Excited to share a new series here on our LinkedIn. We’re highlighting members of the Deep Genomics team - and who better to start this series than our founder and CIO, Brendan Frey! Read more about Brendan’s background, including his previously published work and papers, and his work at University of Toronto. Learn more about Deep Genomics, and find out more about how to join our team, at https://lnkd.in/d8fB4GZ. #deepgenomics #teamspotlight #toronto #bosto
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Research Operations | Product Commercialization | Partnerships & Business Development | Evidence Generation | Enterprise Strategy
If you're interested in the science of predictive intelligence (the prediction of rare events from limited, highly uncertain data in complex systems) read the article recently published by I and peers at Michigan State University! There is relevance not only to diagnostics, genomics, and health outcomes, but for the TRANSLATION of a technical science to a practical, straightforward tool.
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Leveraging PacBio data for WGS germline variant profiling? Microsoft Azure can work with that. Run your analyses , and make new discoveries, faster and more cost effective, on a workflow optimized and scalable for projects big and small. #genomics
Did you know that PacBio now have a range of computational tools designed to take advantage of the unique properties of highly accurate, HiFi long reads within human genomics? Please reach out to me to find out more
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Making Life Science Research Easy! Enabling End-to-End Solutions to bring your solution to market and your vision to life
Dynabeads magnetic beads: Empowering ancient DNA research and beyond. Discover how their role in the Nobel Prize-winning study of Neanderthal genomics has paved the way for advancements in modern healthcare: https://bit.ly/3uVWH5D #Dynabeads #NobelPrize #GenomicAdvancements #NGS
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Dynabeads magnetic beads: Empowering ancient DNA research and beyond. Discover how their role in the Nobel Prize-winning study of Neanderthal genomics has paved the way for advancements in modern healthcare: https://bit.ly/3uVWH5D #Dynabeads #NobelPrize #GenomicAdvancements #NGS
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🤔 What can businesses learn from people’s everyday thoughts? 🌟 Since 1969, Howard Moskowitz has been asking this very question, leading to the development of Mind Genomics – the method fueling our idea battle tests here at ISTS! 💡 To learn more on how you can stress test your venture idea, visit https://istsimulator.io/
The Origins Of The Science Of The Everyday - Mind Genomics | Dr. Howard Moskowitz
https://www.youtube.com/
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Prevailing scientific assumptions often die hard, especially when they fit so neatly into an evolutionary view of life. On this episode of ID The Future, Dr. Casey Luskin discusses the paradigm shift in thinking about "junk DNA": https://lnkd.in/gGFQU_bY #DNA #junkdna #intelligentdesign #evolution
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As science and technology continue to advance at a rapid pace, one of the most remarkable achievements of our time has been the mapping of the human genome. This remarkable feat, accomplished through years of dedicated research and collaboration, has ushered in a new era of understanding about the very foundation of human life. The human genome, composed of approximately 3 billion base pairs, contains the genetic instructions that define who we are. By deciphering this intricate code, scientists have gained unprecedented insights into the genetic underpinnings of human health, disease, and evolution. Through the analysis of the human genome, we now have a deeper understanding of: - The genetic basis of inherited diseases and the potential for targeted therapies - The complex interplay between genes and environmental factors that shape our physical and cognitive traits - The evolutionary history of our species and our shared genetic heritage with other living organisms Moreover, the application of this knowledge has opened up new frontiers in personalized medicine, forensics, and even the exploration of our ancestral origins. By unraveling the mysteries of our DNA, we are empowered to make more informed decisions about our health, unlock new avenues for medical treatment, and gain valuable insights into our collective human story. As we continue to push the boundaries of genomic research, the implications for our understanding of ourselves and our place in the world are truly profound. This scientific breakthrough represents a transformative milestone in the history of humanity, one that will undoubtedly shape the course of our future. #HumanGenome #Genomics #PersonalizedMedicine #Evolution #Science
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Join us to explore #scGPT, the cutting edge of single-cell genomics! Register here: https://lnkd.in/gMzPFRPF While texts are made up of words, cells can be characterized by genes. Based on that idea, scGPT makes use of pre-trained transformers that have been trained on an extensive dataset containing over 33 million single-cell records, efficiently capturing meaningful biological insights into genes and cells. Read the research paper at https://lnkd.in/gQmmXWS2 to learn more about scGPT. We are excited to announce that Dr. Bo Wang, one of the authors behind scGPT, will be presenting at our October 2023 webinar. Come explore this extraordinary AI-driven technology that has the potential to transform biology with us! #BioTuringwebinar #whenAImeetsBiology #singlecell #genomics
Welcome! You are invited to join a webinar: scGPT: Towards Building a Foundation Model for Single-Cell Multi-omics Using Generative Al. After registering, you will receive a confirmation email about joining the webinar.
us02web.zoom.us
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The June issue of my newsletter The Genomics Landscape is out! Read about exciting updates from NHGRI and the field of genomics. I work with my staff to make each newsletter an informative read! Check out the latest issue here: https://lnkd.in/ekN89pDi
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