使用专有和公开可用的数据集进行目标预测的数据探索。

IF 3.8 3区 医学 Q2 CHEMISTRY, MEDICINAL
Chemical Research in Toxicology Pub Date : 2025-05-19 Epub Date: 2025-04-20 DOI:10.1021/acs.chemrestox.4c00347
Aljoša Smajić, Thomas Steger-Hartmann, Gerhard F Ecker, Anke Hackl
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引用次数: 0

摘要

当应用机器学习(ML)方法预测生物活性时,通常从不同的分析或来源收集数据并将其组合成单个数据集。然而,根据数据域和数据来源的不同,同一大分子靶标的生物活性数据可能会显示出很大的数值差异(查看单个化合物),并且涵盖化学空间的不同部分以及生物活性范围(查看整个数据集)。所得到的预测模型的有效性和适用性可能会受到其训练数据检索来源的强烈影响。因此,我们研究了来自拜耳公司和公开可用的ChEMBL数据库的专利药物数据的化学空间和活性/非活性分布,以及它们作为分类模型训练数据时的影响。为此,我们结合不同的ML算法应用了两组不同的描述符。结果显示,两种不同数据源之间的化学空间存在巨大差异,导致模型应用于训练数据以外的领域时,预测性能不理想。所有目标的MCC值在-0.34 ~ 0.37之间,表明在Bayer AG数据上训练的模型在ChEMBL数据上测试时,模型性能不是最优的,反之亦然。这两个数据源之间最近邻的平均谷本相似度表明,31个目标的相似度等于或小于0.3。有趣的是,所有用于评估两个数据源的化学空间重叠以预测模型在其训练数据集之外的适用性的方法都与观察到的性能无关。最后,我们应用了不同的策略来创建基于公共和专有来源的混合训练数据集,使用分析格式(基于细胞和无细胞)信息和谷本相似性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Data Exploration for Target Predictions Using Proprietary and Publicly Available Data Sets.

When applying machine learning (ML) approaches for the prediction of bioactivity, it is common to collect data from different assays or sources and combine them into single data sets. However, depending on the data domains and sources from which these data are retrieved, bioactivity data for the same macromolecular target may show a high variance of values (looking at a single compound) and cover very different parts of the chemical space as well as the bioactivity range (looking at the whole data set). The effectiveness and applicability domain of the resulting prediction models may be strongly influenced by the sources from which their training data were retrieved. Therefore, we investigated the chemical space and active/inactive distribution of proprietary pharmaceutical data from Bayer AG and the publicly available ChEMBL database, and their impact when applied as training data for classification models. For this end, we applied two different sets of descriptors in combination with different ML algorithms. The results show substantial differences in chemical space between the two different data sources, leading to suboptimal prediction performance when models are applied to domains other than their training data. MCC values between -0.34 and 0.37 among all targets were retrieved, indicating suboptimal model performance when models trained on Bayer AG data were tested on ChEMBL data and vice versa. The mean Tanimoto similarity of the nearest neighbors between these two data sources indicated similarities for 31 targets equal to or less than 0.3. Interestingly, all applied methods to assess overlap of chemical space of the two data sources to predict the applicability of models beyond their training data sets did not correlate with observed performances. Finally, we applied different strategies for creating mixed training data sets based on both public and proprietary sources, using assay format (cell-based and cell-free) information and Tanimoto similarities.

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来源期刊
CiteScore
7.90
自引率
7.30%
发文量
215
审稿时长
3.5 months
期刊介绍: Chemical Research in Toxicology publishes Articles, Rapid Reports, Chemical Profiles, Reviews, Perspectives, Letters to the Editor, and ToxWatch on a wide range of topics in Toxicology that inform a chemical and molecular understanding and capacity to predict biological outcomes on the basis of structures and processes. The overarching goal of activities reported in the Journal are to provide knowledge and innovative approaches needed to promote intelligent solutions for human safety and ecosystem preservation. The journal emphasizes insight concerning mechanisms of toxicity over phenomenological observations. It upholds rigorous chemical, physical and mathematical standards for characterization and application of modern techniques.
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