Report: Clinical Genome (ClinGen) Resource - Erin Ramos and Sharon Plon
GGMC Expanding Skills Series: "The Clinical Genome Resource (ClinGen)"
Whole genome sequencing: From sample to report
E08.1 - Using genomic resources to interpret the clinical significance of rare variants
Reading a genomic test report
Variant interpretation: from the clinic to the lab… and back again
WHO Genomics Report Breakdown: Global PGx Opportunities : Live Workshop
GenomeConnect Webinar - Genetics 101 and How to Read Your Lab Report
Genomics on FHIR - Patrick Werner | FHIR DevDays 2025
NACHGR Director's Report (September 2020)
Understanding Genomic Sequencing Video - Brigham and Women's Hospital
ClinGen and ClinVar: Complementary resources - Erin Riggs
GenomeConnect Webinar: How to Read a Genetic Testing Report
ANNUAL REPORT – Genomic Medicine Working Group of NACHGR – Teri Manolio
An Introduction to Resources Facilitating Cancer Variant Interpretation
Genomes2People's MedSeq Project
Presentation - Intro to Genome Analysis (Christina Austin-Tse)
Locus Reference Genomic (LRG) resource
Whole Genome Sequencing: Meet the interpretation team
Webinar #1: Reflections on the Report from the Rare Disease Community
