Celemics and Strand Life Sciences are excited to highlight their strategic collaboration aimed at improving next-generation sequencing (NGS) analysis through an integrated, sample-to-report platform. Together, they deliver clinical-grade genomics reports with assay-specific variant filters, ensuring seamless and efficient workflows for customers across Europe, Asia, and North America.
The partnership combines Celemics’ NGS target enrichment kits and bioinformatics pipeline with Strand’s StrandOmics tertiary analysis platform, ensuring clinical data compliance and secure data residency. As part of its global expansion, Celemics recently opened U.S. offices to better serve growing markets, while Strand continues to support North American clients with advanced genomic solutions.
Over the past 2.5 years, Strand has analyzed various clinical cases for Celemics, leveraging whole exome sequencing for rare diseases and panel-based tests, such as the Hereditary Cancer and OncoRisk Tests. With a three-day turnaround, Strand’s scientists have expertly reviewed over 30,000 variants, providing valuable variant-phenotype associations, even in cases with limited medical data.
Dr. Hyoki Kim, Co-Founder and CEO of Celemics, expressed enthusiasm for the partnership, noting the value of Strand’s expertise in accelerating market integration. Strand CEO Dr. Ramesh Hariharan emphasized their shared goal of expanding NGS-based diagnostics in cancer, rare diseases, and inherited disorders.
Founded in 2010, Celemics specializes in developing reagents and panels for oncology, rare diseases, and biopharma applications. Strand Life Sciences, established in 2000, integrates multiomics research with advanced bioinformatics to offer comprehensive diagnostics and interpretation services globally.