Feedback from Users
Thanks for producing this software. It is helping us very much on our current project (soon to be published) wherein we are sequencing targeted regions in follicular lymphoma specimens which feature very high mutation rates and diversity within samples. We have used SOLiD reads and are about to get some Illumina data, so having a platform that handles both types is a plus. The speed is very impressive and the ability to map to regions with multiple consecutive mutations makes it superior to BFAST (does not handle consecutive mutations well) and SHRiMP (cannot handle too many mutations)..
---John P. Spence(firstname.lastname@example.org), June 20, 2014