Is there a tool that can merge 2 VCF files while taking "representational ambiguity" of multi-allelic variants into account? By: * replaying all variant alleles …
I have imputed VCFs, which I imputed using Beagle for 1000G reference sites (http://bochet.gcc.biostat.washington.edu/beagle/1000_Genomes_phase3_v5a/). From these, I have a bed/bim/fam file that I made using …
Hello, I'm wondering how the designers of software such as [GSNAP][1] which create hash tables of the genome for alignment take into account things like …