RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data.

Tomasz StokowyMateusz GarbulowskiTorunn FiskerstrandRita HoldhusKornel LabunPawel SztromwasserChristian GilissenAlexander HoischenGunnar HougeKjell PetersenInge JonassenVidar M. Steen
Published in: Bioinform. (2016)
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