Using Gene Families For Variant Interpretation & Identification Of Novel Disease-Associated Genes

Using Gene families for variant interpretation & identification of novel disease-associated genes

ClinGen Sequence Variant Interpretation WG: Updates and discussion on variant classification

ClinGen Resource

Presentation - Copy Number Variant Interpretation/Dosage Sensitivity Curation (Erica Andersen)

ClinGen Resource

ACMG AMP guidelines overview and optimization

ClinGen Resource

Presentation - Intro to Genome Analysis (Christina Austin-Tse)

ClinGen Resource

Use of Genetic Variant-Spectrum Evidence in the ACMG/AMP Sequence Variant Interpretation Guidelines

ClinGen Resource

Integrating Functional Studies into Variant Interpretation | Webinar | Ambry Genetics

Comprehensive Genomic Association Data for Genetic Variant Interpretation: A Computational Approach

Progress in Variant Interpretation for Cancer Susceptibility Genes: CanVar-UK Platform

Inherited Cancer Registry (ICARE)

Guidelines for Interpretation of Copy Number Variants - Arushi Batra

Genomics In India

Heidi Rehm: Genomic Variant Interpretation

University of Minnesota Consortium on Law & Values

Integrating Exome Variants with Other Genomic Data and Functional Annotations - David Adams

National Human Genome Research Institute

Finding literature for variant interpretation

ClinGen Resource

Variant Interpretation Challenges & Use Cases | Leveraging Mastermind in the Clinical Lab

Variant interpretation: how to accelerate the adoption of genomic diagnosis in dementia

Interpreting Incidentally Identified Variants in Genes Associated with Heritable Cardiac Disease

ATG Lab Brings New Understanding to Variants of Uncertain Significance | Webinar | Ambry Genetics

Using Large Scale Genomic Databases to Improve Disease Variant Interpretation

Microsoft Research

Presentation - Variant Classification using ACMG/AMP Guidelines (Steven Harrison)

ClinGen Resource

CLICC Day 5: Variant interpretation

South London Cardiovascular Networks