Illumina partners with customers to ensure data security At Illumina, we are proud of our track record of producing high-quality instruments and software suites that meet the changing needs of our diverse customer base. As part of that commitment to quality, we make ongoing efforts to assess our software for potential vulnerabilities and exposures. Most recently, we internally identified a vulnerability affecting Universal Copy Service (UCS), a proprietary software present on certain Illumina instruments. Upon identifying this vulnerability, our team worked diligently to develop mitigations to protect our instruments and customers. We then contacted and worked in close partnership with regulators and customers to address the issue with a simple software update at no cost, requiring little to no downtime for most. Illumina is committed to identifying and appropriately addressing potential vulnerabilities as part of our commitment to delivering quality products and ensuring data security. Regardless of what types of Illumina instruments or software our customers use, they can be assured that we keep the quality and security of our products of greatest importance. We are grateful to our customers for their partnership, and we will continue to proactively work with them to address any potential future concerns.
Alex Aravanis MD PhD’s Post
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I'm excited to announce the launch of Moonwalk Biosciences, a genomic medicine company pioneering precision epigenetic medicines, with $57 million in financing from Alpha Wave Ventures, ARCH Venture Partners, Future Ventures, GV, Khosla Ventures and YK Bioventures. The financing will support continued advancement of Moonwalk’s epigenetic profiling and engineering technology platform and progress its pipeline of epigenetic therapeutics towards the clinic. By targeting the epigenetic code – the software of the genome – Moonwalk aims to reprogram cells to their healthy state, fundamentally enabling a new approach to how therapies are discovered and developed. Moonwalk is the first company that couples an epigenetic discovery platform with precise engineering – opening up the epigenome as a new target space for complex diseases. Learn more here: https://moonwalk.bio/
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Exciting new research shared at ASCO last month supports comprehensive genomic profiling #CGP over single-gene testing as a starting point in treating non-small cell #lungcancer. Thank you to Phillip G. Febbo, MD, Vivek Subbiah, MD, and Prasanth Reddy MD, MPH, FACP for sharing their insights on the changing oncology landscape.
Cancer patients deserve the best care possible in order to have the best outcomes possible. During this year’s ASCO’s Annual Meeting, I sat down with Drs. Vivek Subbiah, MD and Prasanth Reddy MD, MPH, FACP to discuss a study that compared the results from single gene tests to comprehensive genomic profiling. Too often, focused tests deprive patients of valuable information about their tumors. This study, and other evidence, has shown that comprehensive testing provides better clinical insights to guide care. The next step will be to ensure all patients have access to primary CGP. Watch the full conversation below.
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https://www.youtube.com/
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Today we launched DRAGEN v4.2, our most comprehensive and accurate secondary analysis tool to date. Congratulations to the many team members at Illumina who worked on this latest update. Read more about the new targeted callers, machine learning algorithm, and improved accuracy across ethnically diverse samples in v4.2: https://lnkd.in/ggQdsvcm
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Illumina’s Accelerator program for seed-stage companies helped launch 74 companies and attracted more than $1.2B in third party investments over 15 funding cycles. Based on this legacy, we believe the time is right to evolve the Accelerator program by partnering with Illumina Ventures in order to create an even bigger impact on the genomics start-up industry. Congratulations to Illumina Ventures Labs!
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I'm proud of our team’s work on NovaSeq X, XLEAP-SBS Chemistry, and lyophilized reagents - helping sustainably accelerate access to genomics around the world.
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The groundbreaking genome research published last week in Science Magazine will enable conservationists to better understand and potentially slow the patterns of extinction among endangered primates. Learn more about the #WGS study of 809 individuals from 233 different primate species and what genetic mutations tell us about our closest living relatives. https://lnkd.in/gF-2Tgay
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