Error-Controlled Discovery of Protein Interactions via Conformal Calibration

Protein language models (PLMs) are powerful predictors of protein interactions, but strong benchmark performance does not ensure reliable discoveries. We introduce PPI-Caliper, a model-agnostic framework that adapts conformal calibration to select interactions at user-specified false discovery rate (FDR) levels using held-out labels without retraining the predictor. Across five species, two PLM-based predictors, and two human training-data versions for each predictor, PPI-Caliper keeps empirical FDR at or below the target level under in-distribution calibration. Under distribution shift, transferred thresholds tend to become conservative when predictive performance improves, but can fail to control FDR when performance deteriorates. PPI-Caliper connects pre-trained interaction scores to explicit error targets and demonstrates why reliable biological discovery requires evaluating calibration alongside predictive accuracy.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-11-04
DOI
https://doi.org/10.64898/2026.11.03.764142
Primary Topic
Bioinformatics and Genomic Networks
Type
preprint
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preprint

Error-Controlled Discovery of Protein Interactions via Conformal Calibration

丁道云, Han Zhou, Yang Young Lu, Yifan Yang et al.
bioRxiv (Cold Spring Harbor Laboratory)
Bioinformatics and Genomic Networks
preprint

Error-Controlled Discovery of Protein Interactions via Conformal Calibration

丁道云, Han Zhou, Yang Young Lu, Yifan Yang, Lingfeng Shi, Dehan Li
preprint en

Abstract

Protein language models (PLMs) are powerful predictors of protein interactions, but strong benchmark performance does not ensure reliable discoveries. We introduce PPI-Caliper, a model-agnostic framework that adapts conformal calibration to select interactions at user-specified false discovery rate (FDR) levels using held-out labels without retraining the predictor. Across five species, two PLM-based predictors, and two human training-data versions for each predictor, PPI-Caliper keeps empirical FDR at or below the target level under in-distribution calibration. Under distribution shift, transferred thresholds tend to become conservative when predictive performance improves, but can fail to control FDR when performance deteriorates. PPI-Caliper connects pre-trained interaction scores to explicit error targets and demonstrates why reliable biological discovery requires evaluating calibration alongside predictive accuracy.

bioRxiv (Cold Spring Harbor Laboratory)
University of Wisconsin–Madison (US), University of Toronto (CA)
Bioinformatics and Genomic Networks
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