• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

AUPRC:一种用于评估计算机模拟扰动方法在识别差异表达基因方面性能的指标。

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

作者信息

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

机构信息

Department 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.

Department of Biostatistics, Vanderbilt University Medical Center, 2525 West End Avenue, 37203, TN, United States.

出版信息

Brief Bioinform. 2025 Aug 31;26(5). doi: 10.1093/bib/bbaf426.

DOI:10.1093/bib/bbaf426
PMID:40889115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12400816/
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.

摘要

计算机模拟扰动模型,即能够预测细胞对扰动反应的计算方法,为减少对昂贵且耗时的体外实验的需求提供了契机。许多最近提出的模型可预测高维细胞反应,例如基因敲除或药物等扰动下的基因或蛋白质表达。然而,评估计算机模拟性能在很大程度上依赖于诸如(R^{2})之类的指标,这些指标评估的是整体预测准确性,但无法捕捉到诸如鉴定差异表达(DE)基因等具有生物学意义的结果。在本研究中,我们提出了一种新颖的评估框架,该框架引入了AUPRC指标来评估DE基因预测的精确率和召回率。通过将此框架应用于单细胞和伪批量数据集,我们系统地对简单和先进的计算模型进行了基准测试。我们的结果凸显了(R^{2})与AUPRC之间的显著差异,即模型虽能达到较高的(R^{2})值,但在识别DE基因方面却存在困难,这在其较低的AUPRC值中得到体现。这一发现强调了传统评估指标的局限性以及生物学相关评估的重要性。我们的框架提供了对模型能力更全面的理解,推动了计算方法在细胞扰动研究中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94aa/12400816/328a621bc715/bbaf426f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94aa/12400816/48aac829f9ad/bbaf426f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94aa/12400816/f33afec5833a/bbaf426f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94aa/12400816/2b84995d001b/bbaf426f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94aa/12400816/d03c7b4c7d92/bbaf426f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94aa/12400816/e40c54c47299/bbaf426f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94aa/12400816/328a621bc715/bbaf426f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94aa/12400816/48aac829f9ad/bbaf426f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94aa/12400816/f33afec5833a/bbaf426f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94aa/12400816/2b84995d001b/bbaf426f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94aa/12400816/d03c7b4c7d92/bbaf426f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94aa/12400816/e40c54c47299/bbaf426f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94aa/12400816/328a621bc715/bbaf426f6.jpg

相似文献

1
AUPRC: a metric for evaluating the performance of in-silico perturbation methods in identifying differentially expressed genes.AUPRC:一种用于评估计算机模拟扰动方法在识别差异表达基因方面性能的指标。
Brief Bioinform. 2025 Aug 31;26(5). doi: 10.1093/bib/bbaf426.
2
AUC-PR is a More Informative Metric for Assessing the Biological Relevance of In Silico Cellular Perturbation Prediction Models.AUC-PR是一种用于评估计算机细胞扰动预测模型生物学相关性的更具信息量的指标。
bioRxiv. 2025 Mar 11:2025.03.06.641935. doi: 10.1101/2025.03.06.641935.
3
Prescription of Controlled Substances: Benefits and Risks管制药品的处方:益处与风险
4
Short-Term Memory Impairment短期记忆障碍
5
Systemic treatments for metastatic cutaneous melanoma.转移性皮肤黑色素瘤的全身治疗
Cochrane Database Syst Rev. 2018 Feb 6;2(2):CD011123. doi: 10.1002/14651858.CD011123.pub2.
6
Systemic Inflammatory Response Syndrome全身炎症反应综合征
7
The quantity, quality and findings of network meta-analyses evaluating the effectiveness of GLP-1 RAs for weight loss: a scoping review.评估胰高血糖素样肽-1受体激动剂(GLP-1 RAs)减肥效果的网状Meta分析的数量、质量及结果:一项范围综述
Health Technol Assess. 2025 Jun 25:1-73. doi: 10.3310/SKHT8119.
8
Comparison of Two Modern Survival Prediction Tools, SORG-MLA and METSSS, in Patients With Symptomatic Long-bone Metastases Who Underwent Local Treatment With Surgery Followed by Radiotherapy and With Radiotherapy Alone.两种现代生存预测工具 SORG-MLA 和 METSSS 在接受手术联合放疗和单纯放疗治疗有症状长骨转移患者中的比较。
Clin Orthop Relat Res. 2024 Dec 1;482(12):2193-2208. doi: 10.1097/CORR.0000000000003185. Epub 2024 Jul 23.
9
Plug-and-play use of tree-based methods: consequences for clinical prediction modeling.基于树的方法的即插即用:对临床预测模型的影响。
J Clin Epidemiol. 2025 Aug;184:111834. doi: 10.1016/j.jclinepi.2025.111834. Epub 2025 May 19.
10
Stabilizing machine learning for reproducible and explainable results: A novel validation approach to subject-specific insights.稳定机器学习以获得可重复和可解释的结果:一种针对特定个体见解的新型验证方法。
Comput Methods Programs Biomed. 2025 Jun 21;269:108899. doi: 10.1016/j.cmpb.2025.108899.

