05.11.2012 Views

Abstracts Keynote & Plenary

Abstracts Keynote & Plenary

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natural structure is coded in its amino acid<br />

sequence. The way this sequence folds in the 3D space are very important, and can be used for<br />

determining protein function. Protein structures are stored in the Protein Data Bank (PDB). With the<br />

rapid growth of technology, the number of determined protein structures increases every day, so,<br />

retrieving structurally similar proteins using current algorithms takes too long (hours or even days). So,<br />

improving the efficiency of protein structure retrieval and classification methods becomes an important<br />

research issue in bioinformatics community.<br />

In this paper, a novel protein classifier is presented.<br />

Our classifier uses the information about the<br />

conformation of protein structures in 3D space. Namely, the voxel based protein descriptor is used for<br />

representing protein structures. The 3D Discrete Fourier Transform is applied to protein tertiary<br />

structures in order to produce geometry based descriptors. Additionally, some properties of the primary<br />

and secondary structure of the protein are considered, thus forming better integrated descriptor.<br />

Part of the SCOP 1.73 database was used for evaluation of our classifier. The results show that<br />

our<br />

approach achieves more than 78.83% classification accuracy and that it is much faster than other<br />

similar algorithms with comparable accuracy. We provide some experimental results.<br />

Keywords: PDB, SCOP, protein classification, Support Vector Machine (SVM).<br />

OR-021<br />

An Association<br />

Test for Multiple Traits Based on the Generalized Kendall’s Tau<br />

Xueqin Wang<br />

Department of Medical<br />

Statistics and Epidemiology, School of Public Health, Sun Yat-Sen University,<br />

Guangzhou 510080, China<br />

In many genetics studies, especially<br />

in the investigation of mental illness and behavioral disorders, it is<br />

common for researchers to collect multiple phenotypes to characterize the complex disease of interest.<br />

It may be advantageous to analyze those phenotypic measurements simultaneously if they share a<br />

similar genetic mechanism. In this study, we present a nonparametric approach to studying multiple<br />

traits together rather than examining each trait separately. Through simulation we compared the<br />

nominal type I error and power of our proposed test to an existing test, i.e., a generalized family-based<br />

association test. The empirical results suggest that our proposed approach is superior to the existing test<br />

in the analysis of ordinal traits. The advantage is demonstrated on a data set concerning alcohol<br />

dependence. In this application, the use of our methods enhanced the signal of the association test.<br />

OR-022<br />

A Series of Studies for Systems Biology of Complex Diseases<br />

Shaoqi Rao,<br />

Department of Medical Statistics and Epidemiology, School of Public Health, Sun Yat-Sen University,<br />

Guangzhou 510080, China<br />

The central theme of biomedical<br />

domians is how to use modern concepts and methods in systems<br />

biology, and high- throughput omics technologies to unravel the underlying genetic mechnisms for<br />

various complex diseases influential on human health, to discover the key genes or interactions, and<br />

finally to develop new methods and technologies for improved medical diagnosis and treatment. In last<br />

five years, the speaker and his associated bioinformatics team have been actively involved in the<br />

frontiers in cardiovascular genetics, statistical genomics and statistics, bioinformatics and systems<br />

biology. This report briefly describes the recent studies undertaken by this team, separated into: (1)<br />

applied

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