SuperFeat: Quantitative Features Learning from Single-cell RNAseq Data Facilitates Drug Repurposing

Jianmei Zhong, Junyao Yang, Yinghui Song, Zhihua Zhang, Chunming Wang, Renyang Tong, Chenglong Li, Nanhui Yu, Lianhong Zou, Liu Sulai, Pu Jun, Wei Lin
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Abstract

In this study, we have devised a computational framework called Supervised Feature Learning and Scoring (SuperFeat) that allows for the training of a machine learning model and evaluates the canonical cellular status/features in pathological tissues that underlie the progression of disease. This framework also enables the identification of potential drugs that target the presumed detrimental cellular features. This framework was constructed on the basis of an artificial neural network with the gene expression profiles serving as input nodes. The training data comprised single-cell RNA sequencing datasets that encompassed the specific cell lineage during the developmental progression of cell features. A few models of the canonical cancer-involved cellular status/features were tested by such framework. Finally, we have illustrated the drug repurposing pipeline, utilizing the training parameters derived from the adverse cellular status/features, which has yielded successful validation results both in vitro and in vivo. SuperFeat is accessible at https://github.com/weilin-genomics/rSuperFeat.
SuperFeat:从单细胞 RNAseq 数据中学习定量特征有助于药物再利用
在这项研究中,我们设计了一个名为 "监督特征学习和评分(SuperFeat)"的计算框架,它可以训练机器学习模型,并评估病理组织中导致疾病进展的典型细胞状态/特征。该框架还能识别针对假定的有害细胞特征的潜在药物。该框架以人工神经网络为基础,以基因表达谱为输入节点。训练数据包括单细胞 RNA 测序数据集,这些数据集涵盖了细胞特征发展过程中的特定细胞系。通过这种框架测试了一些典型的癌症相关细胞状态/特征模型。最后,我们利用从不利细胞状态/特征中得出的训练参数说明了药物再利用管道,该管道在体外和体内都取得了成功的验证结果。SuperFeat 可通过 https://github.com/weilin-genomics/rSuperFeat 访问。
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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