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      KCI등재 SCOPUS SCIE

      Mutual information and linkage disequilibrium based SNP association study by grouping case‐control

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      https://www.riss.kr/link?id=A104427848

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      다국어 초록 (Multilingual Abstract)

      Two main reasons for the difficulties to search for susceptibility single‐nucleotide polymorphisms (SNPs) underlying genetic diseases are that the findings are not easy to be confirmed and the interactions between potential susceptibility SNPs are n...

      Two main reasons for the difficulties to search for susceptibility single‐nucleotide polymorphisms (SNPs) underlying genetic diseases are that the findings are not easy to be confirmed and the interactions between potential susceptibility SNPs are not clear. Many available association studies usually presented results with significance levels but did not illustrate the stability of the results. In some sense, their performances might be unclear in real practice. In this paper, we develop a novel method based on mutual information theory and linkage disequilibrium by grouping case‐control. Mutual information (MI)is used to test multiple SNPs in combining with disease status.
      Those SNPs contributing the maximum MI are selected as potential susceptibility SNPs. Linkage disequilibrium (LD) analysis is used to extend MI detected result so that both direct and indirect factors can be included in the final result. The purpose of case‐control grouping is to generate a number of data groups by randomly sampling from target samples. Each group is assumed to have almost the same number of individuals (cases and controls), and overlap is allowed among the groups. We apply the method to each data group, and then make comparisons and intersections between the results obtained from each of the groups so as to give the final result.
      We implement the method by continuously grouping until the final result reaches a stable state and a highly significance level. The experimental results indicate that our method to detect susceptibility SNPs in simulated and real data sets has shown remarkable success.

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      참고문헌 (Reference)

      1 Stram DO, "Tag SNP selection for association studies" 27 : 365-374, 2004

      2 Shi YY, "SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci" 15 : 97-98, 2005

      3 Zheng M, "Multipoint linkage‐disequilibrium mapping with haplotype‐block structure" 80 : 112-125, 2007

      4 Hahn LW, "Multifactor dimensionality reduction software for detecting gene‐gene and gene‐environment interactions" 19 : 376-382, 2003

      5 Dempster AP, "Maximum likelihood from incomplete data via the EM algorithm" 39 : 1-38, 1977

      6 Bjarki E, "Linkage Disequilibrim Under Skewed Offspring Distribution Among Individuals in a Population" 178 : 1517-1532, 2008

      7 Barrett JC, "Haploview: analysis and visualization of LD and haplotype maps" 21 : 263-265, 2005

      8 Zhang K, "Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies" 14 : 908-916, 2004

      9 Zhang K, "HapBlock: haplotype block partitioning and tag SNP selection software using a set of dynamic programming algorithms" 21 : 131-134, 2005

      10 Easton DF, "Genome‐wide association study identifies novel breast cancer susceptibility loci" 447 : 1087-1093, 2007

      1 Stram DO, "Tag SNP selection for association studies" 27 : 365-374, 2004

      2 Shi YY, "SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci" 15 : 97-98, 2005

      3 Zheng M, "Multipoint linkage‐disequilibrium mapping with haplotype‐block structure" 80 : 112-125, 2007

      4 Hahn LW, "Multifactor dimensionality reduction software for detecting gene‐gene and gene‐environment interactions" 19 : 376-382, 2003

      5 Dempster AP, "Maximum likelihood from incomplete data via the EM algorithm" 39 : 1-38, 1977

      6 Bjarki E, "Linkage Disequilibrim Under Skewed Offspring Distribution Among Individuals in a Population" 178 : 1517-1532, 2008

      7 Barrett JC, "Haploview: analysis and visualization of LD and haplotype maps" 21 : 263-265, 2005

      8 Zhang K, "Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies" 14 : 908-916, 2004

      9 Zhang K, "HapBlock: haplotype block partitioning and tag SNP selection software using a set of dynamic programming algorithms" 21 : 131-134, 2005

      10 Easton DF, "Genome‐wide association study identifies novel breast cancer susceptibility loci" 447 : 1087-1093, 2007

      11 Saxena R, "Genome‐wide association analysis identifies loci for type 2 diabetes and triglyceride levels" 316 : 1331-1336, 2007

      12 Kimmel G, "GERBIL: Genotype resolution and block identification using likelihood" 102 : 158-162, 2005

      13 Hampe J, "Entropy‐based SNP selection for genetic association studies" 114 : 36-43, 2003

      14 Shannon CE, "A mathematical theory of communication" 27 : 379-423, 1948

      15 Abraham R, "A genome‐wide association study for late‐onset Alzheimer's disease using DNA pooling" 1 : 44-, 2008

      16 Burgner D, "A genomewide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease" 5 : e1000319-, 2009

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2012-05-07 학술지명변경 한글명 : 한국유전학회지 -> Genes & Genomics KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-04-14 학술지명변경 외국어명 : Korean Journal of Genetics -> Genes and Genomics KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2004-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2003-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2002-01-01 평가 등재후보학술지 유지 (등재후보1차) KCI등재후보
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.51 0.12 0.38
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.32 0.27 0.258 0.02
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