Videos - Fabric Genomics

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Featured Videos

Accelerating Precision Medicine with Low-Cost Whole-Genome Sequencing: An Expert Panel Discussion

Rady Grand Rounds Webinar 2023

Additional Videos

Ready to experience Fabric Enterprise?

Featured Videos

Accelerating Precision Medicine with Low-Cost Whole-Genome Sequencing: An Expert Panel Discussion

Rady Grand Rounds Webinar 2023

Additional Videos

Fabric Genomics Overview [2 min]

Implementing and scaling a rapid WGS test at Rady Children’s Institute for Genomic Medicine

Avoiding the common mistakes labs make when launching hereditary cancer panel tests

Achieving Success With Next-Generation Sequencing: AI-Driven Scale and a Strong Reimbursement Strategy

The Bottom Line: Strategies for Labs to Offer Cost-Effective Genetic Testing at Scale

The Need for Speed: How Fabric GEM Will Enhance Rapid Whole Genome Sequencing Interpretation at RCIGM

Fabric GEM: The next great leap in genome interpretation

Accelerating Your NGS Workflow for Rare Disease Diagnosis With Fabric GEM: A novel AI-tool for near-instant identification of disease causing variants

ASHG 2020 CoLab: Expanding the Capabilities of AI in Genome Interpretation: Simultaneous Prioritization of Sequencing and Structural Variants

The Diagnostic Odyssey: Perspectives and Key Learnings from Patient Organisations and Industry

An artificial intelligence method for fast diagnosis of rare genetic disease

Fast turn around time with rapid whole genome sequencing

Phenotypic prioritization with Fabric Enterprise

Amazon Web Service (AWS) Case Study Feature

GEM will find structural variants: A different approach

SV discovery and prioritization with GEM

Applying AI to variant classification

An artificial intelligence method for fast diagnosis of rare genetic disease

Genomics and artificial intelligence as enablers of precision medicine

PMWC 23 "How will Cheap Genome Sequencing Impact Genomic Medicine" - Panel Discussion

Rady Grand Rounds Webinar - AI, Genomes, Electronic Health Records and the NICU - Mark Yandell PhD

ACMG 2023 - Heidi Rehm PhD, and Marina DiStefano PhD, from Broad Institute of MIT and Harvard discuss opportunities for whole genome sequencing in clinical practice

Fabric Turnkey Solution (1 MIN)

Fabric Genomics Overview (2 MIN)

Rapid identification of SVs in WGS data from 60+ rare disease cases (24 MIN)

SV analysis improves diagnostic yield of WGS/WES genetic tests (1 MIN)

Fabric's GEM algorithm overcomes challenges with detecting SVs (1 MIN)

ASHG 2020 CoLab

WGS at Rady Children's Hospital (57 MIN)

Best practices for launching hereditary cancer panel tests (26 MIN)

How to scale NGS testing with a strong reimbursement strategy (55 MIN)

Implementation of whole-exome and panel testing at Cincinnati Children's Hospital (55 MIN)

Strategies for cost-effective NGS testing (40 MIN)

Practical considerations for scalable NGS testing (4 MIN)

Fabric GEM at Rady Children's Institute for Genomic Medicine (12 MIN)

Fabric GEM Introduction (3 MIN)

Keys to successful NGS testing reimbursement (1 MIN)

Panels are a scalable way to generate revenue from NGS (1 MIN)

Cost interpretation savings per NGS panel test (1 MIN)

Fabric's clinical services and tips for launching panel testing (1 MIN)

Accelerating Your NGS Workflow for Rare Disease Diagnosis (41 MIN)

AI genome interpretation for sequencing and structural variants (46 MIN)

Healx Webinar: The Diagnostic Odyssey (1 HR)

An AI method for fast diagnosis of rare disease (41 MIN)

Fast turnaround time with rapid WGS (1 MIN)

Phenotypic prioritization with Fabric Enterprise (1 MIN)

Amazon Web Service Feature (3 MIN)

GEM will find structural variants (3 MIN)

SV discovery and prioritization with GEM (4 MIN)

Applying AI to variant classification (28 MIN)

Rapid WGS of seriously ill children in the NICU (46 MIN)

Highlight: An AI method for fast diagnosis of rare disease (7 MIN)

Genomics and artificial intelligence as enablers of precision medicine (13 MIN)

Ready to experience Fabric Enterprise?

Fabric's clinical services and tips for
launching panel testing (1 MIN)

Healx Webinar:
The Diagnostic Odyssey (1 HR)

Fast turnaround time with rapid WGS
(1 MIN)

Phenotypic prioritization with
Fabric Enterprise (1 MIN)

SV discovery and prioritization with GEM
(4 MIN)

Applying AI to variant classification
(28 MIN)

Rapid WGS of seriously ill children
in the NICU (46 MIN)