Hello
I am working in preprocessing the exome data. I need some inputs in some of the preprocessing steps. I have included the read group...
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Preprocessing exome data for germline variant analysis
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40bp paired reads for novel transcripts identification, which software?
I have some 40bp paired reads RNAseq data, basically that 40 x 2 from each RNA fragment.
It seems to me that, tophat prefers reads that...