start","-",1,9,1,"not_subjected_to_validation" "CRC-9",19,0,38851296,19,39198677,"deletion","347436",9,0,"CHST8","LSM14A","5'-UTR of CHST8(+): 21Kb before coding start","IGR: 156Kb before LSM14A(+)","-",1,9,1,"not_subjected_to_validation" "CRC-1",1,1,48525647,1,49110548,"tandem_dup","584901",9,0,"SPATA6","AGBL4","IGR: 11Kb before SPATA6(-)","Intron of AGBL4(-): 5Kb before exon 6","-",1,9,1,"somatic" "CRC-9",11,0,95738293,11,114578550,"long_range","18840242",9,0,"CCDC82","CADM1","Intron of CCDC82(-): 338bp before exon 8","Intron of CADM1(-): 7Kb after exon 8","Protein fusion: out of frame (CADM1-CCDC82)",0.9996932,8.997239,1,"somatic" "CRC-5",14,1,96522520,14,105644998,"long_range","9122479",9,0,"VRK1","ADAM6","IGR: 189Kb before VRK1(+)","IGR: 138Kb before ADAM6(-)","-",0.9990987,8.991888,1,"not_subjected_to_validation" "CRC-6",5,0,122715537,11,68093742,"inter_chr","NaN",9,0,"CEP120","SAPS3","Intron of CEP120(-): 2Kb before exon 20","Intron of SAPS3(+): 54bp before exon 11","Protein fusion: in frame (SAPS3-CEP120)",0.992469,8.932221,1,"somatic" "CRC-3",10,0,129527238,10,129783714,"deletion","256487",9,0,"CLRN3","MKI67","IGR: 39Kb before CLRN3(-)","IGR: 1Kb before MKI67(-)","-",0.9846154,8.861538,1,"somatic" "CRC-8",8,1,131349063,8,145615642,"long_range","14266500",9,0,"ASAP1","SLC39A4","Intron of ASAP1(-): 31Kb before exon 3","Promoter of SLC39A4(-): 2Kb from tx start","Transcript fusion (ASAP1-SLC39A4)",0.8919821,8.027839,1,"somatic" "CRC-2",4,1,91940220,4,91997779,"tandem_dup","57529",8,0,"FAM190A","FAM190A","Intron of FAM190A(+): 16Kb before exon 8","Intron of FAM190A(+): 42Kb after exon 8","Duplication of 1 exon: in frame",1,8,1,"somatic" "CRC-3",1,0,5275710,3,5187100,"inter_chr","NaN",8,0,"NPHP4","ARL8B","IGR: 570Kb before NPHP4(-)","Intron of ARL8B(+): 77bp before exon 2","-",1,8,1,"somatic" "CRC-3",1,0,5303622,3,8282035,"inter_chr","NaN",8,0,"NPHP4","LMCD1","IGR: 542Kb before NPHP4(-)","IGR: 237Kb before LMCD1(+)","-",1,8,1,"somatic" "CRC-3",1,0,236845686,3,10925011,"inter_chr","NaN",8,0,"LOC339535","SLC6A11","IGR: 135Kb before LOC339535(-)","Intron of SLC6A11(+): 4Kb before exon 7","-",1,8,1,"somatic" "CRC-3",1,0,245408838,3,2802655,"inter_chr","NaN",8,0,"ZNF124","CNTN4","IGR: 7Kb after ZNF124(-)","Intron of CNTN4(+): 34Kb before exon 6","-",1,8,1,"somatic" "CRC-3",2,0,57109389,2,57145561,"deletion","36177",8,0,"CCDC85A","CCDC85A","IGR: 845Kb before CCDC85A(+)","IGR: 881Kb before CCDC85A(+)","-",1,8,1,"somatic" "CRC-3",3,1,3234820,3,6876658,"long_range","3641838",8,0,"CRBN","GRM7","IGR: 38Kb after CRBN(-)","Promoter of GRM7(+): 1Kb from tx start","-",1,8,1,"somatic" "CRC-3",3,0,3777596,3,3813752,"inversion","36172",8,0,"LRRN1","LRRN1","IGR: 39Kb before LRRN1(+)","Promoter of LRRN1(+): 2Kb from tx start","-",1,8,1,"somatic" "CRC-3",3,0,5184088,3,7710801,"long_range","2526704",8,0,"ARL8B","GRM7","Intron of ARL8B(+): 3Kb before exon 2","Intron of GRM7(+): 14Kb after exon 9","Antisense fusion",1,8,1,"somatic" "CRC-3",3,0,60213356,3,60616233,"deletion","403011",8,0,"FHIT","FHIT","Intron of FHIT(-): 238Kb before exon 6","5'-UTR of FHIT(-): 119Kb before coding start","Deletion within transcript",1,8,1,"somatic" "CRC-3",3,0,4787250,3,4815954,"deletion","28738",8,0,"ITPR1","ITPR1","Intron of ITPR1(+): 2Kb after exon 43","Intron of ITPR1(+): 1Kb before exon 51","Deletion of 7 exons: out of frame",1,8,1,"somatic" "CRC-3",3,0,3420430,5,178084387,"inter_chr","NaN",8,0,"CRBN","ZNF354A","IGR: 254Kb before CRBN(-)","Intron of ZNF354A(-): 603bp after exon 4","-",1,8,1,"somatic" "CRC-3",4,0,189926791,4,189997001,"deletion","70210",8,0,"TRIML1","TRIML1","IGR: 629Kb before TRIML1(+)","IGR: 699Kb before TRIML1(+)","-",1,8,0,"somatic" "CRC-3",16,0,6860343,16,6889417,"deletion","29102",8,0,"A2BP1","A2BP1","5'-UTR of A2BP1(+): 182Kb before coding start","5'-UTR of A2BP1(+): 153Kb before coding start","Deletion within transcript",1,8,1,"somatic" "CRC-4",4,0,15473705,4,21781015,"long_range","6307310",8,0,"CD38","GPR125","IGR: 14Kb after CD38(+)","IGR: 217Kb before GPR125(-)","-",1,8,0,"not_subjected_to_validation" "CRC-4",4,1,22192981,16,70670202,"inter_chr","NaN",8,0,"GBA3","TXNL4B","IGR: 111Kb before GBA3(+)","IGR: 6Kb before TXNL4B(-)","-",1,8,1,"not_subjected_to_validation" "CRC-5",20,0,20301047,20,20673624,"inversion","372581",8,0,"INSM1","RALGAPA2","IGR: 4Kb before INSM1(+)","IGR: 32Kb after RALGAPA2(-)","-",1,8,1,"not_subjected_to_validation" "CRC-5",20,0,51919854,20,55967099,"long_range","4047252",8,0,"SUMO1P1","C20orf85","IGR: 5Kb before SUMO1P1(-)","IGR: 192Kb before C20orf85(+)","-",1,8,1,"not_subjected_to_validation" "CRC-5",21,0,32455407,21,41661441,"long_range","9206043",8,0,"NCRNA00159","MX2","IGR: 5Kb after NCRNA00159(+)","5'-UTR of MX2(+): 9Kb before coding start","-",1,8,1,"not_subjected_to_validation" "CRC-6",5,1,114954407,5,125721276,"long_range","10766747",8,0,"TMED7-TICAM2","GRAMD3","Intron of TMED7-TICAM2(-): 10Kb before exon 4","Promoter of GRAMD3(+): 2Kb from tx start","Antisense fusion",1,8,1,"somatic" "CRC-6",5,1,122717021,5,123100394,"inversion","383395",8,0,"CEP120","CSNK1G3","Intron of CEP120(-): 3Kb before exon 20","IGR: 225Kb before CSNK1G3(+)","-",1,8,1,"somatic" "CRC-6",5,0,123100570,11,95790329,"inter_chr","NaN",8,0,"CSNK1G3","JRKL","IGR: 225Kb before CSNK1G3(+)","IGR: 28Kb before JRKL(+)","-",1,8,1,"somatic" "CRC-6",5,1,159754284,11,63010998,"inter_chr","NaN",8,0,"C5orf54","HRASLS5","Exon 2 of C5orf54(-)","Intron of HRASLS5(-): 2Kb after exon 3","Antisense fusion",1,8,1,"somatic" "CRC-7",2,0,224134295,2,224145624,"deletion","11363",8,0,"SCG2","SCG2","IGR: 36Kb before SCG2(-)","IGR: 24Kb before SCG2(-)","-",1,8,1,"somatic" "CRC-8",12,1,8918376,12,80803740,"long_range","71885315",8,0,"A2ML1","CCDC59","Intron of A2ML1(+): 1bp after exon 34","IGR: 467Kb before CCDC59(-)","-",1,8,1,"not_subjected_to_validation" "CRC-8",12,0,16075379,12,20199432,"long_range","4124053",8,0,"DERA","PDE3A","Intron of DERA(+): 1Kb before exon 7","IGR: 214Kb before PDE3A(+)","-",1,8,0,"somatic" "CRC-8",18,0,4158936,22,27395534,"inter_chr","NaN",8,0,"DLGAP1","TTC28","IGR: 289Kb after DLGAP1(-)","Intron of TTC28(-): 10Kb after exon 1","-",1,8,0,"not_detected" "CRC-9",1,0,8797387,1,9136049,"inversion","338667",8,0,"RERE","MIR34A","5'-UTR of RERE(-): 158Kb before coding start","Promoter of MIR34A(-): 2Kb from tx start","-",1,8,1,"not_subjected_to_validation" "CRC-9",1,0,45039229,1,45161555,"deletion","122334",8,0,"PLK3","EIF2B3","Intron of PLK3(+): 18bp after exon 2","Intron of EIF2B3(-): 3Kb after exon 5","Antisense fusion",1,8,1,"not_subjected_to_validation" "CRC-9",1,0,235731091,1,235738451,"deletion","7371",8,0,"RYR2","RYR2","Intron of RYR2(+): 245bp after exon 21","Intron of RYR2(+): 2Kb after exon 23","Deletion of 2 exons: out of frame",1,8,1,"somatic" "CRC-9",2,1,51102563,2,51284945,"inversion","182394",8,0,"NRXN1","NRXN1","Intron of NRXN1(-): 4Kb after exon 3","IGR: 172Kb after NRXN1(-)","-",1,8,1,"not_subjected_to_validation" "CRC-9",2,0,64008040,2,73069020,"long_range","9060985",8,0,"VPS54","SFXN5","Intron of VPS54(-): 6Kb before exon 13","Intron of SFXN5(-): 29bp before exon 10","-",1,8,1,"not_subjected_to_validation" "CRC-9",2,0,104438606,2,104499263,"inversion","60664",8,0,"LOC150568","LOC150568","5'-UTR of LOC150568(+): 57Kb before coding start","IGR: 4Kb after LOC150568(+)","-",1,8,1,"not_subjected_to_validation" "CRC-9",2,0,103568408,2,104431865,"deletion","863464",8,0,"TMEM182","LOC150568","IGR: 823Kb before TMEM182(+)","5'-UTR of LOC150568(+): 64Kb before coding start","-",1,8,1,"not_subjected_to_validation" "CRC-9",2,0,166568539,4,183401410,"inter_chr","NaN",8,0,"SCN1A","MIR1305","Intron of SCN1A(-): 1Kb before exon 21","IGR: 74Kb before MIR1305(+)","-",1,8,1,"somatic" "CRC-9",3,1,115604560,3,116248307,"inversion","643751",8,0,"ZBTB20","ZBTB20","5'-UTR of ZBTB20(-): 51Kb before coding start","5'-UTR of ZBTB20(-): 695Kb before coding start","Antisense fusion",1,8,1,"not_subjected_to_validation" "CRC-9",5,0,46151832,5,46238170,"deletion","86359",8,0,"HCN1","HCN1","IGR: 420Kb after HCN1(-)","IGR: 943Kb before HCN1(-)","-",1,8,1,"not_subjected_to_validation" "CRC-9",5,1,85716865,5,85756895,"tandem_dup","39998",8,0,"NBPF22P","NBPF22P","IGR: 103Kb before NBPF22P(+)","IGR: 143Kb before NBPF22P(+)","-",1,8,1,"not_subjected_to_validation" "CRC-9",6,0,74396691,6,94552489,"long_range","20155819",8,0,"SLC17A5","TSG1","Intron of SLC17A5(-): 5Kb after exon 6","IGR: 10Kb after TSG1(+)","-",1,8,1,"not_subjected_to_validation" "CRC-9",7,0,70453833,7,71023737,"deletion","569900",8,0,"WBSCR17","CALN1","Intron of WBSCR17(+): 15Kb after exon 2","Intron of CALN1(-): 103Kb after exon 5","Antisense fusion",1,8,1,"not_subjected_to_validation" "CRC-9",7,1,63752143,10,99060492,"inter_chr","NaN",8,0,"ZNF107","FRAT1","IGR: 12Kb before ZNF107(+)","IGR: 9Kb before FRAT1(+)","-",1,8,1,"not_subjected_to_validation" "CRC-9",10,1,21725160,10,21781883,"tandem_dup","56723",8,0,"C10orf114","C10orf114","IGR: 98Kb before C10orf114(-)","IGR: 42Kb before C10orf114(-)","-",1,8,0,"not_subjected_to_validation" "CRC-9",10,0,43319085,10,44868178,"long_range","1549062",8,0,"ZNF239","LOC100133308","IGR: 53Kb before ZNF239(-)","IGR: 47Kb before LOC100133308(-)","-",1,8,1,"not_subjected_to_validation" "CRC-9",12,0,43058896,12,43091252,"deletion","32346",8,0,"TMEM117","TMEM117","Intron of TMEM117(+): 2Kb after exon 7","IGR: 21Kb after TMEM117(+)","-",1,8,1,"not_subjected_to_validation" "CRC-9",13,0,34804076,13,35066596,"deletion","262551",8,0,"NBEA","NBEA","Intron of NBEA(+): 17Kb before exon 38","Intron of NBEA(+): 1Kb after exon 48","Deletion of 11 exons: out of frame",1,8,1,"somatic" "CRC-9",13,0,32684864,13,32739820,"deletion","54954",8,0,"STARD13","STARD13","Intron of STARD13(-): 45Kb before exon 2","Intron of STARD13(-): 18Kb after exon 1","Deletion within intron",1,8,1,"not_subjected_to_validation" "CRC-9",13,0,102754623,15,54040273,"inter_chr","NaN",8,0,"SLC10A2","NEDD4","IGR: 260Kb before SLC10A2(-)","Intron of NEDD4(-): 6Kb after exon 2","-",1,8,0,"not_subjected_to_validation" "CRC-9",16,1,55597020,16,55633503,"tandem_dup","36488",8,0,"NLRC5","NLRC5","5'-UTR of NLRC5(+): 15Kb before coding start","Intron of NLRC5(+): 35bp after exon 19","Duplication within transcript",1,8,1,"not_subjected_to_validation" "CRC-9",16,1,64998006,16,64999334,"inversion","1391",8,0,"CDH5","CDH5","IGR: 2Kb after CDH5(+)","IGR: 3Kb after CDH5(+)","-",1,8,1,"not_subjected_to_validation" "CRC-9",19,0,46635225,19,46793744,"deletion","158530",8,0,"ATP5SL","CEACAM21","Intron of ATP5SL(-): 727bp after exon 2","IGR: 19Kb before CEACAM21(+)","-",1,8,1,"not_subjected_to_validation" "CRC-1",13,0,62782087,13,62786569,"deletion","4474",8,0,"OR7E156P","OR7E156P","IGR: 427Kb before OR7E156P(+)","IGR: 423Kb before OR7E156P(+)","-",1,8,1,"not_subjected_to_validation" "CRC-5",9,0,122903651,9,123084825,"deletion","181301",8,0,"CEP110","GSN","Intron of CEP110(+): 3Kb after exon 5","5'-UTR of GSN(+): 