#Research | 𝗘𝗻𝗵𝗮𝗻𝗰𝗶𝗻𝗴 𝘁𝗵𝗲 𝗔𝗿𝗰𝗵𝗶𝘃𝗶𝗻𝗴 𝗼𝗳 𝗚𝗲𝗻𝗲𝘁𝗶𝗰 𝗗𝗮𝘁𝗮 | Led by Dr. Deborah M Leigh from Eidg. Forschungsanstalt WSL, an international team of researchers has achieved a significant milestone in genetic data management. They propose standardized formats for different types of genetic and genomic data, along with the mandatory inclusion of extensive metadata, enhancing data accessibility for researchers worldwide. The research emphasizes the importance of archiving genetic data in these proposed standardized formats. By ensuring comprehensive metadata and adopting these standards retroactively for older data, the research aims to enable more accessible, equitable, and innovative use of genetic data on a global scale. Photo: National Cancer Institute on Unsplash 👉 Learn more >> https://lnkd.in/gHVuWJtM 👉 Original publication >> https://lnkd.in/eSy6QSX8 🇨🇭 Follow #ScienceSwitzerland for the latest news and emerging trends on Swiss science, technology, education, and innovation >> swissinnovation.org Follow us >> Science-Switzerland #Science | #Education | #Research | #Innovation
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This Mission Continues at IndyGeneUS AI!!! This is a major step towards future research studies that will address misdiagnosis of endometriosis, uterine fibroids and PCOS in underrepresented women populations globally. Understanding these conditions at the molecular level will be critical. Extremely honored that IndyGeneUS AI got to work with all the co-authors of this published paper. #genomics #diversitymatters #womenshealth #indygeneus
We are very proud to announce our first paper has been accepted for publication using Digital Twins and Genomics: “The Application of Knowledge Engineering via the use of a Biomimetic Digital Twin Ecosystem, Phenotype Driven Variant Analysis, and Exome Sequencing to Understand the Molecular Mechanisms of Disease.” Authors and affiliations: William G. Kearns (Co-founder/CEO and Chief Scientific Officer of Genzeva and LumaGene); J. Georgios Stamoulis (QIAGEN Digital Insights); Joseph Glick and Lawrence Baisch (RYLTI BioPharma); Andrew Benner, Dalton Brough, Luke Du (Genzeva); Bradford Wilson (IndyGeneUS AI); Laura Kearns (Genzeva and LumaGene); Nicholas Ng, Maya Seshan, and Raymond Anchan (Brigham and Women’s Hospital, Harvard University). Running Title – Digital Twins and Molecular Medicine.
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Labroots Announces the 12th Annual Precision Medicine: Genomics, Genetics & Molecular Diagnostics Virtual Event Series 2024 — PRBuzz.co — Join Labroots on May #15 #2024 for the 12th #Annual #Precision #Medicine #Virtual #Event #Series #exploring the #latest in genomics, #genetics and molecular diagnostics, with keynote #speakers #dynamic #sessions and #opportunities for continuing education. YORBA #LINDA Calif., May #9 2024 Labroots, the leading scientific #social #networking #website and #producer of #educational virtual #events and webinars, proudly announces the upcoming 12th Annual Precision Medicine Virtual Event Series. This #premier virtual #conference scheduled for May 15, 2024, invites worldwide experts and enthusiasts to explore the latest innovations and advancements in precision medicine. This year's event will dive deep into the cutting-edge areas of genomics, genetics, and molecular diagnostics, pivotal in the ongoing revolution of personalized healthcare. With a packed full agenda, renowned speakers and industry leaders will present on transformative topics such as NGS Based Genetic Testing, Genetics and Genomic Based in vitro Diagnostics, AI in Medicine, and much more. Keynote Presentations
