I know this is asking a lot but a change to selscan to be able to read halotype information from multiple chromosomes from a single input file (such as a tped) would be much appreciated.
The logistics of working with draft genomes with thousands of scaffolds w/o chromosome assignment is not trivial :-)
Dear developers,
I know this is asking a lot but a change to selscan to be able to read halotype information from multiple chromosomes from a single input file (such as a tped) would be much appreciated.
The logistics of working with draft genomes with thousands of scaffolds w/o chromosome assignment is not trivial :-)