Fabric Genomics

Don't forget to register for Fabric Genomics' upcoming webinar with Ultima Genomics Learn how clinical researchers using WGS are improving their analysis pipelines and insights from: - Secondary analysis pipelines for UG 100 sequencing data - Accurately detection of copy number variants (CNV), structural variants (SV), and detect variants in segmental duplication regions - Seamless integration of Fabric Enterprise for a full E2E workflow Date: Tuesday, 19th November 2024 Time: 10am PST, 12pm CST, 1pm EST Register here> https://bit.ly/3CyT353 #NGS #Genomics #AI #PrecisionMedicine #Bioinformatics Ilya Soifer, PhD Steven Flygare, PhD Martin G. Reese, PhD

The era of ultra-rapid whole genome #sequencing has arrived! We're excited to see new institutions make rapid #genomics a reality. Contact us if you want to learn how you can too!

??Today?? Catch how leaders are working on providing population genomic medicine at scale! Need a reminder? Add this #ASHG2024 event to your calendar: https://bit.ly/4enERZP #genetics #genomics #wholegenomesequencing

?? Come celebrate the launch of Fabric Enterprise 3.0! ??Join us at booth #414 for a preview of the next generation of Fabric Genomics' GEM AI on Wednesday Nov 6, 12-1 p.m. ?? Add this event to your calendar here: https://bit.ly/3YQCTfV #genomics #genetics #wholegenomesequencing

Most newborns who could benefit from Ultra-Rapid WGS (defined here as 72 hours from sample to answer) do not have access to this revolutionary testing. This is in large part due to the lack of ubiquitous testing apparatus and the challenges of genomic interpretation at scale. In our CoLab session at #ASHG2024, experts in this field will explore the benefits of combining minimal footprint instrumentation and high-quality sequencing developed by Oxford Nanopore Technologies with the AI interpretation GEM algorithm developed by Fabric Genomics. ?? Add this session to your calendar: https://bit.ly/40snXWt #genomics #genentics #wholegenomesequencing

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