17Kb before coding start","Transcript fusion (CEP110-GSN)",0.9984026,7.98722,1,"not_subjected_to_validation" "CRC-3",1,1,237185816,3,8016594,"inter_chr","NaN",8,0,"LOC339535","GRM7","IGR: 475Kb before LOC339535(-)","IGR: 258Kb after GRM7(+)","-",0.9798031,7.838425,1,"somatic" "CRC-3",3,0,4828423,3,7072509,"long_range","2244092",11,0,"ITPR1","GRM7","Intron of ITPR1(+): 276bp after exon 53","Intron of GRM7(+): 91Kb before exon 2","Antisense fusion",0.7032967,7.736264,1,"germline" "CRC-8",2,1,140118350,3,194783965,"inter_chr","NaN",8,0,"LRP1B","OPA1","IGR: 587Kb before LRP1B(-)","IGR: 10Kb before OPA1(+)","-",0.9587171,7.669737,1,"somatic" "CRC-4",3,1,86038783,3,86047882,"inversion","9097",17,0,"CADM2","CADM2","Intron of CADM2(+): 5Kb before exon 5","Intron of CADM2(+): 4Kb after exon 5","-",0.443577,7.540809,1,"somatic" "CRC-9",7,0,63752149,7,64161185,"deletion","409039",10,0,"ZNF107","INTS4L1","IGR: 12Kb before ZNF107(+)","IGR: 78Kb before INTS4L1(+)","-",0.7416799,7.416799,1,"not_subjected_to_validation" "CRC-6",5,0,114954403,5,153955467,"long_range","39001060",8,0,"TMED7-TICAM2","LARP1","Intron of TMED7-TICAM2(-): 9Kb before exon 4","IGR: 117Kb before LARP1(+)","-",0.9197949,7.358359,1,"somatic" "CRC-3",1,1,233923401,1,236536122,"long_range","2612693",7,0,"LYST","LOC339535","Intron of LYST(-): 27bp before exon 47","IGR: 174Kb before LOC339535(-)","-",1,7,1,"somatic" "CRC-3",1,1,5301538,3,6054295,"inter_chr","NaN",7,0,"NPHP4","GRM7","IGR: 544Kb before NPHP4(-)","IGR: 824Kb before GRM7(+)","-",1,7,1,"somatic" "CRC-3",1,1,233714631,3,6880142,"inter_chr","NaN",7,0,"B3GALNT2","GRM7","Intron of B3GALNT2(-): 179bp before exon 4","Intron of GRM7(+): 2Kb after exon 1","Protein fusion: out of frame (B3GALNT2-GRM7)",1,7,1,"somatic" "CRC-3",1,1,245349054,3,3585460,"inter_chr","NaN",7,0,"C1orf229","LRRN1","IGR: 7Kb after C1orf229(-)","IGR: 231Kb before LRRN1(+)","-",1,7,1,"somatic" "CRC-3",1,0,224875793,3,3145867,"inter_chr","NaN",7,0,"ITPKB","TRNT1","IGR: 10Kb before ITPKB(-)","Intron of TRNT1(+): 12bp after exon 2","-",1,7,1,"somatic" "CRC-3",1,0,245288005,5,178130481,"inter_chr","NaN",7,0,"ZNF670","AACSL","Intron of ZNF670(-): 19Kb before exon 2","3'-UTR of AACSL(-): 5Kb after coding stop","-",1,7,1,"somatic" "CRC-3",3,1,2683190,3,2761783,"tandem_dup","78586",7,0,"CNTN4","CNTN4","Intron of CNTN4(+): 70Kb before exon 4","Intron of CNTN4(+): 438bp before exon 5","Duplication of 1 exon: out of frame",1,7,1,"somatic" "CRC-3",3,0,2848467,3,7050326,"long_range","4201890",7,0,"CNTN4","GRM7","Intron of CNTN4(+): 12Kb after exon 6","Intron of GRM7(+): 113Kb before exon 2","Protein fusion: out of frame (CNTN4-GRM7)",1,7,1,"somatic" "CRC-3",3,0,6796695,3,6825146,"deletion","28486",7,0,"GRM7","GRM7","IGR: 81Kb before GRM7(+)","IGR: 53Kb before GRM7(+)","-",1,7,1,"not_detected" "CRC-3",3,0,6263160,5,178758089,"inter_chr","NaN",7,0,"GRM7","ADAMTS2","IGR: 615Kb before GRM7(+)","IGR: 53Kb after ADAMTS2(-)","-",1,7,1,"somatic" "CRC-3",5,0,132903613,5,133396590,"inversion","492964",7,0,"FSTL4","VDAC1","Intron of FSTL4(-): 27Kb after exon 3","IGR: 61Kb before VDAC1(-)","-",1,7,1,"somatic" "CRC-3",6,0,42219015,6,106314863,"long_range","64095836",7,0,"C6orf132","PRDM1","Promoter of C6orf132(-): 330bp from tx start","IGR: 326Kb before PRDM1(+)","-",1,7,1,"somatic" "CRC-3",6,1,27343409,6,108122202,"long_range","80778672",7,0,"PRSS16","SCML4","IGR: 20Kb before PRSS16(+)","IGR: 8Kb before SCML4(-)","-",1,7,1,"somatic" "CRC-3",16,0,6331357,16,7095068,"deletion","763818",7,0,"A2BP1","A2BP1","5'-UTR of A2BP1(+): 711Kb before coding start","Intron of A2BP1(+): 53Kb after exon 4","Deletion within transcript",1,7,1,"somatic" "CRC-4",2,0,53141964,13,61689111,"inter_chr","NaN",7,0,"ASB3","PCDH20","IGR: 609Kb before ASB3(-)","IGR: 807Kb before PCDH20(-)","-",1,7,0,"not_subjected_to_validation" "CRC-4",4,1,14479438,4,14481964,"inversion","2526",7,0,"CPEB2","CPEB2","IGR: 135Kb before CPEB2(+)","IGR: 133Kb before CPEB2(+)","-",1,7,0,"not_subjected_to_validation" "CRC-4",4,0,14543570,16,70665240,"inter_chr","NaN",7,0,"CPEB2","HPR","IGR: 71Kb before CPEB2(+)","Intron of HPR(+): 130bp before exon 2","-",1,7,1,"not_detected" "CRC-4",10,0,133602379,10,133603110,"deletion","731",7,0,"PPP2R2D","PPP2R2D","Intron of PPP2R2D(+): 1Kb before exon 2","Intron of PPP2R2D(+): 415bp before exon 2","Deletion within intron",1,7,0,"not_subjected_to_validation" "CRC-4",10,0,97093914,20,10987822,"inter_chr","NaN",7,0,"SORBS1","JAG1","Intron of SORBS1(-): 2Kb after exon 16","IGR: 422Kb before JAG1(-)","-",1,7,1,"not_subjected_to_validation" "CRC-5",2,0,214002484,2,214241001,"deletion","238517",7,0,"SPAG16","SPAG16","Intron of SPAG16(+): 54Kb after exon 9","Intron of SPAG16(+): 178Kb after exon 10","Deletion of 1 exon: out of frame",1,7,0,"not_detected" "CRC-5",16,0,6524373,16,6768858,"deletion","244506",7,0,"A2BP1","A2BP1","5'-UTR of A2BP1(+): 518Kb before coding start","5'-UTR of A2BP1(+): 273Kb before coding start","Deletion within transcript",1,7,1,"not_detected" "CRC-5",20,1,19298150,20,55620385,"long_range","36322305",7,0,"SLC24A3","ZBP1","Intron of SLC24A3(+): 88Kb after exon 2","Intron of ZBP1(-): 74bp before exon 6","Protein fusion: in frame (ZBP1-SLC24A3)",1,7,1,"not_detected" "CRC-5",20,1,20216240,20,20936467,"inversion","720233",7,0,"C20orf26","PLK1S1","Intron of C20orf26(+): 995bp before exon 23","IGR: 118Kb before PLK1S1(+)","-",1,7,1,"germline" "CRC-5",20,1,44577549,20,57646460,"long_range","13068911",7,0,"ZNF334","PHACTR3","Promoter of ZNF334(-): 2Kb from tx start","Intron of PHACTR3(+): 33Kb after exon 1","Transcript fusion (ZNF334-PHACTR3)",1,7,0,"not_detected" "CRC-5",20,1,15891802,20,55255653,"long_range","39363788",7,0,"MACROD2","BMP7","Intron of MACROD2(+): 4Kb before exon 13","Intron of BMP7(-): 19Kb after exon 1","Protein fusion: in frame (BMP7-MACROD2)",1,7,1,"not_detected" "CRC-6",5,0,123049468,5,132655097,"long_range","9605646",7,0,"CSNK1G3","FSTL4","IGR: 174Kb before CSNK1G3(+)","Intron of FSTL4(-): 21Kb after exon 6","-",1,7,1,"somatic" "CRC-6",5,0,123105121,5,159778023,"long_range","36672899",7,0,"CSNK1G3","SLU7","IGR: 229Kb before CSNK1G3(+)","5'-UTR of SLU7(-): 3Kb before coding start","-",1,7,1,"somatic" "CRC-6",5,1,123116543,5,150142920,"long_range","27026328",7,0,"CSNK1G3","C5orf62","IGR: 241Kb before CSNK1G3(+)","Intron of C5orf62(+): 4Kb after exon 1","-",1,7,1,"somatic" "CRC-6",11,0,58100154,11,60132932,"long_range","2032800",7,0,"LPXN","C11orf64","Intron of LPXN(-): 2Kb after exon 1","IGR: 7Kb before C11orf64(+)","-",1,7,1,"somatic" "CRC-7",7,0,110155845,7,110208050,"deletion","52259",7,0,"IMMP2L","IMMP2L","Intron of IMMP2L(-): 65Kb before exon 6","Intron of IMMP2L(-): 106Kb after exon 5","Deletion within intron",1,7,1,"not_detected" "CRC-8",8,0,38460863,8,38816665,"deletion","355911",7,0,"C8orf86","TACC1","IGR: 27Kb before C8orf86(-)","Intron of TACC1(+): 144bp before exon 9","-",1,7,1,"somatic" "CRC-8",8,0,141533744,8,142816231,"long_range","1282487",7,0,"TRAPPC9","FLJ43860","Intron of TRAPPC9(-): 3Kb before exon 2","IGR: 303Kb before FLJ43860(-)","-",1,7,0,"not_subjected_to_validation" "CRC-8",8,0,144310800,8,144971808,"inversion","661008",7,0,"LY6H","PUF60","3'-UTR of LY6H(-): 242bp after coding stop","Exon 8 of PUF60(-)","-",1,7,0,"somatic" "CRC-8",12,1,16650948,12,20211313,"long_range","3560365",7,0,"LMO3","PDE3A","5'-UTR of LMO3(-): 6Kb before coding start","IGR: 202Kb before PDE3A(+)","-",1,7,0,"somatic" "CRC-8",12,1,57837750,12,79853418,"long_range","22015652",7,0,"LRIG3","LIN7A","IGR: 286Kb before LRIG3(-)","Intron of LIN7A(-): 2Kb after exon 1","-",1,7,1,"not_subjected_to_validation" "CRC-8",12,0,20208549,16,76709098,"inter_chr","NaN",7,0,"PDE3A","WWOX","IGR: 205Kb before PDE3A(+)","Intron of WWOX(+): 3Kb after exon 4","-",1,7,0,"not_detected" "CRC-8",16,0,7082639,16,7480847,"deletion","398212",7,0,"A2BP1","A2BP1","Intron of A2BP1(+): 41Kb after exon 4","Intron of A2BP1(+): 27Kb before exon 2","Deletion of 3 exons: in frame",1,7,1,"somatic" "CRC-9",2,1,44273722,2,73980389,"long_range","29706641",7,0,"PPM1B","ACTG2","5'-UTR of PPM1B(+): 8Kb before coding start","5'-UTR of ACTG2(+): 2Kb before coding start","-",1,7,1,"not_subjected_to_validation" "CRC-9",2,0,104434199,2,104438222,"deletion","4031",7,0,"LOC150568","LOC150568","5'-UTR of LOC150568(+): 61Kb before coding start","5'-UTR of LOC150568(+): 57Kb before coding start","Deletion within transcript",1,7,1,"not_subjected_to_validation" "CRC-9",2,1,239374405,2,239498856,"inversion","124451",7,0,"HDAC4","HDAC4","IGR: 260Kb before HDAC4(-)","IGR: 136Kb before HDAC4(-)","-",1,7,0,"not_subjected_to_validation" "CRC-9",5,1,42766832,5,42776969,"tandem_dup","10072",7,0,"CCDC152","CCDC152","IGR: 26Kb before CCDC152(+)","IGR: 16Kb before CCDC152(+)","-",1,7,1,"not_subjected_to_validation" "CRC-9",5,0,169907652,5,173867232,"long_range","3959585",7,0,"KCNIP1","MSX2","Intron of KCNIP1(+): 43Kb after exon 1","IGR: 217Kb before MSX2(+)","-",1,7,1,"not_subjected_to_validation" "CRC-9",6,1,73115018,6,73136778,"tandem_dup","21742",7,0,"RIMS1","RIMS1","Intron of RIMS1(+): 15Kb after exon 29","Intron of RIMS1(+): 20Kb before exon 30","Duplication within intron",1,7,1,"not_subjected_to_validation" "CRC-9",7,0,54992509,7,55079781,"deletion","87371",7,0,"EGFR","EGFR","IGR: 62Kb before EGFR(+)","Intron of EGFR(+): 25Kb after exon 1","-",1,7,1,"not_subjected_to_validation" "CRC-9",7,0,64852498,7,65010158,"deletion","157694",7,0,"CCT6P1","VKORC1L1","Promoter of CCT6P1(+): 1Kb from tx start","Intron of VKORC1L1(+): 34Kb after exon 1","Transcript fusion (CCT6P1-VKORC1L1)",1,7,1,"somatic" "CRC-9",10,0,6049856,10,43319102,"long_range","37269262",7,0,"IL15RA","ZNF239","Intron of IL15RA(-): 2Kb before exon 2","IGR: 53Kb before ZNF239(-)","-",1,7,1,"not_subjected_to_validation" "CRC-9",10,0,10406810,10,10459380,"deletion","52620",7,0,"SFTA1P","SFTA1P","IGR: 460Kb before SFTA1P(-)","IGR: 407Kb before SFTA1P(-)","-",1,7,1,"not_subjected_to_validation" "CRC-9",11,0,64439799,11,64639130,"deletion","199339",7,0,"ATG2A","TM7SF2","Intron of ATG2A(-): 1Kb after exon 1","Intron of TM7SF2(+): 20bp after exon 7","-",1,7,1,"not_subjected_to_validation" "CRC-9",12,0,44444250,12,44452309,"deletion","8086",7,0,"ARID2","ARID2","Intron of ARID2(+): 33Kb after exon 3","Intron of ARID2(+): 39Kb before exon 4","Deletion within intron",1,7,1,"not_subjected_to_validation" "CRC-9",13,1,36483072,13,36509382,"tandem_dup","26289",7,0,"FAM48A","FAM48A","Intron of FAM48A(-): 277bp before exon 25","Intron of FAM48A(-): 3Kb after exon 9","Duplication of 15 exons: out of frame",1,7,1,"somatic" "CRC-9",15,0,68870523,15,68876290,"deletion","5767",7,0,"LARP6","LARP6","IGR: 40Kb before LARP6(-)","IGR: 35Kb before LARP6(-)","-",1,7,1,"not_subjected_to_validation" "CRC-9",16,0,71559990,16,71598285,"deletion","38345",7,0,"ZFHX3","ZFHX3","5'-UTR of ZFHX3(-): 8Kb before coding start","5'-UTR of ZFHX3(-): 47Kb before coding start","Deletion within