BADGER: biologically-aware interpretable differential gene expression ranking model.

IF 2.8 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Bioinformatics advances Pub Date : 2025-02-18 eCollection Date: 2025-01-01 DOI:10.1093/bioadv/vbaf029
Hajung Kim, Mogan Gim, Seungheun Baek, Soyon Park, Sunkyu Kim, Jaewoo Kang
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引用次数: 0

Abstract

Motivation: Understanding which genes are significantly affected by drugs is crucial for drug repurposing, as drugs targeting specific pathways in one disease might be effective in another with similar genetic profiles. By analyzing gene expression changes in cells before and after drug treatment, we can identify the genes most impacted by drugs.

Results: The Biologically-Aware Interpretable Differential Gene Expression Ranking (BADGER) model is an interpretable model designed to predict gene expression changes resulting from interactions between cancer cell lines and chemical compounds. The model enhances explainability through integration of prior knowledge about drug targets via pathway information, handles novel cancer cell lines through similarity-based embedding, and employs three attention blocks that mimic the cascading effects of chemical compounds. This model overcomes previous limitations of cell line range and explainability constraints in drug-cell response studies. The model demonstrates superior performance over baselines in both unseen cell and unseen pair split evaluations, showing robust prediction capabilities for untested drug-cell line combinations.

Availability and implementation: This makes it particularly valuable for drug repurposing scenarios, especially in developing therapeutic plans for new or resistant diseases by leveraging similarities with other diseases. All code and data used in this study are available at https://github.com/dmis-lab/BADGER.git.

BADGER:生物感知可解释的差异基因表达排序模型。
动机了解哪些基因会受到药物的重大影响对于药物再利用至关重要,因为针对一种疾病的特定通路的药物可能会对具有类似基因特征的另一种疾病有效。通过分析药物治疗前后细胞中基因表达的变化,我们可以确定受药物影响最大的基因:生物感知可解释差异基因表达排名(BADGER)模型是一个可解释的模型,旨在预测癌症细胞系与化合物之间相互作用导致的基因表达变化。该模型通过路径信息整合了有关药物靶点的先验知识,通过基于相似性的嵌入处理新型癌细胞系,并采用了三个模拟化合物级联效应的注意模块,从而增强了可解释性。该模型克服了以往药物-细胞反应研究中细胞系范围和可解释性限制的局限性。该模型在未见细胞和未见配对拆分评估中均表现出优于基线的性能,显示出对未经测试的药物-细胞系组合具有强大的预测能力:这使得它在药物再利用方案中特别有价值,尤其是在利用与其他疾病的相似性为新疾病或耐药性疾病制定治疗计划时。本研究中使用的所有代码和数据可在 https://github.com/dmis-lab/BADGER.git 网站上获取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.60
自引率
0.00%
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