PyViscount: Validating False Discovery Rate Estimation Methods via Random Search Space Partition

Validating false discovery rate (FDR) estimation is an essential but surprisingly understudied aspect of method development in shotgun proteomics. Currently available validation protocols mostly rely on ground truth data sets, which typically involve manipulating the properties of the search space or query spectra used. As a result, comparing estimated FDR and ground truth-based false discovery proportion values may not be representative of the scenarios involving natural data sets encountered in practice. In this study, we introduce PyViscount─a Python tool implementing a novel validation protocol based on random search space partition, which enables generating a quasi ground-truth using unaltered search spaces of unique candidate peptides and generic data sets of experimental query spectra. Furthermore, validation of existing FDR estimation methods by PyViscount is consistent with alternative validation protocols. The presented novel approach to validation free from the need for synthetic data sets or dubious manipulation of the data may be an attractive alternative for proteomics practitioners, allowing them to obtain deeper insights into the performance of existing and new FDR estimation methods.

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Publication Details

Journal
Journal of Proteome Research
Published
2025-02-05
DOI
https://doi.org/10.1021/acs.jproteome.4c00743
Citations
3
Primary Topic
Mass Spectrometry Techniques and Applications
Type
article
Field-Weighted Citation Impact
2.27

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article

PyViscount: Validating False Discovery Rate Estimation Methods via Random Search Space Partition

Henry Lam, Dominik Madej
3 citations
Journal of Proteome Research
Mass Spectrometry Techniques and Applications
2.27
article

PyViscount: Validating False Discovery Rate Estimation Methods via Random Search Space Partition

Henry Lam, Dominik Madej
article en
3 citations

Abstract

Validating false discovery rate (FDR) estimation is an essential but surprisingly understudied aspect of method development in shotgun proteomics. Currently available validation protocols mostly rely on ground truth data sets, which typically involve manipulating the properties of the search space or query spectra used. As a result, comparing estimated FDR and ground truth-based false discovery proportion values may not be representative of the scenarios involving natural data sets encountered in practice. In this study, we introduce PyViscount─a Python tool implementing a novel validation protocol based on random search space partition, which enables generating a quasi ground-truth using unaltered search spaces of unique candidate peptides and generic data sets of experimental query spectra. Furthermore, validation of existing FDR estimation methods by PyViscount is consistent with alternative validation protocols. The presented novel approach to validation free from the need for synthetic data sets or dubious manipulation of the data may be an attractive alternative for proteomics practitioners, allowing them to obtain deeper insights into the performance of existing and new FDR estimation methods.

Journal of Proteome ResearchVol. 24(3)
Hong Kong University of Science and Technology (HK)
Research Grants Council, University Grants Committee
Openalex Percentile: Top 14%
Mass Spectrometry Techniques and Applications
2.27
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