Calls somatic SNVs, indels, and allelic copy number jointly across multiple samples from the same patient. These can be standard tumor/normal pair, longitudinal samples, primary/met, etc. Can also be used for tumor only calling, ideally with a high tumor content and a low tumor content sample.
I'm interested in running lumosvar2 and I think I've successfully run the normal metrics step. For the main step, where is ./lumosVarMain ? This file isn't in the bin directory.
Hi,
I'm interested in running lumosvar2 and I think I've successfully run the normal metrics step. For the main step, where is ./lumosVarMain ? This file isn't in the bin directory.
Thanks.