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  2. Sequencing
  3. Whole-genome resequencing
  4. Variant annotation
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A database and a web interface that is designed to fill the annotation gap left by the high cost of experimental testing for functional significance of protein variants.

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  • (Schaefer et al., 2012) SNPdbe: constructing an nsSNP functional impacts database. Bioinformatics.
    PMID: 22210871
  • Animals
    • Homo sapiens

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