Entering edit mode
5.5 years ago
paumarc
▴
20
Hello
we have been running a pipeline using fastp, bwa-mem, and gatk with hard filtering to perform snp calling on exome seq data. Although the coverage statistics for fastq files is similar, we obtain a huge difference in the number of reads per snp. We wonder if it could be caused by hard filtering. Otherwise, could you suggest any idea of what can be going on?
Thanks in advanced.
I think that adding a bit more details here would increase your chance of getting an answer.