Rapid fine mapping of causative mutations from sets of unordered, contig-sized fragments of genome sequence.
Ghanasyam RallapalliPilar Corredor-MorenoEdward ChalstreyMartin PageDaniel MacLeanPublished in: BMC bioinformatics (2019)
CHERIPIC allows users to rapidly analyse bulk segregant sequence data and we have made it available as a pre-packaged binary with all dependencies for Linux and MacOS and as Galaxy tool.