Trivial to add, but need to handle file size issues carefully. We could potentially move data to cloud, or compute the sequences on the fly by comparing to reference haplotype. We could also provide these sequences in the population-level summary for minimal file size increase, but this would require user to join the two summary files
Trivial to add, but need to handle file size issues carefully. We could potentially move data to cloud, or compute the sequences on the fly by comparing to reference haplotype. We could also provide these sequences in the population-level summary for minimal file size increase, but this would require user to join the two summary files