FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads
FastGT is a program package for whole-genome genotyping of...encing reads. It is written in C and runs in Linux. FastGT uses a list of variant-specif...verage low-cost Linux server. http://bioinfo.ut.ee/FastGT/ https://github.com/bioinfo-...1574 days ago