BioDiscovery White Papers

Topic: Copy Number

Automating Genomic Scar Analysis For Homologous Recombination Deficiency (HRD): A Solution For Clinical Research Labs

Read more about homologous recombination deficiency and how Bionano’s NxClinical analysis software provides an automated genomic scar score.

Optimizing efficiency across cytogenomic applications (GDACyto & GSACyto)

Read more about the latest Illumina’s Infinium Global Diversity Array with Cytogenetics (GDACyto) and Infinium Global Screening Array with Cytogenetics (GSACyto) coupled with BioDiscovery’s NxClinical analysis software.

Optimizing efficiency across cytogenomic applications (GDACyto)

Read more about the latest Illumina Infinium Global Diversity Array with Cytogenetics (GDACyto) coupled with BioDiscovery’s NxClinical analysis software.

Comparison of the BAM (multiscale reference) algorithm to other methods for CNV detection from NGS

Learn more about the various methods that have been proposed to detect CNVs from NGS data in tumor-normal matched paired colon adenocarcinoma samples.

Analyzing NGS Data For Copy Number Events

Next-generation sequencing (NGS) is mainly used to obtain sequence variants (SNVs). However, getting copy number variants (CNVs) from NGS has gained momentum in both research and clinical applications.