
SureSelect Clinical Research Exome
Thoughtfully curated by world-renowned clinical molecular geneticist Dr. Madhuri Hegde, Ph.D., FACMG, formerly of Emory University, CRE V4 provides excellent coverage of targeted non-coding pathogenic sites from ClinVar, HGMD, and ACMG, ancestry single nucleotide variants (SNPs), pharmacogenomic SNPs, a unique design to detect common disease-causing CNVs using a breakpoint detection approach, and other expertly curated disease-relevant content.