Using VarElect to identify a mutated gene potentially linked to congenital diahrrea

In this case study, we demonstrate how VarElect identified a mutated gene that is potentially associated with congenital diarrhea.  We analyzed a list of 512 genes with variants, which have been obtained from next generation sequencing of a whole exome of a subject with congenital diarrhea. VarElect prioritized these genes according to their predicted association with congenital diarrhea, displaying both direct and indirect connections.