Recent Updates
Recently added Catalysts
ILMN Positive Sentiment Score: 82/100

Illumina and Nashville Biosciences Announce Sequencing Agreement with Amgen Illumina Inc. (NASDAQ: ILMN), a global leader in DNA sequencing and array-based technologies, and Nashville Biosciences LLC, a wholly owned...

Key Takeaway: Illumina Inc. and Nashville Biosciences have collaborated on an agreement with Amgen to conduct whole-genome sequencing of approximately 35,000 DNA samples, predominantly from African Americans. This initiative seeks to address the underrepresentation of diverse populations in genomic research and aims to create the largest dataset of its kind. The project is part of a broader multiyear effort to accelerate therapeutic development through extensive genomic data, with insights expected to impact drug discovery and health disparities among underrepresented groups.

Market Sentiment Analysis

POSITIVE FACTORS

  • Agreement will sequence 35,000 diverse genomic DNA samples.
  • Aims to broaden understanding of underrepresented populations in genomic research.
  • Will create a large data set to accelerate drug discovery and therapeutic development.

Full Press Release Details

Whole-genome sequencing of 35,000 de-identified, diverse genomic DNA samples will begin this month
SAN DIEGO , Jan. 9, 2023 /PRNewswire/ -- Illumina Inc. (NASDAQ: ILMN ), a global leader in DNA sequencing and array-based technologies, and Nashville Biosciences LLC, a wholly owned subsidiary of Vanderbilt University Medical Center (VUMC), today announced an agreement with Amgen, a global biopharmaceutical company, to whole-genome sequence approximately 35,000 DNA samples. The sample cohort is primarily made up of DNA from African Americans, who are currently underrepresented in research for the clinical applications of genomics, including drug target discovery. This cohort will be the largest data set of genomes of its kind to date.
Sequencing this set of samples is the first in Illumina and Nashville Biosciences' Alliance for Genomic Discovery (AGD), a multiyear agreement to accelerate therapeutic development through large-scale genomics and establish a preeminent clinico-genomic data set.
Launched in 2022, the AGD aims to whole-genome sequence at least 250,000 de-identified human DNA samples from VUMC's BioVU biobank over two and a half years in collaboration with multiple biopharmaceutical companies. The BioVU samples were extracted from blood collected during routine clinical testing. The patients who provided them consented to research use, and the samples are linked to extensive de-identified clinical data derived from VUMC's electronic medical records.
"The initial cohort will be among the largest sequencing efforts involving African Americans to date," said Leeland Ekstrom , chief executive officer of Nashville Biosciences. "Once complete, this data set will provide a wealth of new information about the human genome and accelerate the study of disease in—and discovery of new therapeutics for—populations less well represented in prior large-scale sequencing efforts. The opportunity to sequence this diverse set of samples will help broaden our understanding for individuals who have been underrepresented in genetic research and continue to experience health disparities."
As part of the agreement announced today, deCODE genetics, a wholly owned subsidiary of Amgen, will perform whole-genome sequencing on the 35,000 samples using Illumina sequencing technologies and will upload the data to the Illumina Connected Analytics platform.
"deCODE's sophisticated human data capabilities are well positioned to sequence these samples and analyze the resulting data to provide a better scientific understanding of disease through the context of human diversity," said Kári Stefánsson, founder of deCODE genetics. "Insights from human data, including both genetics and clinical records, can help inform how medicines may affect different patient populations."
Pharma and biotech collaborators that plan to participate in the AGD and in further sequencing may soon be announced. Researchers will analyze the data for drug discovery and therapy development. The data will also be returned to BioVU to be made available for academic research within the Vanderbilt community.
Illumina is improving human health by unlocking the power of the genome. Its 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. Illumina's 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 Twitter , Facebook , LinkedIn , Instagram , and YouTube .
Nashville Biosciences, a wholly owned subsidiary of Vanderbilt University Medical Center (VUMC), was created to harness the Medical Center's extensive genomic and bioinformatics resources for drug and diagnostics discovery and development. Leveraging Vanderbilt University innovation, Nashville Biosciences serves as a commercial interface between outside companies and the formidable research capabilities housed within VUMC, including BioVU®, one of the world's most comprehensive genetic databases linked to de-identified medical records with years of longitudinal clinical data. This unique asset is one of the largest and highest quality of its kind, providing an opportunity to guide R&D activity in biotech, pharma, diagnostics, medical devices, and other life sciences applications. For more information, please visit nashville.bio .
Investors: Salli Schwartz 858-291-6421 [email protected]
Media: Illumina: David McAlpine 347-327-1336 [email protected]
SOURCE Illumina, Inc.

21 %

Frequently Asked Questions

What is the purpose of whole-genome sequencing in this study?

The sequencing aims to enhance drug target discovery and understand diseases in underrepresented populations.

How many DNA samples will be whole-genome sequenced?

Approximately 35,000 diverse genomic DNA samples will be sequenced.

Which populations are primarily represented in the DNA samples?

The samples primarily consist of DNA from African Americans.

What is the Alliance for Genomic Discovery (AGD)?

AGD is a multiyear agreement to accelerate therapeutic development through large-scale genomics.

Who will perform the whole-genome sequencing?

deCODE genetics, a subsidiary of Amgen, will conduct the whole-genome sequencing.

Last updated: Jan 9, 2023