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J Proteome Res. 2009 Apr;8(4):2106-13. doi: 10.1021/pr8011107.

Statistical calibration of the SEQUEST XCorr function.

Author information

1
Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA.

Abstract

Obtaining accurate peptide identifications from shotgun proteomics liquid chromatography tandem mass spectrometry (LC-MS/MS) experiments requires a score function that consistently ranks correct peptide-spectrum matches (PSMs) above incorrect matches. We have observed that, for the Sequest score function Xcorr, the inability to discriminate between correct and incorrect PSMs is due in part to spectrum-specific properties of the score distribution. In other words, some spectra score well regardless of which peptides they are scored against, and other spectra score well because they are scored against a large number of peptides. We describe a protocol for calibrating PSM score functions, and we demonstrate its application to Xcorr and the preliminary Sequest score function Sp. The protocol accounts for spectrum- and peptide-specific effects by calculating p values for each spectrum individually, using only that spectrum's score distribution. We demonstrate that these calculated p values are uniform under a null distribution and therefore accurately measure significance. These p values can be used to estimate the false discovery rate, therefore, eliminating the need for an extra search against a decoy database. In addition, we show that the pvalues are better calibrated than their underlying scores; consequently, when ranking top-scoring PSMs from multiple spectra, p values are better at discriminating between correct and incorrect PSMs. The calibration protocol is generally applicable to any PSM score function for which an appopriate parametric family can be identified.

PMID:
19275164
PMCID:
PMC2807930
DOI:
10.1021/pr8011107
[Indexed for MEDLINE]
Free PMC Article

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