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Updated: May 3, 2026

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A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes
Published on: May 22, 2018
10.6K
PGP: parallel prokaryotic proteogenomics pipeline for MPI clusters, high-throughput batch clusters and multicore
Andrey Tovchigrechko1, Pratap Venepally, Samuel H Payne
1J. Craig Venter Institute, 9704 Medical Center Drive, Rockville, MD 20850 and Pacific Northwest National Laboratory, 902 Battelle Blvd., Richland, WA 99354, USA.
Bioinformatics (Oxford, England)
|January 29, 2014
Summary
This study releases a new proteogenomic annotation pipeline for prokaryotic genomes. The pipeline improves genome annotation by identifying novel genes and modifications using proteomic data.
Area of Science:
- Genomics
- Proteomics
- Bioinformatics
Background:
- Accurate genome annotation is crucial for understanding prokaryotic biology.
- Existing annotation methods may miss novel genes and post-translational modifications.
- Proteogenomic analysis integrates proteomic data to refine genome annotations.
Purpose of the Study:
- To release a publicly available proteogenomic annotation pipeline.
- To enable improved annotation of prokaryotic genomes.
- To facilitate the discovery of novel biological elements.
Main Methods:
- Development of a proteogenomic annotation pipeline using Python and C++.
- Integration of the Makeflow engine for workflow execution.
- Redesign for parallel Linux computing environments with automated deployment features.
Main Results:
- The pipeline has been used to improve the annotation of 46 prokaryotic genomes.
- Novel genes and post-translational modifications were discovered.
- Erroneous gene annotations were corrected using proteomic mass spectrometry data.
Conclusions:
- The first public release of a proteogenomic annotation pipeline is presented.
- The pipeline enhances prokaryotic genome annotation accuracy and completeness.
- The tool is designed for easy deployment and portability across various computing environments.

