https://www.taxtmi.com/news?id=59138 Illumina's constellation mapped read technology, piloted by GeneDx on 160 DNA samples using NovaSeq X Plus Systems, reportedly identified hard-to-detect variant classes-including large repeat expansions, complex structural variants, homologous-gene and pseudogene-confounded variants, and mosaic aneuploidy-performing at least comparably with orthogonal methods. The technology's workflow features on flow cell library prep and proprietary informatics, supports multiple sample types, and is slated for a commercial product release; the release includes a forward-looking statements caution describing product-development, supplier, manufacturing, and customer-acceptance risks and disclaims any obligation to update projections. en-us Fri, 17 Oct 2025 12:46:03 +0530 Fri, 17 Oct 2025 12:46:03 +0530 TaxTMI RSS Generator https://www.taxtmi.com/news?id=59138 Illumina's constellation mapped read technology, piloted by GeneDx on 160 DNA samples using NovaSeq X Plus Systems, reportedly identified hard-to-detect variant classes-including large repeat expansions, complex structural variants, homologous-gene and pseudogene-confounded variants, and mosaic aneuploidy-performing at least comparably with orthogonal methods. The technology's workflow features on flow cell library prep and proprietary informatics, supports multiple sample types, and is slated for a commercial product release; the release includes a forward-looking statements caution describing product-development, supplier, manufacturing, and customer-acceptance risks and disclaims any obligation to update projections. News - Fri, 17 Oct 2025 12:46:03 +0530 https://www.taxtmi.com/news?id=59138