Hi Everyone
Just as a general rule, if we have a very interesting variant, we have many metrics to judge the variant, from mapping quality to strand bias to coverage ,..etc. If the variant passes most filters on such metrics and fails one, so simply discard just because it fails one? I feel okay to discard if the variant has low mapping quality, even if high coverage and no strand bias, .etc.
But for other metrics, if it fails any, just discard? Could we lose interesting variants then? What do you do?
Thanks
Can you give some details on: which variant caller, which species, what kind of sequencing (exome, wgs, amplicon), control sample available, what kind of variant (SNP, Indel, complex, CNV), and what filter it failed.
I am not talking about specific variant, as i have so many, some of them exome and some of them rnaseq. So, I am asking in general, if a variant fails one metric, do we discard it,, like should it be all good on all metrics? For example high coverage, good mapping quality but QD is low or there is strand bias , etc ?
That's a tradeoff between sensitivity and specificity and entirely depends on the application.