Hi,
Recently, I have used samtools tview -d T -p position data.sort.bam
--reference genome.fasta to get all the reads alignment text file. But it
seems that the maximum read alignment number in tview is about 8000+, and my
remaining aligned reads are not shown. I wonder if the samtools tview has the
maximum read alignment number limitation and how to expand the tview to show
as many alignment reads as possible. Looking forward to your reply, thank you
very much !
Best,
Yudong
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