Hello,
I was wondering whether this tool can reliably handle cancer genomes that contain copy number variations, such as chromosomal arm losses or gains. Can it produce accurate results in these contexts, or is it primarily designed for diploid genomes only?
Hello,
I was wondering whether this tool can reliably handle cancer genomes that contain copy number variations, such as chromosomal arm losses or gains. Can it produce accurate results in these contexts, or is it primarily designed for diploid genomes only?