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Volumn 6, Issue 1, 2013, Pages 29-35

Approaches to the detection of recessive effects using next generation sequencing data from outbred populations

Author keywords

Association; DNA; Sequence

Indexed keywords


EID: 84888807549     PISSN: None     EISSN: 11786949     Source Type: Journal    
DOI: 10.2147/AABC.S44332     Document Type: Article
Times cited : (8)

References (9)
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    • Curtis D. Consideration of plausible genetic architectures for schizophrenia and implications for analytic approaches in the era of next generation sequencing. Psychiatr Genet. 2012; 23(1): 1-10.
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    • Curtis, D.1
  • 2
    • 79952489518 scopus 로고    scopus 로고
    • Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta
    • Becker J, Semler O, Gilissen C, et al. Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta. Am J Hum Genet. 2011; 88(3): 362-371.
    • (2011) Am J Hum Genet. , vol.88 , Issue.3 , pp. 362-371
    • Becker, J.1    Semler, O.2    Gilissen, C.3
  • 3
    • 80053906761 scopus 로고    scopus 로고
    • Deep sequencing reveals 50 novel genes for recessive cognitive disorders
    • Najmabadi H, Hu H, Garshasbi M, et al. Deep sequencing reveals 50 novel genes for recessive cognitive disorders. Nature. 2011; 478(7367):57-63.
    • (2011) Nature , vol.478 , Issue.7367 , pp. 57-63
    • Najmabadi, H.1    Hu, H.2    Garshasbi, M.3
  • 4
    • 84864958219 scopus 로고    scopus 로고
    • A simple method for assessing the strength of evidence for association at the level of the whole gene
    • Curtis D, Vine AE, Knight J. A simple method for assessing the strength of evidence for association at the level of the whole gene. Adv Appl Bioinform Chem. 2008;1:115-120.
    • (2008) Adv Appl Bioinform Chem , vol.1 , pp. 115-120
    • Curtis, D.1    Vine, A.E.2    Knight, J.3
  • 5
    • 84871736050 scopus 로고    scopus 로고
    • Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffold
    • Menelaou A, Marchini J. Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffold. Bioinformatics. 2012; 29(1): 84-91.
    • (2012) Bioinformatics. , vol.29 , Issue.1 , pp. 84-91
    • Menelaou, A.1    Marchini, J.2
  • 6
    • 84871777314 scopus 로고    scopus 로고
    • A rapid method for combined analysis of common and rare variants at the level of a region, gene, or pathway
    • Curtis D. A rapid method for combined analysis of common and rare variants at the level of a region, gene, or pathway. Adv Appl Bioinform Chem. 2012;5:1-9.
    • (2012) Adv Appl Bioinform Chem , vol.5 , pp. 1-9
    • Curtis, D.1
  • 7
    • 61449168010 scopus 로고    scopus 로고
    • A groupwise association test for rare mutations using a weighted sum statistic
    • Madsen BE, Browning SR. A groupwise association test for rare mutations using a weighted sum statistic. PLoS Genet. 2009;5(2):e1000384.
    • (2009) PLoS Genet , vol.5 , Issue.2
    • Madsen, B.E.1    Browning, S.R.2
  • 8
    • 79952467494 scopus 로고    scopus 로고
    • GATES: a rapid and powerful gene-based association test using extended Simes procedure
    • Li MX, Gui HS, Kwan JS, Sham PC. GATES: a rapid and powerful gene-based association test using extended Simes procedure. Am J Hum Genet. 2011; 88(3): 283-293.
    • (2011) Am J Hum Genet. , vol.88 , Issue.3 , pp. 283-293
    • Li, M.X.1    Gui, H.S.2    Kwan, J.S.3    Sham, P.C.4
  • 9
    • 84855295482 scopus 로고    scopus 로고
    • Hierarchical generalized linear models for multiple groups of rare and common variants: jointly estimating group and individual-variant effects
    • Yi N, Liu N, Zhi D, Li J. Hierarchical generalized linear models for multiple groups of rare and common variants: jointly estimating group and individual-variant effects. PLoS Genet. 2011;7(12):e1002382.
    • (2011) PLoS Genet , vol.7 , Issue.12
    • Yi, N.1    Liu, N.2    Zhi, D.3    Li, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.