📣 Announcing Wellcome Connecting Science Engagement and Society as a Saturday Exhibitor at #RAREfest24 Sequencing DNA to Understand How our Bodies Work DNA is the instruction book for our bodies. But how do we read it? And how is our growing understanding of DNA changing medicine? Wellcome Genome Campus are on a mission to enable everyone to explore genomic science and its impact on research, health and society. Drawing on the ground-breaking research taking place on the Wellcome Genome Campus, Connecting Science inspires new thinking, sparks conversation, supports learning, and measures and understands global attitudes and perspectives. https://lnkd.in/eGTtJQqr Join us at RAREfest24 in Cambridge on 23 November, where the Wellcome Genome Campus team will be exploring DNA sequencing practically with real-world examples. “We can’t wait for RAREfest – speaking with people at this festival sparks so many ideas and emotions. It really opens up what DNA science means for them and that changes what it means for us.” To find out more and get your tickets, head over to our website: https://lnkd.in/eWw2X4uf
Cambridge Rare Disease Network (CamRARE)’s Post
More Relevant Posts
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Research Scientist, UArizona / Harvard University (postdoc); Open For Collaboration
Our new paper "PLEKv2: predicting lncRNAs and mRNAs based on intrinsic sequence features and the codingnet model" is published in BMC Genomics. Aimin Li, Haotian Zhou, Siqi Xiong, Junhuai Li, Saurav Mallik, Rong Fei, Yajun Liu, Hongfang Zhou, Xiaofan Wang, Xinhong Hei, Lei Wang, "PLEKv2: predicting lncRNAs and mRNAs based on intrinsic sequence features and the Coding-Net model", BMC Genomics, 25, 756 (2024). https://lnkd.in/gmiZGWhS [Impact Factor: 4.4].
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𝗝𝗼𝗶𝗻 𝘁𝗵𝗲 𝘀𝗶𝗻𝗴𝗹𝗲 𝗰𝗲𝗹𝗹 𝗿𝗲𝘀𝗲𝗮𝗿𝗰𝗵𝗲𝗿 𝗰𝗼𝗺𝗺𝘂𝗻𝗶𝘁𝘆 𝗳𝗼𝗿 𝗶𝗻-𝗽𝗲𝗿𝘀𝗼𝗻 𝗻𝗲𝘁𝘄𝗼𝗿𝗸𝗶𝗻𝗴 𝗮𝘁 𝗦𝗶𝗻𝗴𝗹𝗲 𝗖𝗲𝗹𝗹 𝗕𝗶𝗼𝗹𝗼𝗴𝘆 𝟮𝟬𝟮𝟰 𝗰𝗼𝗻𝗳𝗲𝗿𝗲𝗻𝗰𝗲! #SCB2024 𝗖𝗼𝗻𝗳𝗲𝗿𝗲𝗻𝗰𝗲 𝗱𝗮𝘁𝗲𝘀: 10-12 June 2024 Register for your in-person place by 14 May 2024! ⏰ 📎📎 Click for more details about the programme: bit.ly/48ZARNM Join a global community of biologists, methods developers and systems modellers, for discussion focused on these key questions: - How do cells cooperate and compete in tissues and organs? - How does a cell’s past predict its future? - What are the cell and non-cell autonomous mechanisms of disease? - How can we predict what cells will do next? - What are the evolutionary principles of cellular robustness? - How are complex phenotypes regulated by the genome? Participate in discussion that will shape the landscape of the field. We are looking forward to excellent talks and presentations, including keynotes from: 🗣️ Marianne Bronner, California Institute of Technology, USA 🗣️ Sarah Teichmann, Wellcome Sanger Institute, UK Watch this video to find out more about the benefits of attending a single cell conference in-person: 📽️ https://lnkd.in/gwtCuhvA #SingleCells #SingleCellResearch #MolcularBiology #EvolutionaryBiology #Genomics #AcademicChatter #PhDchat #PhDlife
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There was a lot of 'omics sizzle at this years' AGBT, and I'm not talking about the wicked sun-burns. In this weekend's issue of Omicly, premium members ($5/month) get access to my hot-take on all of the new technology that was announced at this year's conference. Companies I cover include: Ultima Genomics Element Biosciences 10x Genomics Complete Genomics Singular Genomics Nanostring N6Tec Oxford Nanopore PacBio Illumina Volta Labs But if industry tech updates aren't your thing, the free issue includes: 1) 80% of patients with an autoimmune disease are women, we are now beginning to understand why 2) Mass Spec is leading the charge in bringing high-throughput proteomics to a lab near you 3) The "most beautiful experiment in biology" was performed by Meselson and Stahl in 1957 Supporters ($1/month) and above also get access to the Omicly Weekly Reading List! Catch it here: https://buff.ly/49a9e4d
