The project developed a suite of new methods (FAVR) designed to assist the shortlisting of genetic variants under a rare variant-phenotype/disease model. The methods were designed to work with commonl
Genome resequencing of B. subtilis mutant strain resulting from random recombinations between strains NCIB 3610 and RO-NN-1. Strain is mostly RO-NN-1 (~80%) but the rest includes randomly swapped snip
