Mercurial > repos > vimalkumarvelayudhan > riboseqr_wrapper
view test-data/reference.R @ 5:423ad61697c4
Bugfix 1: [triplet] Lengths (frameCounting) if given should be a range (not zero).
readingFrame function fails with subscript out of bounds.
Bugfix 2: [triplet] Check if transcript name in SAM matches the name in FASTA. Produce
an error message if it's not. This fixes the problem where an empty plot is
produced (no bars).
[ribosome_profile] - A proper error message is now produced if an invalid transcript name is
provided.
Updated test data
author | Vimalkumar Velayudhan <vimalkumarvelayudhan@gmail.com> |
---|---|
date | Tue, 27 Oct 2015 12:21:50 +0000 |
parents | |
children |
line wrap: on
line source
# Script used to prepare the input data for Triplet periodicity step. It is done this way # as SAM files were not available for this dataset at the time this release was made library(riboSeqR) fastaCDS <- findCDS(fastaFile='rsem_chlamy236_deNovo.transcripts.fa', startCodon=c("ATG"), stopCodon=c("TAG", "TAA", "TGA")) # RiboSeq file 1-4 are just links to chlamy236_plus_deNovo_plusOnly_Index[17,3,5,7] ribofiles <- paste(c("RiboSeq file 1", "RiboSeq file 2", "RiboSeq file 3", "RiboSeq file 4")) rnafiles <- paste(c("RNASeq file 1", "RNASeq file 2", "RNASeq file 3", "RNASeq file 4")) riboDat <- readRibodata(ribofiles, rnafiles, replicates=c("WT", "WT", "M", "M")) save('riboDat', file='Prepare riboSeqR input (R data file)', compress=FALSE) fCs <- frameCounting(riboDat, fastaCDS) fS <- readingFrame(rC = fCs) #pdf(file="/tmp/Periodicity-plot.pdf") #plotFS(fS, legend.text = c('Frame 0', 'Frame 1', 'Frame 2')) #dev.off() ffCs <- filterHits(fCs, lengths=c(27,28), frames=list(1,0), hitMean = 50, unqhitMean = 10, fS=fS) save('fastaCDS', 'riboDat', 'fCs', 'fS', 'ffCs', file='Metagene analysis (R data file)', compress=FALSE) #pdf(file='/tmp/Metagene-analysis-plot.pdf') #plotCDS(coordinates=ffCs@CDS, riboDat=riboDat, lengths=27) #plotCDS(coordinates=ffCs@CDS, riboDat=riboDat, lengths=28) #dev.off() # #pdf(file='/tmp/Ribosome-profile-plot.pdf') #plotTranscript("CUFF.37930.1", coordinates=ffCs@CDS, riboData=riboDat, length=27, cap=200) #dev.off() # #riboCounts <- sliceCounts(ffCs, lengths = c(27,28), frames = list(0,2)) #rnaCounts <- rnaCounts(riboDat, ffCs@CDS) #save('fastaCDS', 'riboDat', 'fCs', 'fS', 'ffCs', 'riboCounts', 'rnaCounts', file='Robjects.rda')