##put titles/rownames left ##make titles blue ##decrease margins below titles ## put row names in black ##put background rows in. ##change layouts so that it looks better ##get sample numbers in correctly .libPaths('/humgen/gsa-firehose2/pipeline/repositories/StingProduction/R/') suppressMessages(library(gplots)); suppressMessages(library(ReadImages)); suppressMessages(library(gsalib)); suppressMessages(library(ROracle)); cmdargs = gsa.getargs( list( yaml = list(value=NA, doc="pipeline YAML file"), bamlist = list(value=NA, doc="list of BAM files"), evalroot = list(value=NA, doc="VariantEval file"), tearout = list(value=NA, doc="Output path for tearsheet PDF")#, plotout = list(value=NA, doc="Output path for PDF") ), doc="Creates a tearsheet" ); bamlist = scan(cmdargs$bamlist, "character"); squids <- system(paste("grep SQUID ", cmdargs$yaml, ' |grep "C..." -o', sep=""), intern=TRUE) indexed = c(); nonindexed = c(); for (bam in bamlist) { bamheader = system(paste("samtools view -H", bam), intern=TRUE); if (length(bamheader) > 0) { rgs = bamheader[grep("^@RG", bamheader)]; for (rg in rgs) { id = grep("PU:", unlist(strsplit(rg, "\t")), value=TRUE); id = sub("PU:", "", id); id = gsub("XX......", "XX", id) if (length(unlist(strsplit(id, "\\.")))==3){ indexed<-c(indexed, id) } else{ if(length(unlist(strsplit(id, "\\.")))==2){ nonindexed<-c(nonindexed, id) } else{ print(id + " is a strange PU and will result in odd searches") } } } } else { print(sprintf("Could not load '%s'\n", bam)); } } drv = dbDriver("Oracle"); con = dbConnect(drv, "REPORTING/REPORTING@ora01:1521/SEQPROD"); rs = dbSendQuery(con, statement = paste("SELECT * FROM ILLUMINA_PICARD_METRICS")); d = fetch(rs, n=-1); dbHasCompleted(rs); dbClearResult(rs); rs2 = dbSendQuery(con, statement = paste("SELECT * FROM ILLUMINA_SAMPLE_STATUS_AGG")); d2 = fetch(rs2, n=-1); dbHasCompleted(rs2); dbClearResult(rs2); oraCloseDriver(drv); squid_fclanes = sprintf("%s.%s", d$"Flowcell", d$"Lane"); squid_fclanes_indexed = sprintf("%s.%s.%s", d$"Flowcell", d$"Lane", d$"Barcode"); dproj = d[which(squid_fclanes %in% nonindexed),]; dproj = rbind(dproj, d[which(squid_fclanes_indexed %in% indexed),]) dproj = dproj[which(dproj$"Project" %in% unique(squids)),] d2proj = d2[which(d2$"Project" %in% unique(dproj$Project) & d2$"Sample" %in% dproj$"External ID"),]; tearsheet<-function(){ tearsheetdrop <- "~Documents/Sting/R/gsalib/data/tearsheetdrop.jpg" #put the path to the tearsheet backdrop here pdf(file= cmdargs$tearout, width=22, height=17, pagecentre=TRUE, pointsize=24) #define layout postable<-matrix(c(1, 1, 1, 1, 1, 1, rep(c(2, 2, 2, 4, 4, 4), 5), rep(c(3, 3, 3, 4, 4, 4), 3), rep(c(3,3,3,5,5,5), 5), 6,6,6,7,7,7), nrow=15, ncol=6, byrow=TRUE) layout(postable, heights=c(1, rep(.18, 13), 2), respect=FALSE) #prep for title bar drop<-read.jpeg(system.file(tearsheetdrop, package="gsalib")) #plot title bar par(mar=c(0,0,0,0)) plot(drop) text(155, 50, "testing", family="serif", adj=c(0,0), cex=3, col=gray(.25)) # Project summary projects = paste(unique(dproj$"Project"), collapse=", "); used_samples = length(bamlist); unused_samples = 0; sequencing_protocol = "Hybrid selection"; #can this be extracted? bait_design = paste(dimnames(table(dproj$"Bait Set"))[[1]][order(table(dproj$"Bait Set"), decreasing=TRUE)], collapse=", "); if(nchar(bait_design)>50){ bait_design<-strsplit(bait_design, ", ")[[1]][1] } if(nchar(bait_design)>50){ bait_design<-strsplit(bait_design, ".Homo")[[1]][1] } callable_target = paste(na.omit(unique(dproj$"Target Territory")), collapse=", "); table1<-rbind(paste(used_samples," used samples/", unused_samples + used_samples," total samples", sep=""), sequencing_protocol, bait_design, callable_target) rownames(table1)<-c("Samples","Sequencing Protocol", "Bait Design","Callable Target") par(mar=c(0,0,1,0)) textplot(table1, col.rownames="darkblue", show.colnames=FALSE, cex=1.25, valign="top") title(main=sprintf("Project Summary (%s)\n", projects), family="sans", cex.main=1.25, line=-1) # Bases summary reads_per_lane_mean = format(mean(dproj$"PF Reads (HS)", na.rm=TRUE), 8, 3,1, scientific=TRUE); reads_per_lane_sd = format(sd(dproj$"PF Reads (HS)", na.rm=TRUE), 8, 3,1, scientific=TRUE); lanes<-sprintf("%s +/- %s\n", reads_per_lane_mean, reads_per_lane_sd) used_bases_per_lane_mean = format(mean(dproj$"PF HQ Aligned Q20 Bases", na.rm=TRUE),8, 3,1, scientific=TRUE); used_bases_per_lane_sd = format(sd(dproj$"PF HQ Aligned Q20 Bases", na.rm=TRUE), 8, 3,1, scientific=TRUE); lanes<-c(lanes, sprintf("%s +/- %s\n", used_bases_per_lane_mean, used_bases_per_lane_sd)); target_coverage_mean = mean(na.omit(dproj$"Mean Target Coverage")); target_coverage_sd = sd(na.omit(dproj$"Mean Target Coverage")); lanes<-c(lanes, sprintf("%0.2fx +/- %0.2fx\n", target_coverage_mean, target_coverage_sd)); pct_loci_gt_10x_mean = mean(na.omit(dproj$"Target Bases 10x %")); pct_loci_gt_10x_sd = sd(na.omit(dproj$"Target Bases 10x %")); lanes<-c(lanes, sprintf("%0.2f%% +/- %0.2f%%\n", pct_loci_gt_10x_mean, pct_loci_gt_10x_sd)); pct_loci_gt_20x_mean = mean(na.omit(dproj$"Target Bases 20x %")); pct_loci_gt_20x_sd = sd(na.omit(dproj$"Target Bases 20x %")); lanes<-c(lanes,sprintf("%0.2f%% +/- %0.2f%%\n", pct_loci_gt_20x_mean, pct_loci_gt_20x_sd)); pct_loci_gt_30x_mean = mean(na.omit(dproj$"Target Bases 30x %")); pct_loci_gt_30x_sd = sd(na.omit(dproj$"Target Bases 30x %")); lanes<-c(lanes,sprintf("%0.2f%% +/- %0.2f%%\n", pct_loci_gt_30x_mean, pct_loci_gt_30x_sd)); reads_per_sample_mean = format(mean(d2proj$"PF Reads", na.rm=TRUE), 8, 3,1, scientific=TRUE); reads_per_sample_sd = format(sd(d2proj$"PF Reads",na.rm=TRUE), 8, 3,1, scientific=TRUE); samps<-sprintf("%s +/- %s\n", reads_per_sample_mean, reads_per_sample_sd); used_bases_per_sample_mean = format(mean(d2proj$"PF HQ Aligned Q20 Bases", na.rm=TRUE),8, 3,1, scientific=TRUE); used_bases_per_sample_sd = format(sd(d2proj$"PF HQ Aligned Q20 Bases", na.rm=TRUE), 8, 3,1, scientific=TRUE); samps<-c(samps, sprintf("%s +/- %s\n", used_bases_per_sample_mean, used_bases_per_sample_sd)); target_coverage_mean = mean(na.omit(d2proj$"Mean Target Coverage")); target_coverage_sd = sd(na.omit(d2proj$"Mean Target Coverage")); samps<-c(samps, sprintf("%0.2fx +/- %0.2fx\n", target_coverage_mean, target_coverage_sd)); pct_loci_gt_10x_mean = mean(na.omit(d2proj$"Target Bases 10x %")); pct_loci_gt_10x_sd = sd(na.omit(d2proj$"Target Bases 10x %")); samps<-c(samps, sprintf("%0.2f%% +/- %0.2f%%\n", pct_loci_gt_10x_mean, pct_loci_gt_10x_sd)); pct_loci_gt_20x_mean = mean(na.omit(d2proj$"Target Bases 20x %")); pct_loci_gt_20x_sd = sd(na.omit(d2proj$"Target Bases 20x %")); samps<-c(samps, sprintf("%0.2f%% +/- %0.2f%%\n", pct_loci_gt_20x_mean, pct_loci_gt_20x_sd)); pct_loci_gt_30x_mean = mean(na.omit(d2proj$"Target Bases 30x %")); pct_loci_gt_30x_sd = sd(na.omit(d2proj$"Target Bases 30x %")); samps<-c(samps, sprintf("%0.2f%% +/- %0.2f%%\n", pct_loci_gt_30x_mean, pct_loci_gt_30x_sd)); table2<-cbind(lanes, samps) colnames(table2)<-c("Per lane", "Per sample") rownames(table2)<-c("Reads", "Used bases", "Average target coverage", "% loci covered to 10x", "% loci covered to 20x","% loci covered to 30x") par(mar=c(0,0,1,0)) textplot(table2, rmar=1, col.rownames="dark blue", cex=1.25, valign="top") title(main="Bases Summary", family="sans", cex.main=1.25, line=0) # Sequencing summary instrument <- c(); if(length(grep("AAXX", dproj$Flowcell))>0){ instrument <- c(instrument, "Illumina GA2") } if(length(grep("ABXX", dproj$Flowcell))>0){ instrument <- c(instrument, "Illumina HiSeq") } if(length(instrument)>1){ instrument<-paste(instrument[1], instrument[2], sep=" and ") } used_lanes = nrow(dproj); unused_lanes_by_sequencing = 0; #can we get this? unused_lanes_by_analysis = 0; lanes_per_sample_mean = mean(table(dproj$"External ID"), na.rm=TRUE); lanes_per_sample_sd = sd(table(dproj$"External ID"), na.rm=TRUE); lanes_per_sample_median = median(table(dproj$"External ID")); lanes_paired = nrow(subset(dproj, dproj$"Lane Type" == "Paired")); lanes_widowed = nrow(subset(dproj, dproj$"Lane Type" == "Widowed")); lanes_single = nrow(subset(dproj, dproj$"Lane Type" == "Single")); read_length_mean = mean(dproj$"Mean Read Length (P)"); read_length_sd = sd(dproj$"Mean Read Length (P)"); read_length_median = median(dproj$"Mean Read Length (P)"); date = dproj$"Run Date"; # date = sub("JAN", "01", date); # date = sub("FEB", "02", date); # date = sub("MAR", "03", date); # date = sub("APR", "04", date); # date = sub("MAY", "05", date); # date = sub("JUN", "06", date); # date = sub("JUL", "07", date); # date = sub("AUG", "08", date); # date = sub("SEP", "09", date); # date = sub("OCT", "10", date); # date = sub("NOV", "11", date); # date = sub("DEC", "12", date); date = date[order(as.Date(date, format="%d-%m-%Y"))]; start_date = date[1]; end_date = date[length(date)]; table3<-rbind(paste(instrument), used_lanes, sprintf("%s rejected by sequencing, %s by analysis\n", unused_lanes_by_sequencing, unused_lanes_by_analysis), sprintf("%0.1f +/- %0.1f lanes (median=%0.1f)\n", lanes_per_sample_mean, lanes_per_sample_sd, lanes_per_sample_median), sprintf("%s paired, %s widowed, %s single\n", lanes_paired, lanes_widowed, lanes_single), sprintf("%0.1f +/- %0.1f bases (median=%0.1f)\n", read_length_mean, read_length_sd, read_length_median), sprintf("\tSequencing dates: %s to %s\n", start_date, end_date)) rownames(table3)<-c("Sequencer", "Used lanes", "Unused lanes","Used lanes/sample", "Lane parities", "Read lengths", "Sequencing dates") par(mar=c(0,0,1,0)) textplot(table3, rmar=1, col.rownames="dark blue", show.colnames=FALSE, cex=1.25, valign="top") title(main="Sequencing Summary", family="sans", cex.main=1.25, line=0) eval = gsa.read.gatkreport(cmdargs$evalroot) # Variant summary ##TODO: Fix this csv reader eval.counts = eval$CountVariants eval.counts.all = subset(eval.counts, Novelty == "all")$nVariantLoci; eval.counts.known = subset(eval.counts, Novelty == "known")$nVariantLoci; eval.counts.novel = subset(eval.counts, Novelty == "novel")$nVariantLoci; eval.titv = eval$TiTvVariantEvaluator eval.titv.all = subset(eval.titv, Novelty == "all")$tiTvRatio; eval.titv.known = subset(eval.titv, Novelty == "known")$tiTvRatio; eval.titv.novel = subset(eval.titv, Novelty == "novel")$tiTvRatio; table4 = matrix(c(eval.counts.all, eval.counts.known, eval.counts.novel, eval.titv.all, eval.titv.known, eval.titv.novel, "3.0 - 3.2", "3.2 - 3.4", "2.7 - 3.0"), nrow=3); rownames(table4) = c("All", "Known", "Novel"); colnames(table4) = c("Found", "Ti/Tv ratio", "Expected Ti/Tv ratio"); par(mar=c(0,0,0,0)) textplot(table4, rmar=1, col.rownames="dark blue", cex=1.25, valign="top") title(main="Variant Summary", family="sans", cex.main=1.25, line=-2) # # #plots # #fix this reader # eval.bysample = read.csv(paste(cmdargs$evalroot, ".SimpleMetricsBySample.csv", sep=""), header=TRUE, comment.char="#"); # eval.bysample.called = subset(eval.bysample, evaluation_name == "eval" & comparison_name == "dbsnp" & jexl_expression == "none" & filter_name == "called"); # eval.bysample.all = subset(eval.bysample.called, novelty_name == "all"); # eval.bysample.known = subset(eval.bysample.called, novelty_name == "known"); # eval.bysample.novel = subset(eval.bysample.called, novelty_name == "novel"); eval.ac = eval$SimpleMetricsByAC.metrics eval.ac.all = subset(eval.ac, Novelty == "all"); eval.ac.known = subset(eval.ac, Novelty == "known"); eval.ac.novel = subset(eval.ac, Novelty == "novel"); # # eval.func = read.csv(paste(cmdargs$evalroot, ".Functional_Class_Counts_by_Sample.csv", sep=""), header=TRUE, comment.char="#"); # eval.func.called = subset(eval.func, evaluation_name == "eval" & comparison_name == "dbsnp" & jexl_expression == "none" & filter_name == "called"); # eval.func.all = subset(eval.func.called, novelty_name == "all"); # eval.func.known = subset(eval.func.called, novelty_name == "known"); # eval.func.novel = subset(eval.func.called, novelty_name == "novel"); #boxplot(eval.bysample.all$CountVariants, eval.bysample.known$CountVariants, eval.bysample.novel$CountVariants, names=c("All", "Known", "Novel"), ylab="Variants per sample", main="", cex=1.3, cex.lab=1.3, cex.axis=1.3); # par(mar=c(5, 4, 4, 2) + 0.1) # ind = order(eval.bysample.all$CountVariants); # plot(c(1:length(eval.bysample.all$CountVariants)), eval.bysample.all$CountVariants[ind], col="black", cex=1.1, cex.lab=1.1, cex.axis=1.1, main="Variants per Sample", xlab="Sample", ylab="Number of variants", bty="n", ylim=c(0, max(eval.bysample.all$CountVariants))); # points(c(1:length(eval.bysample.known$CountVariants)), eval.bysample.known$CountVariants[ind], col="blue", cex=1.3); # points(c(1:length(eval.bysample.novel$CountVariants)), eval.bysample.novel$CountVariants[ind], col="red", cex=1.3); # legend("right", max(eval.bysample.all$CountVariants)/2, c("All", "Known", "Novel"), col=c("black", "blue", "red"), pt.cex=1.3, pch=21); par(mar=c(5, 4, 4, 2) + 0.1) plot(eval.ac.all$AC, eval.ac.all$n, col="black", type="l", lwd=2, cex=1.1, cex.lab=1.1, cex.axis=1.1, xlab="Allele count", ylab="Number of variants", main="Variants by Allele Count", log="xy", bty="n"); points(eval.ac.known$AC, eval.ac.known$n, col="blue", type="l", lwd=2); points(eval.ac.novel$AC, eval.ac.novel$n, col="red", type="l", lwd=2); legend("topright", c("All", "Known", "Novel"), col=c("black", "blue", "red"), lwd=2); #plot(eval.func.all$Synonymous[ind] / (eval.func.all$Missense + eval.func.all$Nonsense)[ind], ylim=c(0, 2), cex=1.3, cex.lab=1.3, cex.axis=1.3, bty="n", xlab="Sample", ylab="Ratio of synonymous to non-synonymous variants", col="black"); #points(eval.func.known$Synonymous[ind] / (eval.func.known$Missense + eval.func.known$Nonsense)[ind], cex=1.3, col="blue"); #points(eval.func.novel$Synonymous[ind] / (eval.func.novel$Missense + eval.func.novel$Nonsense)[ind], cex=1.3, col="red"); #legend("topright", c("All", "Known", "Novel"), col=c("black", "blue", "red"), pt.cex=1.3, pch=21); dev.off() } tearsheet() # Plots plots<-function(){ # eval.bysample = read.csv(paste(cmdargs$evalroot, ".SimpleMetricsBySample.csv", sep=""), header=TRUE, comment.char="#"); # eval.bysample.called = subset(eval.bysample, evaluation_name == "eval" & comparison_name == "dbsnp" & jexl_expression == "none" & filter_name == "called"); # eval.bysample.all = subset(eval.bysample.called, novelty_name == "all"); # eval.bysample.known = subset(eval.bysample.called, novelty_name == "known"); # eval.bysample.novel = subset(eval.bysample.called, novelty_name == "novel"); eval.ac = eval$SimpleMetricsByAC.metrics eval.ac.all = subset(eval.ac.called, Novelty == "all"); eval.ac.known = subset(eval.ac.called, Novelty == "known"); eval.ac.novel = subset(eval.ac.called, Novelty == "novel"); # # eval.func = read.csv(paste(cmdargs$evalroot, ".Functional_Class_Counts_by_Sample.csv", sep=""), header=TRUE, comment.char="#"); # eval.func.called = subset(eval.func, evaluation_name == "eval" & comparison_name == "dbsnp" & jexl_expression == "none" & filter_name == "called"); # eval.func.all = subset(eval.func.called, novelty_name == "all"); # eval.func.known = subset(eval.func.called, novelty_name == "known"); # eval.func.novel = subset(eval.func.called, novelty_name == "novel"); pdf(file= cmdargs$plotout, width=22, height=17, pagecentre=TRUE, pointsize=24) # # boxplot(eval.bysample.all$CountVariants, eval.bysample.known$CountVariants, eval.bysample.novel$CountVariants, names=c("All", "Known", "Novel"), ylab="Variants per sample", main="", cex=1.3, cex.lab=1.3, cex.axis=1.3); # # ind = order(eval.bysample.all$CountVariants); # plot(c(1:length(eval.bysample.all$CountVariants)), eval.bysample.all$CountVariants[ind], col="black", cex=1.3, cex.lab=1.3, cex.axis=1.3, xlab="Sample", ylab="Number of variants", bty="n", ylim=c(0, max(eval.bysample.all$CountVariants))); # points(c(1:length(eval.bysample.known$CountVariants)), eval.bysample.known$CountVariants[ind], col="blue", cex=1.3); # points(c(1:length(eval.bysample.novel$CountVariants)), eval.bysample.novel$CountVariants[ind], col="red", cex=1.3); # legend(0, max(eval.bysample.all$CountVariants)/2, c("All", "Known", "Novel"), col=c("black", "blue", "red"), pt.cex=1.3, pch=21); plot(eval.ac.all$AC, eval.ac.all$n, col="black", type="l", lwd=2, cex=1.3, cex.lab=1.3, cex.axis=1.3, xlab="Allele count", ylab="Number of variants", main="", log="xy", bty="n"); points(eval.ac.known$AC, eval.ac.known$n, col="blue", type="l", lwd=2); points(eval.ac.novel$AC, eval.ac.novel$n, col="red", type="l", lwd=2); legend("topright", c("All", "Known", "Novel"), col=c("black", "blue", "red"), lwd=2); # # plot(eval.func.all$Synonymous[ind] / (eval.func.all$Missense + eval.func.all$Nonsense)[ind], ylim=c(0, 2), cex=1.3, cex.lab=1.3, cex.axis=1.3, bty="n", xlab="Sample", ylab="Ratio of synonymous to non-synonymous variants", col="black"); # points(eval.func.known$Synonymous[ind] / (eval.func.known$Missense + eval.func.known$Nonsense)[ind], cex=1.3, col="blue"); # points(eval.func.novel$Synonymous[ind] / (eval.func.novel$Missense + eval.func.novel$Nonsense)[ind], cex=1.3, col="red"); # legend("topright", c("All", "Known", "Novel"), col=c("black", "blue", "red"), pt.cex=1.3, pch=21); dev.off(); }