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Read more about homologous recombination deficiency and how Bionano’s NxClinical analysis software provides an automated genomic scar score.
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.
Read more about the latest Illumina Infinium Global Diversity Array with Cytogenetics (GDACyto) coupled with BioDiscovery’s NxClinical analysis software.
Learn more about the various methods that have been proposed to detect CNVs from NGS data in tumor-normal matched paired colon adenocarcinoma samples.
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.
Explore the use of LogR and B-allele frequency values from SNP arrays to interpret the underlying biology of tumor samples, along with limitations of this approach.