Closed souravnayak closed 5 years ago
It should work reasonably well in practice. Compared to a true haploid model, the diploid scoring model genotype confidence for a variant will grow more slowly as a function of depth, but that should only matter for low-depth sequencing. If you're actually evaluating a pooled sample then you might consider the tumor-only calling mode instead.
I am working with haploid microbial genome. I have a set of genome sequenced. I want to look for structural variations within the population. Can I use MANTA for calling the SVs?