Hi there, I filtered my PE reads based on strict parameters, but now i want to make good use of the good quality (unpaired PE) reads. What i should do? the unpaired PE and paired PE have been mapped to the reference genome and been converted to BAM files. Can i merge them by samtools? Thanks
Question: Can I Merge The Good Quality (Unpaired Pe ) Bam File And Paired Pe Bam File With Samtools?
6.1 years ago by
waswangs • 0
waswangs • 0 wrote:
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