June 23, 2021. Register for the free webinar in partnership with Dark Daily and get access to the post-webinar recording. Learn effective strategies for implementing tertiary analysis tools and a scalable interpretation workflow.
Register now for this March 9th GenomeWeb webinar on lessons learned from successful clinical implementation of NGS panel testing at Cincinnati Children’s Hospital Medical Center
Join us in this November 12th webinar with XIFIN, Inc. Learn best practices to implement and scale NGS panel testing in your lab.
A novel AI-tool for near-instant identification of disease causing variants. Register now for the October 22nd Webinar to see a powerful new algorithm, Fabric GEM,
In this webinar, Francisco De La Vega will introduce the Fabric GEM AI algorithm and demonstrate how it significantly simplifies and improves disease-causing variant identification
Labs from every sector- private, reference, hospital, and academic- may be considering expansion of their test offering to include next generation sequencing (NGS). However, before
In this presentation by Fabric Genomics, Dr. Katarzyna (Kasia) Ellsworth, Associate Laboratory Director at Rady Children’s Institute for Genomic Medicine, discusses the launching and scaling
Genomic medicine’s growth is transforming healthcare, delivering precision diagnoses and targeted therapies. Artificial intelligence approaches are needed to help clinicians cope with the rapidly increasing
Martin Reese speaks on a panel on the state of genomics and its role in healthcare. Moderated by Rasu Shrestha, Chief Innovation Officer at UPMC, the Webinar was hosted by the Center for Connected Medicine. Other panelists included Jill Hagenkord (Chief Medical Officer at Color), Mylynda B. Massart (Co-Investigator at All of Us Pennsylvania), and Houman Modarres (Senior Director of IP networks at Nokia).
August 28-31st. Come learn about our gene prioritization algorithm that analyzes both SNVs and SVs in a single step, enabling rapid identification of causal variants for rare genetic diseases.
June 14-18th. Join us at AMP Europe 2021 to learn more about our novel AI-based solution, GEM in our poster “An Artificial Intelligence Based Approach for Rapid Diagnosis of NICU Patients.”
June 10th. Join us for this year’s free Precision Medicine Leadership Summit on Precision Medicine & Rare Disease. Dr. Jeanette McCarthy, MPH, PhD will speak on “Strategies for Improving the Diagnostic Yield of WGS/WES in Rare Disease.”
April 21-23th – Visit our virtual booth and learn from international genomics leaders. See how we partnered with Rady Children’s Hospital to achieve world-record diagnostic
April 13-16th – Join us for this year’s ACMG Annual Clinical Genetics Meeting in a fully virtual format and watch our Product Theaters presentation.
October 27-30th – Visit Fabric Genomics at the world’s largest online gathering of human genetics and genomics professionals.
Register now for the upcoming Translational Dx summit and see our presentation “Avoiding the common mistakes labs make when launching hereditary cancer panel tests“ Wednesday,
