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Volumn 3, Issue 6, 2008, Pages

Copy number variation detection via high-density SNP genotyping

Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; ANALYTIC METHOD; ANALYTICAL PARAMETERS; ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; COMPUTER PROGRAM; DATA ANALYSIS; DNA MICROARRAY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DUPLICATION; GENE FREQUENCY; GENE IDENTIFICATION; GENE NUMBER; GENE PROBE; GENOME ANALYSIS; GENOTYPE; HIDDEN MARKOV MODEL; HUMAN GENOME; INHERITANCE; MATHEMATICAL ANALYSIS; MATHEMATICAL COMPUTING; MICROARRAY ANALYSIS; SIGNAL PROCESSING; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 55249101708     PISSN: None     EISSN: 15596095     Source Type: Journal    
DOI: 10.1101/pdb.top46     Document Type: Article
Times cited : (20)

References (22)
  • 1
    • 34347339520 scopus 로고    scopus 로고
    • Methods and strategies for analyzing copy number variation using DNA microarrays
    • Carter, N.P. 2007. Methods and strategies for analyzing copy number variation using DNA microarrays. Nat. Genet. 39: Suppl: S16-S21.
    • (2007) Nat. Genet , vol.39 , Issue.SUPPL.
    • Carter, N.P.1
  • 5
    • 31144469134 scopus 로고    scopus 로고
    • Structural variation in the human genome
    • Feuk, L., Carson, A.R., and Scherer, S.W. 2006. Structural variation in the human genome. Nat. Rev. Genet. 7: 85-97.
    • (2006) Nat. Rev. Genet , vol.7 , pp. 85-97
    • Feuk, L.1    Carson, A.R.2    Scherer, S.W.3
  • 7
    • 34547756934 scopus 로고    scopus 로고
    • Copy-number variations and human disease
    • Hegele, R.A. 2007. Copy-number variations and human disease. Am. J. Hum. Genet. 81: 414-415.
    • (2007) Am. J. Hum. Genet , vol.81 , pp. 414-415
    • Hegele, R.A.1
  • 13
    • 33646163019 scopus 로고    scopus 로고
    • BioHMM: A heterogeneous hidden Markov model for segmenting array CGH data
    • Marioni, J.C., Thorne, N.P., and Tavaré, S. 2006. BioHMM: A heterogeneous hidden Markov model for segmenting array CGH data. Bioinformatics 22: 1144-1146.
    • (2006) Bioinformatics , vol.22 , pp. 1144-1146
    • Marioni, J.C.1    Thorne, N.P.2    Tavaré, S.3
  • 16
    • 17344371740 scopus 로고    scopus 로고
    • High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
    • Pinkel, D., Segraves, R., Sudar, D., Clark, S., Poole, I., Kowbel, D., Collins, C., Kuo, W.L., Chen, C., Zhai, Y., et al. 1998. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nat. Genet. 20: 207-211.
    • (1998) Nat. Genet , vol.20 , pp. 207-211
    • Pinkel, D.1    Segraves, R.2    Sudar, D.3    Clark, S.4    Poole, I.5    Kowbel, D.6    Collins, C.7    Kuo, W.L.8    Chen, C.9    Zhai, Y.10
  • 19
    • 33645072440 scopus 로고    scopus 로고
    • Service, R.F. 2006. Gene sequencing. The race for the $1000 genome. Science 311: 1544-1546.
    • Service, R.F. 2006. Gene sequencing. The race for the $1000 genome. Science 311: 1544-1546.
  • 21
    • 84935113569 scopus 로고
    • Error bounds for convolutional codes and an asymptotically optimum decoding algorithm
    • Viterbi, A.J. 1967. Error bounds for convolutional codes and an asymptotically optimum decoding algorithm. IEEE Trans. Inf. Theory 13: 260-269.
    • (1967) IEEE Trans. Inf. Theory , vol.13 , pp. 260-269
    • Viterbi, A.J.1
  • 22
    • 35948984173 scopus 로고    scopus 로고
    • PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
    • Wang, K., Li, M., Hadley, D., Liu, R., Glessner, J., Grant, S.F.A., Hakonarson, H., and Bucan, M. 2007. PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res. 17: 1665-1674.
    • (2007) Genome Res , vol.17 , pp. 1665-1674
    • Wang, K.1    Li, M.2    Hadley, D.3    Liu, R.4    Glessner, J.5    Grant, S.F.A.6    Hakonarson, H.7    Bucan, M.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.