Methods in genomic variant calling

(1:8:40)

SNPs and variant calling

(4:4)

NGS - Genome Variant analysis – Variant calling (3 of 5)

(1:5:15)

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

(48:3)

Variant calling tutorial

(7:10)

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

(17:44)

MPG Primer: High throughput sequencing and variant calling pipelines (2017)

(54:20)

MPG Primer: Sequence variant calling and data handling (2018)

(50:45)

Pangenome Bio Hacking 2025 Workshop - Day 3

(3:44:55)

W8: Variant Calling with GATK - Day 1

(1:57:21)

BroadE: GATK - Introduction to Variant Discovery

(33:25)

BroadE: Introduction to data processing and variant detection for next-generation DNA sequencing

(28:48)

Sequencing, Variant Calling, and Cancer Genomics

(50:20)

Kishwar Shafin - Accurate variant calling and de novo assembly with nanopore reads

(20:16)

Overcoming Challenges of Somatic RNA Variant Calling in Solid Tumors

(17:25)

3. Introduction to Variant Discovery

(25:46)

Small-Variant Calling and Annotation

(32:9)

Fritz Sedlazeck: Rapid structural variant calling across AllOfUs using Oxford Nanopore sequencing

(11:55)