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Labroots Announces the 12th Annual Precision Medicine: Genomics, Genetics & Molecular Diagnostics Virtual Event Series 2024 — MediaContacts.co — Join Labroots on May #15 #2024 for the 12th #Annual #Precision #Medicine #Virtual #Event #Series #exploring the #latest in genomics, #genetics and molecular diagnostics, with keynote #speakers #dynamic #sessions and #opportunities for continuing education. YORBA #LINDA Calif., May #9 2024 Labroots, the leading scientific #social #networking #website and #producer of #educational virtual #events and webinars, proudly announces the upcoming 12th Annual Precision Medicine Virtual Event Series. This #premier virtual #conference scheduled for May 15, 2024, invites worldwide experts and enthusiasts to explore the latest innovations and advancements in precision medicine. This year's event will dive deep into the cutting-edge areas of genomics, genetics, and molecular diagnostics, pivotal in the ongoing revolution of personalized healthcare. With a packed full agenda, renowned speakers and industry leaders will present on transformative topics such as NGS Based Genetic Testing, Genetics and Genomic Based in vitro Diagnostics, AI in Medicine, and much more. Keynote Presentations
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This video below showcases the following: - How Oxford Nanopore Technologies' partnership with PRECISE and Novogene is driving significant advancements in genetic research and healthcare, particularly for ethnically diverse Asian populations that are often underrepresented in genomic databases. This collaboration has the potential to transform healthcare by enabling early disease prediction in Asia, opening new frontiers in precision medicine on a global scale. - Sequencing at Scale capabilities: Leveraging our fleet of high-output PromethION sequencers to deliver long-read data for 10,000 genomes within a 12-month timeframe. - Showcasing the advantages of the technologies: smaller footprint (accessible), faster and automated high-throughput barcoded library preparation, qLIMS (end-to-end sample management) and the ability to generate complete and highly accurate long genome sequence reads. - Oxford Nanopore is proud to be involved in this programme (Learn more: https://bit.ly/3XsUZTk). Together we think we can have a dramatic impact on healthcare outcomes through precision medicine, at a population scale for the Singaporean population. Thanks to all the key stakeholders involved in this effort. Thomas Bray - 唐睿, man chun leong, Justin Lee, Sheanne Weixuan Soh, Diana Koh, Dalya Tay, Kingsley Tan (陈礼杰), Rodrigo Toro Jimenez, Balamurugan Periaswamy, Wesley Tan, Lin Jin, @Zhenzhen Lei #precisionmedicine #oxfordnanopore #novogene #sequencingatscale
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The Cambridge AI Club for Biomedicine returns on 7th March, and this time Dr. Fatima Baldo and I will be discussing Knowledge Graphs. We'll share insights on the practical applications and challenges of implementing them in various domains. In my presentation, I'll explore the intersection of Knowledge Graphs and Graph Databases in the fascinating world of Graphs. Next, I'll discuss transforming our data into #FAIRdata to gain wisdom. Then, I'll take a glimpse into AstraZeneca's current graph realm, and how using Federated Queries to overcome silos helps us increase the value of our data. The final part will focus on how we utilise #GenerativeAI to support scientists and professionals in having engaging conversations about the content of their very own Knowledge Graphs! Let's get together and exchange ideas. I do hope to see you there! #CambridgeAIClub #Biomedicine #KnowledgeGraphs #AI
