Variant Interpretation

1:00:34

Variant Interpretation in Cancer Susceptibility Genes

1:01:59

Panel Presentation: Mitigating Variability in Somatic Variant Interpretation with Live Q&A

0:43:44

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

0:34:51

MPG Primer: Rare Variant Interpretation (2024)

0:42:09

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

0:37:58

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

1:00:04

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

0:44:54

AI-Driven Literature Curation for Determining Genomic Variant Pathogenicity

1:33:13

Heidi Rehm: Genomic Variant Interpretation

1:00:59

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

0:24:41

How to use population frequency data in variant interpretation process

0:48:03

WGS Variant Calling: Variant calling with GATK - Part 1 | Detailed NGS Analysis Workflow

1:10:28

Dr. Bryan Gall - Variant Interpretation: The Achilles Heel of Clinical Genetics and Genomics

0:03:18

AION Demo | AI-driven Variant Interpretation

0:49:49

Variant interpretation, literature curation, and clinical trials, oh my! How to simplify somatic...

0:27:48

E15.1 Variant Interpretation in Hereditary Colorectal Cancer Syndromes Lessons Learned from INSIGHT

1:07:23

Variant Interpretations in NGS

0:04:08

Varsome, Clinical Variant Interpretation Tool

0:04:27

Somatic Variant Classification with VarSome

0:05:24

How to use population frequency data in variant interpretation process

0:40:29

Introduction to the ACMG & AMP Guidelines for Interpretation of Sequence Variants - Abhinav Jain

0:18:04

Coordinating Variant Interpretation Knowledgebases

0:11:13

CanVar-UK Variant Interpretation Platform Updates

0:30:47

Clinical Interpretation of Genomic Variants - What we need to keep in mind - Dr. Vinod Scaria