Generative Topographic Mapping (GTM): Universal Tool for Data Visualization, Structure-Activity Modeling and Dataset Comparison

被引:108
作者
Kireeva, N. [1 ,2 ]
Baskin, I. I. [1 ,3 ]
Gaspar, H. A. [1 ]
Horvath, D. [1 ]
Marcou, G. [1 ]
Varnek, A. [1 ]
机构
[1] Univ Strasbourg, Lab Infochim, CNRS, UMR 7177, F-67000 Strasbourg, France
[2] Inst Phys Chem & Electrochem RAS, Moscow 119991, Russia
[3] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119991, Russia
关键词
Generative topographic maps; Dimensionality reduction; Manifold learning; Data visualization; Predicting activity profiles; Comparison of databases; Bhattacharyya kernel; LIKELIHOOD;
D O I
10.1002/minf.201100163
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Here, the utility of Generative Topographic Maps (GTM) for data visualization, structure-activity modeling and database comparison is evaluated, on hand of subsets of the Database of Useful Decoys (DUD). Unlike other popular dimensionality reduction approaches like Principal Component Analysis, Sammon Mapping or Self-Organizing Maps, the great advantage of GTMs is providing data probability distribution functions (PDF), both in the high-dimensional space defined by molecular descriptors and in 2D latent space. PDFs for the molecules of different activity classes were successfully used to build classification models in the framework of the Bayesian approach. Because PDFs are represented by a mixture of Gaussian functions, the Bhattacharyya kernel has been proposed as a measure of the overlap of datasets, which leads to an elegant method of global comparison of chemical libraries.
引用
收藏
页码:301 / 312
页数:12
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