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With the rapid development of mass spectrometry-based proteomics, the volume of phosphoproteomic data has increased substantially. However, accurate localization of phosphorylation sites and standardized statistical validation remain critical analytical bottlenecks. To address the lack of standardized cross-algorithm evaluation, we introduce onsite, a unified and open-source Python framework. onsite integrates an alanine-decoy strategy to estimate the false localization rate (FLR) across three algorithms: AScore, PhosphoRS, and pyLucXor. This modular architecture efficiently processes large-scale data sets and enables global FLR calculation. Benchmarking on the standard synthetic phosphopeptide data set PXD000138 highlighted distinct interalgorithmic variations. Using the same 5% global FLR threshold, pyLucXor localized the most target sites (28,353). It also reached a high accuracy (91.22%) against the known ground truth, resulting in the largest number of correctly localized sites (25,865). Reanalysis of the highly fractionated, large-scale PXD012255 data set further demonstrated that native integration of onsite into the quantms pipeline enables scalable processing and provides a standardized framework for FLR control in large-scale phosphoproteomics.
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Yue et al. (2026) studied this question.
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