Entering edit mode
2.8 years ago
MH85
▴
10
Hi everyone,
I have a mapping of PE reads to reference with a mean coverage of about 100 x. I need to sample (extract) reads across the alignment randomly to reduce coverage. Optimally but not necessarily, if there is heterozygote SNP, extract reads of both alleles.
Is there any way how to do it?
Thanks a lot in advance Milos
Thank you very much, Pierre!!! This is exactly what I need.