Hi, I am working with dUTP bases stranded RNA-Seq paired end data. After aligning with STAR , I would like to convert my bam files to bigwig. I am trying to use bamCoverage but cannot use the --filterRNAstrand in Galaxy. Please can anyone help . Thanks
why are you unable to use
--filterRNAstrand
? Do you get an error when trying to use this parameter? If so, what is the error?Hi , In usegalaxy.eu instance there is no option for --filterRNAstrand. Hence I cannot filter them.
Sounds like
deeptools
on that galaxy instance is out of date.All
--filterRNAStrand
really does is selects reads that have mapped to one strand and returns a bigwig file with coverage of those reads. (–filterRNAstrand=forward keeps minus-strand reads, which originally came from genes on the forward strand using a dUTP-based method)You can do this yourself using
samtools view
to select the minus-strand reads from your BAM file and use that as input tobamCoverage
to generate your plus-strand coverage bigwig file, then repeat with plus-strand reads.Its not that simple with paired-end reads (because usually, the mates are on different strands), see How To Separate Illumina Based Strand Specific Rna-Seq Alignments By Strand