transcript",1,7,1,"somatic" "CRC-9",16,0,77933377,19,206782,"inter_chr","NaN",7,0,"MAF","PPAP2C","IGR: 252Kb before MAF(-)","IGR: 25Kb before PPAP2C(-)","-",1,7,1,"not_subjected_to_validation" "CRC-9",19,0,47499594,19,48282158,"deletion","782667",7,0,"PRR19","PSG2","5'-UTR of PRR19(+): 6Kb before coding start","IGR: 4Kb after PSG2(-)","-",1,7,1,"not_subjected_to_validation" "CRC-9",19,0,61168652,19,62536242,"long_range","1367633",7,0,"NLRP8","ZNF543","Intron of NLRP8(+): 767bp before exon 5","IGR: 2Kb after ZNF543(+)","-",1,7,1,"not_subjected_to_validation" "CRC-9",19,1,61105029,19,62536136,"long_range","1431098",7,0,"NLRP13","ZNF543","Intron of NLRP13(-): 190bp after exon 9","IGR: 2Kb after ZNF543(+)","-",1,7,1,"not_subjected_to_validation" "CRC-9",2,0,44275170,2,218605280,"long_range","174330120",7,0,"PPM1B","IL8RBP","5'-UTR of PPM1B(+): 7Kb before coding start","IGR: 27Kb before IL8RBP(-)","-",1,7,1,"not_subjected_to_validation" "CRC-1",3,0,152629038,6,48862147,"inter_chr","NaN",7,0,"MED12L","MUT","Intron of MED12L(+): 2Kb before exon 42","IGR: 645Kb before MUT(-)","-",1,7,1,"not_subjected_to_validation" "CRC-1",16,1,5695418,16,5700880,"tandem_dup","5459",7,0,"A2BP1","A2BP1","IGR: 314Kb before A2BP1(+)","IGR: 308Kb before A2BP1(+)","-",1,7,1,"not_subjected_to_validation" "CRC-1",16,1,7402271,16,7511019,"tandem_dup","108722",7,0,"A2BP1","A2BP1","Intron of A2BP1(+): 79Kb after exon 1","Intron of A2BP1(+): 3Kb after exon 2","Duplication of 1 exon: in frame",1,7,1,"not_detected" "CRC-3",1,1,236540834,3,2921314,"inter_chr","NaN",7,0,"LOC339535","CNTN4","IGR: 169Kb before LOC339535(-)","Intron of CNTN4(+): 2Kb after exon 3","-",0.9999339,6.999537,1,"somatic" "CRC-6",16,0,6653874,16,7661265,"long_range","1007391",7,0,"A2BP1","A2BP1","5'-UTR of A2BP1(+): 388Kb before coding start","Intron of A2BP1(+): 295bp before exon 10","Deletion within transcript",0.9987922,6.991546,0,"somatic" "CRC-3",3,0,6987679,5,178930532,"inter_chr","NaN",7,0,"GRM7","RUFY1","Intron of GRM7(+): 109Kb after exon 1","Intron of RUFY1(+): 1Kb after exon 5","Antisense fusion",0.9950537,6.965376,1,"somatic" "CRC-7",2,0,223648811,2,223695622,"deletion","46803",7,0,"KCNE4","KCNE4","IGR: 24Kb before KCNE4(+)","IGR: 71Kb before KCNE4(+)","-",0.9780186,6.84613,1,"not_subjected_to_validation" "CRC-9",17,1,60352268,19,33786036,"inter_chr","NaN",7,0,"LRRC37A3","LOC148145","IGR: 7Kb after LRRC37A3(-)","IGR: 362Kb before LOC148145(+)","-",0.975039,6.825273,1,"not_subjected_to_validation" "CRC-7",5,0,116920917,5,116990452,"deletion","69526",7,0,"SEMA6A","SEMA6A","IGR: 1Mb before SEMA6A(-)","IGR: 1Mb before SEMA6A(-)","-",0.9672391,6.770674,1,"not_detected" "CRC-9",17,0,60394603,17,60493368,"inversion","98824",7,0,"FLJ32065","GNA13","3'-UTR of FLJ32065(-): 8Kb after coding stop","IGR: 58Kb before GNA13(-)","-",0.9600025,6.720017,1,"not_subjected_to_validation" "CRC-5",20,0,17966076,20,19535593,"long_range","1569517",7,0,"OVOL2","SLC24A3","Intron of OVOL2(-): 4Kb after exon 3","Intron of SLC24A3(+): 21Kb after exon 6","-",0.8888889,6.222222,0,"not_detected" "CRC-2",2,1,126884337,2,191184610,"long_range","64300273",6,0,"GYPC","NAB1","IGR: 246Kb before GYPC(+)","IGR: 37Kb before NAB1(+)","-",1,6,0,"not_detected" "CRC-3",1,1,224887091,3,3721322,"inter_chr","NaN",6,0,"ITPKB","LRRN1","3'-UTR of ITPKB(-): 2Kb after coding stop","IGR: 95Kb before LRRN1(+)","-",1,6,1,"somatic" "CRC-3",1,0,235853269,3,6891109,"inter_chr","NaN",6,0,"RYR2","GRM7","Intron of RYR2(+): 434bp before exon 39","Intron of GRM7(+): 12Kb after exon 1","Antisense fusion",1,6,1,"somatic" "CRC-3",3,0,5951264,3,5988489,"deletion","37275",6,0,"EDEM1","EDEM1","IGR: 747Kb before EDEM1(+)","IGR: 784Kb before EDEM1(+)","-",1,6,1,"somatic" "CRC-3",3,1,6737767,3,7245547,"tandem_dup","507767",6,0,"GRM7","GRM7","IGR: 140Kb before GRM7(+)","Intron of GRM7(+): 70Kb before exon 3","-",1,6,1,"somatic" "CRC-3",5,1,171852562,9,106961714,"inter_chr","NaN",6,0,"SH3PXD2B","SLC44A1","IGR: 38Kb after SH3PXD2B(-)","IGR: 85Kb before SLC44A1(+)","-",1,6,0,"somatic" "CRC-3",6,1,51486682,6,53732426,"long_range","2245745",6,0,"PKHD1","LRRC1","IGR: 101Kb before PKHD1(-)","IGR: 35Kb before LRRC1(+)","-",1,6,1,"somatic" "CRC-3",6,0,65842350,6,106542981,"long_range","40700600",6,0,"EYS","PRDM1","Intron of EYS(-): 18Kb before exon 13","IGR: 98Kb before PRDM1(+)","-",1,6,1,"somatic" "CRC-3",6,1,75292810,6,104494212,"long_range","29201487",6,0,"COL12A1","HACE1","IGR: 558Kb before COL12A1(-)","IGR: 788Kb before HACE1(-)","-",1,6,1,"somatic" "CRC-3",6,0,44587618,6,65789992,"long_range","21202374",6,0,"CDC5L","EYS","IGR: 124Kb before CDC5L(+)","Intron of EYS(-): 26Kb before exon 14","-",1,6,0,"somatic" "CRC-3",6,0,42007977,6,107965922,"long_range","65957950",6,0,"BYSL","SOBP","Intron of BYSL(+): 99bp before exon 7","Intron of SOBP(+): 4Kb after exon 4","Protein fusion: out of frame (BYSL-SOBP)",1,6,1,"somatic" "CRC-3",6,0,25748686,6,41403970,"long_range","15655317",6,0,"SCGN","NCR2","IGR: 12Kb before SCGN(+)","IGR: 8Kb before NCR2(+)","-",1,6,1,"somatic" "CRC-3",6,1,64543890,6,107883335,"long_range","43339445",6,0,"EYS","PDSS2","Intron of EYS(-): 2Kb after exon 40","Intron of PDSS2(-): 4Kb after exon 1","Protein fusion: in frame (EYS-PDSS2)",1,6,0,"somatic" "CRC-3",8,0,120453230,8,120750651,"deletion","297523",6,0,"NOV","TAF2","IGR: 45Kb before NOV(+)","IGR: 61Kb before TAF2(-)","-",1,6,1,"somatic" "CRC-3",16,0,5683449,16,5776175,"deletion","92793",6,0,"A2BP1","A2BP1","IGR: 326Kb before A2BP1(+)","IGR: 233Kb before A2BP1(+)","-",1,6,1,"somatic" "CRC-3",16,0,6523054,16,6622896,"deletion","99906",6,0,"A2BP1","A2BP1","5'-UTR of A2BP1(+): 519Kb before coding start","5'-UTR of A2BP1(+): 419Kb before coding start","Deletion within transcript",1,6,1,"somatic" "CRC-3",16,1,27857950,16,31733613,"long_range","3875601",6,0,"GSG1L","ZNF267","Intron of GSG1L(-): 24Kb after exon 2","IGR: 59Kb before ZNF267(+)","-",1,6,1,"germline" "CRC-5",2,0,203119194,2,203125009,"deletion","5941",6,0,"BMPR2","BMPR2","Intron of BMPR2(+): 4Kb after exon 10","Intron of BMPR2(+): 616bp before exon 11","Deletion within intron",1,6,1,"not_subjected_to_validation" "CRC-5",5,0,163551083,5,163604862,"deletion","53860",6,0,"MAT2B","MAT2B","IGR: 686Kb before MAT2B(+)","IGR: 740Kb before MAT2B(+)","-",1,6,1,"not_subjected_to_validation" "CRC-5",10,0,60323738,10,60324504,"deletion","843",6,0,"LOC728640","LOC728640","IGR: 179Kb before LOC728640(+)","IGR: 180Kb before LOC728640(+)","-",1,6,1,"not_subjected_to_validation" "CRC-5",14,0,96491766,14,105726656,"long_range","9234829",6,0,"VRK1","ADAM6","IGR: 158Kb before VRK1(+)","IGR: 220Kb before ADAM6(-)","-",1,6,1,"not_subjected_to_validation" "CRC-5",16,0,6358079,16,6509555,"deletion","151533",6,0,"A2BP1","A2BP1","5'-UTR of A2BP1(+): 684Kb before coding start","5'-UTR of A2BP1(+): 532Kb before coding start","Deletion within transcript",1,6,1,"not_detected" "CRC-5",16,0,6790263,16,6908457,"deletion","118194",6,0,"A2BP1","A2BP1","5'-UTR of A2BP1(+): 252Kb before coding start","5'-UTR of A2BP1(+): 134Kb before coding start","Deletion within transcript",1,6,0,"germline" "CRC-5",16,0,6624211,16,6748900,"deletion","124788",6,0,"A2BP1","A2BP1","5'-UTR of A2BP1(+): 418Kb before coding start","5'-UTR of A2BP1(+): 293Kb before coding start","Deletion within transcript",1,6,1,"not_detected" "CRC-5",19,0,14104030,19,14492217,"deletion","388277",6,0,"ASF1B","DNAJB1","Intron of ASF1B(-): 4Kb after exon 1","Promoter of DNAJB1(-): 2Kb from tx start","Transcript fusion (DNAJB1-ASF1B)",1,6,1,"not_subjected_to_validation" "CRC-5",20,0,15102340,20,15116291,"deletion","13997",6,0,"MACROD2","MACROD2","Intron of MACROD2(+): 56Kb before exon 6","Intron of MACROD2(+): 42Kb before exon 6","Deletion within intron",1,6,1,"not_detected" "CRC-5",20,0,19425518,20,62173477,"long_range","42747959",6,0,"SLC24A3","TCEA2","Intron of SLC24A3(+): 19Kb before exon 3","Intron of TCEA2(+): 190bp before exon 10","Protein fusion: out of frame (SLC24A3-TCEA2)",1,6,0,"not_detected" "CRC-5",20,0,25329589,20,25674516,"deletion","344973",6,0,"GINS1","FAM182B","IGR: 7Kb before GINS1(+)","IGR: 18Kb before FAM182B(-)","-",1,6,1,"not_detected" "CRC-5",20,1,34784080,20,46820205,"long_range","12036125",6,0,"NDRG3","PREX1","5'-UTR of NDRG3(-): 528bp before coding start","Intron of PREX1(-): 22Kb before exon 2","Transcript fusion (NDRG3-PREX1)",1,6,0,"not_subjected_to_validation" "CRC-5",20,1,41422640,20,44615002,"long_range","3192361",6,0,"SFRS6","C20orf123","IGR: 97Kb before SFRS6(+)","Promoter of C20orf123(-): 2Kb from tx start","-",1,6,1,"not_detected" "CRC-5",20,1,41845331,20,44647244,"long_range","2801966",6,0,"GTSF1L","SLC13A3","IGR: 57Kb before GTSF1L(-)","Intron of SLC13A3(-): 2Kb before exon 9","-",1,6,1,"not_detected" "CRC-5",20,0,41857543,20,48977376,"long_range","7119832",6,0,"GTSF1L","ADNP","IGR: 69Kb before GTSF1L(-)","5'-UTR of ADNP(-): 23Kb before coding start","-",1,6,1,"not_detected" "CRC-5",20,1,51671637,20,51859438,"tandem_dup","187778",6,0,"ZNF217","SUMO1P1","IGR: 55Kb before ZNF217(-)","IGR: 65Kb before SUMO1P1(-)","-",1,6,1,"not_subjected_to_validation" "CRC-5",21,1,30705099,21,44192799,"long_range","13487675",6,0,"KRTAP13-3","AGPAT3","IGR: 14Kb before KRTAP13-3(-)","5'-UTR of AGPAT3(+): 11Kb before coding start","-",1,6,1,"not_subjected_to_validation" "CRC-6",5,0,122747926,5,123116614,"inversion","368701",6,0,"CEP120","CSNK1G3","Intron of CEP120(-): 662bp after exon 12","IGR: 241Kb before CSNK1G3(+)","-",1,6,1,"not_subjected_to_validation" "CRC-6",16,0,6708036,16,6921294,"deletion","213348",6,0,"A2BP1","A2BP1","5'-UTR of A2BP1(+): 334Kb before coding start","5'-UTR of A2BP1(+): 121Kb before coding start","Deletion within transcript",1,6,1,"somatic" "CRC-7",12,0,16574454,12,116295989,"long_range","99721535",6,0,"LMO3","NOS1","IGR: 18Kb before LMO3(-)","IGR: 12Kb after NOS1(-)","-",1,6,0,"somatic" "CRC-7",17,1,24460967,18,35588775,"inter_chr","NaN",6,0,"MYO18A","LOC647946","Intron of MYO18A(-): 56bp after exon 19","Promoter of LOC647946(-): 3Kb from tx start","Transcript fusion (MYO18A-LOC647946)",1,6,1,"somatic" "CRC-7",20,1,23404752,20,23808935,"tandem_dup","404142",6,0,"CST8","CST5","IGR: 15Kb before CST8(+)","Promoter of CST5(-): 523bp from tx start","-",1,6,1,"somatic" "CRC-8",2,0,139446082,2,140084574,"inversion","638492",6,0,"NXPH2","LRP1B","IGR: 303Kb before NXPH2(-)","IGR: 621Kb before LRP1B(-)","-",1,6,0,"somatic" "CRC-8",8,0,131473980,8,143854697,"long_range","12380755",6,0,"ASAP1","LYNX1","Intron of ASAP1(-): 9Kb after exon 1","5'-UTR of LYNX1(-): 322bp before coding start","-",1,6,1,"somatic" "CRC-8",12,1,29977766,12,70278761,"long_range","40300995",6,0,"TMTC1","ZFC3H1","IGR: 433Kb before TMTC1(-)","IGR: 11Kb before ZFC3H1(-)","-",1,6,0,"somatic" "CRC-8",12,0,41972536,12,65962291,"long_range","23989827",6,0,"ADAMTS20","CAND1","IGR: 62Kb before ADAMTS20(-)","Intron of CAND1(+): 185bp after exon 2","-",1,6,1,"not_subjected_to_validation" "CRC-8",13,0,63986312,14,55086853,"inter_chr","NaN",6,0,"OR7E156P","C14orf33","IGR: 