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  5. Whole-genome resequencing
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OMIC
00185

SNPdbe

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.

Specifications

Restrictions to use:
None
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Publications

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

Classification

  • Animals
    • Homo sapiens

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