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Biclustering strategies for genetic marker selection in gynecologic tumor cell lines

机译:妇科肿瘤细胞系遗传标记选择的聚类策略

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Over the past few decades great interest has been focused on cell lines derived from tumors, because of their usability as models to understand the biology of cancer. At the same time, advanced technologies such as DNA-microarrays have been broadly used to study the expression level of thousands of genes in primary tumors or cancer cell lines in a single experiment. Results from microarray analysis approaches have provided valuable insights into the underlying biology and proven useful for tumor classification, prognostication and prediction. Our approach utilizes biclustering methods for the discovery of genes with coherent expression across a subset of conditions (cell lines of a tumor type). More specifically, we present a novel modification on Cheng & Church's algorithm that searches for differences across the studied conditions, but also enforces consistent intensity characteristics of each cluster within each condition. The application of this approach on a gynecologic panel of cell lines succeeds to derive discriminant groups of compact bi-clusters across four types of tumor cell lines. In this form, the proposed approach is proven efficient for the derivation of tumor-specific markers.
机译:在过去的几十年中,由于它们可用作理解癌症生物学模型的用途,因此人们对由肿瘤衍生的细胞系引起了极大的兴趣。同时,诸如DNA微阵列之类的先进技术已被广泛用于在单个实验中研究数千种基因在原发性肿瘤或癌细胞系中的表达水平。微阵列分析方法的结果为基础生物学提供了宝贵的见解,并被证明对肿瘤的分类,预后和预测有用。我们的方法利用双聚类分析方法来发现在部分条件(肿瘤类型的细胞系)中具有一致表达的基因。更具体地说,我们对Cheng&Church算法提出了一种新颖的修改形式,可以搜索研究条件之间的差异,而且还可以在每个条件下强制每个聚类的强度特征一致。这种方法在妇科细胞系中的应用成功地在四种类型的肿瘤细胞系中获得了紧凑的双簇的判别组。以这种形式,已证明所提出的方法对于衍生肿瘤特异性标记物是有效的。

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