777Kb before OR7E156P(+)","IGR: 26Kb before C14orf33(-)","-",1,6,1,"not_subjected_to_validation" "CRC-9",1,0,116798641,1,116875831,"deletion","77193",6,0,"C1orf203","CD58","IGR: 49Kb before C1orf203(-)","Intron of CD58(-): 4Kb after exon 3","-",1,6,1,"not_subjected_to_validation" "CRC-9",1,0,62852260,1,63249104,"deletion","396834",6,0,"DOCK7","ATG4C","Intron of DOCK7(-): 5Kb after exon 14","IGR: 227Kb before ATG4C(+)","-",1,6,1,"not_subjected_to_validation" "CRC-9",2,0,115572742,2,116072645,"deletion","499938",6,0,"DPP10","DPP10","Intron of DPP10(+): 211Kb before exon 2","Intron of DPP10(+): 73Kb after exon 5","Deletion of 4 exons: in frame",1,6,1,"somatic" "CRC-9",2,1,166566882,2,232331823,"long_range","65764915",6,0,"SCN1A","PDE6D","Intron of SCN1A(-): 305bp after exon 21","Intron of PDE6D(-): 20Kb before exon 2","Antisense fusion",1,6,1,"somatic" "CRC-9",5,0,160050875,5,160077517,"deletion","26689",6,0,"ATP10B","ATP10B","5'-UTR of ATP10B(-): 3Kb before coding start","5'-UTR of ATP10B(-): 30Kb before coding start","Deletion within transcript",1,6,1,"not_subjected_to_validation" "CRC-9",7,0,100504584,7,100598643,"deletion","94113",6,0,"TRIM56","C7orf52","IGR: 11Kb before TRIM56(+)","IGR: 2Kb before C7orf52(-)","-",1,6,1,"not_subjected_to_validation" "CRC-9",7,1,110450270,7,110464796,"tandem_dup","14511",6,0,"IMMP2L","IMMP2L","Intron of IMMP2L(-): 59Kb before exon 4","Intron of IMMP2L(-): 74Kb before exon 4","Duplication within intron",1,6,1,"somatic" "CRC-9",7,0,146629492,7,146655605,"inversion","26146",6,0,"CNTNAP2","CNTNAP2","Intron of CNTNAP2(+): 1Kb after exon 9","Intron of CNTNAP2(+): 27Kb after exon 9","Antisense fusion",1,6,1,"not_subjected_to_validation" "CRC-9",10,0,6061019,10,44399911,"long_range","38338939",6,0,"IL15RA","CXCL12","Promoter of IL15RA(-): 824bp from tx start","IGR: 207Kb before CXCL12(-)","-",1,6,1,"not_subjected_to_validation" "CRC-9",13,1,82480512,13,82903824,"inversion","423334",6,0,"SLITRK1","SLITRK1","IGR: 869Kb before SLITRK1(-)","IGR: 445Kb before SLITRK1(-)","-",1,6,1,"not_subjected_to_validation" "CRC-9",16,1,66400586,19,11525758,"inter_chr","NaN",6,0,"TSNAXIP1","ELOF1","5'-UTR of TSNAXIP1(+): 12Kb before coding start","Intron of ELOF1(-): 68bp after exon 3","-",1,6,0,"not_subjected_to_validation" "CRC-9",17,0,16078795,17,16103350,"deletion","24648",6,0,"PIGL","PIGL","Intron of PIGL(+): 635bp after exon 2","Intron of PIGL(+): 25Kb after exon 2","Deletion within intron",1,6,1,"somatic" "CRC-9",17,0,31004775,17,31212527,"deletion","207812",6,0,"AP2B1","C17orf66","Intron of AP2B1(+): 3Kb after exon 13","Intron of C17orf66(-): 2Kb after exon 8","Antisense fusion",1,6,1,"not_subjected_to_validation" "CRC-9",20,0,8758913,20,8830215,"deletion","71347",6,0,"PLCB1","PLCB1","Intron of PLCB1(+): 40Kb after exon 31","IGR: 17Kb after PLCB1(+)","-",1,6,1,"not_subjected_to_validation" "CRC-9",13,1,102754616,15,54039352,"inter_chr","NaN",6,0,"SLC10A2","NEDD4","IGR: 260Kb before SLC10A2(-)","Intron of NEDD4(-): 7Kb after exon 2","-",1,6,1,"not_subjected_to_validation" "CRC-1",1,0,106459391,1,107445011,"deletion","985625",6,0,"PRMT6","NTNG1","IGR: 941Kb before PRMT6(+)","IGR: 39Kb before NTNG1(+)","-",1,6,1,"not_subjected_to_validation" "CRC-1",2,0,205513638,2,205776156,"deletion","262524",6,0,"PARD3B","PARD3B","Intron of PARD3B(+): 24Kb before exon 3","Intron of PARD3B(+): 10Kb after exon 14","Deletion of 12 exons: out of frame",1,6,1,"somatic" "CRC-6",5,1,123049810,5,132586703,"long_range","9536864",6,0,"CSNK1G3","FSTL4","IGR: 174Kb before CSNK1G3(+)","Intron of FSTL4(-): 1Kb after exon 11","-",0.9999898,5.999939,1,"somatic" "CRC-7",10,0,52404509,10,52618615,"deletion","214144",6,0,"PRKG1","PRKG1","IGR: 16Kb before PRKG1(+)","Intron of PRKG1(+): 36Kb after exon 2","-",0.9916129,5.949677,1,"somatic" "CRC-3",16,0,6749075,16,6769575,"deletion","20500",6,0,"A2BP1","A2BP1","5'-UTR of A2BP1(+): 293Kb before coding start","5'-UTR of A2BP1(+): 272Kb before coding start","Deletion within transcript",0.9846154,5.907692,0,"somatic" "CRC-4",8,1,34934614,20,19302106,"inter_chr","NaN",6,0,"UNC5D","SLC24A3","IGR: 278Kb before UNC5D(+)","Intron of SLC24A3(+): 92Kb after exon 2","-",0.9846154,5.907692,1,"somatic" "CRC-5",20,1,42185520,20,44673129,"long_range","2487627",6,0,"JPH2","SLC13A3","Intron of JPH2(-): 5Kb before exon 3","Intron of SLC13A3(-): 488bp before exon 3","Antisense fusion",0.9846154,5.907692,1,"not_detected" "CRC-8",16,0,7137539,16,7629747,"deletion","492219",6,0,"A2BP1","A2BP1","Intron of A2BP1(+): 95Kb after exon 4","Intron of A2BP1(+): 9Kb after exon 8","Deletion of 4 exons: out of frame",0.9846154,5.907692,1,"somatic" "CRC-5",20,0,43573771,20,55897456,"long_range","12323675",8,0,"SPINT3","PMEPA1","IGR: 744bp before SPINT3(-)","IGR: 241Kb before PMEPA1(-)","-",0.7032967,5.626374,1,"not_subjected_to_validation" "CRC-4",20,1,11064575,20,25287646,"long_range","14223071",6,0,"JAG1","ABHD12","IGR: 498Kb before JAG1(-)","Intron of ABHD12(-): 20Kb before exon 2","-",0.8888889,5.333333,0,"not_detected" "CRC-4",16,0,74937229,16,76382447,"long_range","1445213",8,0,"CNTNAP4","VAT1L","Intron of CNTNAP4(+): 9Kb before exon 3","Intron of VAT1L(+): 2Kb after exon 1","Protein fusion: out of frame (CNTNAP4-VAT1L)",0.6612911,5.290329,1,"somatic" "CRC-2",7,1,110830874,7,113284620,"long_range","2453697",5,0,"IMMP2L","PPP1R3A","Intron of IMMP2L(-): 84Kb after exon 3","IGR: 20Kb before PPP1R3A(-)","-",1,5,1,"somatic" "CRC-3",6,1,25214697,6,27085335,"long_range","1870520",5,0,"CMAH","C6orf41","3'-UTR of CMAH(-): 31Kb after coding stop","5'-UTR of C6orf41(+): 14Kb before coding start","-",1,5,1,"somatic" "CRC-3",6,0,27858841,6,106939044,"long_range","79080203",5,0,"HIST1H2BL","ATG5","IGR: 24Kb before HIST1H2BL(-)","IGR: 59Kb after ATG5(-)","-",1,5,0,"somatic" "CRC-3",6,0,34975611,6,106940055,"long_range","71964444",5,0,"ANKS1A","ATG5","Intron of ANKS1A(+): 10Kb after exon 1","IGR: 60Kb after ATG5(-)","-",1,5,0,"somatic" "CRC-3",6,0,39862557,6,40074147,"deletion","211630",5,0,"DAAM2","MOCS1","IGR: 6Kb before DAAM2(+)","IGR: 94Kb before MOCS1(-)","-",1,5,1,"somatic" "CRC-3",6,1,41068797,6,49850765,"long_range","8781883",5,0,"UNC5CL","PGK2","IGR: 34Kb before UNC5CL(-)","IGR: 11Kb before PGK2(-)","-",1,5,1,"somatic" "CRC-3",6,1,41989443,6,51716875,"long_range","9727330",5,0,"MED20","PKHD1","Intron of MED20(-): 3Kb after exon 2","Intron of PKHD1(-): 272bp after exon 60","Protein fusion: in frame (MED20-PKHD1)",1,5,1,"somatic" "CRC-3",6,0,51799583,6,52648225,"inversion","848642",5,0,"PKHD1","TMEM14A","Intron of PKHD1(-): 4Kb after exon 52","5'-UTR of TMEM14A(+): 2Kb before coding start","Transcript fusion (TMEM14A-PKHD1)",1,5,0,"somatic" "CRC-3",7,0,65024392,7,153522286,"long_range","88497894",5,0,"VKORC1L1","DPP6","Intron of VKORC1L1(+): 27Kb before exon 2","Intron of DPP6(+): 141Kb after exon 1","Antisense fusion",1,5,0,"somatic" "CRC-3",8,1,128170553,8,128473966,"tandem_dup","303360",5,0,"POU5F1B","POU5F1B","IGR: 326Kb before POU5F1B(+)","IGR: 23Kb before POU5F1B(+)","-",1,5,1,"somatic" "CRC-4",10,1,97093694,20,10987662,"inter_chr","NaN",5,0,"SORBS1","JAG1","Intron of SORBS1(-): 2Kb before exon 17","IGR: 421Kb before JAG1(-)","-",1,5,0,"not_subjected_to_validation" "CRC-5",3,0,60447588,3,60727192,"deletion","279640",5,0,"FHIT","FHIT","Intron of FHIT(-): 50Kb after exon 5","5'-UTR of FHIT(-): 229Kb before coding start","Deletion within transcript",1,5,1,"not_detected" "CRC-5",3,0,164579895,3,165309234,"deletion","729339",5,0,"SI","SI","IGR: 2Mb before SI(-)","IGR: 870Kb before SI(-)","-",1,5,0,"not_subjected_to_validation" "CRC-5",10,1,52458424,10,52491221,"tandem_dup","32797",5,0,"PRKG1","PRKG1","Intron of PRKG1(+): 37Kb after exon 1","Intron of PRKG1(+): 70Kb after exon 1","Duplication within intron",1,5,0,"not_detected" "CRC-5",16,0,6812787,16,6836236,"deletion","23510",5,0,"A2BP1","A2BP1","5'-UTR of A2BP1(+): 229Kb before coding start","5'-UTR of A2BP1(+): 206Kb before coding start","Deletion within transcript",1,5,1,"not_detected" "CRC-5",20,0,16755867,20,61178959,"long_range","44423065",5,0,"OTOR","HAR1B","IGR: 79Kb before OTOR(+)","IGR: 18Kb before HAR1B(-)","-",1,5,1,"not_subjected_to_validation" "CRC-5",20,0,20179612,20,23103421,"long_range","2923896",5,0,"C20orf26","CD93","Intron of C20orf26(+): 685bp before exon 20","IGR: 95Kb before CD93(-)","-",1,5,1,"not_detected" "CRC-5",20,0,36374009,20,44513069,"long_range","8139075",5,0,"BPI","LOC100240726","Intron of BPI(+): 238bp after exon 5","IGR: 13Kb before LOC100240726(-)","-",1,5,1,"not_subjected_to_validation" "CRC-5",20,0,39103474,20,56226363,"long_range","17122889",5,0,"TOP1","PPP4R1L","Intron of TOP1(+): 12Kb after exon 2","IGR: 15Kb before PPP4R1L(-)","-",1,5,0,"not_subjected_to_validation" "CRC-5",20,0,49368760,20,51500322,"long_range","2131587",5,0,"NFATC2","TSHZ2","IGR: 72Kb before NFATC2(-)","3'-UTR of TSHZ2(+): 194Kb after coding stop","-",1,5,1,"not_detected" "CRC-5",20,1,56121371,20,56340979,"tandem_dup","219537",5,0,"C20orf85","RAB22A","IGR: 38Kb before C20orf85(+)","Intron of RAB22A(+): 11Kb before exon 3","-",1,5,1,"not_subjected_to_validation" "CRC-5",20,0,47507010,20,60236232,"long_range","12729185",5,0,"KCNB1","HRH3","Intron of KCNB1(-): 25Kb after exon 1","IGR: 7Kb after HRH3(-)","-",1,5,1,"not_subjected_to_validation" "CRC-5",21,1,21019520,21,26475692,"long_range","5456172",5,0,"C21orf131","APP","IGR: 17Kb before C21orf131(-)","IGR: 11Kb after APP(-)","-",1,5,0,"not_subjected_to_validation" "CRC-5",21,0,26148984,21,41578865,"long_range","15429915",5,0,"APP","FAM3B","IGR: 26Kb before APP(-)","IGR: 32Kb before FAM3B(+)","-",1,5,1,"not_detected" "CRC-6",3,0,60693024,3,60995416,"deletion","302451",5,0,"FHIT","FHIT","5'-UTR of FHIT(-): 195Kb before coding start","5'-UTR of FHIT(-): 498Kb before coding start","Deletion within transcript",1,5,1,"somatic" "CRC-6",5,0,103605990,11,130254634,"inter_chr","NaN",5,0,"NUDT12","SNX19","IGR: 694Kb before NUDT12(-)","Intron of SNX19(-): 108bp after exon 10","-",1,5,1,"somatic" "CRC-6",5,1,153429264,11,95785181,"inter_chr","NaN",5,0,"MFAP3","JRKL","IGR: 31Kb before MFAP3(+)","IGR: 22Kb before JRKL(+)","-",1,5,1,"not_subjected_to_validation" "CRC-6",8,1,36536789,8,36560279,"inversion","23507",5,0,"KCNU1","KCNU1","IGR: 224Kb before KCNU1(+)","IGR: 201Kb before KCNU1(+)","-",1,5,1,"not_subjected_to_validation" "CRC-7",16,1,976541,16,67374427,"long_range","66397976",5,0,"SOX8","CDH1","3'-UTR of SOX8(+): 1Kb after coding stop","Intron of CDH1(+): 19Kb before exon 3","-",1,5,1,"somatic" "CRC-7",20,0,23403008,20,24121128,"inversion","718197",5,0,"CST8","GGTLC1","IGR: 17Kb before CST8(+)","IGR: 207Kb before GGTLC1(-)","-",1,5,1,"not_detected" "CRC-8",8,1,143703297,8,145610872,"long_range","1907504",5,0,"ARC","SLC39A4","IGR: 14Kb before ARC(-)","Intron of SLC39A4(-): 126bp after exon 5","-",1,5,1,"somatic" "CRC-8",9,1,9719565,9,9759191,"tandem_dup","39582",5,0,"PTPRD","PTPRD","5'-UTR