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Volumn 26, Issue 17, 2010, Pages 2208-2209

CNVineta: A data mining tool for large case-control copy number variation datasets

Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; ARTICLE; COMPUTER PROGRAM; DATA MINING; DNA MICROARRAY; GENE DOSAGE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; HUMAN GENOME; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 77955863414     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btq356     Document Type: Article
Times cited : (6)

References (10)
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    • (2008) Nat. Genet. , vol.40 , pp. 1245-1252
    • Barnes, C.1
  • 2
    • 34247877877 scopus 로고    scopus 로고
    • QuantiSNP: an objective Bayes hidden-Markov model to detect and accurately map copy number variation using SNP genotyping data
    • Colella, S. et al. (2007) QuantiSNP: an objective Bayes hidden-Markov model to detect and accurately map copy number variation using SNP genotyping data. Nucleic Acids Res., 35, 2013-2025.
    • (2007) Nucleic Acids Res. , vol.35 , pp. 2013-2025
    • Colella, S.1
  • 3
    • 79959503826 scopus 로고    scopus 로고
    • The International Hap Map Project
    • International HapMap Consortium
    • International HapMap Consortium (2003) The International HapMap Project. Nature, 426, 789-796.
    • (2003) Nature , vol.426 , pp. 789-796
  • 5
    • 70349956433 scopus 로고    scopus 로고
    • Finding the missing heritability of complex diseases
    • Manolio, T.A. et al. (2009) Finding the missing heritability of complex diseases. Nature, 461, 747-753.
    • (2009) Nature , vol.461 , pp. 747-753
    • Manolio, T.A.1
  • 6
    • 50449091647 scopus 로고    scopus 로고
    • Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease
    • McCarroll, S.A. et al. (2008) Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease. Nat. Genet., 40, 1107-1112.
    • (2008) Nat. Genet. , vol.40 , pp. 1107-1112
    • McCarroll, S.A.1
  • 7
    • 33746512512 scopus 로고    scopus 로고
    • Principal components analysis corrects for stratification in genome-wide association studies
    • Price, A.L. et al. (2006) Principal components analysis corrects for stratification in genome-wide association studies. Nat. Genet., 38, 904-909.
    • (2006) Nat. Genet. , vol.38 , pp. 904-909
    • Price, A.L.1
  • 8
    • 70350004083 scopus 로고    scopus 로고
    • Comparing CNV detection methods for SNP arrays
    • Winchester, L. et al. (2009) Comparing CNV detection methods for SNP arrays. Brief. Funct. Genomic Proteomic, 8, 353-356.
    • (2009) Brief. Funct. Genomic Proteomic , vol.8 , pp. 353-356
    • Winchester, L.1
  • 9
    • 84969213492 scopus 로고    scopus 로고
    • Genome-wide association study of 14, 000 cases of seven common diseases and 3, 000 shared controls
    • WTCCC
    • WTCCC (2007) Genome-wide association study of 14, 000 cases of seven common diseases and 3, 000 shared controls. Nature, 447, 661-678.
    • (2007) Nature , vol.447 , pp. 661-678
  • 10
    • 70350221909 scopus 로고    scopus 로고
    • Copy number variation in human health, disease, and evolution
    • Zhang, F. et al. (2009) Copy number variation in human health, disease, and evolution. Annu. Rev. Genomics Hum. Genet., 10, 451-481.
    • (2009) Annu. Rev. Genomics Hum. Genet. , vol.10 , pp. 451-481
    • Zhang, F.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.