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Bioinformatics. 2011 Feb 15;27(4):441-8. doi: 10.1093/bioinformatics/btq695. Epub 2010 Dec 15.

Using bioinformatics to predict the functional impact of SNVs.

Author information

1
Department of Molecular Cell and Developmental Biology, University of California, Santa Cruz, CA, USA.

Abstract

MOTIVATION:

The past decade has seen the introduction of fast and relatively inexpensive methods to detect genetic variation across the genome and exponential growth in the number of known single nucleotide variants (SNVs). There is increasing interest in bioinformatics approaches to identify variants that are functionally important from millions of candidate variants. Here, we describe the essential components of bioinformatics tools that predict functional SNVs.

RESULTS:

Bioinformatics tools have great potential to identify functional SNVs, but the black box nature of many tools can be a pitfall for researchers. Understanding the underlying methods, assumptions and biases of these tools is essential to their intelligent application.

PMID:
21159622
PMCID:
PMC3105482
DOI:
10.1093/bioinformatics/btq695
[Indexed for MEDLINE]
Free PMC Article

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