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    RISS 인기검색어

      최신 Single Nucleotide Polymorphism (SNP) 분석법의 원리 및 유전자 연구 응용법 = Principle And Application of Single Nucleotide Polymorphism (SNP) Analysis

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      https://www.riss.kr/link?id=A60248001

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      부가정보

      다국어 초록 (Multilingual Abstract)

      This mini review describes the principles, protocols, and applications of three commercially available Single Nucleotide Polymorphism (SNP) genotyping platforms, the TaqMan® SNP Genotyping Assay, SNPlexTM Genotyping System and Gene Chip Assay. These ...

      This mini review describes the principles, protocols, and applications of three commercially available Single Nucleotide Polymorphism (SNP) genotyping platforms, the TaqMan® SNP Genotyping Assay, SNPlexTM Genotyping System and Gene Chip Assay. These technologies meet the requirements of multiple SNP applications in genetics research including diseases based on genetic background. This article also describes a set of SNP selection guide and useful web sites for SNP informations. Overall, the TaqMan assay format is suitable for low- to mid-throughput applications in which a high assay conversion rate, simple assay workflow, and low cost of automation are desirable. The SNPlex Genotyping System, on the other hand, is well suited for SNP applications in which throughput and cost-efficiency are essential, e.g., applications requiring either the testing of large numbers of SNPs and samples, or the flexibility to select various SNP subsets. Gene Chip Assay is powerful tool to analyze whole SNPs and has benefit to find new SNPs involved diseases or phenotype but has a defect that it is costly. In the conclusion, this article suggests the appropriate methods for the desired experiments by comparing with these three SNPs technologies.

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      목차 (Table of Contents)

      • 서론
      • TaqMan® 방식의 SNP Genotyping Assay
      • SNPlexTM Genotyping System
      • Gene Chip Assay
      • SNP Probe의 선정 및 design
      • 서론
      • TaqMan® 방식의 SNP Genotyping Assay
      • SNPlexTM Genotyping System
      • Gene Chip Assay
      • SNP Probe의 선정 및 design
      • SNP analysis의 방향과 응용
      • 결론
      • 참고문헌
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      참고문헌 (Reference)

      1 박미선, "한우 판별용 SNP 마커조합 (SNP MARKERS FOR DISCRIMINATION OF HANWOO)"

      2 Miller MP, "Understanding human disease mutations through the use of interspecific genetic variation" 10 : 2319-2328, 2001

      3 Venter JC, "The sequence of the human genome" 291 : 1304-1351, 2001

      4 Risch N, "The future of genetic studies of complex human diseases" 273 : 1516-1517, 1996

      5 McGuigan FE, "Single nucleotide polymorphism detection: allelic discrimination using TaqMan" 12 : 133-136, 2002

      6 Shastry BS, "SNPs and haplotypes: genetics markers for disease and drug response" 11 : 379-382, 2003

      7 Shastry BS, "Role of SNP/haplotype map in gene discovery and drug development: an overview" 62 : 142-150, 2004

      8 Evans WE, "Pharmacogenomics: the inherited basis for interindividual differences in drug response" 2 : 9-39, 2001

      9 Livak KJ, "Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization" 4 : 357-362, 1995

      10 BRLMM, "Improved Genotype Calling Method for the GeneChip Human Mapping 500K Array Set"

      1 박미선, "한우 판별용 SNP 마커조합 (SNP MARKERS FOR DISCRIMINATION OF HANWOO)"

      2 Miller MP, "Understanding human disease mutations through the use of interspecific genetic variation" 10 : 2319-2328, 2001

      3 Venter JC, "The sequence of the human genome" 291 : 1304-1351, 2001

      4 Risch N, "The future of genetic studies of complex human diseases" 273 : 1516-1517, 1996

      5 McGuigan FE, "Single nucleotide polymorphism detection: allelic discrimination using TaqMan" 12 : 133-136, 2002

      6 Shastry BS, "SNPs and haplotypes: genetics markers for disease and drug response" 11 : 379-382, 2003

      7 Shastry BS, "Role of SNP/haplotype map in gene discovery and drug development: an overview" 62 : 142-150, 2004

      8 Evans WE, "Pharmacogenomics: the inherited basis for interindividual differences in drug response" 2 : 9-39, 2001

      9 Livak KJ, "Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization" 4 : 357-362, 1995

      10 BRLMM, "Improved Genotype Calling Method for the GeneChip Human Mapping 500K Array Set"

      11 Emilien G, "Impact of genomics on drug discovery and clinical medicine" 93 : 391-423, 2000

      12 Hirschhorn JN, "Genome-wide association studies for common diseases and complex traits" 6 : 95-108, 2005

      13 Subramanian S, "Evolutionary anatomies of position and types o f disease a ssociated and n eutral amino a cid mutations in the human genome" 7 : 306-312, 2006

      14 6)Afonina I, "Efficient priming of PCR with short oligonucleotides conjugated to a minor groove binder" 25 : 2657-2660, 1997

      15 Botstein D, "Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease" 33 : 228-237, 2003

      16 Francisco MDLV, "Assessment of two flexible and compatible SNP genotyping platforms: TaqMan® SNP Genotyping Assays and the SNPlexTM Genotyping System" 573 : 111-135, 2005

      17 Livak KJ, "Allelic discrimination using fluorogenic probes and the 5nuclease assay" 14 : 143-149, 1999

      18 Rabbee N, "A genotype calling algorithm for affymetrix SNP arrays" 22 : 7-12, 2006

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2018-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2017-01-01 평가 등재후보학술지 유지 (계속평가) KCI등재후보
      2015-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.02 0.02 0.03
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.04 0.04 0.21 0
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