Whole Genome Sequence Analysis

When you are working with whole genome sequencing data, finding the information you need can be a daunting challenge. This course offers both theoretical and hands-on training so you can learn the main tools used to do alignment, variant calling, annotation, and visualization. You’ll learn how to go from raw FASTQ reads to annotated variants (VCF files).

Intermediate Level: This is an intermediate workshop in the Whole Genome and Exome Analysis series. Prior experience with command line is required.

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