Fabric Genomics

Speakers from organizations at the forefront of combined monogenic and polygenic research will present their work leveraging emerging knowledge and their vision for providing genomic medicine care at population scale. They will share updates on developing tools, establishing large cohorts with high diversity, and putting a “rare and common” paradigm into clinical practice. Add this #ASHG2024 event to your calendar: https://bit.ly/4hsRntY #genetics #genomics #wholegenomesequencing

We're excited to be heading to Denver! We have so much in store for the American Society of Human Genetics, from the latest AI-driven innovations for rare diseases, hereditary conditions, and the NICU. Check out our busy schedule with our world-class leading laboratory collaborators from Broad Clinical Labs, Galatea Bio Inc., Nurture Genomics, Gene Kids (Intermountain Health) and BadgerSeq, including many posters from partners and customers at: https://bit.ly/4hm7l9c #Genetics #WholeGenomeSequencing #PrecisionMedicine #ASHG2024

What an incredible first day at #ICoNS24! We are so happy to be back surrounded by industry leaders and friends making newborn sequencing a reality. Martin G. Reese Dr. Mark Yandell Michael Vishnevetsky Dr. Ammira Al-Shabeeb AKIL #newbornsequencing #WGS #wholegenomesequencing

Whole Genome Sequencing (WGS) is well established for rapid diagnosis of critically ill newborns in the NICU and is now being advocated for population-scale Newborn Genome Sequencing (NGS) of healthy infants. In contrast to current approaches to variant prioritization and interpretation that model the data, GEM Transformer is an AI Intelligent Agent that models the human reviewer’s actions when interpreting WGS results. One of GEM Transformer’s most innovative features is its ability to solve simple cases on its own so a human reviewer will only be required for difficult-to-interpret cases. Catch Dr. Mark Yandell's presentation on GEM Transformer today! #ICoNS24 #GeneticTesting #NewbornScreening #WholeGenomeSequencing #RareDisease

Fabric is a proud sponsor of the International Consortium on Newborn Sequencing (ICoNS) 🌟 Presentations we are watching: Panel: NBSeq in 3/5/10 Years Moderator: Dr. Robert Green MD, MPH, BabySeq Time: Oct. 9 @ 9:40am Title: AI-enabled, Automated Interpretation for the NICU and Population Newborn Screening that is fast, accurate, and scalable Speaker: Dr. Mark Yandell, U. of Utah Time: Oct. 9 @ 10:20am Title: Rapid Care at Scale Speaker: Dr. Stephen Kingsmore, Rady Children's Hospital Time: Oct. 9 @ 10:40am Top Abstract: Genomic Newborn Screening for Variants in Cancer Predisposition Genes Associated with Increased Risk for Developing Early Onset Childhood Cancers: A Retrospective Approach to Developing Evidence-Based Gene Lists Speaker: Dr. Richard Parad, Brigham and Women's Hospital Time: Oct. 9 @ 1:50pm Fireside Chat: NBSeq in Greece: A National Initiative Moderator: Dr. Holly Peay, EarlyCheck Speakers: Adonis Georgiadis, Minister of Health of Greece; Dr. Petros Tsipouras, FirstSteps Time: Oct. 10 @ 11:30am Which presentations will you be watching? Meet our team at Booth #6. #WGS #newbornscreening #newbornsequencing

🧬 Fabric Genomics is a proud sponsor of the International Consortium on Newborn Sequencing (ICoNS). Meet us in New York, Oct 9-10, to see how leading programs are now accessing #WGS testing using Fabric's AI to meet the time-critical needs of our youngest patients. Schedule a meeting with one of our team: > CEO, Martin G. Reese > SVP of Business Development & Commercial Operations, Michael Vishnevetsky > VP of Clinical Operations and Clinical Genomics, Samuel Strom, PhD FACMG #ICoNS24 #GeneticTesting #NewbornScreening #NewbornSequencing #RareDisease

🧬 The Fabric Genomics team will be at National Society of Genetic Counselors' Annual Conference, September 17-21 in New Orleans, LA. Meet us at booth #318 to discuss how Fabric’s solutions accelerate accurate clinical interpretation by automating variant classification and clinical report generation. #ClinicalInterpretation #PrecisionMedicine #Genomics #Healthcare

Great meeting - back in San Diego next year! #AGBTPH

📢 descendantsDNA, has announced a new agreement with Broad Clinical Labs (BCL) to advance human longevity through cutting-edge genomics. BCL will provide whole genome sequencing and other genomic services for descendantsDNA, and, through an existing agreement, Fabric Genomics will provide its Fabric Enterprise software to analyze whole genomes. Fabric Genomics is transforming healthcare through its AI-driven interpretation of the human genome. Michael Vishnevetsky, Vice President of Business Development for Fabric stated, “As part of our existing partnership with descendantsDNA and the Broad Clinical Laboratory, we are excited to support this new collaboration and the prospects for preventative patient care through the use of genomics.” 👉 Read more about the agreement on Fabric's website: https://lnkd.in/dKs3Vn5V #longevity #humangenomics #WGS #genomicinterpretation #genomes #AIhealthcare

🧬 Join our presentation at AGBT - Advances in Genome Biology and Technology Precision Health! Title: A Framework to Advance Pediatric Precision Medicine at Scale Presenter: Martin Tristani-Firouzi, MD Where: Adams Ballroom, Thursday 09/05, 2:35 - 2:50 PM Discover how the "Primary Children’s Gene Kids" program at Intermountain Primary Children’s Hospital utilizes innovative computational tools and AI, from the University of Utah Health and Fabric Genomics, to support and scale accurate diagnostics in infants with rare genetic disorders. Don't miss out on learning about this transformative approach in pediatric healthcare! Join the talk or visit our team at booth #200. #Pediatrics #PrecisionMedicine #Genomics #Healthcare