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Volumn 60, Issue , 2016, Pages 319-327

FMFilter: A fast model based variant filtering tool

Author keywords

Next generation sequencing; Rare diseases; Variant filtering

Indexed keywords

BUDGET CONTROL; GENES; GRAPHICAL USER INTERFACES;

EID: 84959283631     PISSN: 15320464     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jbi.2016.02.013     Document Type: Article
Times cited : (5)

References (15)
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  • 2
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    • WKGGSeq: a comprehensive strategy-based and disease-targeted online framework to facilitate exome sequencing studies of inherited disorders
    • Li M.J., Deng J., Wang P., Yang W., Ho S.L., Sham P.C., Wang J., Li M. wKGGSeq: a comprehensive strategy-based and disease-targeted online framework to facilitate exome sequencing studies of inherited disorders. Human Mutation 2015, 36:496-503.
    • (2015) Human Mutation , vol.36 , pp. 496-503
    • Li, M.J.1    Deng, J.2    Wang, P.3    Yang, W.4    Ho, S.L.5    Sham, P.C.6    Wang, J.7    Li, M.8
  • 9
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    • De novo mutations in human genetic disease
    • Veltman J.A., Brunner H.G. De novo mutations in human genetic disease. Nat. Rev. Genet. 2012, 13:565-575.
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    • Veltman, J.A.1    Brunner, H.G.2
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    • A map of human genome variation from population scale sequencing
    • The 1000 Genomes Project Consortium A map of human genome variation from population scale sequencing. Nature 2010, 467:1061-1073.
    • (2010) Nature , vol.467 , pp. 1061-1073


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.