Variant read depth

[Akazhiel]

Hello!

I've noticed the number of reads supporting the variant is reported, but I'd like to ask if there's any plans of implementing the reporting of the reference reads for each variant reported? So as to be able to compute the read depth and do some filtering based on allele frequency and so.

Best regards,

Jonatan

[nealplatt]

I agree. This would be very helpful.