Join Cincinnati Children’s Hospital’s Jaime Lopes and Fabric Genomics’ Jeanette McCarthy on September 23 for a presentation on the hospital’s transition to a streamlined variant interpretation workflow that utilizes Fabric Genomics’ software.
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April 14. VP Jeanette McCarthy presents as part of the Duke Center for Applied Genomics & Precision Medicine’s Spring 2022 Forum. Register now.
With increased payer scrutiny, labs need to know how to offer NGS tests that cost-effectively satisfy coverage requirements. Vice President of Precision Medicine Jeanette McCarthy shares strategies for developing such tests from design to reporting with Precision Medicine Incident’s Live Briefings on March 1 at 12p.m. ET.
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
March 14th, 2023 – Join us for this year’s ACMG in Salt Lake City. Learn more about Fabric Genomics on our Learning Lounge presentation.
Join Cincinnati Children’s Hospital’s Jaime Lopes and Fabric Genomics’ Jeanette McCarthy on September 23 for a presentation on the hospital’s transition to a streamlined variant interpretation workflow that utilizes Fabric Genomics’ software.
We will be at Precision Medicine World Conference in Silicon Valley. Visit our booth D2824 and participate on track 4 on June 29 at the Sequencing in the Neonatal and Pediatric Intensive Care, to hear industry leaders discussing genome-scale sequencing and how it could have widespread availability in pediatric care.
Watch our corporate satellite talk to learn more about our applications of whole-genome sequencing and artificial intelligence in detecting rare hereditary diseases and in newborn screening.
April 14. VP Jeanette McCarthy presents as part of the Duke Center for Applied Genomics & Precision Medicine’s Spring 2022 Forum. Register now.
May 10-11, 2022. CEO Martin Reese presenting on “Understanding how the Intersection of Artificial Intelligence with WGS Will Advance Precision Medicine and Improve Patient Care.”
March 24th, 2022 – Join us for this year’s ACMG Annual Clinical Genetics Meeting in a fully virtual format and watch our Product Theaters presentation.
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,
