Significance Analysis of Spectral Count Data in Label-free Shotgun Proteomics

Spectral counting has become a commonly used approach for measuring protein abundance in label-free shotgun proteomics. At the same time, the development of data analysis methods has lagged behind. Currently most studies utilizing spectral counts rely on simple data transforms and posthoc correction...

Full description

Saved in:
Bibliographic Details
Published inMolecular & cellular proteomics Vol. 7; no. 12; pp. 2373 - 2385
Main Authors Choi, Hyungwon, Fermin, Damian, Nesvizhskii, Alexey I.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.12.2008
American Society for Biochemistry and Molecular Biology
Subjects
Online AccessGet full text
ISSN1535-9476
1535-9484
1535-9484
DOI10.1074/mcp.M800203-MCP200

Cover

More Information
Summary:Spectral counting has become a commonly used approach for measuring protein abundance in label-free shotgun proteomics. At the same time, the development of data analysis methods has lagged behind. Currently most studies utilizing spectral counts rely on simple data transforms and posthoc corrections of conventional signal-to-noise ratio statistics. However, these adjustments can neither handle the bias toward high abundance proteins nor deal with the drawbacks due to the limited number of replicates. We present a novel statistical framework (QSpec) for the significance analysis of differential expression with extensions to a variety of experimental design factors and adjustments for protein properties. Using synthetic and real experimental data sets, we show that the proposed method outperforms conventional statistical methods that search for differential expression for individual proteins. We illustrate the flexibility of the model by analyzing a data set with a complicated experimental design involving cellular localization and time course.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
To whom correspondence should be addressed: Dept. of Pathology, University of Michigan, 1301 Catherine, 4237 MS1, Ann Arbor, Michigan 48109. E-mail: nesvi@med.umich.edu
ISSN:1535-9476
1535-9484
1535-9484
DOI:10.1074/mcp.M800203-MCP200