Welcome to our dedicated page for Illumina news (Ticker: ILMN), a resource for investors and traders seeking the latest updates and insights on Illumina stock.
Illumina Inc (ILMN), a global leader in genomic sequencing technologies, provides critical tools advancing precision medicine and life science research. This dedicated news hub offers investors and industry professionals centralized access to official press releases, financial disclosures, and strategic updates directly from the company.
Track developments across key areas including quarterly earnings, sequencing platform innovations, and global health partnerships. Stay informed about regulatory milestones, product launches, and collaborations shaping the future of genomic analysis. Bookmark this page for unfiltered access to Illumina's latest announcements, enabling data-driven decisions in the rapidly evolving biotechnology sector.
Illumina (NASDAQ: ILMN) has announced a co-development agreement with SomaLogic to integrate the SomaScan® Proteomics Assay with its next-generation sequencing (NGS) platforms. This collaboration aims to enhance the high throughput proteomics market, enabling researchers to analyze thousands of samples for over 10,000 protein targets efficiently and cost-effectively. The partnership taps into the estimated $50 billion proteomics market, allowing Illumina to utilize its extensive NGS technology to boost multiomic research capabilities. Discussions regarding this partnership will take place at the J.P. Morgan Healthcare Conference on January 10, 2022.
Illumina (NASDAQ: ILMN) announced that its executives will present at the J.P. Morgan Annual Healthcare Conference on January 10, 2022. The presentation is set for 12:45 PM PT, followed by a Q&A session starting around 1:05 PM PT. Interested parties can access the live webcast via the Investor Info section on illumina.com. A replay will be available for at least 30 days post-event. Illumina continues to lead in DNA sequencing and array-based technologies, impacting various sectors such as life sciences and clinical markets.
Illumina (NASDAQ: ILMN) partners with Gretel.ai to create privacy-protected synthetic genomic data. This collaboration aims to enhance medical research by providing immediate access to statistically accurate genomic datasets without lengthy approval processes. The partnership demonstrates new use cases for synthetic data in genomics, promising advancements in drug discovery and genetic disorder treatment. With a focus on compliance with GDPR and CCPA, this initiative is poised to accelerate DNA sequencing analysis and medical breakthroughs for various health challenges, including COVID-19.
Illumina (NASDAQ:ILMN) announces support for a national precision medicine study in Norway called IMPRESS-Norway. This initiative aims to evaluate blood-based comprehensive genomic profiling (CGP) for selecting cancer therapies and assess its cost-effectiveness in the public healthcare system. The study will involve a sub-study of 500 patients, comparing solid tissue biopsies with blood samples. If successful, this could make less invasive CGP testing more accessible, enhancing patient participation in clinical trials. The analysis will utilize Illumina's DRAGEN software.
GRAIL, LLC has partnered with Alignment Health Plan to provide Medicare Advantage members in California and North Carolina access to Galleri®, a multi-cancer early detection blood test. Starting January 1, 2022, new and existing members can obtain the test, which detects over 50 cancers, many of which lack standard screenings. The initiative aims to enhance cancer detection among seniors, thereby potentially reducing late-stage diagnoses.
Illumina and Sequoia Capital China announced the first startups joining their Intelligent Healthcare Genomics Incubator in Shanghai, aimed at fostering genomics innovation. The selected companies, Mobidrop Biotechnology and Sequanta Technologies, will benefit from funding, business guidance, and access to Illumina's sequencing systems. This initiative highlights Illumina's commitment to developing China's genomics landscape and supports their localization strategy. Startups will be selected biannually, with applications for the next cycle open until March 1, 2022.
Illumina and Genetic Alliance launched the iHope™ Genetic Health program, a $120 million initiative to enhance access to whole-genome sequencing for patients with genetic diseases. The program aims to serve tens of thousands of individuals globally, focusing on underprivileged regions, particularly over one-third of resources directed towards Africa. This partnership will create networks of clinics and labs, enabling precision genomic diagnoses. Applications for genome sequencing will open in February 2022, improving diagnostic access for over 300 million individuals affected by genetic disorders worldwide.
Illumina reported third-quarter 2021 results featuring revenues of $1,108 million, a 40% increase year-over-year. GAAP net income was $317 million ($2.08 per diluted share), boosted by a $900 million gain from GRAIL. Non-GAAP earnings were $221 million ($1.45 per diluted share). R&D expenses rose to $436 million, while SG&A expenses surged to $879 million. Despite operational cash flow of $(272) million, Illumina anticipates revenue growth of approximately 36% for 2021. Meanwhile, the GRAIL acquisition is expected to drive market expansion.
Illumina (NASDAQ: ILMN) announced its sequencing and bioinformatics solutions are being used by HostSeq, part of Canada's COVID-19 Genomics Network, to analyze the genetic factors affecting COVID-19 susceptibility by sequencing genomes from up to 10,000 patients. This initiative aims to identify biomarkers to predict severe disease and assist in developing therapeutics. Illumina's Connected Analytics platform will ensure secure data sharing among researchers across Canada's leading facilities, supporting the HostSeq and VirusSeq programs. These efforts are crucial for public health insights and guiding COVID-19 responses.
Illumina (NASDAQ: ILMN) announced a collaboration with Israel's Ministry of Health for a pilot program implementing whole-genome sequencing (WGS) in NICUs for critically-ill infants suspected of genetic disorders. The initiative, starting this month, spans 18 hospitals and aims to provide faster diagnostics by replacing traditional tests. The program may lead to national reimbursement for WGS in Israel, enhancing clinical management and reducing NICU stays. Experts highlight the potential for improved decision-making in urgent neonatal situations.