Illumina to preview newest innovations in NGS and multiomic technologies at the American Society of Human Genetics Annual Meeting
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New, groundbreaking technology delivers
Illumina 's most comprehensive genome yet ; early results fromBroad 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
First-of-its-kind technology streamlines whole-genome workflows, expands genomic insights
In a mainstage presentation on
Additionally, constellation mapped read technology will deliver Illumina's most comprehensive whole genome yet, adding long-range information to Illumina's proven, highly accurate XLEAP-SBS™ chemistry. The expanded insights from this proprietary technology will resolve challenging genic regions, such as pseudogenes, while generating ultra-long phased data and providing a high-resolution view of complex structural variation.
"These are unprecedented, breakthrough technologies that will power our future comprehensive whole-genome solutions," Barnard said. "We believe this solution could be the de facto genome of the future, offering expanded information and simplicity for labs."
Barnard will be joined on stage by
The first product based on constellation mapped read technology is set to begin early access in the first half of 2025.
On
Proteomics enables the observation of direct cellular function to gain insights on protein-driven disease traits, and the inclusion of proteomics in Illumina's NGS portfolio provides visibility into the entire biological process. The presentation will highlight the early access solution's ability to identify and quantify more than 6000 human proteins and its readout compatibility with NovaSeq™ X and NovaSeq 6000 Systems to enable multiomics on a single platform—a key differentiator from existing proteomics methodologies.
Kamel Lahouel, PhD, assistant professor in the Early Detection and Prevention Division at
When it launches in early 2025,
Leading single-cell technology: Fluent PIPseq™ V
On
Additional updates
Barnard's presentation on
"We look forward to expanding on these innovations with our customers and peers at ASHG," Barnard said. "We also look forward to sharing our latest instruments, the MiSeq™ i100 Series, with our fellow NGS enthusiasts at our booth."
Illumina's new MiSeq i100 Series will be on display at booth 503 during the meeting, and Illumina will be presenting scientific findings in five poster presentations and abstracts.
Use of forward-looking statements
This release may contain forward-looking statements that involve risks and uncertainties. Among the important factors to which our business is subject that could cause actual results to differ materially from those in any forward-looking statements are: (i) challenges inherent in developing and launching new products and services, including modifying and scaling manufacturing operations, and reliance on third-party suppliers for critical components; (ii) our ability to manufacture robust instrumentation and consumables; and (iii) the acceptance by customers of our newly launched products, which may or may not meet our and their expectations, together with other factors detailed in our filings with the
About Illumina
Illumina is improving human health by unlocking the power of the genome. Our focus on innovation has established us as a global leader in DNA sequencing and array-based technologies, serving customers in the research, clinical, and applied markets. Our products are used for applications in the life sciences, oncology, reproductive health, agriculture, and other emerging segments. To learn more, visit illumina.com and connect with us on X, Facebook, LinkedIn, Instagram, TikTok, and YouTube.
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