of PTPRD(-): 996Kb before coding start","5'-UTR of PTPRD(-): 1Mb before coding start","Duplication within transcript",1,5,1,"somatic" "CRC-8",10,0,89933831,10,89936027,"deletion","2235",5,0,"RNLS","RNLS","IGR: 90Kb before RNLS(-)","IGR: 88Kb before RNLS(-)","-",1,5,1,"not_subjected_to_validation" "CRC-8",12,0,33024245,12,61395121,"long_range","28370839",5,0,"PKP2","PPM1H","IGR: 189Kb before PKP2(-)","Intron of PPM1H(-): 5Kb after exon 6","-",1,5,1,"not_subjected_to_validation" "CRC-9",1,1,17133567,1,29709831,"long_range","12576281",5,0,"CROCC","PTPRU","Intron of CROCC(+): 2Kb before exon 9","IGR: 274Kb before PTPRU(+)","-",1,5,1,"not_subjected_to_validation" "CRC-9",2,0,49869312,2,50476113,"deletion","606832",5,0,"NRXN1","NRXN1","IGR: 130Kb before NRXN1(-)","Intron of NRXN1(-): 70Kb after exon 17","-",1,5,1,"not_subjected_to_validation" "CRC-9",2,0,81049192,2,166566725,"long_range","85517441",5,0,"CTNNA2","SCN1A","IGR: 320Kb after CTNNA2(+)","Intron of SCN1A(-): 591bp after exon 21","-",1,5,1,"somatic" "CRC-9",2,0,185287266,2,185323083,"deletion","35815",5,0,"ZNF804A","ZNF804A","Intron of ZNF804A(+): 115Kb after exon 1","Intron of ZNF804A(+): 116Kb before exon 2","Deletion within intron",1,5,1,"not_subjected_to_validation" "CRC-9",2,0,81047917,4,183399746,"inter_chr","NaN",5,0,"CTNNA2","MIR1305","IGR: 318Kb after CTNNA2(+)","IGR: 72Kb before MIR1305(+)","-",1,5,1,"somatic" "CRC-9",4,1,92337716,4,92367215,"tandem_dup","29428",5,0,"FAM190A","FAM190A","Intron of FAM190A(+): 112Kb after exon 10","Intron of FAM190A(+): 141Kb after exon 10","Duplication within intron",1,5,1,"somatic" "CRC-9",5,0,160094531,5,161765775,"long_range","1671304",5,0,"ATP10B","GABRG2","5'-UTR of ATP10B(-): 47Kb before coding start","IGR: 339Kb before GABRG2(+)","-",1,5,1,"not_subjected_to_validation" "CRC-9",6,0,162879207,6,162933037,"deletion","53884",5,0,"PARK2","PARK2","Intron of PARK2(-): 95Kb before exon 2","Intron of PARK2(-): 136Kb after exon 1","Deletion within intron",1,5,1,"somatic" "CRC-9",7,0,99541921,7,99594256,"deletion","52408",5,0,"AP4M1","C7orf43","Exon 13 of AP4M1(+)","Promoter of C7orf43(-): 14bp from tx start","Antisense fusion",1,5,1,"not_subjected_to_validation" "CRC-9",7,0,144811952,7,146606927,"long_range","1794977",5,0,"CNTNAP2","CNTNAP2","IGR: 632Kb before CNTNAP2(+)","Intron of CNTNAP2(+): 21Kb before exon 9","-",1,5,1,"not_subjected_to_validation" "CRC-9",11,1,97007864,11,97060596,"tandem_dup","52682",5,0,"JRKL","JRKL","IGR: 1Mb before JRKL(+)","IGR: 1Mb before JRKL(+)","-",1,5,1,"not_subjected_to_validation" "CRC-9",15,0,68167552,15,68866713,"deletion","699171",5,0,"TLE3","LARP6","Intron of TLE3(-): 6Kb after exon 4","IGR: 44Kb before LARP6(-)","-",1,5,1,"not_subjected_to_validation" "CRC-9",16,0,64991696,16,64999866,"deletion","8166",5,0,"CDH5","CDH5","Intron of CDH5(+): 474bp before exon 11","IGR: 4Kb after CDH5(+)","-",1,5,1,"not_subjected_to_validation" "CRC-9",17,0,21085930,17,21354828,"deletion","269005",5,0,"C17orf103","C17orf51","3'-UTR of C17orf103(-): 1Kb after coding stop","IGR: 17Kb before C17orf51(-)","-",1,5,1,"not_subjected_to_validation" "CRC-9",17,0,23164224,17,23221315,"deletion","57138",5,0,"NOS2","C17orf108","IGR: 56Kb before NOS2(-)","IGR: 8Kb before C17orf108(-)","-",1,5,1,"not_subjected_to_validation" "CRC-9",20,0,31443993,20,31463927,"deletion","20013",5,0,"CDK5RAP1","SNTA1","Intron of CDK5RAP1(-): 214bp before exon 5","Intron of SNTA1(-): 43bp before exon 5","Protein fusion: out of frame (SNTA1-CDK5RAP1)",1,5,1,"somatic" "CRC-1",1,1,17061559,2,219423871,"inter_chr","NaN",5,0,"CROCC","WNT6","IGR: 59Kb before CROCC(+)","IGR: 9Kb before WNT6(+)","-",1,5,0,"not_subjected_to_validation" "CRC-1",3,0,103617318,12,116296736,"inter_chr","NaN",5,0,"ZPLD1","NOS1","IGR: 19Kb before ZPLD1(+)","IGR: 13Kb after NOS1(-)","-",1,5,0,"not_detected" "CRC-1",3,0,11360291,16,2440449,"inter_chr","NaN",5,0,"ATG7","CCNF","Intron of ATG7(+): 2Kb after exon 11","Intron of CCNF(+): 532bp after exon 13","Antisense fusion",1,5,0,"not_subjected_to_validation" "CRC-1",4,1,96796176,13,62449256,"inter_chr","NaN",5,0,"PDHA2","OR7E156P","IGR: 184Kb before PDHA2(+)","IGR: 760Kb before OR7E156P(+)","-",1,5,0,"not_subjected_to_validation" "CRC-1",10,0,106788205,10,106789099,"deletion","892",5,0,"SORCS3","SORCS3","Intron of SORCS3(+): 5Kb before exon 5","Intron of SORCS3(+): 4Kb before exon 5","Deletion within intron",1,5,1,"not_subjected_to_validation" "CRC-9",20,0,9675822,20,12110734,"long_range","2434921",5,0,"PAK7","BTBD3","5'-UTR of PAK7(-): 103Kb before coding start","IGR: 264Kb before BTBD3(+)","-",0.9993012,4.996506,1,"somatic" "CRC-9",19,0,3181460,19,6448952,"long_range","3267523",5,0,"BRUNOL5","TUBB4","Intron of BRUNOL5(+): 5Kb after exon 1","Intron of TUBB4(-): 2Kb before exon 4","Antisense fusion",0.9984026,4.992013,1,"not_subjected_to_validation" "CRC-3",6,1,25188883,6,108126806,"long_range","82937923",5,0,"CMAH","SCML4","IGR: 391bp before CMAH(-)","IGR: 3Kb before SCML4(-)","-",0.9956407,4.978204,0,"somatic" "CRC-3",9,0,26169650,9,26330710,"deletion","161065",5,0,"TUSC1","C9orf82","IGR: 501Kb after TUSC1(-)","IGR: 500Kb before C9orf82(-)","-",0.9783539,4.89177,1,"somatic" "CRC-3",3,0,6017124,3,7294182,"long_range","1277074",5,0,"EDEM1","GRM7","IGR: 813Kb before EDEM1(+)","Intron of GRM7(+): 21Kb before exon 3","-",0.9773231,4.886616,1,"not_detected" "CRC-9",2,1,103332442,2,184097725,"long_range","80765281",5,0,"TMEM182","NUP35","IGR: 588Kb before TMEM182(+)","IGR: 400Kb before NUP35(+)","-",0.9561072,4.780536,1,"not_subjected_to_validation" "CRC-6",8,1,127318815,8,129338694,"long_range","2019863",5,0,"FAM84B","MIR1208","IGR: 315Kb before FAM84B(-)","IGR: 107Kb before MIR1208(+)","-",0.9250575,4.625288,1,"not_subjected_to_validation" "CRC-9",7,0,33793145,7,34420122,"deletion","626981",5,0,"BMPER","NPSR1","IGR: 118Kb before BMPER(+)","IGR: 244Kb before NPSR1(+)","-",0.9040385,4.520192,1,"not_subjected_to_validation" "CRC-7",3,1,181787058,12,3478351,"inter_chr","NaN",14,0,"TTC14","PRMT8","IGR: 16Kb before TTC14(+)","Intron of PRMT8(+): 7Kb after exon 1","-",0.3009994,4.213992,1,"somatic" "CRC-2",2,1,191186399,2,217755002,"long_range","26568603",4,0,"NAB1","DIRC3","IGR: 36Kb before NAB1(+)","IGR: 102Kb before DIRC3(-)","-",1,4,0,"somatic" "CRC-3",1,1,233787690,3,3273593,"inter_chr","NaN",4,0,"GNG4","CRBN","Intron of GNG4(-): 6Kb before exon 4","IGR: 107Kb before CRBN(-)","-",1,4,1,"somatic" "CRC-3",1,1,235861396,3,8292875,"inter_chr","NaN",4,0,"RYR2","LMCD1","Exon 42 of RYR2(+)","IGR: 226Kb before LMCD1(+)","-",1,4,0,"somatic" "CRC-3",4,0,190416476,4,190601298,"deletion","184847",4,0,"FRG1","FRG1","IGR: 683Kb before FRG1(+)","IGR: 498Kb before FRG1(+)","-",1,4,1,"somatic" "CRC-3",6,0,25200375,6,106934554,"long_range","81734229",4,0,"CMAH","ATG5","3'-UTR of CMAH(-): 46Kb after coding stop","IGR: 54Kb after ATG5(-)","-",1,4,1,"somatic" "CRC-3",6,1,26432414,6,107228180,"long_range","80795769",4,0,"HIST1H4H","QRSL1","IGR: 39Kb before HIST1H4H(-)","IGR: 5Kb after QRSL1(+)","-",1,4,1,"somatic" "CRC-3",6,0,27301141,6,42271311,"long_range","14970170",4,0,"PRSS16","GUCA1B","IGR: 22Kb before PRSS16(+)","Promoter of GUCA1B(-): 639bp from tx start","-",1,4,0,"somatic" "CRC-3",6,1,27763751,6,36305598,"long_range","8541857",4,0,"HIST1H2BL","BRPF3","IGR: 119Kb before HIST1H2BL(-)","Intron of BRPF3(+): 526bp before exon 13","-",1,4,1,"somatic" "CRC-3",6,0,34533687,6,107337718,"long_range","72804031",4,0,"PACSIN1","LOC553137","IGR: 8Kb before PACSIN1(+)","IGR: 13Kb before LOC553137(-)","-",1,4,0,"somatic" "CRC-3",6,0,36280941,6,44076259,"long_range","7795318",4,0,"BRPF3","C6orf223","Intron of BRPF3(+): 372bp after exon 3","Promoter of C6orf223(+): 58bp from tx start","Antisense fusion",1,4,0,"somatic" "CRC-3",6,0,38222706,6,40183593,"long_range","1960835",4,0,"ZFAND3","MOCS1","Intron of ZFAND3(+): 5Kb before exon 6","IGR: 203Kb before MOCS1(-)","-",1,4,1,"somatic" "CRC-3",6,1,39865154,6,105413847,"long_range","65548693",4,0,"DAAM2","HACE1","IGR: 4Kb before DAAM2(+)","Intron of HACE1(-): 288bp after exon 1","-",1,4,0,"somatic" "CRC-3",6,0,40017876,6,49266572,"long_range","9248735",4,0,"MOCS1","MUT","IGR: 8Kb after MOCS1(-)","IGR: 240Kb before MUT(-)","-",1,4,1,"somatic" "CRC-3",6,0,41792828,6,58797510,"long_range","17004680",4,0,"TFEB","GUSBL2","5'-UTR of TFEB(-): 26Kb before coding start","IGR: 443Kb before GUSBL2(-)","-",1,4,1,"somatic" "CRC-3",6,1,42150556,6,107161417,"long_range","65010861",4,0,"TAF8","RTN4IP1","Intron of TAF8(+): 2Kb before exon 8","Intron of RTN4IP1(-): 4Kb before exon 5","-",1,4,0,"somatic" "CRC-3",6,1,127469928,6,128781518,"long_range","1311592",4,0,"RSPO3","PTPRK","IGR: 12Kb before RSPO3(+)","Intron of PTPRK(-): 21Kb before exon 2","-",1,4,1,"somatic" "CRC-3",9,1,10517409,9,10571170,"tandem_dup","53761",4,0,"PTPRD","PTPRD","5'-UTR of PTPRD(-): 2Mb before coding start","5'-UTR of PTPRD(-): 2Mb before coding start","Duplication within transcript",1,4,0,"somatic" "CRC-3",10,0,19393206,10,19397392,"inversion","4245",4,0,"ARL5B","ARL5B","IGR: 405Kb before ARL5B(+)","IGR: 409Kb before ARL5B(+)","-",1,4,1,"somatic" "CRC-3",20,0,15034059,20,15057086,"deletion","23137",4,0,"MACROD2","MACROD2","Intron of MACROD2(+): 125Kb before exon 6","Intron of MACROD2(+): 101Kb before exon 6","Deletion within intron",1,4,1,"somatic" "CRC-4",6,0,48438107,6,48604253,"deletion","166146",4,0,"C6orf138","C6orf138","IGR: 484Kb before C6orf138(-)","IGR: 460Kb after C6orf138(-)","-",1,4,0,"not_subjected_to_validation" "CRC-4",8,0,137736983,8,138443498,"deletion","706515",4,0,"KHDRBS3","FAM135B","IGR: 1Mb before KHDRBS3(+)","IGR: 768Kb before FAM135B(-)","-",1,4,0,"not_subjected_to_validation" "CRC-4",8,1,40398218,20,36806255,"inter_chr","NaN",4,0,"ZMAT4","ACTR5","IGR: 109Kb before ZMAT4(-)","IGR: 4Kb before ACTR5(+)","-",1,4,0,"not_subjected_to_validation" "CRC-5",3,0,25867941,12,3478298,"inter_chr","NaN",4,0,"OXSM","PRMT8","IGR: 61Kb before OXSM(+)","Intron of PRMT8(+): 7Kb after exon 1","-",1,4,1,"not_detected" "CRC-5",7,0,110324513,7,110479629,"deletion","155218",4,0,"IMMP2L","IMMP2L","Intron of IMMP2L(-): 10Kb before exon 5","Intron of IMMP2L(-): 89Kb before exon 4","Deletion of 1 exon: in frame",1,4,1,"not_detected" "CRC-5",9,1,109301784,9,109305854,"tandem_dup","4070",4,0,"KLF4","KLF4","IGR: 15Kb before KLF4(-)","IGR: 19Kb before KLF4(-)","-",1,4,0,"not_subjected_to_validation" "CRC-5",14,1,48934972,14,48961186,"inversion","26248",4,0,"RPS29","RPS29","IGR: 179Kb before RPS29(-)","IGR: 153Kb before RPS29(-)","-",1,4,1,"not_subjected_to_validation" "CRC-5",16,1,5841388,16,5869228,"tandem_dup","27840",4,0,"A2BP1","A2BP1","IGR: 168Kb before A2BP1(+)","IGR: 140Kb before A2BP1(+)","-",1,4,0,"not_subjected_to_validation" "CRC-5",16,1,6616499,16,6629640,"tandem_dup","13141",4,0,"A2BP1","A2BP1","5'-UTR of A2BP1(+): 426Kb before coding start","5'-UTR of A2BP1(+): 412Kb before coding start","Duplication within