Webinar

Conferences

CONFERENCE

ACMG 2023

March 24 2022, Virtual

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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.

CONFERENCE

ACMG 2022

March 24 2022, Virtual

Read More

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.

News & Press

WEBINAR | May 16, 2022

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

Diagnostic sequencing for rare disease using whole genome/exome sequencing is becoming a routine part of care for critically ill newborns as well as children with undiagnosed diseases. This is possible due to advances in genome sequencing and AI methods that provide intelligent data analysis. At Fabric, we are leveraging our GEM AI technology, currently used by labs for diagnostic sequencing, for identifying disease-causing variants among ostensibly healthy individuals in the screening setting. Potential applications, including the use of GEM for genome-wide newborn screening, carrier testing and adult hereditary risk profiling, will be discussed.

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WEBINAR | January 21, 2019

PMWC 2019 talk: Genomics and artificial intelligence as enablers of precision medicine

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 volumes of genomic data. Dr. Francisco De La Vega, Senior Vice President of Genomics at Fabric Genomics, spoke at Precision Medicine World Conference (PMWC) 2019 and talked about how AI …

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WEBINAR | March 21, 2019

Implementing and scaling a rapid whole genome sequencing test at Rady Children’s Institute for Genomic Medicine

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 clinical NGS testing in a children’s hospital environment, utilizing Fabric Enterprise for the rapid interpretation of genomic data to decrease turnaround time and increase diagnostic yield. Rady is advancing rapid …

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WEBINAR | September 5, 2019

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

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 implementing NGS, there are a number of factors that lab leaders must carefully consider to ensure that successful implementation and sustainability of their NGS program. Join XIFIN and Fabric Genomics …

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WEBINAR | March 18, 2020

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

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 over prior methods, substantially reducing genome interpretation time in the diagnosis of monogenic disease, and could allow cost-effective, automated reanalysis of undiagnosed cases over time. 

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WEBINAR | February 25, 2022

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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