Sign in
BioinformaticsbioRxiv
Preprint

diagFDR: Verifiable False Discovery Rate Reporting in Proteomics via Scope, Calibration, and Stability Diagnostics

Marie ChioniD, Alexandre GodmeriD, Thibaut DouchéiD, Mariette MatondoiD, Quentin Giai GianettoiD

Abstract

AO_SCPLOWBSTRACTC_SCPLOWIn mass spectrometry-based proteomics, false discovery rate (FDR) control underpins the credibility of peptide and protein identifications. In contemporary workflows, including multi-run Data Independent Acquisition (DIA), deep learning-assisted scoring, library-free searches, and extensive post-processing, the statement "1% FDR" has become increasingly ambiguous, potentially referring to different statistical entities, multiple-testing scopes, and null models. We propose a standardized framework requiring explicit specification of three complementary properties: "scope", meaning which statistical universe is controlled; "calibration", meaning whether confidence measures behave consistently with their intended interpretation on the reported unit; and "stability", meaning whether acceptance thresholds and resulting identification lists remain robust to perturbations. Building on routine target/decoy outputs, we introduce pipeline-agnostic diagnostics that audit internal coherence of scores, q-values, and posterior error probabilities, quantify tail support and cutoff fragility, and test plausibility of target-decoy assumptions. We further complement internal checks with external validation via entrapment, which measures empirical false positives on knownabsent sequences. We highlight a "granularity paradox": as scoring becomes more discriminative, decoy matches can become so sparse near stringent cutoffs that the numerical support for decoy-based estimation deteriorates, making reported FDR thresholds increasingly fragile despite improved separation between the distributions of target and decoy scores. Applications to DIA-NN and MS2Rescore show that scope and aggregation choices can materially alter both estimated error rates and list reproducibility. We provide a practical reporting checklist and an open-source R package (diagFDR, available from CRAN) that generates diagnostic reports from standard software outputs. As a minimal verifiable reporting standard, we recommend that any "FDR = %" claim specify the controlled unit and scope, report tail support at the operating cutoff, and make decoy-inclusive outputs available for independent verification. HighlightsO_LIFDR claims can be misleading without explicit scope, calibration, and stability assessment. C_LIO_LIdiagFDR introduces pipeline-agnostic diagnostics from standard software outputs. C_LIO_LIThe granularity paradox shows sparse decoy tails can make stringent cutoffs numerically fragile. C_LIO_LICase studies show that scope misuse and rescoring can affect both error rates and stability. C_LIO_LIdiagFDR produces reviewer-ready reports and a practical reporting checklist. C_LI

PDFDOI

02 /Specification & Classification

Click any tag to browse matching papers

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.

Similarity Map
SelectedSame fieldCross-field
THISYarbro '26Couté '20Lin '24Debrie '23Freestone '25Wen '25
70% semantic matchBioinformatics
Jay M. Yarbro, Ya Huang, Vishwajeeth Pagala+8 more·bioRxiv·Jun 2, 2026