The Cambridge AI Club for Biomedicine is back on 7th March, and this time we'll be exploring the theme of "Knowledge Graphs." Our speakers for the evening, Dr Fatima Baldo (Milner Therapeutics Institute) and Dr Antonio Fabregat Mundo (AstraZeneca), will guide us through the practical applications and challenges of implementing Knowledge Graphs in various domains. Following the talks, feel free to join for pizza, drinks and casual networking: connect with fellow attendees and share your thoughts on the evolving landscape of Knowledge Graphs. A big thanks to our organising committee: Dr Namshik Han, Prof Florian Markowetz, Holly Giles, PhD, Dr Susanne Bornelöv, Dr William Prew, Dr Ines Prata Machado, Nicholas Marios Katritsis, Sofia Radrizzani, Dr Dr Gehad Youssef, Dr Fatima Baldo, Dr Alessandra Cardinali, Seokjun Lee, Dash Tirtharaj, Anna-Maria P., Joanna Du And to our sponsors for the continued support: Milner Therapeutics Institute, Cancer Research UK Cambridge Institute, CardiaTec Biosciences There is no need to sign up, see you on the 7th of March! https://lnkd.in/dP728xmM #knowledgegraphs #ai #bioinformatics #event
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📢 Unlocking Spatial Biology: Overcoming Challenges with MACSima™ 🔍 The article discusses the challenges in spatial biology and how they can be overcome using the MACSima™ Platform. 🧬 Spatial biology combines different "omics" techniques to gain a deeper understanding of human health and disease. 🌟 The MACSima™ Platform enables the staining and imaging of a large number of targets, providing valuable insights into the tissue microenvironment. 🔬 Solid tumor cancers are particularly challenging, but the MACSima™ Platform can help characterize the tumor microenvironment. 🔍 Miltenyi Biotec offers a wide range of immunologically relevant antibodies for use with the MACSima™ Platform. 🧪 The platform also includes advanced informatics tools for data analysis and interpretation. 💡 By increasing marker availability, reducing panel optimization time, and enabling simple data analysis, the challenges in spatial biology can be addressed effectively. #BioprocessUpdates #SpatialBiology #MACSimaPlatform #OmicsTechniques #TissueMicroenvironment #SolidTumorCancers #ImmunologicallyRelevantAntibodies #DataAnalysis #InformaticsTools #MarkerAvailability #PanelOptimization #DataInterpretation #SpatialBiologyChallenges #MACSimaInsights #MiltenyiBiotec #DataAnalysisTools ▷ Read the full article here: 📎 https://lnkd.in/dkwib9CP
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𝐀𝐝𝐯𝐚𝐧𝐜𝐢𝐧𝐠 𝐏𝐫𝐞𝐜𝐢𝐬𝐢𝐨𝐧 𝐌𝐞𝐝𝐢𝐜𝐢𝐧𝐞 𝐰𝐢𝐭𝐡 𝐍𝐆𝐒 𝐒𝐚𝐦𝐩𝐥𝐞 𝐏𝐫𝐞𝐩𝐚𝐫𝐚𝐭𝐢𝐨𝐧 📌𝐃𝐨𝐰𝐧𝐥𝐨𝐚𝐝 𝐅𝐫𝐞𝐞 𝐏𝐃𝐅𝐬 𝐚𝐭: https://lnkd.in/dCkB6eE8 (𝙐𝙨𝙚 𝘾𝙤𝙧𝙥𝙤𝙧𝙖𝙩𝙚 𝙈𝙖𝙞𝙡 𝙄𝙙 𝙛𝙤𝙧 𝙌𝙪𝙞𝙘𝙠 𝙍𝙚𝙨𝙥𝙤𝙣𝙨𝙚) In the #world of #genomics, precision starts with the right sample preparation. #Next #Generation #Sequencing (NGS) Sample Preparation is revolutionizing the way we approach genetic analysis, ensuring that each sample is optimized for the most accurate and reliable results. Whether it's advancing #cancer research, unlocking the mysteries of rare diseases, or pushing the boundaries of personalized medicine, #NGS sample preparation is the critical first step. As we continue to innovate in this space, the potential to improve patient outcomes and accelerate scientific discovery is immense. 🔬 𝐖𝐡𝐲 𝐍𝐆𝐒 𝐒𝐚𝐦𝐩𝐥𝐞 𝐏𝐫𝐞𝐩𝐚𝐫𝐚𝐭𝐢𝐨𝐧 𝐌𝐚𝐭𝐭𝐞𝐫𝐬: ✔ 𝐏𝐫𝐞𝐜𝐢𝐬𝐢𝐨𝐧: Every detail counts in capturing the full genetic landscape. ✔ 𝐄𝐟𝐟𝐢𝐜𝐢𝐞𝐧𝐜𝐲: Streamlined processes lead to faster, more reliable outcomes. ✔ 𝐈𝐧𝐧𝐨𝐯𝐚𝐭𝐢𝐨𝐧: Advanced techniques are paving the way for new discoveries in healthcare, diagnostics, and personalized medicine. Let's drive the future of healthcare together by focusing on the foundation—perfecting the NGS sample preparation process. 🌟 📌𝐒𝐨𝐮𝐫𝐜𝐞: NASA GeneLab 📌𝐃𝐢𝐬𝐜𝐥𝐚𝐢𝐦𝐞𝐫: I don't intend any copyright (DM me for credit & removal) #NGS #Genomics #PrecisionMedicine #HealthcareInnovation #NextGenSequencing #LifeSciences #NGS #Genomics #SamplePreparation #PrecisionMedicine #Innovation #Healthcare #Biotech
