Search For Missing Variants In Large Exome Sequencing Projects By Optimization Of...

Search for Missing Variants in Large Exome Sequencing Projects by Optimization of...

Secondary or Incidental Findings from Exome Sequence Data - Jennifer Johnston

National Human Genome Research Institute

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

National Human Genome Research Institute

Danny E. Miller: Sequencing resolves complex SVs and identifies missing pathogenic variants in u...

Oxford Nanopore Technologies

Filtering Strategies for Identifying Germline Variants that Cause Disease - Leslie Biesecker

National Human Genome Research Institute

Using Large Scale Genomic Databases to Improve Disease Variant Interpretation

Microsoft Research

Utilizing exome sequencing analysis in solving rare genetic disorders - Júlia Baptista, PhD, Exeter

Twist Bioscience

Variant Annotation and Viewing Exome Sequencing Data - Jamie Teer

National Human Genome Research Institute

Deanna Church - Dissecting the diagnostic yield of exome sequencing

Long Reads to Identify Hidden Structural Variants in Rare Disease

Optimizing CNV Search Through Mastermind

Improved mutation detection with targeted sequencing

Twist Bioscience

Accelerating Time to Discovery with Whole Exome Sequencing on the Research Analysis Platform

[Webinar] HiFi Long-read Sequencing for Rare & Inherited Diseases

Pinar Bayrak Toydemir - Exome Sequencing as a Diagnostic Tool

The Need for Speed: Ultra Rapid Genome Sequencing for Critical Care | DoM Grand Rounds | 24 Aug 2022

Stanford Department of Medicine

Robert Nussbaum - Keynote Presentation - Variant interpretation in Molecular Diagnostics..

MIA: Ronen Mukamel, Imputed repeat polymorphisms point to variants driving genetic associations

Broad Institute

Matthew Lebo - Genome and exome sequencing in a clinical laboratory

Ryan Mills - Exploring Complex Structural Genomic Variation using Next Gen Sequencing