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bio-variant-annotation

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Comprehensive variant annotation using bcftools annotate/csq, VEP, SnpEff, and ANNOVAR. Add database annotations, predict functional consequences, and assess clinical significance. Use when annotating variants with functional and clinical information.

When to use

• annotating variants with functional and clinical information
• adding database annotations
• predicting functional consequences
• assessing clinical significance
• adding rsIDs from dbSNP
• predicting coding effects and impact severity
• annotating variants with gene effects

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