Hi guys,
This forum is awesome. I recently just started using software for seq data analysis. One question I have right now is how can I obtain the reads that map with 100% identity (no mismatches) to a reference genome. I have BAM files available, and was thinking that SAMTools is the way to do it, but I haven't figured it out yet.
If someone could point me to a useful reference or give me some guidance I'll be extremely grateful.
Thanks!
-Sakti
This forum is awesome. I recently just started using software for seq data analysis. One question I have right now is how can I obtain the reads that map with 100% identity (no mismatches) to a reference genome. I have BAM files available, and was thinking that SAMTools is the way to do it, but I haven't figured it out yet.
If someone could point me to a useful reference or give me some guidance I'll be extremely grateful.
Thanks!
-Sakti
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