With a continued focus on customers, BioDiscovery moves from a sales and support departmental structure to a holistic team filled with Customer Success Managers.
Low Pass Genome Sequencing (LP-GS) for detection of CNVs as a replacement to constitutional microarray analysis. The team evaluated a number of different tools and found NxClinical to have superiority in CNV detection and classification.
Take a look at how Nexus Copy Number handles the different “Raw Data” and the three steps to analyzing the data.
WES and SNP arrays detect concordant gene-level alterations. Learn how CNV detection from whole-exome sequencing (WES) compares with SNP microarray.
Learn more about CNV analysis by reading this review of the challenges with detecting copy number variations with next-generation sequencing.
Learn why Nexus Copy Number is the exclusive software solution for the analysis of OncoScan™ data due to its advanced algorithm and ease of use.