transcript",1,4,0,"germline" "CRC-5",20,1,36645955,20,57060755,"long_range","20414800",4,0,"ADIG","SLMO2","Intron of ADIG(+): 2Kb before exon 2","IGR: 19Kb before SLMO2(-)","-",1,4,0,"not_subjected_to_validation" "CRC-5",20,0,46305736,20,47124838,"deletion","819174",4,0,"LOC284749","CSE1L","IGR: 116Kb before LOC284749(+)","Intron of CSE1L(+): 113bp after exon 11","-",1,4,1,"not_subjected_to_validation" "CRC-5",20,1,59793897,20,61395415,"long_range","1601518",4,0,"CDH4","COL20A1","Intron of CDH4(+): 12Kb after exon 4","5'-UTR of COL20A1(+): 1Kb before coding start","-",1,4,0,"not_subjected_to_validation" "CRC-5",21,0,28403410,21,41553317,"long_range","13149976",4,0,"C21orf94","BACE2","IGR: 96Kb before C21orf94(+)","Intron of BACE2(+): 2Kb after exon 7","-",1,4,1,"not_detected" "CRC-5",21,1,32290524,21,41579070,"long_range","9288526",4,0,"HUNK","FAM3B","Intron of HUNK(+): 433bp after exon 10","IGR: 31Kb before FAM3B(+)","-",1,4,1,"not_detected" "CRC-5",21,1,26151596,21,26475923,"inversion","324304",4,0,"APP","APP","IGR: 23Kb before APP(-)","IGR: 11Kb after APP(-)","-",1,4,1,"not_detected" "CRC-6",1,1,200980692,3,66383929,"inter_chr","NaN",4,0,"KDM5B","SLC25A26","Intron of KDM5B(-): 917bp after exon 16","Intron of SLC25A26(+): 8Kb after exon 2","Antisense fusion",1,4,0,"not_subjected_to_validation" "CRC-6",3,1,59959993,3,59994869,"tandem_dup","34754",4,0,"FHIT","FHIT","Intron of FHIT(-): 12Kb after exon 7","Intron of FHIT(-): 20Kb before exon 6","Duplication of 2 exons: out of frame",1,4,1,"somatic" "CRC-6",3,1,176312186,3,176314409,"tandem_dup","2223",4,0,"NAALADL2","NAALADL2","Intron of NAALADL2(+): 14Kb after exon 2","Intron of NAALADL2(+): 17Kb after exon 2","Duplication within intron",1,4,0,"not_subjected_to_validation" "CRC-6",4,0,92535699,4,92625911,"deletion","90212",4,0,"FAM190A","FAM190A","Intron of FAM190A(+): 203Kb before exon 11","Intron of FAM190A(+): 113Kb before exon 11","Deletion within intron",1,4,0,"not_detected" "CRC-6",5,1,122756417,11,100152883,"inter_chr","NaN",4,0,"CEP120","FLJ32810","Intron of CEP120(-): 476bp after exon 7","Intron of FLJ32810(+): 7Kb after exon 2","Antisense fusion",1,4,0,"not_subjected_to_validation" "CRC-6",14,1,76714077,14,76720824,"tandem_dup","6747",4,0,"TMEM63C","TMEM63C","IGR: 4Kb before TMEM63C(+)","5'-UTR of TMEM63C(+): 34Kb before coding start","-",1,4,0,"not_subjected_to_validation" "CRC-6",17,1,19246777,17,19257957,"inversion","11180",4,0,"RNF112","RNF112","IGR: 8Kb before RNF112(+)","Intron of RNF112(+): 43bp before exon 7","-",1,4,0,"not_subjected_to_validation" "CRC-8",1,0,196022165,1,196062879,"inversion","40636",4,0,"DENND1B","DENND1B","IGR: 11Kb after DENND1B(-)","IGR: 52Kb after DENND1B(-)","-",1,4,1,"not_subjected_to_validation" "CRC-8",3,1,194273514,3,195052334,"tandem_dup","778798",4,0,"HRASLS","LOC100128023","IGR: 168Kb before HRASLS(+)","IGR: 141Kb before LOC100128023(-)","-",1,4,1,"not_subjected_to_validation" "CRC-8",3,1,194714158,3,194814804,"inversion","100573",4,0,"ATP13A4","OPA1","Intron of ATP13A4(-): 929bp after exon 2","Intron of OPA1(+): 381bp before exon 2","Protein fusion: out of frame (ATP13A4-OPA1)",1,4,1,"somatic" "CRC-8",3,0,194773769,3,194806115,"inversion","32296",4,0,"OPA1","OPA1","IGR: 20Kb before OPA1(+)","Intron of OPA1(+): 9Kb before exon 2","-",1,4,1,"somatic" "CRC-8",4,0,144621415,4,144626028,"deletion","4613",4,0,"GAB1","SMARCA5","IGR: 6Kb after GAB1(+)","IGR: 28Kb before SMARCA5(+)","-",1,4,0,"not_subjected_to_validation" "CRC-8",5,0,114842995,12,83369694,"inter_chr","NaN",4,0,"FEM1C","SLC6A15","IGR: 42Kb before FEM1C(-)","IGR: 408Kb before SLC6A15(-)","-",1,4,0,"not_detected" "CRC-8",12,1,42430331,16,76709265,"inter_chr","NaN",4,0,"PUS7L","WWOX","Intron of PUS7L(-): 2Kb before exon 3","Intron of WWOX(+): 3Kb after exon 4","Antisense fusion",1,4,1,"somatic" "CRC-9",1,0,241862197,1,242050663,"deletion","188499",4,0,"AKT3","AKT3","Intron of AKT3(-): 5Kb after exon 5","Intron of AKT3(-): 22Kb after exon 1","Deletion of 4 exons: out of frame",1,4,1,"somatic" "CRC-9",2,1,47634647,2,238394406,"long_range","190759740",4,0,"KCNK12","RBM44","Intron of KCNK12(-): 16Kb after exon 1","Intron of RBM44(+): 27bp before exon 6","Protein fusion: out of frame (KCNK12-RBM44)",1,4,1,"somatic" "CRC-9",2,0,51257816,2,51284768,"inversion","27008",4,0,"NRXN1","NRXN1","IGR: 145Kb after NRXN1(-)","IGR: 172Kb after NRXN1(-)","-",1,4,1,"not_subjected_to_validation" "CRC-9",3,1,166700996,3,166716105,"tandem_dup","15109",4,0,"BCHE","BCHE","IGR: 272Kb before BCHE(-)","IGR: 257Kb before BCHE(-)","-",1,4,-1,"not_subjected_to_validation" "CRC-9",5,0,26635380,5,26707346,"deletion","72008",4,0,"CDH9","CDH9","IGR: 281Kb before CDH9(-)","IGR: 209Kb before CDH9(-)","-",1,4,1,"not_subjected_to_validation" "CRC-9",5,0,76887978,5,76965860,"deletion","77904",4,0,"OTP","OTP","IGR: 72Kb before OTP(-)","Intron of OTP(-): 3Kb after exon 2","-",1,4,1,"not_subjected_to_validation" "CRC-9",7,1,23797054,7,156704913,"long_range","132907822",4,0,"STK31","UBE3C","Exon 22 of STK31(+)","Intron of UBE3C(+): 1Kb before exon 15","Protein fusion: mid-exon (UBE3C-STK31)",1,4,1,"somatic" "CRC-9",7,0,63752426,10,100056448,"inter_chr","NaN",4,0,"ZNF107","LOXL4","IGR: 12Kb before ZNF107(+)","IGR: 59Kb before LOXL4(-)","-",1,4,1,"not_subjected_to_validation" "CRC-9",11,0,47540615,11,47574645,"deletion","34030",4,0,"PTPMT1","C1QTNF4","Promoter of PTPMT1(+): 3Kb from tx start","Promoter of C1QTNF4(-): 2Kb from tx start","Antisense fusion",1,4,0,"not_subjected_to_validation" "CRC-9",12,0,56051182,12,56549506,"deletion","498333",4,0,"R3HDM2","MIR26A2","IGR: 61Kb after R3HDM2(-)","IGR: 45Kb before MIR26A2(-)","-",1,4,1,"not_subjected_to_validation" "CRC-9",13,0,112034882,13,112047173,"deletion","12453",4,0,"C13orf28","C13orf28","IGR: 44Kb before C13orf28(+)","IGR: 31Kb before C13orf28(+)","-",1,4,1,"not_subjected_to_validation" "CRC-9",16,0,54870015,16,78261006,"long_range","23391034",4,0,"GNAO1","MAF","Intron of GNAO1(+): 2Kb after exon 3","IGR: 76Kb before MAF(-)","-",1,4,1,"not_subjected_to_validation" "CRC-9",20,0,14895495,20,15024126,"deletion","128703",4,0,"MACROD2","MACROD2","Intron of MACROD2(+): 263Kb before exon 6","Intron of MACROD2(+): 134Kb before exon 6","Deletion within intron",1,4,1,"somatic" "CRC-1",1,0,215453630,2,104800929,"inter_chr","NaN",4,0,"GPATCH2","POU3F3","IGR: 217Kb before GPATCH2(-)","IGR: 37Kb before POU3F3(+)","-",1,4,0,"not_subjected_to_validation" "CRC-1",2,0,241140187,15,77522092,"inter_chr","NaN",4,0,"ANKMY1","KIAA1024","Intron of ANKMY1(-): 817bp after exon 3","5'-UTR of KIAA1024(+): 13Kb before coding start","Transcript fusion (KIAA1024-ANKMY1)",1,4,0,"not_subjected_to_validation" "CRC-1",3,1,152628865,6,48862164,"inter_chr","NaN",4,0,"MED12L","MUT","Intron of MED12L(+): 2Kb before exon 42","IGR: 645Kb before MUT(-)","-",1,4,0,"not_subjected_to_validation" "CRC-1",5,1,149189702,8,72761696,"inter_chr","NaN",4,0,"PPARGC1B","MSC","Intron of PPARGC1B(+): 821bp before exon 4","IGR: 155Kb before MSC(-)","-",1,4,0,"not_subjected_to_validation" "CRC-1",5,0,31785394,16,6909262,"inter_chr","NaN",4,0,"PDZD2","A2BP1","IGR: 49Kb before PDZD2(+)","5'-UTR of A2BP1(+): 133Kb before coding start","-",1,4,0,"not_detected" "CRC-1",6,1,10890712,12,95552637,"inter_chr","NaN",4,0,"MAK","C12orf63","Intron of MAK(-): 2Kb after exon 10","IGR: 13Kb before C12orf63(+)","-",1,4,0,"not_subjected_to_validation" "CRC-1",6,0,136664585,14,66675470,"inter_chr","NaN",4,0,"MAP7","GPHN","IGR: 41Kb before MAP7(-)","Intron of GPHN(+): 4Kb before exon 18","-",1,4,0,"not_subjected_to_validation" "CRC-9",6,1,163054940,6,163119918,"tandem_dup","64972",4,0,"PARK2","PACRG","Intron of PARK2(-): 14Kb after exon 1","Intron of PACRG(+): 35Kb before exon 3","Antisense fusion",0.9999836,3.999935,1,"somatic" "CRC-3",6,1,43747579,6,106932132,"long_range","63184507",4,0,"MRPS18A","ATG5","Exon 6 of MRPS18A(-)","IGR: 52Kb after ATG5(-)","-",0.9999274,3.999709,1,"somatic" "CRC-6",8,0,9981488,8,10335594,"deletion","354106",4,0,"MSRA","MSRA","Intron of MSRA(+): 32Kb after exon 1","IGR: 12Kb after MSRA(+)","-",0.9998082,3.999233,0,"not_subjected_to_validation" "CRC-9",6,0,157104253,6,158111862,"long_range","1007609",4,0,"ARID1B","SNX9","IGR: 37Kb before ARID1B(+)","IGR: 52Kb before SNX9(+)","-",0.9997807,3.999123,1,"not_subjected_to_validation" "CRC-9",1,0,5816357,1,6351304,"deletion","534947",4,0,"NPHP4","ACOT7","IGR: 29Kb before NPHP4(-)","Intron of ACOT7(-): 17Kb after exon 1","-",0.9991374,3.996549,0,"not_subjected_to_validation" "CRC-9",11,1,6339706,11,6422181,"tandem_dup","82459",4,0,"SMPD1","TRIM3","IGR: 29Kb before SMPD1(+)","IGR: 4Kb before TRIM3(-)","-",0.9991374,3.996549,1,"not_subjected_to_validation" "CRC-3",6,1,42328572,6,65141693,"long_range","22813068",4,0,"TRERF1","EYS","Intron of TRERF1(-): 2Kb after exon 13","Intron of EYS(-): 14Kb after exon 29","Protein fusion: out of frame (TRERF1-EYS)",0.9985211,3.994084,1,"somatic" "CRC-8",8,1,123968554,8,143066749,"long_range","19098184",4,0,"ZHX2","NCRNA00051","5'-UTR of ZHX2(+): 64Kb before coding start","IGR: 211Kb before NCRNA00051(+)","-",0.9984841,3.993936,1,"somatic" "CRC-6",16,0,71296251,16,71581646,"deletion","285395",4,0,"ZFHX3","ZFHX3","IGR: 78Kb before ZFHX3(-)","5'-UTR of ZFHX3(-): 30Kb before coding start","-",0.9980234,3.992093,0,"not_detected" "CRC-3",2,0,151790755,9,135957853,"inter_chr","NaN",4,0,"RBM43","WDR5","IGR: 22Kb before RBM43(-)","IGR: 33Kb before WDR5(+)","-",0.9846154,3.938462,0,"not_subjected_to_validation" "CRC-3",6,0,40441124,6,54387076,"long_range","13946006",4,0,"TDRG1","TINAG","IGR: 13Kb before TDRG1(+)","IGR: 24Kb after TINAG(+)","-",0.9846154,3.938462,1,"somatic" "CRC-3",7,0,153522268,8,76589412,"inter_chr","NaN",4,0,"DPP6","HNF4G","Intron of DPP6(+): 141Kb after exon 1","IGR: 25Kb before HNF4G(+)","-",0.9846154,3.938462,0,"somatic" "CRC-5",19,0,13671507,20,52197867,"inter_chr","NaN",4,0,"CCDC130","CYP24A1","IGR: 48Kb before CCDC130(+)","IGR: 6Kb before CYP24A1(-)","-",0.9846154,3.938462,0,"not_subjected_to_validation" "CRC-1",3,0,160034190,11,86641093,"inter_chr","NaN",4,0,"MFSD1","TMEM135","IGR: 4Kb after MFSD1(+)","Intron of TMEM135(+): 16Kb after exon 6","-",0.9846154,3.938462,0,"not_subjected_to_validation" "CRC-3",5,1,87253239,8,91569923,"inter_chr","NaN",4,0,"TMEM161B","TMEM64","IGR: 274Kb before TMEM161B(-)","IGR: 133Kb before TMEM64(-)","-",0.9706382,3.882553,0,"not_subjected_to_validation" "CRC-3",3,1,60532986,3,60541605,"tandem_dup","8602",4,0,"FHIT","FHIT","5'-UTR of FHIT(-): 35Kb before coding start","5'-UTR of FHIT(-): 44Kb before coding start","Duplication within transcript",0.8884696,3.553878,1,"somatic" "CRC-4",7,0,124026928,14,58290310,"inter_chr","NaN",4,0,"GPR37","DACT1","IGR: 146Kb before GPR37(-)","IGR: 116Kb before DACT1(+)","-",0.8752137,3.500855,1,"not_subjected_to_validation" "CRC-7",2,0,15375353,8,56732714,"inter_chr","NaN",13,0,"NBAS","TMEM68","Intron of NBAS(-): 9Kb before exon 39","IGR: 81Kb before