Topic: Copy Number

BioDiscovery’s NxClinical software augments PerkinElmer Genomics newborn screening and genomic testing services in labs around the world

PerkinElmer Genomics has selected BioDiscovery's NxClinical software as its choice for genomic data analysis for its services.

BioDiscovery releases Nexus Copy Number 10.0, a single solution for copy number estimation from arrays, WES, WGS, shallow, and targeted sequencing

Nexus Copy Number 10.0 is a highly robust, intuitive, and multi-platform software for both copy number calling and downstream statistical analyses. A key feature of Nexus Copy Number is its ability to derive high quality copy number calls from many flavors of NGS (whole exome, whole genome, shallow, targeted panel, and normal depth of coverage sequencing).

BioDiscovery launches NxClinical 4.1, a comprehensive system allowing interpretation of variants of any size from SNVs to large CNVs

NxClinical 4.1 is a unique software solution for integration of copy number, sequence variants, and allelic changes obtained from microarray and NGS technologies. NxClinical 4.1 allows combined analysis and interpretation of all genomic variants on a single, platform agnostic system.

Thermo Fisher Scientific and BioDiscovery form software development partnership providing an end-to-end solution for cancer researchers

BioDiscovery, a leader in copy number analysis software, created a new tailored software solution (Nexus Express for OncoScan) for copy number detection and downstream analysis for the OncoScan™ CNV Assay. The assay plus software solution allows researchers performing solid tumor analysis a high-quality, complete, end-to-end solution from raw data to discovery for difficult FFPE samples.

BioDiscovery Inc. Forms Partnership with Be Creative Lab (Beijing) Co. Ltd. For Distribution of NxClinical Software

BioDiscovery announced today an agreement with Be Creative Lab in Beijing, China to be the exclusive reseller and distributor of BioDiscovery products in China.

BioDiscovery launches NxClinical 4.0, a unique system allowing analysis and interpretation of CNV, SNV, and AOH from a single NGS assay

BioDiscovery launches NxClinical 4.0, a unique system allowing analysis and interpretation of CNV, SNV, and AOH from a single NGS assay.

BioDiscovery releases Nexus Copy Number 9.0 with improved copy number estimation from NGS, including targeted panels and shallow sequencing

The new features in Nexus Copy Number 9.0 really enhance the usability of WES, WGS, targeted panels and low-pass sequencing for copy number analysis.

BioDiscovery releases Nexus Copy Number 8.0 with cutting-edge features: estimation of copy number and allelic events from NGS data

Nexus Copy Number 8.0 is derivation of copy number from NGS results. BAM (pooled reference), detects copy number from WES, WGS, and targeted NGS panels.

BioDiscovery’s Nexus Copy Number software helps accelerate cancer gene discovery

See how Nexus Copy Number has been used at North Carolina State University to detect copy number changes by CGH analysis in Canines.