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SNAP is a method for evaluating effects of single amino acid substitutions on protein function. It was developed by Yana Bromberg in Rost Lab, at Columbia University, New York.

Single Nucleotide Polymorphisms (SNPs) represent a very large portion of all genetic variations. SNPs found in the coding regions of genes are often non-synonymous, changing a single amino acid in the encoded protein sequence. SNPs are either "neutral" in the sense that the resulting point-mutated protein is not functionally discernible from the wild-type, or they are "non-neutral" in that the mutant and wild-type differ in function. The ability to identify non-neutral substitutions in an ocean of SNPs could significantly aid targeting disease causing detrimental mutations, as well as SNPs that increase the fitness of particular phenotypes.

SNAP is a neural-network based method that uses in silico derived protein information (e.g. secondary structure, conservation, solvent accessibility, etc.) in order to make predictions regarding functionality of mutated proteins. The network takes protein sequences and lists of mutants as input, returning a score for each substitution. These scores can then be translated into binary predictions of effect (present/absent) and reliability indices (RI). SNAP returns its results to the user via e-mail.

NOTE: Reliability Indices are somewhat correlated with severity of change (as described in the paper referenced below). However, users are urged to take care in using them directly as severity classifiers.

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If you find SNAP useful for your research, please cite:
  • SNAP: predict effect of non-synonymous polymorphisms on function.
    Yana Bromberg and Burkhard Rost
    Nucleic Acids Research, 2007, Vol. 35, No. 11 3823-3835 (PubMed)
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Copyright © 2010 Yana Bromberg and Brukhard Rost, ROSTLAB all rights reserved. | The use of this service is free for academia all others should inquire about a commercial license by writing to biosof llc