Department of Electrical and Computer Engineering, Division of Systems Engineering, Boston University, Boston, MA, USA.
Department of Electrical and Computer Engineering, Division of Systems Engineering, Boston University, Boston, MA, USA; Department of Biomedical Engineering, and Faculty of Computing and Data Sciences, Boston University, Boston, MA, USA.
Comput Biol Med. 2024 Apr;172:108312. doi: 10.1016/j.compbiomed.2024.108312. Epub 2024 Mar 16.
Personalized drug response prediction is an approach for tailoring effective therapeutic strategies for patients based on their tumors' genomic characterization. While machine learning methods are widely employed in the literature, they often struggle to capture drug-cell line relations across various cell lines. In addressing this challenge, our study introduces a novel listwise Learning-to-Rank (LTR) model named Inversion Transformer-based Neural Ranking (ITNR). ITNR utilizes genomic features and a transformer architecture to decipher functional relationships and construct models that can predict patient-specific drug responses. Our experiments were conducted on three major drug response data sets, showing that ITNR reliably and consistently outperforms state-of-the-art LTR models.
个性化药物反应预测是一种根据肿瘤的基因组特征为患者量身定制有效治疗策略的方法。虽然机器学习方法在文献中得到了广泛应用,但它们往往难以捕捉不同细胞系中药物-细胞系关系。在解决这一挑战时,我们的研究引入了一种名为基于反转 Transformer 的神经排序(Inversion Transformer-based Neural Ranking,ITNR)的新型列表式学习排序(Learning-to-Rank,LTR)模型。ITNR 利用基因组特征和 Transformer 架构来破译功能关系,并构建能够预测患者特定药物反应的模型。我们在三个主要的药物反应数据集上进行了实验,结果表明 ITNR 可靠且一致地优于最先进的 LTR 模型。