Hi all , I am working on RNA -seq Data analysis. I have reads for specific gene in a bam format which I was extracted using samtools command. That bam file contain 37 reads. I want merge these overlap reads and make into single file. Is there any tool available to do this ? Pls let me know ? (It is a pair end seq reads).
Question: How to merge the reads into single file
3.7 years ago by
Bioblazer • 50
Bioblazer • 50 wrote:
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