Genomic Variant Interpretation

0:05:15

Introduction to Genomic Variant Interpretation for Clinicians

0:43:44

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

1:33:13

Heidi Rehm: Genomic Variant Interpretation

0:55:29

Interpreting Genomic Variants for Inherited Cancer Risk and ELSI Considerations

0:04:19

Genomic Variants: Innocent Until Proven Guilty

0:30:20

Using Large Scale Genomic Databases to Improve Disease Variant Interpretation

0:37:36

OICR Mondays - Genomic Interpretation of Variants

0:30:47

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

0:14:50

The Untold Genetic Story of the Inuit People

0:37:58

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

0:44:54

AI-Driven Literature Curation for Determining Genomic Variant Pathogenicity

0:07:22

Introduction to the Genomic Variant Analysis and Clinical Interpretation Course 2020 - Vinod Scaria

0:21:47

Clinical Perspectives: Optimized Variant Interpretation with the Mastermind Genomic Search Engine

0:54:26

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

0:14:20

How to interpret the human genome | Alisha Holloway | TEDxClaremontColleges

0:12:15

Streamline Genomic Analysis with BaseSpace™ Variant Interpreter

1:02:33

FOCUS ON Principles for efficient and proportionate analysis of genomic variants

0:23:11

Clinical Perspectives: Optimized Variant Interpretation with the Mastermind Genomic Search Engine

0:54:53

Sharing Data about Genomic Variants: A Clinical and Scientific Imperative

0:30:11

E08.1 - Using genomic resources to interpret the clinical significance of rare variants

0:52:28

MPG Primer: ExAC & gnomAD: Using large genomic data sets to interpret human genetic variation (2017)

0:57:57

Towards Precision Medicine: Advances in Informatics for Genomic Variants Analysis

1:02:54

Webinar: Mining Genomic Literature for Variant Interpretation and Gene Panel Design

0:09:12

ACMG guidelines 2015: How to interpret genomic variants? [Today's paper]