Events - Fabric Genomics



Integrated End-to-End Solutions for Hereditary NGS Panel Testing

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.

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ASHG 2023

Come and meet our team at ASHG 2023, Washington, DC | November 1-5, 2023. Our team will be at booth 1215 presenting our AI-powered solutions for rapid, accurate genomic data analysis.

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AGBT Precision Health, 2023

Come and meet our senior team at AGBT Precision Health 2023, September 7-9, 2023, San Diego, CA. As well as sponsoring the welcome reception, you will be able to find our team at booth 101. We will also be delivering a company presentation on Saturday 9th at 12:30pm.

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ESHG, 2023

June 10-13, 2023, Glasgow, Scotland – Don’t miss our Head of Customer Success, Vanisha Mistry, PhD, who will be presenting: ”Enabling Rapid Clinical WGS & WES Analysis and Interpretation with an Advanced AI-Driven Platform”

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2023 Executive War College

April 25-26, New Orleans, LA – Join us as we discuss best practices for panel design, gene curation and variant interpretation and how Fabric software and clinical interpretation services are helping labs deploy NGS testing at scale.

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ACMG 2023

March 14th, 2023 – Join us for this year’s ACMG in Salt Lake City. Learn more about Fabric Genomics on our Learning Lounge presentation.

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Precision Medicine World Conference 2022

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.

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ACMG 2022

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.

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ESHG 2021

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.

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AMP Europe 2021

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.”

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PMLS Virtual Series 2021

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.”

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Read About Our Recent Partnerships: DNA Nexus | Oxford Nanopore Technologies
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