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	NGS-Intro 10: Variant Calling Workflow \| GATK Best Practices (NBISweden) View
	BroadE: GATK/Introduction to High-Throughput Sequencing data formats and methods (2015) (Broad Institute) View
	1. Introduction to GATK Workshop 2017 (Chipster Tutorials) View
	Variant Calling workflow using Galaxy (Lawrence Uy) View
	Overcoming Challenges of Somatic RNA Variant Calling in Solid Tumors (Cancer Genomics Consortium) View
	9. Genotype Refinement Workflow (Chipster Tutorials) View
	Calling All Variants with HiFi reads (PacBio) View
	Next Generation Sequencing Workflow (COG-Train) View
	Getting Started with Targeted NGS with TruSeq® Custom Amplicon Low-Input on the MiniSeqTM System (Illumina) View
	Human genome variant calling on chromosome 20 with HaplotypeCaller and FreeBayes (Olga Babic) View