NGS 28: Clinvar

preview_player
Показать описание

  1. Advanced VnPathoinformatics
Рекомендации по теме
NGS 28: Clinvar 0:24:26

NGS 28: Clinvar

The NCBI Minute: 0:09:54

The NCBI Minute: Find All Variants with ClinVar

ClinVar Miner 0:34:46

ClinVar Miner

WGS Variant Calling: 0:43:24

WGS Variant Calling: Variant Filtering and Annotation - Part 2 | Detailed NGS Analysis Workflow

Automated Variant Classification 0:27:01

Automated Variant Classification in QIAGEN Clinical Insight Shows Near Perfect..

A Sample to 0:32:29

A Sample to Insight Solution for Detection and Classification of Challenging Pathogenic

Optimizing Drug Development: 0:03:28

Optimizing Drug Development: An overview of the Human Somatic Variant Database (HSMD)

NGS: Target-Enrichment Strategies 2:00:41

NGS: Target-Enrichment Strategies Enable Precision Medicine

Call and filter 0:01:20

Call and filter variants with FreeBayes and the VCFlib toolkit

Elaine Lyon - 0:59:39

Elaine Lyon - Clinical Interpretation of Sequence Variants

Clinical Genomicist Workspace 0:43:06

Clinical Genomicist Workspace CGW Accelerate Your NGS Testing with an End to End Integrated Workspa

DNASTAR - Achieving 0:47:28

DNASTAR - Achieving Highly Accurate NGS Variant Calling Webinar

Assuring the Quality 1:01:28

Assuring the Quality and Reliability of Clinical Sequencing: Understanding CAP NGS Accredidation

Detection and Interpretation 0:47:31

Detection and Interpretation of Complex Myeloid Leukemia Mutations

Exon-level array: Bridging 0:59:33

Exon-level array: Bridging the gap between chromosomal microarray and next-gen sequencing

EmilyFarrow- Pediatric genetics 0:59:42

EmilyFarrow- Pediatric genetics - Applications of NGS in the Clinic

Big data, Complex 1:06:14

Big data, Complex NGS workflows, Simplified for South Africa

Somatic Variant Calling 0:37:30

Somatic Variant Calling with Mutect2 | GATK Best Practices Tutorial

varvis® webinar series: 1:12:14

varvis® webinar series: The challenge of variant interpretation

Using Mastermind to 0:08:57

Using Mastermind to Speed up Your Variant Interpretation Process | MGZ Medical & Genetics Center

Hack Your Genome 4:12:21

Hack Your Genome Workshop

Genetic diagnostics in 1:25:32

Genetic diagnostics in the era of NGS

Lecture 49 : 0:30:44

Lecture 49 : NGS Technology - Bioinformatics and data analysis-II

How to submit 0:13:40

How to submit the Sequence Read Archive (SRA) data in NCBI