Hi all,
For several reasons I have BAM files made of multiple samples (identified by ID/SM tags). I've noticed that delly warns about this:
Warning: Multiple sample names (@RG:SM) present in the BAM file!
and that the resulting bcf includes genotypes for a single sample, the first found in the BAM header. I've read that delly performs joint calling, hence is it correct to assume that the results are derived from the analysis of all reads in the BAM file?
In principle I can separate samples in different files, but since I'm not really interested in individual genotypes but only in SV definitions I'd like to know if I'm doing right.
d