Workshop: Variant Prioritization with OpenCRAVAT

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In this workshop, we will show how to perform genomic variant interpretation and analysis using OpenCRAVAT, a biologist-friendly open source software framework for the annotation of human genetic variation.

For more information, visit our Online Program Planner.

Learning Objectives:

  1. Design an analysis workflow for variants identified in human genomes.
  2. Identify multiple phenotypic consequences of selected rare and common human genetic variants provided by the workshop.
  3. Evaluate the limits of current tools for genetic variant interpretation.
  4. Construct a high-throughput workflow to analyze genetic variation in a large case-only cohort.


Key:

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Introduction
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Open to view video.
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Introduction
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Open to download resource.
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Quickstart Guide
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Session One: Identify Multiple Phenotypic Consequences of Selected Rare and Common Human Genetic Variants
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Open to view video.
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Session One
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Open to download resource.
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Session Two: Design an Analysis Workflow for Variants Identified in Human Genomes
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Open to view video.
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Session Two
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Open to download resource.
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Session Three: Evaluate the Limits of Current Tools for Genetic Variant Interpretation
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Open to view video.
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Session Three
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Open to download resource.
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