Bruno Mendes Moro Conque, A. Kashiwabara, Fabricio M. Lopes
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The edges are estimated by observing the respective adjacency among the nucleotides in the genomic sequence. These complex network measures are extracted and adopted in order to generate a feature vector for each genomic sequence. For each biological sequence, the entropy, sum of entropy and its maximum value are also adopted. A dataset containing 3 different genomic sequences: coding, intergenic and TSS (Transcriptional Starter Sites) were adopted in order to evaluate the proposed approach. The results were obtained by the following classification methods: Random Forest with 91.2%, followed by J48 with 89.1% and SVM with 84.8% of accuracy without including any source of a priori information, i.e., considering only the genomic sequences. These results indicate the suitability, effectiveness and robustness of the proposed feature extraction approach for the classification of the adopted classes of genomic sequences.","PeriodicalId":275095,"journal":{"name":"2016 9th International Congress on Image and Signal Processing, BioMedical Engineering and Informatics (CISP-BMEI)","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2016-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"A feature extraction approach based on complex networks for genomic sequences recognition\",\"authors\":\"Bruno Mendes Moro Conque, A. Kashiwabara, Fabricio M. Lopes\",\"doi\":\"10.1109/CISP-BMEI.2016.7853010\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The development of new genomic sequencing techniques leads to a generation of a huge volume of biological data. In this context, it is important to develop new pattern recognition methods and improve its accuracy in order to support the analysis of these huge volume of data. In particular, a valuable information of the genomic sequences is its nucleotides organization. This work presents an effective feature extraction approach for genomic sequences from complex networks, which is based on mapping the genomic sequences in its representation as complex networks. The nodes of the networks are defined by the combination of nucleotides, dinucleotides or trinucleotides within the sequence by adopting the parameters: Word Size (W S) and Step (ST). The edges are estimated by observing the respective adjacency among the nucleotides in the genomic sequence. These complex network measures are extracted and adopted in order to generate a feature vector for each genomic sequence. For each biological sequence, the entropy, sum of entropy and its maximum value are also adopted. A dataset containing 3 different genomic sequences: coding, intergenic and TSS (Transcriptional Starter Sites) were adopted in order to evaluate the proposed approach. The results were obtained by the following classification methods: Random Forest with 91.2%, followed by J48 with 89.1% and SVM with 84.8% of accuracy without including any source of a priori information, i.e., considering only the genomic sequences. 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引用次数: 1
摘要
新的基因组测序技术的发展导致了大量生物数据的产生。在此背景下,开发新的模式识别方法并提高其准确性,以支持对这些海量数据的分析是非常重要的。特别是,基因组序列的一个有价值的信息是它的核苷酸组织。本文提出了一种从复杂网络中提取基因组序列特征的有效方法,该方法基于将基因组序列的表示映射为复杂网络。网络的节点由序列内核苷酸、二核苷酸或三核苷酸的组合来定义,采用参数:Word Size (W S)和Step (ST)。通过观察基因组序列中核苷酸之间各自的邻接性来估计边缘。这些复杂的网络度量被提取并用于生成每个基因组序列的特征向量。对于每个生物序列,也采用熵、熵和及其最大值。采用了包含3个不同基因组序列的数据集:编码序列、基因间序列和转录起始位点(TSS),以评估所提出的方法。在不考虑任何先验信息来源,即只考虑基因组序列的情况下,采用随机森林(Random Forest)的准确率为91.2%,J48的准确率为89.1%,SVM的准确率为84.8%。这些结果表明了所提出的特征提取方法对所采用的基因组序列分类的适用性、有效性和鲁棒性。
A feature extraction approach based on complex networks for genomic sequences recognition
The development of new genomic sequencing techniques leads to a generation of a huge volume of biological data. In this context, it is important to develop new pattern recognition methods and improve its accuracy in order to support the analysis of these huge volume of data. In particular, a valuable information of the genomic sequences is its nucleotides organization. This work presents an effective feature extraction approach for genomic sequences from complex networks, which is based on mapping the genomic sequences in its representation as complex networks. The nodes of the networks are defined by the combination of nucleotides, dinucleotides or trinucleotides within the sequence by adopting the parameters: Word Size (W S) and Step (ST). The edges are estimated by observing the respective adjacency among the nucleotides in the genomic sequence. These complex network measures are extracted and adopted in order to generate a feature vector for each genomic sequence. For each biological sequence, the entropy, sum of entropy and its maximum value are also adopted. A dataset containing 3 different genomic sequences: coding, intergenic and TSS (Transcriptional Starter Sites) were adopted in order to evaluate the proposed approach. The results were obtained by the following classification methods: Random Forest with 91.2%, followed by J48 with 89.1% and SVM with 84.8% of accuracy without including any source of a priori information, i.e., considering only the genomic sequences. These results indicate the suitability, effectiveness and robustness of the proposed feature extraction approach for the classification of the adopted classes of genomic sequences.