Skip to main content

BioDiscovery NxClinical 4.0

BioDiscovery recently launched NxClinical 4.0, software for the interrogation of copy number, sequence variants, and allelic changes obtained from a single next-generation sequencing assay. The software incorporates all these genomic variations into a single database where a compound heterozygous event can easily be detected with interactive browser view and advanced filtering schemas that quickly narrow down the list of potential causal variants, the company said.