Hello all,
I'm going to demultiplex a run with a sample sheet in which there are entries and adapter sequences in the sheet with no corresponding...
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how to get the count of reads mapped to rRNA regions?
Hi all,
I just mapped the RNA-Seqs by Tophat and got the output file accepted_hit.bam. I also have gtf file. I want to count the reads...
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samtools sorting issue or HTSeq-count problem?
Hello all,
This has puzzled me for days and I couldnt find any explanation on the internet.
I noticed HTSeq-count gives the reads...