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Proteoforms: Unlocking Biology’s Next Frontier. The evolving field of proteomics is at a pivotal moment, with proteoforms emerging as the new currency of precision biology. As described in the article by Lloyd M. Smith and Neil Kelleher, proteoforms — the various molecular forms of proteins — hold the key to unlocking complex biological functions. Yet, the current paradigm of studying proteins often falls short. While traditional 'bottom-up' methods fragment proteins to infer identities, these approaches can’t capture the full complexity of proteoforms. We need new technologies capable of characterizing these variants with the same depth that next-generation sequencing (NGS) brought to DNA. This is where Lunar Bio comes in. Our platform is designed to map proteoforms directly, offering deep granularity and overcoming the limitations highlighted by the authors. Imagine a world where every form of a protein can be tracked and studied, revealing precise insights into disease mechanisms, potential drug targets, and biomarkers that drive personalized medicine. The possibilities extend far beyond identifying known post-translational modifications (PTMs) like phosphorylation or glycosylation. We aim to uncover the untapped "dark matter" of biology, providing insights into the proteoform networks that underpin diseases like Alzheimer’s and cancer. By establishing a comprehensive atlas of proteoforms, we’re not just changing the way proteins are studied; we’re laying the foundation for a new era in drug discovery and diagnostics. At Lunar Bio, we believe that understanding proteoforms is the next step in transforming healthcare. Just as NGS unlocked genomics, we aim to unlock proteomics — one proteoform at a time. Check out the full article to dive deeper into the challenges and promises of proteoform research, and join us in pioneering a new era of precision medicine! https://lnkd.in/ea2pEBzi #Proteomics #Proteoforms #PrecisionMedicine #BiomarkerDiscovery #LunarBio #DrugDiscovery #Diagnostics
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At the Human Cell Atlas General Meeting, 10x Genomics announced plans to make single cell analysis more affordable. They aim to offer large-scale analysis at $0.01 per cell, launching this quarter, with capabilities for up to 2.5 million cells per run, making it ideal for high-throughput applications like CRISPR screens. The company is focused on reducing costs to make single cell analysis accessible for all researchers. Upcoming products will allow small-scale experiments at about $560 per sample, encouraging wider adoption in biological research. 10x Genomics has also introduced cost-saving innovations like the Chromium GEM-X, which improves efficiency and lowers per-cell costs, and the affordable $25,000 Chromium Xo instrument. These efforts help maintain their leadership in single cell technology. Read the full article on Pathology News: https://lnkd.in/e5zQQc9k #digitalpathology #pathologynews
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Exciting news in the field of genomics... The National Human Genome Research Institute (NHGRI) has committed $6.7 million to develop faster, cheaper, and more accurate sequencing technologies. These advancements have the potential to revolutionize healthcare, research, and medicine. 👏 👏 Check out the link below for more information. 👇 https://lnkd.in/eVVTEdGW In addition, Oxford Nanopore Technologies announced breakthrough performance data and new platform updates at their annual conference. Their direct RNA sequencing technology supports the emergence of RNA-based therapies, and they are driving towards democratizing sequencing technology for everyone, everywhere. 👏 👏 Learn more about their impressive updates in the link below.👇 https://lnkd.in/ei-g9Fmt These advancements underscore a thrilling era of innovation in genomics! #Genomics #DNASequencing #RNAResearch #Biotechnology #Innovation
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