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Volumn 43, Issue 9, 2015, Pages

MultiSNV: A probabilistic approach for improving detection of somatic point mutations from multiple related tumour samples

Author keywords

[No Author keywords available]

Indexed keywords

BAYES THEOREM; DNA MUTATIONAL ANALYSIS; EVALUATION STUDY; GENE FREQUENCY; GENETICS; HUMAN; KIDNEY CARCINOMA; KIDNEY TUMOR; NEOPLASM; POINT MUTATION; PROCEDURES; STATISTICAL MODEL;

EID: 84936876772     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkv135     Document Type: Article
Times cited : (33)

References (15)
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    • JointSNVMix: A probabilistic model for accurate detection of somatic mutations in normal/tumour paired next-generation sequencing data
    • Roth, A., Ding, J., Morin, R.D., Crisan, A., Ha, G., Giuliany, R., Bashashati, A., Hirst, M., Turashvili, G., Oloumi, A. et al. (2012) JointSNVMix: a probabilistic model for accurate detection of somatic mutations in normal/tumour paired next-generation sequencing data. Bioinformatics, 28, 907-913.
    • (2012) Bioinformatics , vol.28 , pp. 907-913
    • Roth, A.1    Ding, J.2    Morin, R.D.3    Crisan, A.4    Ha, G.5    Giuliany, R.6    Bashashati, A.7    Hirst, M.8    Turashvili, G.9    Oloumi, A.10
  • 11
    • 66449114324 scopus 로고    scopus 로고
    • SNP detection for massively parallel whole-genome resequencing
    • Li, R., Li, Y., Fang, X., Yang, H., Wang, J., Kristiansen, K. and Wang, J. (2009) SNP detection for massively parallel whole-genome resequencing. Genome Res., 19, 1124-1132.
    • (2009) Genome Res. , vol.19 , pp. 1124-1132
    • Li, R.1    Li, Y.2    Fang, X.3    Yang, H.4    Wang, J.5    Kristiansen, K.6    Wang, J.7
  • 12
    • 0036852246 scopus 로고    scopus 로고
    • Neighboring-nucleotide effects on single nucleotide polymorphisms: A study of 2.6 million polymorphisms across the human genome
    • Zhao, Z. and Boerwinkle, E. (2002) Neighboring-nucleotide effects on single nucleotide polymorphisms: a study of 2.6 million polymorphisms across the human genome. Genome Res., 12, 1679-1686.
    • (2002) Genome Res. , vol.12 , pp. 1679-1686
    • Zhao, Z.1    Boerwinkle, E.2
  • 15
    • 84905576523 scopus 로고    scopus 로고
    • Integrating mapping-, assembly-and haplotype-based approaches for calling variants in clinical sequencing applications
    • Rimmer, A., Phan, H., Mathieson, I., Iqbal, Z., Twigg, S.R.F., Wilkie, A.O.M., McVean, G., Lunter, G. and WGS500 Consortium. (2014) Integrating mapping-, assembly-and haplotype-based approaches for calling variants in clinical sequencing applications. Nat. Genet., 46, 912-918.
    • (2014) Nat. Genet. , vol.46 , pp. 912-918
    • Rimmer, A.1    Phan, H.2    Mathieson, I.3    Iqbal, Z.4    Twigg, S.R.F.5    Wilkie, A.O.M.6    McVean, G.7    Lunter, G.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.