AUPRC: a metric for evaluating the performance of <i>in-silico</i> perturbation methods in identifying differentially expressed genes

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.

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Publication Details

Journal
Briefings in Bioinformatics
Published
2025-08-31
DOI
https://doi.org/10.1093/bib/bbaf426
Citations
1
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.81

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article

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

Ehsan Irajizad, Hongxu Zhu, Amir Asiaee, Han Liang et al.
1 citations
Briefings in Bioinformatics
Single-cell and spatial transcriptomics
0.81
article

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

Ehsan Irajizad, Hongxu Zhu, Amir Asiaee, Han Liang, James P. Long, Jun Li, Kim‐Anh Do, Leila Azinfar
article en
1 citations

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.

Briefings in BioinformaticsVol. 26(5)
The University of Texas MD Anderson Cancer Center (US), Vanderbilt University Medical Center (US), The University of Texas Health Science Center at Houston (US)
National Institutes of Health, National Cancer Institute, National Center for Advancing Translational Sciences
Openalex Percentile: Top 24%
Single-cell and spatial transcriptomics
0.81
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