Hello, I am trying to get readcounts of coordinates of a gene I found on ucsc genome browser on some bam files I have. Is there some sort of protocol on how to use either bam-readcounts or "R" to do this quick analysis. I am new to linux and bioinformatics in general.
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See this thread (an oldie) but should give you what you need: http://sourceforge.net/p/samtools/ma...sage/27419954/
If you want the bare minimum steps (replace chr1:1234-2345 with actual coordinates of your gene, you may have to make sure that chromosome name matches what is in your bam e.g. chr1 vs 1).
Code:$ samtools index input.bam $ samtools view input.bam chr1:1234-2345 | wc -l
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Last edited by blancha; 11-24-2015, 09:40 AM.
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