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DCGene: A Novel Predicting Approach of the Disease Related Genes on Functional Annotation

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Emerging Intelligent Computing Technology and Applications (ICIC 2009)

Part of the book series: Lecture Notes in Computer Science ((LNTCS,volume 5754))

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Abstract

Disease Candidate Genes (DCGene) is an advanced system for predicting the disease related genes, It is a novel computational approach by using the GO annotation information. The performance of the DCGene is evaluated in a set containing 1057 test samples, on both the local region and genome scale. In the local region scale, for 397 of 1057 (37.6%) samples, the disease-associated genes are at the top 1 of the out put gene prioritization list, and if the top 9 genes are all considered, 754(71.3%) disease-associated genes are included in the result. In the genome scale, 55% of the disease-relevant genes are included in the top scoring 3%, and 74% of the disease-relevant genes are included in the top 15%. The performance of the DCGene is demonstrated to be significant better than the others by comparison with the other systems and methods.

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References

  1. Lander, E.S., Linton, L.M., et al.: Initial Sequencing and Analysis of the Human Genome. Nature 409, 860–921 (2001)

    Article  Google Scholar 

  2. Venter, J.C., Adams, M.D., Myers, E.W., et al.: The Sequence of the Human Genome. Science 291, 1304–1351 (2001)

    Article  Google Scholar 

  3. McCarthy, M.I., Smedley, D., Hide, W.: New Methods for Finding Disease-susceptibility Genes: Impact and Potential. Genome Biology 4, 119 (2003)

    Article  Google Scholar 

  4. Perez-Iratxeta, C., Bork, P., Andrade, M.A.: Association of Genes to Genetically Inherited Diseases Using Data Mining. Nature Genetics 31, 316–319 (2002)

    Google Scholar 

  5. Perez-Iratxeta, C., Matthias, W., Bork, P., et al.: G2D: A Tool for Mining Genes Associated with Disease. BMC Genetics 6, 45 (2005)

    Article  Google Scholar 

  6. Turner, F.S., Clutterbuck, D.R., Semple, C.A.: POCUS: Mining Genomic Sequence Annotation to Predict Disease Genes. Genome Biology 4, R75 (2003)

    Article  Google Scholar 

  7. Freudenberg, J., Propping, P.: A Similarity-based Method for Genome-wide Prediction of Disease-relevant Human Genes. Bioinformatics 18(Suppl. 2), S110–S115 (2002)

    Google Scholar 

  8. Adie, E.A., Adams, R.R., Evans, K.L., Porteous, D.J., Pickard, B.S.: SUSPECTS: Enabling Fast and Effective Prioritization of Positional Candidates. Bioinformatics 22, 773–777 (2006)

    Article  Google Scholar 

  9. Aerts, S.: Gene Prioritization through Genomic Data Fusion. Nat. Biotechnol. 24, 537–544 (2006)

    Article  Google Scholar 

  10. Franke, L., Bakel, H., Fokkens, L., Jong, E.D., Egmont-Petersen, M., Wijmenga, C.: Reconstruction of a Functional Human Gene Network, with an Application for Prioritizing Positional Candidate Genes. Am. J. Hum. Genet. 78, 1011–1025 (2006)

    Article  Google Scholar 

  11. Ashburner, M., et al.: Gene Ontology: Tool for the Unification of Biology. Nature Genetics 25, 25–29 (2000)

    Article  Google Scholar 

  12. Hamosh, A., Scott, A.F., Amberger, J.S.: Online Mendelian Inheritance in Man (OMIM), a Knowledgebase of Human Genes and Genetic Disorders. Nucleic Acids Research 33, D514–D517 (2005)

    Article  Google Scholar 

  13. Pruitt, K.D., Maglott, D.R.: RefSeq and LocusLink: NCBI Gene-centered Resources. Nucleic Acids Res. 29(1), 137–140 (2001)

    Article  Google Scholar 

  14. Botstein, D., Risch, N.: Discovering Genotypes Underlying Human Phenotypes: Past Successes for Mendelian Disease, Future Approaches for Complex Disease. Nature genetics supplement 33, 228–237 (2003)

    Article  Google Scholar 

  15. Lehmann, A.R.: The Xeroderma Pigmentosum Group D(XPD) Gene: One Gene, Two Functions, Three Diseases. Genes & Development 15, 15–23 (2001)

    Article  Google Scholar 

  16. Nemeth, A.H.: The Genetics of Primary Dystonias and Related Disorders. Brain 125, 695–721 (2002)

    Article  Google Scholar 

  17. Van Steensel, M.A., Celli, J., Van Bokhoven, J.H., et al.: Probing the Gene eXpression Database for Candidate Genes. European Journal of Human Genetics 7, 910–919 (1999)

    Article  Google Scholar 

  18. Van Driel, M.A., Cuelenaere, K., Kemmeren, P.P., et al.: A New Web-based Data Mining Tool for the Identification of Candidate Genes for Human Genetic Disorders. European Journal of Human Genetics 11, 57–63 (2003)

    Article  Google Scholar 

  19. Kondrashov, F.A., Ogurtsov, A.Y., Kondrashov, A.S.: Bioinformatical Assay of Human Gene Morbidity. Nucleic Acids Res. 32(5), 1731–1737 (2004)

    Article  Google Scholar 

  20. Lopez-Bigas, N., Ouzounis, C.A.: Genome-wide Identification of Genes Likely to be Involved in Human Genetic Disorder. Nucleic Acids Res. 32(10), 3108–3114 (2004)

    Article  Google Scholar 

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Fang, Y., Wang, H. (2009). DCGene: A Novel Predicting Approach of the Disease Related Genes on Functional Annotation. In: Huang, DS., Jo, KH., Lee, HH., Kang, HJ., Bevilacqua, V. (eds) Emerging Intelligent Computing Technology and Applications. ICIC 2009. Lecture Notes in Computer Science, vol 5754. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-04070-2_101

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  • DOI: https://doi.org/10.1007/978-3-642-04070-2_101

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-04069-6

  • Online ISBN: 978-3-642-04070-2

  • eBook Packages: Computer ScienceComputer Science (R0)

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