Join our expert team at ASHG and discover how we can support you expanding your WGS and WES testing with confidence.
Meet Us Booth #1215Learn 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.
Industry Education SessionTitle: Accelerating biomedical research while also supporting clinical implementation and return of results with both WGS and a blended genome-exome
Speakers:
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
CoLabTitle: Long-Read Rapid Whole Genome Sequencing for NICU/PICU applications
Speakers:
Kamran Shazand, PhD, Director of Genomics Institute, Shriners Children’s
Sean Hofherr, PhD, FACMG Chief Operating Officer and Clinical Director, Fabric Genomics
David Kulp, PhD, Vice 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 HourFabric 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.
