# HG changeset patch # User iuc # Date 1551376852 18000 # Node ID 64c5c1bbbdbeb53bb4f6a67c59f1b7a2ef32c92a # Parent 9fec5dd8fbb9b103cbc1195af1f329d4f60d8eaa planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/raceid3 commit 71e6b205841c83391ea8fc69e10eac03f212f4d6 diff -r 9fec5dd8fbb9 -r 64c5c1bbbdbe scripts/cluster.R --- a/scripts/cluster.R Thu Nov 22 04:45:41 2018 -0500 +++ b/scripts/cluster.R Thu Feb 28 13:00:52 2019 -0500 @@ -1,5 +1,5 @@ #!/usr/bin/env R -VERSION = "0.2" +VERSION = "0.3" args = commandArgs(trailingOnly = T) @@ -23,10 +23,10 @@ sc <- do.call(filterdata, c(sc, filt)) ## Get histogram metrics for library size and number of features - raw.lib <- log(colSums(as.matrix(sc@expdata))) - raw.feat <- log(rowSums(as.matrix(sc@expdata))) - filt.lib <- log(colSums(getfdata(sc))) - filt.feat <- log(rowSums(getfdata(sc))) + raw.lib <- log10(colSums(as.matrix(sc@expdata))) + raw.feat <- log10(rowSums(as.matrix(sc@expdata)>0)) + filt.lib <- log10(colSums(getfdata(sc))) + filt.feat <- log10(rowSums(getfdata(sc)>0)) br <- 50 ## Determine limits on plots based on the unfiltered data @@ -47,10 +47,17 @@ ## feat.x_lim <- c(0,betterrange(max(tmp.feat$breaks))) par(mfrow=c(2,2)) - print(hist(raw.lib, breaks=br, main="ExpData Log(LibSize)")) # , xlim=lib.x_lim, ylim=lib.y_lim) - print(hist(raw.feat, breaks=br, main="ExpData Log(NumFeat)")) #, xlim=feat.x_lim, ylim=feat.y_lim) - print(hist(filt.lib, breaks=br, main="FiltData Log(LibSize)")) # , xlim=lib.x_lim, ylim=lib.y_lim) - print(hist(filt.feat, breaks=br, main="FiltData Log(NumFeat)")) # , xlim=feat.x_lim, ylim=feat.y_lim) + print(hist(raw.lib, breaks=br, main="RawData Log10(LibSize)")) # , xlim=lib.x_lim, ylim=lib.y_lim) + print(hist(raw.feat, breaks=br, main="RawData Log10(NumFeat)")) #, xlim=feat.x_lim, ylim=feat.y_lim) + print(hist(filt.lib, breaks=br, main="FiltData Log10(LibSize)")) # , xlim=lib.x_lim, ylim=lib.y_lim) + tmp <- hist(filt.feat, breaks=br, main="FiltData Log10(NumFeat)") # , xlim=feat.x_lim, ylim=feat.y_lim) + print(tmp) # required, for extracting midpoint + unq <- unique(filt.feat) + if (length(unq) == 1){ + text(tmp$mids, table(filt.feat)[[1]] - 100, pos=1, paste(format(10^unq, scientific=T, digits=3), + " Features in all Cells", sep=""), cex=0.8) + } + if (filt.use.ccorrect){ par(mfrow=c(2,2)) diff -r 9fec5dd8fbb9 -r 64c5c1bbbdbe test-data/intestinal.filter.pdf Binary file test-data/intestinal.filter.pdf has changed diff -r 9fec5dd8fbb9 -r 64c5c1bbbdbe test-data/intestinal_advanced.filter.pdf Binary file test-data/intestinal_advanced.filter.pdf has changed diff -r 9fec5dd8fbb9 -r 64c5c1bbbdbe test-data/matrix.filter.pdf Binary file test-data/matrix.filter.pdf has changed