利用核苷酸性质组成特征预测人类Pol II启动子

Q2 Medicine
Wen-Lin Huang, C. Tung, Shinn-Ying Ho
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引用次数: 1

摘要

RNA聚合酶II (RNA polymerase II, Pol II)启动子是调控蛋白质编码基因差异转录的关键区域。RNA聚合酶II (Pol II)启动子的鉴定是基因组注释中最具挑战性的问题之一。虽然已经开发了许多启动子预测方法和工具,但它们尚未从大规模DNA序列中提取信息特征以提高预测准确性。提出了一种挖掘信息核苷酸属性组成(NPC)特征的预测方法ProPolyII,用于设计基于支持向量机的分类器。使用现有的数据集驼峰(1872个人类启动子和1870个非启动子)来评估ProPolyII的启动子预测。ProPolyII产生70个信息丰富的NPC特征,训练和测试准确率分别为99.1%和95.1%。这70个NPC特征包括46个4-mer基序,3个核苷酸特性和21个全局描述符。该方法的准确率分别高于promm - machine(94.9%和91.1%)和M1(97.4%和93.6%),前者分别使用了前128个4-mer motif和36个全局描述符。与其他方法相比,ProPolyII具有较高的预测性能,可用于启动子的识别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human Pol II promoter prediction by using nucleotide property composition features
RNA polymerase II (Pol II) promoter is a key region that regulates differential transcription of protein coding genes. The identification of the RNA polymerase II (Pol II) promoter is one of the most challenging problems in genome annotation. Though many promoter prediction methods and tools have been developed, they have not yet extracted informative features from large-scale DNA sequences to improve predictive accuracy. A prediction method ProPolyII, which involves mining informative nucleotide property composition (NPC) features, is proposed to design a support vector machine-based classifier. An existing data set HumP (1872 human promoters and 1870 non-promoters) is used to evaluate ProPolyII for promoter prediction. ProPolyII yields 70 informative NPC features with training and test accuracies of 99.1% and 95.1%, respectively. The 70 NPC features consist of 46 4-mer motifs, 3 nucleotide properties and 21 global descriptors. The accuracies are better than those of Prom-Machine (94.9% and 91.1%) and M1 (97.4% and 93.6%) which uses top 128 4-mer motifs and 36 global descriptors, respectively. The high predictive performance indicates that ProPolyII can be beneficial in the identification of promoters comparative to other methods.
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来源期刊
In Silico Biology
In Silico Biology Computer Science-Computational Theory and Mathematics
CiteScore
2.20
自引率
0.00%
发文量
1
期刊介绍: The considerable "algorithmic complexity" of biological systems requires a huge amount of detailed information for their complete description. Although far from being complete, the overwhelming quantity of small pieces of information gathered for all kind of biological systems at the molecular and cellular level requires computational tools to be adequately stored and interpreted. Interpretation of data means to abstract them as much as allowed to provide a systematic, an integrative view of biology. Most of the presently available scientific journals focus either on accumulating more data from elaborate experimental approaches, or on presenting new algorithms for the interpretation of these data. Both approaches are meritorious.
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