Happy National DNA Day! 🧬 Today, we celebrate the breakthroughs that have propelled our understanding in genetics and genomics, and guide our future innovations. Historically, structural variants have posed considerable challenges for study, despite being a significant source of variation within the human genome. With new and innovative technologies, like electronic genome mapping, researchers can now dive deeper into understanding genetic diseases, rare diseases, cancers, and much more. Celebrate National DNA Day with us and learn more about structural variants and electronic genome mapping here 👉 https://lnkd.in/geAc_3iZ #DNADay #DNA #Genomics #GenomicResearch #DNASequencing
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Edinburgh University scientists have been awarded £46.3m by the Medical Research Council for research into the "dark genome". The work will include research into the 98% of DNA which is underexplored, ultimately aiming to help people living with genetic conditions and cancer. The dark genome – which was previously referred to as “junk” DNA - is hoped could help provide new insights into complex genetic diseases. #genomics #funding #genetictesting #DNA #genetics
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Join this webinar from BioSkryb Genomics to learn about a groundbreaking method of whole genome amplification. 🧪🔬 Learn how primary template-directed amplification enables high-precision sequencing of individual cell genomes, uncovering genetic variation, somatic mutations and their impact on disease development. Webinar Speaker: Dr. Charles Gawad, MD, PhD, Associate Professor, Stanford University 👉 Reserve your spot now: https://buff.ly/3q9cL1r #SingleCellSequencing #Genomics #WholeGenomeSequencing
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Experienced Biotech, Diagnostics, and Genomics Professional - Currently looking for new opportunities.
UPCOMING WEBINAR: Assessing HiFi genomes as first-tier analysis in rare disease genetic research "Discover how highly accurate long-read sequencing (HiFi sequencing) on the PacBio Revio system is reshaping human genetics, uncovering variants inaccessible with short-read sequencing. In this webinar, professor Lisenka Vissers demonstrates how they confidently identified, using HiFi reads, a wide range of mutations – sequencing genomes with ~30-fold coverage of mutation-positive controls and rare disease cohorts." Sign up here: https://lnkd.in/gAG2h42g If you can't make the date, you will be sent a link to a recording shortly after the event provided you still have signed up. #RareDisease #Clinical #Genomics #HumanGenentics #HiFiSequencing #Revio #LRS #PacBio
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Investigating Genomics and Multi-Omics Sciences to Impact Neurodegeneration and Pharmacoresponse | Computational Biologist @ Columbia University
📣 Excited to share our latest paper about multiple system atrophy. Our research dives deep into the genetic of this rare and understudied neurodegenerative disorder. Special thanks to Dr. Sonja Scholz #NIH #NINDS and her amazing team and collaborators at #NIA, particularly to Ruth Chia and Anindita Ray! Read the full paper here! https://lnkd.in/enNbcfwz #Research #Science #Neurodegeneration #Genetics
Genome sequence analyses identify novel risk loci for multiple system atrophy
sciencedirect.com
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Chief, Section of Colorectal and Pelvic Reconstructive Surgery, Director- Comprehensive Colorectal Center, Program Director- pediatric surgery fellowship, Children's Mercy Hospital, University Missouri Kansas City
Better diagnoses for more kids: Ana Cohen, PhD, CMRI's asst. dir. of molecular genetics, talked to Global Genes about a new pilot to bring cutting-edge genetic testing to rural pediatric populations. Read more about the collab with Salina Pediatric Care.
Expanding Access to Genome Sequencing in Rural Populations
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Exploring the Genomics of Alzheimer's, discover how genetic research is unveiling the mysteries of Alzheimer's disease, paving the way for innovative treatments and early interventions. #genomics #alzheimersresearch #unlockingthegenome #geneticscience
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🔬 Exciting new research has uncovered genetic clues to the cause of restless leg syndrome (RLS)! ➡️Read more: https://bit.ly/3x4TKAA 🧬 This condition, prevalent among older adults, has long puzzled scientists. 🧑🔬 The breakthrough could lead to better identification of those at highest risk 🩺 and pave the way for new treatment options. 💡 Stay tuned as we explore these genetic insights to improve patient care. Credit: Nature Genetics #TUM #DNA #HealthcareInnovation #Genetics #RestlessLegSyndrome #meded #eMednews
Genetic Clues to Restless Leg Syndrome Uncovered - eMedNews
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Better diagnoses for more kids: Ana Cohen, PhD, CMRI's asst. dir. of molecular genetics, talked to Global Genes about a new pilot to bring cutting-edge genetic testing to rural pediatric populations. Read more about the collab with Salina Pediatric Care.
Expanding Access to Genome Sequencing in Rural Populations
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Celebrate the beauty of diversity and the power of genetics on this Albinism Awareness Day. Understanding albinism starts with knowing your genes. MyDNA offers cutting-edge genetic tests to help uncover the mysteries of conditions like Oculocutaneous Albinism (OCA) and guide you toward informed healthcare decisions. Explore our Multigene Panel Testing (OCA panel) or Whole Exome Sequencing by NGS. For family members, Sanger Sequencing is available for detailed screening. Genetic testing is recommended when: 1. Recurrence risk is a concern and prenatal diagnosis is being considered. 2. Signs of systemic involvement are present. Empower yourself with personalized insights to optimize your well-being 💪. Visit our website now(https://lnkd.in/gyM9taTg) and explore our customized DNA tests. #AlbinismAwarenessDay #Albinism #GeneticTesting #MyDNA #MultigenePanel #WholeExomeSequencing #SangerSequencing #GeneticHealth #GeneticDiversity #OCA #PrenatalDiagnosis #GeneticCounseling #HealthcareDecisions #FamilyHealth #GeneticScreening #MyDNA #MyDNAGeneProactive #MyDNAGeneProactivekids
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🎉 Excited to share our latest article titled "Computational Prediction of Crucial Genes Involved in Gonorrhea Infection and Neoplastic Cell Transformation: A Multiomics Approach"! Delving into the forefront of research, this work aims to illuminate critical genetic factors shaping our understanding of infection and cellular transformation. Dive into the insights and let's spark conversations on the future of genomic medicine together! 🧬💡 #Genomics #Research #Healthcare #Innovation
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