Evidence map›Paper›PMID 40889115›Full record

ArticleBriefings in bioinformatics2025

AUPRC: a metric for evaluating the performance of in-silico perturbation methods in identifying differentially expressed genes.

Hongxu Zhu, Amir Asiaee, Leila Azinfar, Jun Li, Han Liang, Ehsan Irajizad, Kim-Anh Do, James P Long

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Hongxu ZhuDepartment of Biostatistics and Data Science, The University of Texas Health Science Center at Houston School of Public Health, 1200 Pressler St., 77030, TX, United States.ORCID 0000-0003-3774-4495
Amir AsiaeeDepartment of Biostatistics, Vanderbilt University Medical Center, 2525 West End Avenue, 37203, TN, United States.
Leila AzinfarDepartment of Biostatistics, Vanderbilt University Medical Center, 2525 West End Avenue, 37203, TN, United States.
Jun LiDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, 7007 Bertner Ave., 77030, TX, United States.
Han LiangDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, 7007 Bertner Ave., 77030, TX, United States.
Ehsan IrajizadDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, 7007 Bertner Ave., 77030, TX, United States.
Kim-Anh DoDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, 7007 Bertner Ave., 77030, TX, United States.
James P LongDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, 7007 Bertner Ave., 77030, TX, United States.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DIANE BODURKA · 1985 to 2026
$290.8M
Tropism Enhanced Oncolytic Adenovirus for the Treatment of Brain TumorsP50CA127001 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Juan Fueyo, FREDERICK F LANG · 2008 to 2026
$41.2M
Center for Clinical and Translational SciencesUM1TR004906 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Maria Eulalia Fernandez, LORNA H. MCNEILL · 2024 to 2026
$16.7M
Causal Effect Estimation of Regulatory MoleculesR00HG011367 · NHGRI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ASIAEETAHERI, AMIR · 2021 to 2023
$734k
NCATS NIH HHS UM1 TR004906NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA127001NHGRI NIH HHS R00 HG011367
6 · The paper itself

Abstract

In silico perturbation models, computational methods that can predict cellular responses to perturbations, present an opportunity to reduce the need for costly and time-intensive in vitro experiments. Many recently proposed models predict high-dimensional cellular responses, such as gene or protein expression to perturbations such as gene knockout or drugs. However, evaluating in silico performance has largely relied on metrics such as $R^{2}$, which assess overall prediction accuracy but fail to capture biologically significant outcomes like the identification of differentially expressed (DE) genes. In this study, we present a novel evaluation framework that introduces the AUPRC metric to assess the precision and recall of DE gene predictions. By applying this framework to both single-cell and pseudo-bulked datasets, we systematically benchmark simple and advanced computational models. Our results highlight a significant discrepancy between $R^{2}$ and AUPRC, with models achieving high $R^{2}$ values but struggling to identify DE genes, as reflected in their low AUPRC values. This finding underscores the limitations of traditional evaluation metrics and the importance of biologically relevant assessments. Our framework provides a more comprehensive understanding of model capabilities, advancing the application of computational approaches in cellular perturbation research.

Indexed as

Computational BiologyComputer SimulationGene Expression ProfilingGene Expression RegulationAlgorithmsHumanscellular perturbation experimentsdifferentially expressed genesevaluation metricsin silico models

Identifiers

PMID40889115
PMCPMC12400816

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.