TMEM68(-)","-",0.2496006,3.244808,0,"not_subjected_to_validation" "CRC-3",16,1,34872868,16,46364585,"long_range","11491700",7,0,"LOC146481","ABCC12","IGR: 304Kb before LOC146481(-)","IGR: 310Kb before ABCC12(-)","-",0.4608088,3.225662,1,"somatic" "CRC-3",1,0,236231922,1,237182872,"inversion","950924",3,0,"ZP4","LOC339535","IGR: 120Kb before ZP4(-)","IGR: 473Kb before LOC339535(-)","-",1,3,1,"somatic" "CRC-3",1,1,244869048,3,7582747,"inter_chr","NaN",3,0,"CNST","GRM7","Intron of CNST(+): 3Kb before exon 7","Intron of GRM7(+): 12Kb before exon 8","-",1,3,1,"somatic" "CRC-3",6,1,25774577,6,46056103,"long_range","20281526",3,0,"SCGN","CLIC5","Intron of SCGN(+): 1Kb after exon 4","Intron of CLIC5(-): 25Kb before exon 2","Protein fusion: in frame (CLIC5-SCGN)",1,3,0,"somatic" "CRC-3",6,1,33209107,6,107004069,"long_range","73794878",3,0,"HLA-DPB2","AIM1","IGR: 4Kb after HLA-DPB2(+)","IGR: 62Kb before AIM1(+)","-",1,3,1,"somatic" "CRC-3",6,1,39521662,6,107849873,"long_range","68328211",3,0,"KIF6","PDSS2","Intron of KIF6(-): 15Kb before exon 14","Intron of PDSS2(-): 37Kb after exon 1","Antisense fusion",1,3,0,"somatic" "CRC-3",6,1,50600569,6,53546383,"long_range","2945814",3,0,"TFAP2D","GCLC","IGR: 189Kb before TFAP2D(+)","IGR: 29Kb after GCLC(-)","-",1,3,0,"somatic" "CRC-3",6,0,55600617,6,63329817,"long_range","7729200",3,0,"HMGCLL1","KHDRBS2","IGR: 49Kb after HMGCLL1(-)","IGR: 276Kb after KHDRBS2(-)","-",1,3,0,"somatic" "CRC-3",6,0,33418159,6,107985099,"long_range","74566907",3,0,"LYPLA2P1","SOBP","IGR: 22Kb before LYPLA2P1(-)","Intron of SOBP(+): 24Kb after exon 4","-",1,3,1,"somatic" "CRC-3",8,0,123860547,8,123862069,"deletion","1522",3,0,"ZHX2","ZHX2","Promoter of ZHX2(+): 3Kb from tx start","Promoter of ZHX2(+): 1Kb from tx start","Deletion within transcript",1,3,0,"somatic" "CRC-5",3,1,85745454,3,97636406,"long_range","11891023",3,0,"CADM2","EPHA6","Intron of CADM2(+): 113Kb before exon 2","IGR: 380Kb before EPHA6(+)","-",1,3,1,"not_detected" "CRC-5",5,1,59972540,5,60013608,"tandem_dup","41068",3,0,"DEPDC1B","DEPDC1B","Intron of DEPDC1B(-): 2Kb after exon 6","Intron of DEPDC1B(-): 5Kb after exon 2","Duplication of 4 exons: out of frame",1,3,0,"not_detected" "CRC-5",5,0,77512507,5,171390480,"long_range","93877973",3,0,"AP3B1","STK10","Intron of AP3B1(-): 580bp after exon 8","IGR: 11Kb before STK10(-)","-",1,3,0,"not_subjected_to_validation" "CRC-5",20,0,25363537,20,56640403,"long_range","31276804",3,0,"GINS1","STX16","Intron of GINS1(+): 7Kb before exon 6","IGR: 19Kb before STX16(+)","-",1,3,1,"not_detected" "CRC-5",20,0,49388941,20,61289732,"long_range","11900791",3,0,"NFATC2","YTHDF1","IGR: 52Kb before NFATC2(-)","IGR: 7Kb before YTHDF1(-)","-",1,3,0,"not_detected" "CRC-6",4,0,92475038,4,92502563,"deletion","27525",3,0,"FAM190A","FAM190A","Intron of FAM190A(+): 249Kb after exon 10","Intron of FAM190A(+): 236Kb before exon 11","Deletion within intron",1,3,0,"somatic" "CRC-6",8,1,41693481,8,41694385,"inversion","904",3,0,"ANK1","ANK1","Intron of ANK1(-): 147bp after exon 13","Intron of ANK1(-): 8bp before exon 12","Antisense fusion",1,3,0,"somatic" "CRC-6",8,0,43103766,8,60011734,"long_range","16907968",3,0,"SGK196","TOX","IGR: 6Kb after SGK196(+)","Intron of TOX(-): 3Kb after exon 3","-",1,3,0,"not_subjected_to_validation" "CRC-6",20,0,14461408,20,15021576,"deletion","560168",3,0,"MACROD2","MACROD2","Intron of MACROD2(+): 39Kb after exon 4","Intron of MACROD2(+): 137Kb before exon 6","Deletion of 1 exon: in frame",1,3,0,"somatic" "CRC-8",3,1,106703281,3,107759420,"long_range","1056060",3,0,"ALCAM","LOC100302640","Intron of ALCAM(+): 18Kb before exon 2","IGR: 552Kb before LOC100302640(-)","-",1,3,1,"not_subjected_to_validation" "CRC-8",8,1,143087726,8,144958438,"long_range","1870712",3,0,"NCRNA00051","SCRIB","IGR: 190Kb before NCRNA00051(+)","Intron of SCRIB(-): 124bp before exon 22","-",1,3,0,"somatic" "CRC-8",12,0,25854473,12,78605905,"long_range","52751494",3,0,"RASSF8","PAWR","IGR: 149Kb before RASSF8(+)","Intron of PAWR(-): 2Kb after exon 2","-",1,3,1,"somatic" "CRC-9",2,0,50943751,2,51284605,"deletion","340928",3,0,"NRXN1","NRXN1","Intron of NRXN1(-): 60Kb after exon 4","IGR: 171Kb after NRXN1(-)","-",1,3,1,"not_subjected_to_validation" "CRC-9",7,1,146600206,7,146636950,"inversion","36731",3,0,"CNTNAP2","CNTNAP2","Intron of CNTNAP2(+): 28Kb before exon 9","Intron of CNTNAP2(+): 9Kb after exon 9","-",1,3,1,"not_subjected_to_validation" "CRC-1",11,0,24625796,11,24627392,"deletion","1596",3,0,"LUZP2","LUZP2","Intron of LUZP2(+): 81Kb before exon 2","Intron of LUZP2(+): 80Kb before exon 2","Deletion within intron",1,3,0,"somatic" biovizBase/inst/extdata/crc1-missense.csv0000644000126300012640000001264212227067714022047 0ustar00biocbuildphs_compbio"Hugo_Symbol","Entrez_Gene_Id","Center","NCBI_Build","Chromosome","Start_position","End_position","Strand","Variant_Classification","Variant_Type","Reference_Allele","Tumor_Seq_Allele1","Tumor_Seq_Allele2" "TARDBP","23435","Broad",36,"chr1",11003085,11003085,"+","Missense","SNP","G","G","A" "INADL","10207","Broad",36,"chr1",62352395,62352395,"+","Missense","SNP","T","T","G" "CFH","3075","Broad",36,"chr1",194960885,194960885,"+","Missense","SNP","G","G","A" "CYS1","192668","Broad",36,"chr2",10116508,10116508,"-","Missense","SNP","C","C","T" "RASGRP3","25780","Broad",36,"chr2",33617747,33617747,"+","Missense","SNP","C","C","T" "C2orf78","388960","Broad",36,"chr2",73894280,73894280,"+","Missense","SNP","T","T","C" "FER1L5","90342","Broad",36,"chr2",96732769,96732769,"+","Missense","SNP","T","T","G" "TTN","7273","Broad",36,"chr2",179160267,179160267,"-","Missense","SNP","C","C","T" "IGFBP5","3488","Broad",36,"chr2",217251189,217251189,"-","Missense","SNP","C","C","T" "RAF1","5894","Broad",36,"chr3",12620699,12620699,"-","Missense","SNP","G","G","A" "LTF","4057","Broad",36,"chr3",46472880,46472880,"-","Missense","SNP","C","C","T" "PPP2R3A","5523","Broad",36,"chr3",137203130,137203130,"+","Missense","SNP","A","A","C" "PCCB","5096","Broad",36,"chr3",137457429,137457429,"+","Missense","SNP","C","C","A" "KLHL6","89857","Broad",36,"chr3",184708629,184708629,"-","Missense","SNP","G","G","A" "PAK2","5062","Broad",36,"chr3",198024055,198024055,"+","Missense","SNP","A","A","T" "SLC10A7","84068","Broad",36,"chr4",147434591,147434591,"-","Missense","SNP","G","G","A" "ACSL1","2180","Broad",36,"chr4",185915412,185915412,"-","Missense","SNP","A","A","C" "CMYA5","202333","Broad",36,"chr5",79070342,79070342,"+","Missense","SNP","C","C","A" "FAM81B","153643","Broad",36,"chr5",94775579,94775579,"+","Missense","SNP","G","G","A" "PCDHGC3","5098","Broad",36,"chr5",140838266,140838266,"+","Missense","SNP","T","T","G" "AKD1","221264","Broad",36,"chr6",109992724,109992724,"-","Missense","SNP","C","C","T" "C6orf204","387119","Broad",36,"chr6",118993492,118993492,"-","Missense","SNP","G","G","A" "POT1","25913","Broad",36,"chr7",124286401,124286401,"-","Missense","SNP","A","A","C" "GRM8","2918","Broad",36,"chr7",125960456,125960456,"-","Missense","SNP","A","A","C" "KIAA1539","80256","Broad",36,"chr9",35097658,35097658,"-","Missense","SNP","A","A","C" "BAAT","570","Broad",36,"chr9",103164773,103164773,"-","Missense","SNP","G","G","T" "ABL1","25","Broad",36,"chr9",132745783,132745783,"+","Missense","SNP","C","C","A" "SEC16A","9919","Broad",36,"chr9",138481305,138481305,"-","Missense","SNP","C","C","T" "ITIH5","80760","Broad",36,"chr10",7661761,7661761,"-","Missense","SNP","C","C","T" "ITPRIP","85450","Broad",36,"chr10",106064683,106064683,"-","Missense","SNP","T","T","G" "IRF7","3665","Broad",36,"chr11",603430,603430,"-","Missense","SNP","G","G","A" "TRIM34","53840","Broad",36,"chr11",5610148,5610148,"+","Missense","SNP","A","A","C" "IPO7","10527","Broad",36,"chr11",9420281,9420281,"+","Missense","SNP","G","G","T" "ANO3","63982","Broad",36,"chr11",26495005,26495005,"+","Missense","SNP","C","C","T" "OR8H2","390151","Broad",36,"chr11",55629818,55629818,"+","Missense","SNP","G","G","A" "CEP164","22897","Broad",36,"chr11",116737834,116737834,"+","Missense","SNP","C","C","A" "CASC1","55259","Broad",36,"chr12",25165980,25165980,"-","Missense","SNP","G","G","T" "KRAS","3845","Broad",36,"chr12",25289548,25289548,"-","Missense","SNP","C","C","T" "DDX11","1663","Broad",36,"chr12",31142142,31142142,"+","Missense","SNP","G","G","C" "PUS7L","83448","Broad",36,"chr12",42434771,42434771,"-","Missense","SNP","T","T","A" "PAN2","9924","Broad",36,"chr12",55006974,55006974,"-","Missense","SNP","T","T","G" "LOC643677","643677","Broad",36,"chr13",102199348,102199348,"-","Missense","SNP","G","G","A" "ZFP106","64397","Broad",36,"chr15",40503502,40503502,"-","Missense","SNP","C","C","T" "BBS4","585","Broad",36,"chr15",70816269,70816269,"+","Missense","SNP","A","A","C" "UBFD1","56061","Broad",36,"chr16",23481033,23481033,"+","Missense","SNP","C","C","G" "MAP2K3","5606","Broad",36,"chr17",21149010,21149010,"+","Missense","SNP","G","G","A" "TOP2A","7153","Broad",36,"chr17",35812691,35812691,"-","Missense","SNP","T","T","C" "ROCK1","6093","Broad",36,"chr18",16788810,16788810,"-","Missense","SNP","C","C","T" "NFATC1","4772","Broad",36,"chr18",75322338,75322338,"+","Missense","SNP","G","G","A" "OR10H3","26532","Broad",36,"chr19",15713495,15713495,"+","Missense","SNP","G","G","T" "TMEM147","10430","Broad",36,"chr19",40730140,40730140,"+","Missense","SNP","C","C","T" "SAE1","10055","Broad",36,"chr19",52338664,52338664,"+","Missense","SNP","G","G","A" "PPP2R1A","5518","Broad",36,"chr19",57407795,57407795,"+","Missense","SNP","G","G","A" "GZF1","64412","Broad",36,"chr20",23298287,23298287,"+","Missense","SNP","A","A","C" "EFCAB8","388795","Broad",36,"chr20",31012946,31012946,"+","Missense","SNP","C","C","T" "PTPRT","11122","Broad",36,"chr20",40223536,40223536,"-","Missense","SNP","C","C","T" "CASS4","57091","Broad",36,"chr20",54467136,54467136,"+","Missense","SNP","G","G","A" "GTPBP5","26164","Broad",36,"chr20",60201983,60201983,"+","Missense","SNP","C","C","T" "CHAF1B","8208","Broad",36,"chr21",36688774,36688774,"+","Missense","SNP","C","C","T" "LCA5L","150082","Broad",36,"chr21",39699770,39699770,"-","Missense","SNP","T","T","G" "CHEK2","11200","Broad",36,"chr22",27437953,27437953,"-","Missense","SNP","C","C","A" "FAM47A","158724","Broad",36,"chrX",34059280,34059280,"-","Missense","SNP","C","C","T" biovizBase/man/0000755000126300012640000000000012227067713015014 5ustar00biocbuildphs_compbiobiovizBase/man/GCcontent.Rd0000644000126300012640000000253012227067713017167 0ustar00biocbuildphs_compbio\name{GCcontent} \alias{GCcontent} \title{GC content computation for BSgenome} \usage{ GCcontent(obj, ..., view.width, as.prob = TRUE) } \description{Compute GC content in a certain region of a BSgenome object} \details{GC content is an interesting variable may be related to various biological questions. So we need a way to compute GC content in a certain region of a reference genome. GCcontent function is a wrapper around getSeq function in BSgenome package and \code{letterFrequency}, \code{letterFrequencyInSlidingView} in Biostrings package. if the \code{view.width} is specified, the GC content will be computed in the sliding view} \value{Numeric value indicate count or percentage} \author{Tengfei Yin} \arguments{\item{obj}{BSgenome object} \item{...