hello!
Currently I am working with a large set of STAR mapped reads, the output is in sam format. I would like to remap, but was wondering if its possible to do this using the SAM files without converting the sam files to fastq and then mapping. Any help would be appreciated.
Currently I am working with a large set of STAR mapped reads, the output is in sam format. I would like to remap, but was wondering if its possible to do this using the SAM files without converting the sam files to fastq and then mapping. Any help would be appreciated.
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