本文引用的文献

1
Deep-learning-based gene perturbation effect prediction does not yet outperform simple linear baselines.基于深度学习的基因扰动效应预测尚未超越简单的线性基线。
Nat Methods. 2025 Aug;22(8):1657-1661. doi: 10.1038/s41592-025-02772-6. Epub 2025 Aug 4.
2
Interpretable identification of cancer genes across biological networks via transformer-powered graph representation learning.通过基于Transformer的图表示学习在生物网络中对癌症基因进行可解释识别。
Nat Biomed Eng. 2025 Mar;9(3):371-389. doi: 10.1038/s41551-024-01312-5. Epub 2025 Jan 9.
3
Large-scale foundation model on single-cell transcriptomics.
单细胞转录组学的大规模基础模型。
Nat Methods. 2024 Aug;21(8):1481-1491. doi: 10.1038/s41592-024-02305-7. Epub 2024 Jun 6.
4
scPRAM accurately predicts single-cell gene expression perturbation response based on attention mechanism.scPRAM 基于注意力机制准确预测单细胞基因表达扰动响应。
Bioinformatics. 2024 May 2;40(5). doi: 10.1093/bioinformatics/btae265.
5
scGPT: toward building a foundation model for single-cell multi-omics using generative AI.scGPT:迈向使用生成式人工智能构建单细胞多组学基础模型
Nat Methods. 2024 Aug;21(8):1470-1480. doi: 10.1038/s41592-024-02201-0. Epub 2024 Feb 26.
6
scPerturb: harmonized single-cell perturbation data.scPerturb:协调的单细胞扰动数据。
Nat Methods. 2024 Mar;21(3):531-540. doi: 10.1038/s41592-023-02144-y. Epub 2024 Jan 26.
7
Learning single-cell perturbation responses using neural optimal transport.利用神经最优传输学习单细胞扰动响应。
Nat Methods. 2023 Nov;20(11):1759-1768. doi: 10.1038/s41592-023-01969-x. Epub 2023 Sep 28.
8
Predicting transcriptional outcomes of novel multigene perturbations with GEARS.用 GEARS 预测新型多基因扰动的转录结果。
Nat Biotechnol. 2024 Jun;42(6):927-935. doi: 10.1038/s41587-023-01905-6. Epub 2023 Aug 17.
9
Improved prediction of gene expression through integrating cell signalling models with machine learning.通过将细胞信号模型与机器学习相结合来提高基因表达预测。
BMC Bioinformatics. 2022 Aug 6;23(1):323. doi: 10.1186/s12859-022-04787-8.
10
Differential Expression Analysis of Single-Cell RNA-Seq Data: Current Statistical Approaches and Outstanding Challenges.单细胞RNA测序数据的差异表达分析:当前的统计方法与突出挑战
Entropy (Basel). 2022 Jul 18;24(7):995. doi: 10.3390/e24070995.