PepC: Proteomics software for identifying differentially expressed proteins based on spectral counting

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Abstract

Summary: Identifying biologically significant changes in protein abundance between two conditions is a key issue when analyzing proteomic data. One widely used approach centers on spectral counting, a label-free method that sums all the tandem mass spectra for a protein observed in an analysis. To assess the significance of the results, we recently combined the t-test and G-test, with random permutation analysis, and we validated this approach biochemically. To automate the statistical method, we developed PepC, a software program that balances the trade-off between the number of differentially expressed proteins identified and the false discovery rate. This tool can be applied to a wide range of proteomic datasets, making data analysis rapid, reproducible and easily interpretable by proteomics specialists and non-specialists alike. Availability and implementation: The software is implemented in Java. It has been added to the Trans Proteomic Pipeline project's 'Petunia' web interface, but can also be run as a command line program. The source code is GNU Lesser General Public License and the program is freely available on the web. http://sashimi.svn.sourceforge.net/viewvc/sashimi/trunk/trans_proteomic_pipeline/src/Quantitation/Pepc. Contact: levb@u.washington.edu; brian.pratt@insilicos.com. © The Author(s) 2010. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org.

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APA

Heinecke, N. L., Pratt, B. S., Vaisar, T., & Becker, L. (2010). PepC: Proteomics software for identifying differentially expressed proteins based on spectral counting. Bioinformatics, 26(12), 1574–1575. https://doi.org/10.1093/bioinformatics/btq171

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