Meet Us at ASHG 2023
EXHIBIT DATES: November 2-4
Washington, DC, Booth #1215

Join our expert team at ASHG and discover how we can support you expanding your WGS and WES testing with confidence.

Icon - usability Meet Us Booth #1215

Learn more about Fabric Genomics and its best in-class clinical interpretation solution.

Our team will be on hand to answer all your questions. Find out how customers like Rady Children’s Institute and the Broad Clinical Lab are using Fabric Genomics to accelerate their WGS and WES testing. Plus, learn about the $1K sample-to-report clinical WGS service.

Book A Meeting


Industry Education Session

Fri 11/03, 3:30 to 4:30pm, Room 144A

Title: Accelerating biomedical research while also supporting clinical implementation and return of results with both WGS and a blended genome-exome


Diana M. Toledo, PhD, HCLD, Associate Lab Director at Broad Institute of MIT and Harvard 
Robert C. Green, MD, MPH Professor, Medicine, Harvard Medical School Geneticist, Medicine, Brigham and Women’s Hospital
Sean Hofherr, PhD, FACMG, Chief Operating Officer and Clinical Director, Fabric Genomics
Elizabeth Rountree, Diagnostics Lead, COMBINEDBrain



Icon - lightbulb CoLab

Thu 11/02, 4:30 – 5:00pm, CoLab Theater 1

Title: Long-Read Rapid Whole Genome Sequencing for NICU/PICU applications

Kamran Shazand,
PhD, Director of Genomics Institute, Shriners Children’s
Sean Hofherr, PhD, FACMG Chief Operating Officer and Clinical Director, Fabric Genomics
David Kulp, PhDVice President of Bioinformatics, Fabric Genomics

We will be launching an early access program available to event attendees, join us to learn more.


Fabric-Broad Happy Hour

Friday Evening 11/03

Fabric Genomics and Broad Clinical Labs are delighted to welcome you to a cocktail reception. Take this opportunity to learn more about our $1K sample-to-report clinical WGS service and network with your peers. 

Spacing is limited! Please register via the button below in order to attend.

Register Here

Learn about the $1K sample-to-report clinical WGS service. Visit our booth!

Discover More

Poster Presentation

Title: Leveraging AI to improve variant prioritization algorithms and scale whole genome analysis

Shana White, PhD, Fabric Genomics

Saturday 11/04 – 2:15 to 4:15pm


Platform talk – Rady’s

Title: A pilot prospective study of BeginNGS, an artificial intelligence-enabled genome sequencing system for newborn screening of 412 childhood genetic diseases

Kasia Ellsworth, PhD, FACMG, Rady Children’s Institute for Genomic Medicine

Thursday 11/02 – 9:45 to 10:00am

Poster Presentation

Title: N-of-1 personalized medicine: Identification of a putative small fiber peripheral polyneuropathy- causing mutation in the glycolytic intermediate enzyme, PHGDH

Max Glanz, PhD, University of Florida

Thursday 11/02 – 3:00 to 5:00pm