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Volumn 27, Issue 13, 2011, Pages 1873-1875

famCNV: Copy number variant association for quantitative traits in families

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; COMPUTER PROGRAM; COPY NUMBER VARIATION; FAMILY; GENE FREQUENCY; GENERAL ASPECTS OF DISEASE; GENETIC ASSOCIATION; GENETICS; HUMAN; PHENOTYPE; QUANTITATIVE TRAIT;

EID: 79959419881     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btr264     Document Type: Note
Times cited : (10)

References (17)
  • 1
    • 0033909546 scopus 로고    scopus 로고
    • Ageneral test of association for quantitative traits in nuclear families
    • Abecasis,G.R. et al. (2000)Ageneral test of association for quantitative traits in nuclear families. Am. J. Hum. Genet., 66, 279-292.
    • (2000) Am. J. Hum. Genet. , vol.66 , pp. 279-292
    • Abecasis, G.R.1
  • 2
    • 0028058128 scopus 로고
    • Robust variance-components approach for assessing genetic linkage in pedigrees
    • Amos,C.I. (1994) Robust variance-components approach for assessing genetic linkage in pedigrees. Am. J. Hum. Genet., 54, 535-543.
    • (1994) Am. J. Hum. Genet. , vol.54 , pp. 535-543
    • Amos, C.I.1
  • 3
    • 35048838105 scopus 로고    scopus 로고
    • Genomewide rapid association using mixed model and regression: a fast and simple method for genomewide pedigree-based quantitative trait loci association analysis
    • Aulchenko,Y.S. et al. (2007) Genomewide rapid association using mixed model and regression: a fast and simple method for genomewide pedigree-based quantitative trait loci association analysis. Genetics, 177, 577-578.
    • (2007) Genetics , vol.177 , pp. 577-578
    • Aulchenko, Y.S.1
  • 4
    • 63349103940 scopus 로고    scopus 로고
    • ALK7 expression is specific for adipose tissue, reduced in obesity and correlates to factors implicated in metabolic disease
    • Carlsson,L.M. et al. (2009) ALK7 expression is specific for adipose tissue, reduced in obesity and correlates to factors implicated in metabolic disease. Biochem. Biophys. Res. Commun., 382, 309-314.
    • (2009) Biochem. Biophys. Res. Commun. , vol.382 , pp. 309-314
    • Carlsson, L.M.1
  • 5
    • 77954733893 scopus 로고    scopus 로고
    • cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs
    • Coin,L.J. et al. (2010) cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs. Nat. Methods, 7, 541-546.
    • (2010) Nat. Methods , vol.7 , pp. 541-546
    • Coin, L.J.1
  • 7
    • 0012057129 scopus 로고
    • Measurement of inequality of incomes
    • Gini,C. (1921) Measurement of inequality of incomes. Econ. J., 31, 124-126.
    • (1921) Econ. J. , vol.31 , pp. 124-126
    • Gini, C.1
  • 8
    • 67349182343 scopus 로고    scopus 로고
    • Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
    • Glessner,J.T. et al. (2009) Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature, 459, 569-573.
    • (2009) Nature , vol.459 , pp. 569-573
    • Glessner, J.T.1
  • 9
    • 63449117467 scopus 로고    scopus 로고
    • Segmental copy number variation shapes tissue transcriptomes
    • Henrichsen,C.N. et al. (2009) Segmental copy number variation shapes tissue transcriptomes. Nat. Genet., 41, 424-429.
    • (2009) Nat. Genet. , vol.41 , pp. 424-429
    • Henrichsen, C.N.1
  • 10
    • 42249103276 scopus 로고    scopus 로고
    • On the analysis of copy-number variations in genomewide association studies: a translation of the family-based association test
    • Ionita-Laza,I. et al. (2008) On the analysis of copy-number variations in genomewide association studies: a translation of the family-based association test. Genet. Epidemiol., 32, 273-284.
    • (2008) Genet. Epidemiol. , vol.32 , pp. 273-284
    • Ionita-Laza, I.1
  • 11
    • 34347353237 scopus 로고    scopus 로고
    • Copy-number variation and association studies of human disease
    • McCarroll,S.A. and Altshuler,D.M. (2007) Copy-number variation and association studies of human disease. Nat. Genet., 39, S37-S42.
    • (2007) Nat. Genet. , vol.39
    • McCarroll, S.A.1    Altshuler, D.M.2
  • 12
    • 59149097625 scopus 로고    scopus 로고
    • Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations
    • Meyre,D. et al. (2009) Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. Nat. Genet., 41, 157-159.
    • (2009) Nat. Genet. , vol.41 , pp. 157-159
    • Meyre, D.1
  • 13
    • 33748272115 scopus 로고    scopus 로고
    • High-resolution genomic profiling of chromosomal aberrations using infinium whole-genome genotyping
    • Peiffer,D.A. et al. (2006) High-resolution genomic profiling of chromosomal aberrations using infinium whole-genome genotyping. Genome Res., 16, 1136-1148.
    • (2006) Genome Res. , vol.16 , pp. 1136-1148
    • Peiffer, D.A.1
  • 14
    • 34548292504 scopus 로고    scopus 로고
    • PLINK: a tool set for whole-genome association and populationbased linkage analyses
    • Purcell,S. et al. (2007) PLINK: a tool set for whole-genome association and populationbased linkage analyses. Am. J. Hum. Genet., 81, 559-575.
    • (2007) Am. J. Hum. Genet. , vol.81 , pp. 559-575
    • Purcell, S.1
  • 15
    • 0042424602 scopus 로고    scopus 로고
    • Statistical significance for genomewide studies
    • Storey,J.D. and Tibshirani,R. (2003) Statistical significance for genomewide studies. Proc. Natl Acad. Sci. USA, 100, 9440-9445.
    • (2003) Proc. Natl Acad. Sci. USA , vol.100 , pp. 9440-9445
    • Storey, J.D.1    Tibshirani, R.2
  • 16
    • 33846978695 scopus 로고    scopus 로고
    • Relative impact of nucleotide and copy number variation on gene expression phenotypes
    • Stranger,B.E. et al. (2007) Relative impact of nucleotide and copy number variation on gene expression phenotypes. Science, 315, 848-853.
    • (2007) Science , vol.315 , pp. 848-853
    • Stranger, B.E.1
  • 17
    • 76249116215 scopus 로고    scopus 로고
    • A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
    • Walters,R.G. et al. (2010) A new highly penetrant form of obesity due to deletions on chromosome 16p11.2. Nature, 463, 671-675.
    • (2010) Nature , vol.463 , pp. 671-675
    • Walters, R.G.1


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