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	BroadE: GATK/Variant calling and joint genotyping (2015) (Broad Institute) View
	Application Tutorial: Introduction to Variant Detection with HiFi Reads (PacBio) View
	Variant Analysis Tutorial (Lal Research Group) View
	seqr: Variant search (Broad Institute) View
	BroadE: Statistical Genetics - Rare variants (Broad Institute) View
	Introducing Ingenuity Variant Analysis (Ingenuity Web Apps) View
	NGS - Genome Variant analysis – Variant annotation (5 of 5) (SIB - Swiss Institute of Bioinformatics) View
	SNPs and variant calling (DnA lab short read sequencing workshop) View
	Varsome, Clinical Variant Interpretation Tool (Pakistan Science TV) View
	The NCBI Minute: Find All Variants with ClinVar (National Library of Medicine) View