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  • FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads

FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads

http://bioinfo.ut.ee/FastGT/

FastGT is a program package for whole-genome genotyping of genome variants directly from raw sequencing reads. It is written in C and runs in Linux. FastGT uses a list of variant-specific k-mer pairs that are unique in human genome, counts the frequency of k-mers in sequencing data and predicts the genotype. All this takes less than 1 hour on average low-cost Linux server.

http://bioinfo.ut.ee/FastGT/

https://github.com/bioinfo-ut/GenomeTester4/