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Updated: May 5, 2026

A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes
Published on: May 22, 2018
Database construction and peptide identification strategies for proteogenomic studies on sequenced genomes
Celine Hernandez, Patrice Waridel, Manfredo Quadroni1
1Protein Analysis Facility (Center for Integrative Genomics, UniL); Vital-IT Group (Swiss Institute of Bioinformatics), Batiment Genopode, University of Lausanne, 1015 Lausanne, Switzerland. Celine.Hernandez@isb-sib.ch.
Mass-spectrometry based proteomics validates genome annotations by confirming predicted gene products. This review covers proteogenomic strategies, database construction, and statistical analysis for accurate protein identification.
Area of Science:
- Genomics
- Proteomics
- Bioinformatics
Background:
- High-throughput DNA sequencing generates vast genomic data, necessitating accurate genome annotation.
- Gene prediction software requires experimental validation for functional gene product confirmation.
Purpose of the Study:
- To review strategies for Mass Spectrometry (MS)-based proteogenomics experiments.
- To guide the validation of genome annotations using proteomic data.
Main Methods:
- Discusses bottom-up proteogenomics approaches.
- Evaluates various genomic database construction strategies (whole genome, ORF, cDNA, EST, RNA-Seq).
- Covers statistical assessment of peptide identifications and mapping back to genomic information.
Main Results:
- Highlights the strengths and weaknesses of different database construction methods.
- Emphasizes the importance of statistical rigor in peptide identification.
- Provides references for tools used in proteogenomic data analysis.
Conclusions:
- MS-based proteomics is crucial for validating genome annotations.
- Careful database selection and statistical analysis are key for successful proteogenomic studies.
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