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dc.contributor.authorHan, Bing
dc.contributor.authorChen, Xue-wen
dc.contributor.authorWang, Xinkun
dc.contributor.authorMichaelis, Elias K.
dc.date.accessioned2015-05-11T16:13:13Z
dc.date.available2015-05-11T16:13:13Z
dc.date.issued2009-06-01
dc.identifier.citationHan, B., Chen, X., Wang, X. & Michaelis, E. K. (2009) Integrating Multiple Microarray Data for Cancer Pathway Analysis. Journal of Biomedicine and Biotechnology. http://www.dx.doi.org/10.1155/2009/707580en_US
dc.identifier.urihttp://hdl.handle.net/1808/17682
dc.descriptionThis is the publisher's version, also available electronically from "http://www.hindawi.com".en_US
dc.description.abstractPrevious applications of microarray technology for cancer research have mostly focused on identifying genes that are differentially expressed between a particular cancer and normal cells. In a biological system, genes perform different molecular functions and regulate various biological processes via interactions with other genes thus forming a variety of complex networks. Therefore, it is critical to understand the relationship (e.g., interactions) between genes across different types of cancer in order to gain insights into the molecular mechanisms of cancer. Here we propose an integrative method based on the bootstrapping Kolmogorov-Smirnov test and a large set of microarray data produced with various types of cancer to discover common molecular changes in cells from normal state to cancerous state. We evaluate our method using three key pathways related to cancer and demonstrate that it is capable of finding meaningful alterations in gene relations.en_US
dc.publisherHindawi Publishing Corporationen_US
dc.titleIntegrating Multiple Microarray Data for Cancer Pathway Analysisen_US
dc.typeArticle
kusw.kuauthorWang, Xinkun
kusw.kuauthorMichaelis, Elias K.
kusw.kudepartmentPharmacology & Toxicologyen_US
dc.identifier.doi10.1155/2009/707580
dc.identifier.orcidhttps://orcid.org/0000-0003-1377-0509
kusw.oaversionScholarly/refereed, publisher version
kusw.oapolicyThis item meets KU Open Access policy criteria.
dc.rights.accessrightsopenAccess


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