{"title":"机器学习驱动数据评估,优化高通量筛选流水线","authors":"Joshua Hesse, Davide Boldini, Stephan A. Sieber","doi":"10.1021/acs.jcim.4c01547","DOIUrl":null,"url":null,"abstract":"In the rapidly evolving field of drug discovery, high-throughput screening (HTS) is essential for identifying bioactive compounds. This study introduces a novel application of data valuation, a concept for evaluating the importance of data points based on their impact, to enhance drug discovery pipelines. Our approach improves active learning for compound library screening, robustly identifies true and false positives in HTS data, and identifies important inactive samples in an imbalanced HTS training, all while accounting for computational efficiency. We demonstrate that importance-based methods enable more effective batch screening, reducing the need for extensive HTS. Machine learning models accurately differentiate true biological activity from assay artifacts, streamlining the drug discovery process. Additionally, importance undersampling aids in HTS data set balancing, improving machine learning performance without omitting crucial inactive samples. These advancements could significantly enhance the efficiency and accuracy of drug development.","PeriodicalId":44,"journal":{"name":"Journal of Chemical Information and Modeling ","volume":"24 1","pages":""},"PeriodicalIF":5.6000,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Machine Learning-Driven Data Valuation for Optimizing High-Throughput Screening Pipelines\",\"authors\":\"Joshua Hesse, Davide Boldini, Stephan A. Sieber\",\"doi\":\"10.1021/acs.jcim.4c01547\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In the rapidly evolving field of drug discovery, high-throughput screening (HTS) is essential for identifying bioactive compounds. This study introduces a novel application of data valuation, a concept for evaluating the importance of data points based on their impact, to enhance drug discovery pipelines. Our approach improves active learning for compound library screening, robustly identifies true and false positives in HTS data, and identifies important inactive samples in an imbalanced HTS training, all while accounting for computational efficiency. We demonstrate that importance-based methods enable more effective batch screening, reducing the need for extensive HTS. Machine learning models accurately differentiate true biological activity from assay artifacts, streamlining the drug discovery process. Additionally, importance undersampling aids in HTS data set balancing, improving machine learning performance without omitting crucial inactive samples. These advancements could significantly enhance the efficiency and accuracy of drug development.\",\"PeriodicalId\":44,\"journal\":{\"name\":\"Journal of Chemical Information and Modeling \",\"volume\":\"24 1\",\"pages\":\"\"},\"PeriodicalIF\":5.6000,\"publicationDate\":\"2024-10-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Information and Modeling \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.jcim.4c01547\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Information and Modeling ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.jcim.4c01547","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Machine Learning-Driven Data Valuation for Optimizing High-Throughput Screening Pipelines
In the rapidly evolving field of drug discovery, high-throughput screening (HTS) is essential for identifying bioactive compounds. This study introduces a novel application of data valuation, a concept for evaluating the importance of data points based on their impact, to enhance drug discovery pipelines. Our approach improves active learning for compound library screening, robustly identifies true and false positives in HTS data, and identifies important inactive samples in an imbalanced HTS training, all while accounting for computational efficiency. We demonstrate that importance-based methods enable more effective batch screening, reducing the need for extensive HTS. Machine learning models accurately differentiate true biological activity from assay artifacts, streamlining the drug discovery process. Additionally, importance undersampling aids in HTS data set balancing, improving machine learning performance without omitting crucial inactive samples. These advancements could significantly enhance the efficiency and accuracy of drug development.
期刊介绍:
The Journal of Chemical Information and Modeling publishes papers reporting new methodology and/or important applications in the fields of chemical informatics and molecular modeling. Specific topics include the representation and computer-based searching of chemical databases, molecular modeling, computer-aided molecular design of new materials, catalysts, or ligands, development of new computational methods or efficient algorithms for chemical software, and biopharmaceutical chemistry including analyses of biological activity and other issues related to drug discovery.
Astute chemists, computer scientists, and information specialists look to this monthly’s insightful research studies, programming innovations, and software reviews to keep current with advances in this integral, multidisciplinary field.
As a subscriber you’ll stay abreast of database search systems, use of graph theory in chemical problems, substructure search systems, pattern recognition and clustering, analysis of chemical and physical data, molecular modeling, graphics and natural language interfaces, bibliometric and citation analysis, and synthesis design and reactions databases.