PyViscount:通过随机搜索空间分区验证错误发现率估计方法

IF 3.6 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Dominik Madej,  and , Henry Lam*, 
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引用次数: 0

摘要

验证错误发现率(FDR)估计是枪弹蛋白质组学方法开发的一个重要方面,但令人惊讶的是,这方面的研究却很少。目前可用的验证方案大多依赖于地面实况数据集,而地面实况数据集通常涉及对搜索空间或所使用的查询光谱的属性进行操作。因此,比较估计的 FDR 值和基于地面实况的错误发现比例值可能并不能代表实际中遇到的涉及自然数据集的情况。在本研究中,我们介绍了 PyViscount─ 一种基于随机搜索空间分区的 Python 工具,该工具实现了一种新颖的验证协议,可使用未改变的候选肽搜索空间和实验查询光谱的通用数据集生成准基本真实值。此外,PyViscount 对现有 FDR 估计方法的验证与其他验证协议是一致的。所介绍的新型验证方法无需合成数据集或对数据进行可疑处理,对蛋白质组学从业人员来说可能是一种有吸引力的替代方法,使他们能够更深入地了解现有的和新的 FDR 估计方法的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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来源期刊
Journal of Proteome Research
Journal of Proteome Research 生物-生化研究方法
CiteScore
9.00
自引率
4.50%
发文量
251
审稿时长
3 months
期刊介绍: Journal of Proteome Research publishes content encompassing all aspects of global protein analysis and function, including the dynamic aspects of genomics, spatio-temporal proteomics, metabonomics and metabolomics, clinical and agricultural proteomics, as well as advances in methodology including bioinformatics. The theme and emphasis is on a multidisciplinary approach to the life sciences through the synergy between the different types of "omics".
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