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Published online before print April 21, 2008
Genome Research, DOI: 10.1101/gr.074344.107
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Methods and Resources

Comparative proteogenomics: Combining mass spectrometry and comparative genomics to analyze multiple genomes

Nitin Gupta1,4, Jamal Benhamida2, Vipul Bhargava2, Daniel Goodman2, Elisabeth Kain2, Ian Kerman2, Ngan Nguyen2, Noah Ollikainen2, Jesse Rodriguez2, Jian Wang2, Mary S Lipton3, Margaret Romine3, Vineet Bafna2, Richard D Smith3, and Pavel A Pevzner2

1 University of California San Diego; 2 UCSD; 3 PNNL

Recent proliferation of low-cost DNA sequencing techniques will soon lead to an explosive growth in the number of sequenced genomes and will turn manual annotations into a luxury. Mass spectrometry recently emerged as a valuable technique for proteogenomic annotations that improves on the state-of-the-art in predicting genes and other features. However, previous proteogenomic approaches were limited to a single genome and did not take advantage of analyzing mass spectrometry data from multiple genomes at once. We show that such comparative proteogenomics approach (like comparative genomics) allows one to address the problems that remained beyond the reach of the traditional "single proteome" approach in mass-spectrometry. In particular, we show how comparative proteogenomics addresses the notoriously difficult problem of "one-hit-wonders" in proteomics, improves on the existing gene prediction tools in genomics and allows identification of rare post-translational modifications. We therefore argue that complementing DNA sequencing projects by comparative proteogenomics projects can be a viable approach to improve both genomic and proteomic annotations.


Correspondence: 4 E-mail: ngupta{at}ucsd.edu


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