{"title":"Statistical discrimination of breast cancer microarray data","authors":"Gautam Kumar, Tapobarata Lahiri, Rajnish Kumar","doi":"10.1109/BSB.2016.7552136","DOIUrl":null,"url":null,"abstract":"Recently published literatures indicate that, a consistent and precise classification system of microarray data is very essential for the successful identification of genes responsible for a cancer subtype and early treatment of cancer. However, in common clinical practice, diagnostic assertion of malignancies mostly relies on the morphological examination of tissues and clinical tests. In spite of the recent progress of treatment that uses semiempirical approaches involving computation methods, there are still uncertainties in cancer identification and diagnosis. High density oligonucleotide chips and genomic microarray data are being used progressively more in cancer research by generating huge expression data for thousands of genes simultaneously that poses problem of mining specific genes responsible for characterization of a specific cancer subtype. In this backdrop, we briefly address the impact of various statistical methods and their relative performances for the identification of potential probes and Discriminant genes for the breast cancer. We used Fisher's Discriminant Ratio (FDR), two tailed T-Test and vector norm on raw expression data and for each of the probe generated from the difference data accounting for up and down regulation of expression for each probes for various samples. The result indicates the potential of these methods to identify genes responsible for manifestation of breast cancer which is also well supported by the published result of experiments. The success of this approach not only gives the benefit of identification of cancer specific genes but also may help building of efficient classifier on the basis of these genes for automatic diagnostics of cancer.","PeriodicalId":363820,"journal":{"name":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","volume":"157 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2016-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/BSB.2016.7552136","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
Recently published literatures indicate that, a consistent and precise classification system of microarray data is very essential for the successful identification of genes responsible for a cancer subtype and early treatment of cancer. However, in common clinical practice, diagnostic assertion of malignancies mostly relies on the morphological examination of tissues and clinical tests. In spite of the recent progress of treatment that uses semiempirical approaches involving computation methods, there are still uncertainties in cancer identification and diagnosis. High density oligonucleotide chips and genomic microarray data are being used progressively more in cancer research by generating huge expression data for thousands of genes simultaneously that poses problem of mining specific genes responsible for characterization of a specific cancer subtype. In this backdrop, we briefly address the impact of various statistical methods and their relative performances for the identification of potential probes and Discriminant genes for the breast cancer. We used Fisher's Discriminant Ratio (FDR), two tailed T-Test and vector norm on raw expression data and for each of the probe generated from the difference data accounting for up and down regulation of expression for each probes for various samples. The result indicates the potential of these methods to identify genes responsible for manifestation of breast cancer which is also well supported by the published result of experiments. The success of this approach not only gives the benefit of identification of cancer specific genes but also may help building of efficient classifier on the basis of these genes for automatic diagnostics of cancer.
最近发表的文献表明,一个一致和精确的微阵列数据分类系统对于成功识别癌症亚型的基因和癌症的早期治疗至关重要。然而,在常见的临床实践中,恶性肿瘤的诊断断言大多依赖于组织形态学检查和临床试验。尽管近年来使用涉及计算方法的半经验方法的治疗取得了进展,但在癌症的识别和诊断中仍然存在不确定性。高密度寡核苷酸芯片和基因组微阵列数据正在越来越多地用于癌症研究,同时产生数千个基因的大量表达数据,这给挖掘特定癌症亚型特征的特定基因带来了问题。在此背景下,我们简要地讨论了各种统计方法及其相对性能对乳腺癌潜在探针和判别基因鉴定的影响。我们使用Fisher’s Discriminant Ratio (FDR)、双尾t检验和矢量范数对原始表达数据和从差异数据生成的每个探针进行分析,以解释不同样本中每个探针的表达上下调节。这一结果表明,这些方法有潜力识别出与乳腺癌表现有关的基因,这也得到了已发表的实验结果的很好支持。该方法的成功不仅有利于癌症特异性基因的识别,而且有助于在这些基因的基础上建立有效的分类器,用于癌症的自动诊断。