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🌟 Don't Forget to Register! 🌟 Our "Single Cell Genomics Event" with 10x Genomics and Asst. Prof. Tolga Sutlu is just around the corner! If you haven't registered yet, now is the time. This event is a unique chance to explore groundbreaking advancements in genomics, connect with experts, and expand your knowledge in this exciting field. Seats are filling up fast, so make sure to secure your spot! 🔗 Register now: https://lnkd.in/drZkKm7D Looking forward to seeing you there and diving deep into the world of single cell genomics! #10xgenomics #singlecellsequencing #genomics
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Attending #PMWC next week! Excited to connect with other professionals and learn about the latest innovations in precision medicine. If you're also attending, let's connect and meet in person! Phase Genomics
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🌟 Exciting News from NanoString! 🌟 We're thrilled to introduce the CosMx Human 6K Discovery Panel – a revolutionary tool in single-cell spatial analysis, is now shipping! Get ready to explore over 6,000 RNA targets and unlock secrets in nearly every human biological pathway. 📍 Join Us at AGBT 2024! 📍 📅 February 5-8 | 📍 Orlando, Florida 🔍 Highlights: -Be among the first to witness whole transcriptome imaging with CosMx SMI – a new era in spatial biology! -Discover how the CosMx Human 6K Discovery Panel, equipped with advanced cell segmentation algorithms, can transform your spatial analysis. 🌐 Exclusive Session Alert! 🌐 Don't miss our 'Morning Buzz' session at 8:00 AM ET, February 6th, in the NanoString suite (Curacao 1) at AGBT. Hear firsthand from leading spatial opinion leaders about the future of 6K and High Plex spatial multiomics. #SpatialMultiomics #SpatialBiology #AGBT2024 https://bit.ly/48Y6ff2 #SingleCellImaging #SpatialMultiomics #CellSegmentation #SpatialBiology This post may include information regarding CosMx™ SMI products for RNA detection, which products are not available in the member states of the European Unified Patent Court, as further described here - https://bit.ly/498JPIB.
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Reflecting on the monumental impact of the Human Genome Project—a landmark endeavor that mapped out our genetic blueprint nearly two decades ago. This ambitious project not only unraveled the intricacies of our DNA but also paved the way for groundbreaking advancements in bioinformatics. Today, we continue to harness the wealth of data generated by this endeavor, driving discoveries in personalized medicine, disease understanding, and beyond. Proud to be part of a field that continues to unlock the secrets encoded within our genome, shaping the future of healthcare and scientific innovation. #HumanGenomeProject #Bioinformatics #GenomicRevolution
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NEW: Our own Professor Sunduz Keles, a leading researcher at the intersection of statistics and genomics, has been awarded funding from the Chan Zuckerberg Initiative! Prof. Keles and Prof. Emery Bresnick from the UW School of Medicine and Public Health will lead a project entitled "Multi-Modal Single Cell Data Tensors For Gene-Enhancer Links." The team will work to develolp new methods for understanding the complex relationship between genes and cells. Learn more about this leading-edge work: https://ow.ly/vjKX50SShQZ #BiomedicalInformatics #GenomicsResearch
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Pleased to share that our paper ("Differences in 5'untranslated regions highlight the importance of translational regulation of dosage sensitive genes") is now published and available at: https://lnkd.in/dTkWMUCM. To explore 5'UTR architecture and how variants within them may create or disturb upstream open reading frames (uORFs), check out vUTR https://lnkd.in/dYF-9-Z8
