Closed RADIOMUMM closed 7 months ago
Is it possible for Clair3 to use the BAM files split by chromosome for calling variant separately and finally merge the resulting VCF files to reduce the run time? Or is there any other way to reduce the runtime?
Clair3 do splitting into 5Mbp chucks for parallel processing by default.
Is it possible for Clair3 to use the BAM files split by chromosome for calling variant separately and finally merge the resulting VCF files to reduce the run time? Or is there any other way to reduce the runtime?