- New, groundbreaking technology delivers Illumina’s most comprehensive genome yet; early results from Broad Clinical Labs demonstrate a highly simplified workflow, ultra-long phasing, high-resolution insights into complex genomic variation, and enhanced long-range information
- Illumina and customers will also showcase new details on complete proteomics solution and latest data on Fluent single-cell technology
, /PRNewswire/ — Illumina, Inc. (NASDAQ: ILMN), a global leader in DNA sequencing and array-based technologies, today announced that it will present updates on several key innovations in whole-genome sequencing, proteomics, and single-cell technology at the American Society of Human Genetics (ASHG) Annual Meeting next week in Denver. The latest details will be presented alongside new data from key opinion leaders in next-generation sequencing (NGS), illustrating the potential impact of Illumina’s emerging innovations.
First-of-its-kind technology streamlines whole-genome workflows, expands genomic insights
In a mainstage presentation on November 6, Steve Barnard, PhD, chief technology officer, will reveal new details on the company’s constellation mapped read technology, originally announced in the company’s August 2024…