Events - Fabric Genomics

Events

Webinars

Protected: Unlock the full-potential of whole genome sequencing for genetic screening and diagnosis

May 16, 2022

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WEBINAR: A Universal AI-based Whole Genome Sequencing Solution for Genetic Screening and Diagnosis

April 7, 2022

April 14. VP Jeanette McCarthy presents as part of the Duke Center for Applied Genomics & Precision Medicine’s Spring 2022 Forum. Register now.

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

February 25, 2022

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.

Best Practices for Launching Profitable, Efficient NGS Tests for Hereditary Risk

June 9, 2021

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.

Implementation of Whole-Exome and Virtual Panel Testing for Rare Disease at a Children’s Hospital

February 1, 2021

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

Achieving Success With Next-Generation Sequencing: AI-Driven Scale and a Strong Reimbursement Strategy

October 28, 2020

Join us in this November 12th webinar with XIFIN, Inc. Learn best practices to implement and scale NGS panel testing in your lab.

Accelerating Your NGS Workflow for Rare Disease Diagnosis With Fabric GEM

October 19, 2020

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,

Near-instant identification of rare disease genes: A retrospective study of seriously ill children in the NICU using rapid WGS

March 18, 2020

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

Pathway to Success with Next Generation Sequencing- Reimbursement Insight and IT Strategies

September 5, 2019

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

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.

European Human Genetics Conference 2022

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.

WEBINAR: A Universal AI-based Whole Genome Sequencing Solution for Genetic Screening and Diagnosis

April 14. VP Jeanette McCarthy presents as part of the Duke Center for Applied Genomics & Precision Medicine’s Spring 2022 Forum. Register now.

Artificial Intelligence in Healthcare & Diagnostics Conference

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.”

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.

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.

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.”

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.”

Join us at the Frontiers in Pediatric Genomic Medicine Conference-2021

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

ACMG 2021 Virtual Meeting

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.

American Society of Human Genetics (ASHG) 2020

October 27-30th – Visit Fabric Genomics at the world’s largest online gathering of human genetics and genomics professionals.

TranslationalDx: Advances in Multi-omic Oncology Virtual Summit

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,

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