BioDiscovery News

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Ambry Genetics Selects BioDiscovery’s NxClinical Software for Analysis, Management, and Reporting of Copy Number Events in its Clinical Genomics Workflow

Ambry Genetics selects BioDiscovery’s NxClinical software for analysis, management, and reporting of copy number events in its clinical genomics workflow.

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Illumina Selects BioDiscovery’s NxClinical Software for Data Visualization, Management and Interpretation for its CytoSeq ™ assay, an NGS-based Solution for Detection of CNVs, AOH, and SNVs

Illumina Selects BioDiscovery’s NxClinical Software for Data Visualization, Management and Interpretation for its CytoSeq ™ assay, an NGS-based Solution for Detection of CNVs, AOH, and SNVs

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BioDiscovery launches NxClinical™ 2.0 software for improved genetic data analysis, interpretation, management, and reporting

NxClinical 2.0 is a flexible, platform-agnostic database solution for efficient analysis, interpretation, and reporting of variations.

Ambry Genetics Selects BioDiscovery’s NxClinical Software for Analysis, Management, and Reporting of Copy Number Events in its Clinical Genomics Workflow

Ambry Genetics selects BioDiscovery’s NxClinical software for analysis, management, and reporting of copy number events in its clinical genomics workflow.

Illumina Selects BioDiscovery’s NxClinical Software for Data Visualization, Management and Interpretation for its CytoSeq ™ assay, an NGS-based Solution for Detection of CNVs, AOH, and SNVs

Illumina Selects BioDiscovery’s NxClinical Software for Data Visualization, Management and Interpretation for its CytoSeq ™ assay, an NGS-based Solution for Detection of CNVs, AOH, and SNVs

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.

CombiMatrix implements BioDiscovery’s NxClinical software for higher efficiency to process and report cytogenomic testing results

CombiMatrix is now using BioDiscovery’s NxClinical software for analysis, management, and interpretation of copy number events in its clinical workflow.

Lurie Children’s Hospital of Chicago adopts BioDiscovery’s NxClinical software in its Genetics Laboratories

Recognized leader in research and education, and one of the top pediatric providers in the Midwest recently started using NxClinical.

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.

BioDiscovery and AKESOgen announce their co-marketing partnership

A genomics services provider for clinical trials, testing, and research will now be working with BioDiscovery in a co-marketing partnership.

BioDiscovery launches NxClinical™ 2.0 software for improved genetic data analysis, interpretation, management, and reporting

NxClinical 2.0 is a flexible, platform-agnostic database solution for efficient analysis, interpretation, and reporting of variations.

BioDiscovery Launches NxClinical™ for Complete Case Review and Reporting for Genetics Labs

NxClinical focuses on improving efficiency and quality through multi-user collaborative communication, audit-trail features, and automation.

BioDiscovery awarded National Institutes of Health SBIR Grant to Improve TCGA Copy Number Profiles

BioDiscovery awarded grant to make further discoveries into tumorigenesis and disease progression and provide a validation set for studies.