Analysis of Important Gene Ontology Terms and Biological Pathways Related to Pancreatic Cancer.

Pancreatic cancer is a serious disease that results in more than thirty thousand deaths around the world per year. To design effective treatments, many investigators have devoted themselves to the study of biological processes and mechanisms underlying this disease. However, it is far from complete....

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Publicado en:BioMed Research International Vol. 2016; pp. 1 - 11
Autores principales: Yin, Hang, Wang, ShaoPeng, Zhang, Yu-Hang, Cai, Yu-Dong, Liu, Hailin
Formato: equations & formulas research tables/charts Journal Article
Publicado: Wiley-Blackwell 11/9/2016
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 11/9/2016
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      pub: Wiley-Blackwell
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        10.1155/2016/7861274
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        atl: Analysis of Important Gene Ontology Terms and Biological Pathways Related to Pancreatic Cancer.
      aug:
        au:
          Yin, Hang
          Wang, ShaoPeng
          Zhang, Yu-Hang
          Cai, Yu-Dong
          Liu, Hailin
        affil: Department of Gastroenterology, Ninth People’s Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200011, China
      sug:
        subj:
          Pancreatic Neoplasms Familial and Genetic
          Ontologies
          Genetic Research
          Bioinformatics
          Descriptive Statistics
          P-Value
          Pancreatic Neoplasms Classification
          Signal Transduction
          Protein Kinases
          Funding Source
      ab: Pancreatic cancer is a serious disease that results in more than thirty thousand deaths around the world per year. To design effective treatments, many investigators have devoted themselves to the study of biological processes and mechanisms underlying this disease. However, it is far from complete. In this study, we tried to extract important gene ontology (GO) terms and KEGG pathways for pancreatic cancer by adopting some existing computational methods. Genes that have been validated to be related to pancreatic cancer and have not been validated were represented by features derived from GO terms and KEGG pathways using the enrichment theory. A popular feature selection method, minimum redundancy maximum relevance, was employed to analyze these features and extract important GO terms and KEGG pathways. An extensive analysis of the obtained GO terms and KEGG pathways was provided to confirm the correlations between them and pancreatic cancer.
      pubtype: Academic Journal
      doctype:
        equations & formulas
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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