Fabric Genomics
@FabricGenomics
Fabric Genomics - AI‑Driven Clinical Insights for Genomic Data
Don't miss our presentation at #ACMGmtg24 annual meeting! Title: BadgerSeq: Developing a decentralized model for ultra-rapid long-read whole genome sequencing, with speakers from @nanopore and @uwmadison. Learning Lounge: Friday 03/15, 10:30 AM – 11:00 AM

#GalateaBio and #FabricGenomics team up to deliver comprehensive #genetictesting for common #geneticdiseases. By combining their capabilities, the partnership offers both rare variant and PRS reporting using the #BroadClinicalLab Blended Genome-Exome. bit.ly/3ZMe6Ke

Don't miss our poster session tomorrow: "AI-supported Identification of Disease-Gene Relationship Publications" Friday 21/03, 10:30 – 11:30AM Add to calendar: bit.ly/4ht8WJ5 #ACMGMtg25

Reminder: our exhibit theater presentation is tomorrow: "Why AI Matters in Today's Clinical Genomics - Accelerating Testing with Fabric GEM, a Cutting-Edge and Clinical Proven AI Tool" Exhibit Theater #2 Thur, 3/20, 12:30PM Add to calendar: bit.ly/4iVmbU7 #ACMGMtg25

🌟 Come celebrate the launch of Fabric Enterprise 3.0! 📍Join us at booth #414 on Wednesday Nov 6, 12-1 p.m. 📅 Add this event to your calendar here: bit.ly/4hBF0Me #genomics #genetics #wholegenomesequencing

We're excited to be heading to Denver! We have so much in store for #ASHG24, from the latest AI-driven innovations for rare diseases, hereditary conditions, and the NICU. Check out our busy schedule at: bit.ly/3A9La5e #Genetics #WholeGenomeSequencing #PrecisionMedicine
🧬 The Fabric Genomics team will be at @agbt Precision Health. Meet us at booth 200 and learn how Fabric Genomics is scaling precision medicine for pediatrics in genetic testing programs for top children's hospitals!

We are thrilled to welcome Sam Strom to the Fabric Genomics team as our new VP of Clinical Operations and Clinical Genomics! Sam is a true innovator in the field, bringing years of expertise that will drive our mission forward. #genomics #WGS #genomesequencing

Exciting news! With a grant from the WARREN ALPERT FOUNDATION, @Intermountain Primary Children's Hospital announces creation of “Primary Children’s Gene Kids” a 3-year, major pediatric genomics initiative to help children with genetic conditions. #WGS bit.ly/3Wvkyme
The Fabric team will be at #ESHG2024. We're delighted to have partnered with @nanopore to pair long-read ultra-rapid whole genome sequencing with AI based interpretation for the NICU. Find us at Oxford Nanopore's booth #310, to learn more!

Heading to the Executive War College? Join Michael Vishnevetsky for an expert presentation on using Fabric Genomics' software and Clinical Services to help children's hospital labs to implement rapid and ultra-rapid WGS for kids in the NICU/PICU. #ExecutiveWarCollege

🌟 We're very happy to share the exciting news of Vanisha Mistry's promotion to VP of Customer Success! She's been an incredible force on our team for many years, embodying dedication, creativity, and unwavering expertise every single day. Congratulations Vanisha!

Don't miss our presentation at #ACMG2024 meeting. Implementing WGS on infants admitted to the CICU at @Intermountain Health's Primary Children’s Hospital in collaboration with the @BroadGenomics Clinical Labs and #FabricGenomics 03/14, 11:15 AM – 11:45 AM bit.ly/4bVpqIk

Today, on @rarediseaseday we stand together to raise awareness and support for those facing uncommon challenges. We're dedicated to making a difference in the lives of individuals and families affected by rare diseases. 🤝 #Genomics #PrecisionMedicine #RareDiseases

We are attending the #ACMG2024 Annual Meeting. Visit our website to learn more about our exciting schedule of events. bit.ly/42WKABJ. Meet our team at booth #806 and learn about our $1K sample-to-report clinical WGS service. #WGS #genomics #ACMG24

If you're at @agbt, don't miss this talk on the exciting progress towards population scale newborn sequencing by @radychildrens Institute for Genomic Medicine: Leveraging population databases & machine learning models to scale whole genome newborn sequencing, 06/02, 4:40-5pm
