DISCOVAR has been released!

We are pleased to announce that DISCOVAR is now available to download .

DISCOVAR is a variant caller and genome assembler from the Broad Institute. It uses the latest low cost sequencing data, and can generate highly accurate variant calls for individual humans, or assemble small genomes de novo (with support for large genomes to follow). We expect it will be particularly valuable for understanding human Mendelian disease, but equally suited to investigating the biology of other organisms.

Find out more about DISCOVAR, and please check out the FAQ and help too.