📣 Calling all ISV 2024 attendees in Porto, Portugal! Make sure to catch our CTO Ivan Limongelli as he takes the stage for a panel discussion on "Enhancing genomic variant interpretation with machine learning models" tomorrow at 1:50pm! It's an opportunity not to be missed, so mark your calendars and join the conversation! 📚For more information on the program: https://lnkd.in/epqdKPqZ #ISV2024 #AIingenomics #enGenome
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Using microarrays, our senior researcher Piotr Lisik can examine 50,000 genes from Atlantic salmon at one go. Indeed, this amazing tool can "turn genes into pixels, and pixels into knowledge". Scroll our post below for more fascinating numbers and facts. #SkrettingInnovates
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GDC 2.0 centers around the idea of building cohorts, or custom groups of cases for genomic analysis. Use the Cohort Builder tool to create and modify cohorts, import and export cohorts, and load cohorts for analysis using the GDC’s other tools https://buff.ly/3OGTHAC #NCIGDC #ResearchDiscovery
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Join our webinar on June 26 to learn about DRAGEN v4.3's next-gen multi-genome reference, new mosaic caller, and specialized MRJD callers. Discover how these innovations can enhance your genomic analysis accuracy and efficiency!
Illumina DRAGEN v4.3: Comprehensive coverage with leading edge innovations
illumina.com
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enabling digital services for Student Loan related activities while maintaining the highest security standard, the most compliant personal data protection and customer-centric data-driven innovation.
Exciting news in genomics data compression! We've just published a new blog post on arXiv (2404.02163v1) introducing FastqZip, an enhanced reference-based compression framework for FASTQ format files. Our work showcases FastqZip's ability to achieve a higher compression ratio than state-of-the-art algorithms, enabling more efficient storage and archiving of next-generation sequencing data. Learn more about this innovative approach: https://bit.ly/4aDr0NB
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What if you could: 🔵 Investigate thousands of genes at subcellular resolution. 🔵 Discover more than ever before with deeper cellular and spatial insights. 🔵 Explore your data with nearly instant results. Find out with Xenium, and take your ‘what if’ to ‘what next’. https://bit.ly/3EsTQSI
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Will you be at #ASHG23? Meet me at Booth 511 for a demo of #MastermindGSE and learn how we’re making genomic information actionable. We will be unveiling a game-changing update so stop by for your personal demo!
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Join our webinar on June 26 to learn about DRAGEN v4.3's next-gen #multigenomemapping, new mosaic caller, and specialized callers. Discover how these innovations can enhance your genomic analysis accuracy and coverage!
Illumina DRAGEN v4.3: Comprehensive coverage with leading edge innovations
illumina.com
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The 1st NovaSeq X Plus right here in the heartlands of #SoutheastAsia! See how we're bringing greater access to genomics services and discover the exciting capabilities the #NovaSeqXPlus offers to researchers. Our journey is just getting started. Watch what Thomas Neo at Illumina and Justin Lee at Novogene AMEA (APAC, Middle-East & Africa) have to say. https://lnkd.in/gxyGcPHj
Now with Greater Access to Genomics Services with Southeast Asia's First NovaSeq X Plus!
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Some great insights in to the impacts machine learning advancements are having on the Life Sciences industry.
Roger Wahman, Chief Technology Office, explores how machine learning is revolutionizing the life sciences industry, from disease identification, image analysis, to human genome mapping. Read more: https://lnkd.in/gqu-VD3z #ValueReimagined #artificialintelligence #lifesciences
