The newly formed partnership will enable clinical genomics laboratories to move from sample to evidence-backed analysis to actionable clinical reports using a push-button solution.
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”
Turning genomic data into Clinical Insight Powered by the most advanced AI algorithms, Fabric’s software and clinical services speeds up diagnostics across a range of clinical applications. Learn More Latest News Whole Genome Sequencing Intermountain Primary Children’s Hospital implements WGS for children with Congenital Heart Disease (CHD) Newborn Screening PlumCare and Fabric partner for Greece’s …
Data Sheet Download Data Sheet AI-driven tool for fast diagnosis of rare genetic diseases Benefits of Fabric GEM Fabric GEM is the fastest, most accurate interpretation solution available. Fabric GEM uniquely goes beyond filtering and ranking to provide a complete decision support platform. Fabric GEM’s unprecedented accuracy gives you the speed you need to scale …
Data Sheet Download Data Sheet A Seamless End-to-End Clinical NGS Analysis Solution, Fully Integrated with Fabric Enterprise Fabric Enterprise is an end-to-end precision medicine platform for genomic data analysis, interpretation, and clinical reporting. The platform enables labs to easily offer a more extensive diagnostic menu of reimbursable panels, as well as support whole exome and …
Turn raw genomic data into clinical insights with Fabric Enterprise Your comprehensive platform for NGS analysis, interpretation, and clinical reporting – powered by Fabric AI. Fabric GEM for Rare Disease Fabric ACE for Hereditary Risk Fabric Enterprise is a turnkey, scalable platform that speeds up clinical genomic analysis Request Demo Providing fast, accurate results for …
Discover the most advanced analysis toolkits for clinical genomics Schedule a demo Panels Validated across >100K variants Fabric ACE, empowered by artificial intelligence, delivers industry-leading speed and accuracy in genomic panel interpretation. Download WGS/WES 15 minute clinical review Fabric GEM combines deep genetic, phenotypic, and clinical data to achieve accurate causal gene candidate determination. Download …
Advanced hereditary risk screening at scale Inherited Cancer Cardiac Risk Newborn Screening ACMG Incidental Findings Fabric’s AI reduces turnaround time for analysis of NGS hereditary panels to minutes Try a demo Fabric’s Artificial Intelligence Classification Engine (ACE) synthesizes knowledge from disparate datasets to rapidly automate clinical reporting for all common hereditary risk panels Comprehensive coverage of most common genetic panels …
Fabric Genomics Partnerships Key industry leaders enabling AI-driven precision medicine SEE PARTNERS Fabric Featured Partners Roche As complementary pioneers in sequencing, Roche offers streamlined sample prep and Fabric Genomics offers robust analytics. We’ve partnered to provide a complete, end-to-end solution for a variety of genomic research areas, including rare disease and hereditary screening.Learn more XIFIN, …
XIFIN, Inc. + Fabric Genomics Fabric Genomics and XIFIN partner to expand access to clinical genomics EXPLORE AI-DRIVEN INSIGHT Expanding access to genomic testing Fabric Enterprise and XIFIN LIS together provide a seamless informatics solution for NGS testing. Now, clinical labs can quickly adopt advanced molecular genomic testing with a complete, best-in-class and integrated …
Roche + Fabric Genomics Roche and Fabric partner to deliver a rapid, end-to-end workflow from sample preparation to meaningful insight EXPLORE AI-DRIVEN INSIGHT Removing obstacles to success There can be many obstacles to success in next-generation sequencing and removing those could revolutionize research. First, an optimal workflow can help you get the most out of …
Meet Fabric GEM™ Webinar Demo 10:00 AM PT July 7th, 2020 Fabric GEM™ builds upon VAAST and Phevor, achieving near-instant identification of disease-causing variants in WGS & WES for rare disease diagnosis. Watch the Webinar APPLY FOR EARLY ACCESS Overview Fabric Genomics is excited to introduce the next-generation of our industry-leading AI for fast rare …
Meet Fabric GEM™ Webinar Demo 10:00 AM PT July 7th, 2020 Fabric GEM™ builds upon VAAST and Phevor, achieving near-instant identification of disease-causing variants in WGS & WES for rare disease diagnosis. Fabric GEM Early Access Program Open Now APPLY FOR EARLY ACCESS Overview Fabric Genomics is excited to introduce the next-generation of our industry-leading …
Truly accelerated genomic interpretation Fabric GEM utilizes AI to enable accurate and near-instant identification of disease-causing genes in WGS & WES REQUEST A DEMO More needles. Less haystack. Setting a new standard for diagnostic accuracy, Fabric GEM delivers advanced AI to rank the disease-causing variant at the top after a multi-dimensional analysis of all variants. …
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 …
New England Journal of Medicine publication showcases technology-driven variant detection platforms in accurately identifying causative genetic mutations
BLOG By Jeanette McCarthy, MPH, PhD By Martin Reese & Laura Yecies DOWNLOAD AS A PDF DOWNLOAD AS A PDF It has been nearly a decade since whole genome sequencing was first used clinically to diagnose a child with a rare idiopathic disease.1 Since then, thousands of rare disease patients have benefited from advances in …
BLOG By Laura Yecies By Martin Reese & Laura Yecies DOWNLOAD AS A PDF Precision medicine is a form of medicine that uses information about a person’s own genes or proteins to prevent, diagnose, or treat disease.1 When we think of precision medicine, we often focus on cancer and the recent efforts to specifically target …
BLOG By Charlene Son Rigby By Martin Reese & Laura Yecies Genomics provides the opportunity to realize the promise of personalized medicine, with tests scaling from single genes to comprehensive panels, exomes and whole genomes. Whole genome and whole exome sequencing provide a wealth of information to potentially identify the cause of disease in an …
Fabric Genomics and Genomenon announced today that they have entered into a partnership with the goal of further strengthening clinical genomic interpretation and variant classification. Fabric Genomics speeds and scales genomic interpretation by combining the most advanced AI algorithms with automated workflows, while Genomenon’s literature search engine facilitates comprehensive literature review, which is advantageous for …
