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一种改进的 k-TSP 算法及其在基于 LC-MS 的肝癌和慢性肝病代谢组学研究中的应用。

A modified k-TSP algorithm and its application in LC-MS-based metabolomics study of hepatocellular carcinoma and chronic liver diseases.

机构信息

School of Computer Science & Technology, Dalian University of Technology, 116024 Dalian, China.

Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Sep 1;966:100-8. doi: 10.1016/j.jchromb.2014.05.044. Epub 2014 Jun 2.

Abstract

In systems biology, the ability to discern meaningful information that reflects the nature of related problems from large amounts of data has become a key issue. The classification method using top scoring pairs (TSP), which measures the features of a data set in pairs and selects the top ranked feature pairs to construct the classifier, has been a powerful tool in genomics data analysis because of its simplicity and interpretability. This study examined the relationship between two features, modified the ranking criteria of the k-TSP method to measure the discriminative ability of each feature pair more accurately, and correspondingly, provided an improved classification procedure. Tests on eight public data sets showed the validity of the modified method. This modified k-TSP method was applied to our serum metabolomics data derived from liquid chromatography-mass spectrometry analysis of hepatocellular carcinoma and chronic liver diseases. Based on the 27 selected feature pairs, HCC and chronic liver diseases were accurately distinguished using the principal component analysis, and certain profound metabolic disturbances related to liver disease development were revealed by the feature pairs.

摘要

在系统生物学中,从大量数据中辨别出反映相关问题本质的有意义信息已成为一个关键问题。使用最高分对(TSP)的分类方法,通过成对地测量数据集的特征并选择排名最高的特征对来构建分类器,由于其简单性和可解释性,已成为基因组学数据分析的有力工具。本研究检验了两个特征之间的关系,修改了 k-TSP 方法的排名标准,以更准确地衡量每个特征对的判别能力,并相应地提供了一种改进的分类程序。对八个公共数据集的测试表明了该改进方法的有效性。该改进的 k-TSP 方法应用于我们从肝细胞癌和慢性肝病的液相色谱-质谱分析中获得的血清代谢组学数据。基于 27 个选定的特征对,使用主成分分析准确地区分了 HCC 和慢性肝病,并通过特征对揭示了与肝病发展相关的某些深刻的代谢紊乱。

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