Phenoxome: ranking pathogenic variants provided phenotypic context
A comprehensive computational framework to prioritize genetic variants based upon the likelihood of the variant being pathogenic given the phenotype of the patient.
A comprehensive computational framework to prioritize genetic variants based upon the likelihood of the variant being pathogenic given the phenotype of the patient.
Identifying potential drug repurposing candidates by community detection on heterogeneous networks.
A computational classifier to distinguish sequencing artifacts from bona fide variants from next-generation sequencing data in pediatric tumors.
A computational workbench to prioritize miRNAs provided disease context represented by messengerRNA targets.