}{Arguments passed to getSeq method for BSgenome package.} \item{view.width}{ Passed to \code{letterFrequencyInSlidingView}, the constant (e.g. 35, 48, 1000) size of the "window" to slide along \code{obj}. The specified \code{letters} are tabulated in each window of length \code{view.width}. The rows of the result (see value) correspond to the various windows.} \item{as.prob}{ If TRUE return percentage of GC content, otherwise return counts.} } \examples{ library(BSgenome.Hsapiens.UCSC.hg19) GCcontent(Hsapiens, GRanges("chr1", IRanges(1e6, 1e6 + 1000))) } biovizBase/man/addStepping-method.Rd0000644000126300012640000000543412227067713021031 0ustar00biocbuildphs_compbio\name{addStepping-method} \alias{addStepping} \alias{addStepping,GenomicRanges-method} \usage{ \S4method{addStepping}{GenomicRanges}(obj, group.name, extend.size = 0, fix = "center", group.selfish = TRUE) } \title{Adding disjoint levels to a GenomicRanges object} \description{Adding disjoint levels to a GenomicRanges object} \details{This is a tricky question, for example, pair-end RNA-seq data could be represented as two set of GenomicRanges object, one indicates the read, one indicates the junction. At the same time, we need to make sure pair-ended read are shown on the same level, and nothing falls in between. For better visualization of the data, we may hope to add invisible extended buffer to the reads, so closely neighbored reads will be on the different levels.} \arguments{\item{obj}{A GenomicRanges object} \item{group.name}{Column name in the elementMetadata which specify the grouping information of all the entries. If provided, this will make sure all intervals belong to the same group will try to be on the same level and nothing falls in between.} \item{extend.size}{Adding invisible buffered region to the GenomicRanges object, if it's 10, then adding 5 at both end. This make the close neighbors assigned to the different levels and make your eyes easy to identify.} \item{fix}{ "start", "end", or "center"(default) passed to \code{resize}, denoting what to use as an anchor for each element of obj, and add extend.size to it's current width. } \item{group.selfish}{ Passed to \code{addStepping}, control whether to show each group as unique level or not. If set to \code{FALSE}, if two groups are not overlapped with each other, they will probably be layout in the same level to save space. } } \value{A modified GenmicRanges object with \code{stepping} as one column.} \docType{methods} \author{Tengfei Yin} \examples{ library(GenomicRanges) set.seed(1) N <- 500 ## sample GRanges 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)) ## grouping and extending 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) } biovizBase/man/aes-utils.Rd0000644000126300012640000000102412227067713017206 0ustar00biocbuildphs_compbio\name{parseArgsForAes} \alias{parseArgsForAes} \alias{parseArgsForNonAes} \title{Utils for parsing (un)evaluated arguments} \description{ Utilities for parsing (un)evaluated arguments } \usage{ parseArgsForAes(args) parseArgsForNonAes(args) } \arguments{ \item{args}{ arguments list. } } \value{ For \code{parseArgsForAes} return a unevaluated arguments. For \code{parseArgsNonForAes} return a evaluated/quoted arguments. } \examples{ args <- alist(a = color, b = "b") # parseArgsForAes(args) } \author{Tengfei Yin} biovizBase/man/biovizBase-package.Rd0000644000126300012640000000127212227067713020773 0ustar00biocbuildphs_compbio\name{biovizBase-package} \alias{biovizBase-package} \alias{biovizBase-package} \title{biovizBase is a package which provides utilities and color scheme...} \description{biovizBase is a package which provides utilities and color scheme for higher level graphic package which aim to visualize biological data especially genetic data.} \details{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.} \alias{biovizBase} \docType{package} biovizBase/man/colorBlindSafePal.Rd0000644000126300012640000000636012227067713020633 0ustar00biocbuildphs_compbio\name{colorBlindSafePal} \alias{colorBlindSafePal} \alias{genBrewerBlindPalInfo} \alias{genDichromatPalInfo} \alias{genBlindPalInfo} \alias{blind.pal.info} \alias{brewer.pal.blind.info} \alias{dichromat.pal.blind.info} \title{Color blind safe palette generator} \description{ This function help users create a function based on specified color blind safe palette. And the returned function could be used for color generation. } \usage{ genDichromatPalInfo() genBrewerBlindPalInfo() genBlindPalInfo() colorBlindSafePal(palette) blind.pal.info brewer.pal.blind.info dichromat.pal.blind.info } \arguments{ \item{palette}{ A index numeric value or character. Please see \code{blind.pal.info}, the palette could be "pal_id" or names the row in which users could specify the palette you want to use. } } \value{ A color generating function with arguments \code{n} and \code{repeatable}. \code{n} specifying how many different discrete colors you want to get from them palette, and if repeatable turned on and set to TRUE, you can specify n even larger than maximum color. The color will be repeated following the same order. } \details{ We get those color-blind safe palette based on \url{http://colorbrewer2.org/} and \url{http://geography.uoregon.edu/datagraphics/color_scales.htm} those color are implemented in two packages, RColorBrewer and dichromat. But RColorBrewer doesn't provide subset of color-blind safe palette info. And dichromat doesn't group color based on "quality", "sequential" and "divergent", so we pick those color manually and create a combined palette, blind.pal.info. \code{colorBlindSafePal} will return a function, this function will take two arguments, \code{n} and \code{repeatable}. if n is smaller than 3(n >= 3 is required by RColorBrewer), we use 3 instead and return a color vector. 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.Rd0000644000126300012640000000102012227067713020272 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000072712227067713016731 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000337512227067713020053 0ustar00biocbuildphs_compbio\name{crunch} \alias{crunch} \alias{crunch,TranscriptDb-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 TranscriptDb, GAligment and BamFile. } \usage{ \S4method{crunch}{TranscriptDb}(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}{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{TranscriptDb}, \code{GAligment} and \code{BamFile}. } \item{which}{ GRanges object. For TranscriptDb object, could aslo be a list. } \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{readGAlignmentsFromBam}. } } \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") } \author{Tengfei Yin} biovizBase/man/darned_hg19_subset500.Rd0000644000126300012640000000074112227067713021204 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000061412227067713022051 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000145612227067713016704 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000057612227067713017457 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000001076712227067713017526 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000075012227067713020211 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000441612227067713016702 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000205612227067713017117 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000210112227067713017524 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000143612227067713017036 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000055412227067713017527 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000057412227067713020370 0ustar00biocbuildphs_compbio\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/isIdeogram.Rd0000644000126300012640000000077012227067713017372 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000275712227067713021034 0ustar00biocbuildphs_compbio\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(Rsamtools) bamfile <- system.file("extdata", "SRR027894subRBM17.bam", package="biovizBase") ## get index of junction read which(isJunctionRead(cigar(readGAlignmentsFromBam(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.Rd0000644000126300012640000000105412227067713020540 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000113412227067713016223 0ustar00biocbuildphs_compbio\name{getYLab-method} \alias{getYLab} \alias{getYLab,TranscriptDb-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}{TranscriptDb}(obj) \S4method{getXLab}{GRanges}(obj) \S4method{getXLab}{GRangesList}(obj) \S4method{getXLab}{GAlignments}(obj) } \arguments{ \item{obj}{ A \code{TranscriptDb} object. } } \value{ a string. } \author{Tengfei Yin} biovizBase/man/maxGap-method.Rd0000644000126300012640000000175112227067713020002 0ustar00biocbuildphs_compbio\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/pileupAsGRanges.Rd0000644000126300012640000000330412227067713020334 0ustar00biocbuildphs_compbio\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 PileupParam 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{PileupParam}.} \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{PileupParam}.} } \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.Rd0000644000126300012640000000356012227067713022635 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000115312227067713020377 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000224512227067713016375 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000073512227067713017267 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000355512227067713021215 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000420112227067713021332 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000071112227067713021221 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000121612227067713021244 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000001440112227067713017316 0ustar00biocbuildphs_compbio\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.Rd0000644000126300012640000000163512227067713023033 0ustar00biocbuildphs_compbio\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/0000755000126300012640000000000012253761745015035 5ustar00biocbuildphs_compbiobiovizBase/src/R_init_biovizBase.c0000644000126300012640000000044212253761745020602 0ustar00biocbuildphs_compbio#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.c0000644000126300012640000000313412253761745017503 0ustar00biocbuildphs_compbio#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; } biovizBase/src/bin_offsets.h0000644000126300012640000000007612253761745017512 0ustar00biocbuildphs_compbio#include SEXP scan_bam_bin_offsets(SEXP bytes);