Meet our team at Frontiers in Pediatric Genomic Medicine 2025 to see how our partners are using rapid WGS and Fabric’s AI interpretation platform to deliver time-critical, accurate genetic testing in the NICU – helping infants get the answers they need, when they need them.
ACMG 2024 Learning Lounge Presentation: Implementing WGS on infants admitted to the CICU at Intermountain Primary Children’s Hospital in collaboration with the Broad Clinical Labs and Fabric Genomics
A GenomeWeb On Demand Webinar, Sponsored by Fabric Genomics and Illumina
Watch our on-demand webinar delivered by Mark Yandell as part of Rady Children’s Institute for Genomic Medicine’s Rapid Precision Medicine Grand Rounds series: ‘AI, Genomes, Electronic Health Records and the NICU’
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
Fabric Genomics is at the forefront of AI-driven genomic interpretation. Meet us at booth #415 to learn more about our:
– $1000 clinical genome provided in collaboration with Broad Clinical labs
– integrated sample-to-report rapid nanopore sequencing analysis platform for neonatal/pediatric intensive care units to support clinicians in acute settings
– and more!
Meet our team at booth #414 and learn how Fabric is empowering fast, accurate genomic interpretation at a price that empowers adoption today.
Meet us at ICoNS and learn how our AI-enabled, automated interpretation platform for NICU and population newborn sequencing is fast, accurate and scalable.
Meet us at booth #318 to discuss how Fabric’s solutions accelerate accurate clinical interpretation by automating variant classification and clinical report generation.
Meet us at booth #200. Don’t miss a presentation by pediatric cardiologist Dr. Martin Tristiani-Firouzi on September 5 at 2:35pm, “A Framework to Advance Pediatric Precision Medicine at Scale”. He will be sharing how he uses Fabric’s AI and Broad Clinical Labs’ sequencing solutions to expand access to genetic testing for infants at Intermountain Primary Children’s Hospital.
Please join Michael Vishnevetsky, SVP of Business Development, as he presents a Master Class on Wednesday, May 1, from 8:30 to 9:20 AM.
Discover how Fabric Genomics’ software and Clinical Services can empower children’s hospital labs to implement rapid and ultra-rapid whole genome sequencing for NICU/PICU patients.
Additionally, Michael will also participate in a panel discussion on “Business and Marketing Strategies for Genetic Laboratories in the Current Market” on Tuesday, April 30, from 3:45 PM to 4:35 PM.
Come and meet our team at ACMG 2024, Toronto, Canada | March 13-15, 2024. Our team will be at booth 806. Learn more about Fabric Genomics and its best in-class clinical interpretation solution and clinical services.
Come and meet us at PMWC. Our team will be at Booth #B928. Plus, don’t miss our talks to learn more about the significance of AI in interpreting vast datasets and its importance in clinical practice.
– Shana White, Fabric Genomics. Jan 25, Day 2: 10 AM – Showcase Track S2
– Dr. Mark Yandell, University of Utah (invited talk). Jan 24, Day 1: 9:45 AM Track – AI and Data Science in Clinical Practice Track
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.
Come and meet our team at Global Genomic Medicine Consortium (G2MC) 2023, October 2-4, Geneva, Switzerland
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.
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”
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.
April 19-20, La Jolla, California – Join us and discover how GEM AI can revolutionize diagnosis in NICUs and PICUs by overcoming the challenges of genomic variant interpretation, leading to improved outcomes and more equitable care.
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.
