BroadE: GATK - Introduction to High-Throughput Sequencing Data

(27:30)

BroadE: GATK - Introduction to Variant Discovery

(33:25)

BroadE: Introduction to the GATK (2015)

(17:53)

BroadE: GATK/Introduction to High-Throughput Sequencing data formats and methods (2015)

(13:41)

BroadE: Overview of GATK \u0026 best practices

(22:5)

BroadE: Introduction to NGS for GATK

(39:12)

BroadE: GATK - Introduction to Germline Variant Discovery

(22:34)

BroadE: GATK - Genotype Refinement

(34:3)

W8: Variant Calling with GATK - Day 1

(1:57:21)

W8: Variant Calling with GATK - Day 2

(1:27:46)

BroadE: GATK/Mapping, processing and duplicate marking with Picard tools (2015)

(27:13)

BroadE: GATK - Haplotype Caller

(33:54)

Methods in genomic variant calling

(1:8:40)

NGS-Intro 9: Whole Genome Sequencing \u0026 Variant Calling Workflow

(20:36)

Calling Variants With Mutect

(1:4:23)

Copy number variation and the secret of life - with Aoife McLysaght

(53:35)

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

(43:24)

BroadE: XHMM: Discovery and Genotyping of Copy Number Variation from Exome Read Depth 07102013 13

(1:9:43)

BroadE: GATK - JointCalling

(41:52)

BroadE: GATK/Genotype refinement (2015)

(20:51)

BroadE: GATK - Somatic SNVs and Indels

(23:27)

BroadE: GATK/Introduction to variant discovery: calling cohorts (2015)

(17:41)

BroadE: GATK - Somatic Copy Number Alterations

(47:19)

BroadE: GATK/Variant calling and joint genotyping (2015)

(17:44)

BroadE: Introduction to the GATK \u0026 GSA best practices

(19:3)

BroadE: GATK - Introduction to Data Pre-processing

(1:12:10)

BroadE: GATK/Mapping and processing RNAseq

(18:52)

BroadE: GATK/Introduction to working with variants (2015)

(29:40)