Dataset Information

Ligand Classifier of Adaptively Boosting Ensemble Decision Stumps (LiCABEDS) and its application on modeling ligand functionality for 5HT-subtype GPCR families.

ABSTRACT: Advanced high-throughput screening (HTS) technologies generate great amounts of bioactivity data, and this data needs to be analyzed and interpreted with attention to understand how these small molecules affect biological systems. As such, there is an increasing demand to develop and adapt cheminformatics algorithms and tools in order to predict molecular and pharmacological properties on the basis of these large data sets. In this manuscript, we report a novel machine-learning-based ligand classification algorithm, named Ligand Classifier of Adaptively Boosting Ensemble Decision Stumps (LiCABEDS), for data-mining and modeling of large chemical data sets to predict pharmacological properties in an efficient and accurate manner. The performance of LiCABEDS was evaluated through predicting GPCR ligand functionality (agonist or antagonist) using four different molecular fingerprints, including Maccs, FP2, Unity, and Molprint 2D fingerprints. Our studies showed that LiCABEDS outperformed two other popular techniques, classification tree and Naive Bayes classifier, on all four types of molecular fingerprints. Parameters in LiCABEDS, including the number of boosting iterations, initialization condition, and a "reject option" boundary, were thoroughly explored and discussed to demonstrate the capability of handling imbalanced data sets, as well as its robustness and flexibility. In addition, the detailed mathematical concepts and theory are also given to address the principle behind statistical prediction models. The LiCABEDS algorithm has been implemented into a user-friendly software package that is accessible online at http://www.cbligand.org/LiCABEDS/ .

SUBMITTER: Ma C

PROVIDER: S-EPMC3065508 | biostudies-literature | 2011 Mar

REPOSITORIES: biostudies-literature

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Ligand Classifier of Adaptively Boosting Ensemble Decision Stumps (LiCABEDS) and its application on modeling ligand functionality for 5HT-subtype GPCR families.

Ma Chao C Wang Lirong L Xie Xiang-Qun XQ

Journal of chemical information and modeling 20110307 3

Advanced high-throughput screening (HTS) technologies generate great amounts of bioactivity data, and this data needs to be analyzed and interpreted with attention to understand how these small molecules affect biological systems. As such, there is an increasing demand to develop and adapt cheminformatics algorithms and tools in order to predict molecular and pharmacological properties on the basis of these large data sets. In this manuscript, we report a novel machine-learning-based ligand clas ...[more]

PMID: 21381738

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Project description:BackgroundAutomated, image based high-content screening is a fundamental tool for discovery in biological science. Modern robotic fluorescence microscopes are able to capture thousands of images from massively parallel experiments such as RNA interference (RNAi) or small-molecule screens. As such, efficient computational methods are required for automatic cellular phenotype identification capable of dealing with large image data sets. In this paper we investigated an efficient method for the extraction of quantitative features from images by combining second order statistics, or Haralick features, with curvelet transform. A random subspace based classifier ensemble with multiple layer perceptron (MLP) as the base classifier was then exploited for classification. Haralick features estimate image properties related to second-order statistics based on the grey level co-occurrence matrix (GLCM), which has been extensively used for various image processing applications. The curvelet transform has a more sparse representation of the image than wavelet, thus offering a description with higher time frequency resolution and high degree of directionality and anisotropy, which is particularly appropriate for many images rich with edges and curves. A combined feature description from Haralick feature and curvelet transform can further increase the accuracy of classification by taking their complementary information. We then investigate the applicability of the random subspace (RS) ensemble method for phenotype classification based on microscopy images. A base classifier is trained with a RS sampled subset of the original feature set and the ensemble assigns a class label by majority voting.ResultsExperimental results on the phenotype recognition from three benchmarking image sets including HeLa, CHO and RNAi show the effectiveness of the proposed approach. The combined feature is better than any individual one in the classification accuracy. The ensemble model produces better classification performance compared to the component neural networks trained. For the three images sets HeLa, CHO and RNAi, the Random Subspace Ensembles offers the classification rates 91.20%, 98.86% and 91.03% respectively, which compares sharply with the published result 84%, 93% and 82% from a multi-purpose image classifier WND-CHARM which applied wavelet transforms and other feature extraction methods. We investigated the problem of estimation of ensemble parameters and found that satisfactory performance improvement could be brought by a relative medium dimensionality of feature subsets and small ensemble size.ConclusionsThe characteristics of curvelet transform of being multiscale and multidirectional suit the description of microscopy images very well. It is empirically demonstrated that the curvelet-based feature is clearly preferred to wavelet-based feature for bioimage descriptions. The random subspace ensemble of MLPs is much better than a number of commonly applied multi-class classifiers in the investigated application of phenotype recognition.

Dataset Information

Ligand Classifier of Adaptively Boosting Ensemble Decision Stumps (LiCABEDS) and its application on modeling ligand functionality for 5HT-subtype GPCR families.

Publications

Ligand Classifier of Adaptively Boosting Ensemble Decision Stumps (LiCABEDS) and its application on modeling ligand functionality for 5HT-subtype GPCR families.

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