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Volumn 27, Issue 4, 2016, Pages 125-128

Monitoring error rates in Illumina sequencing

Author keywords

Bioinformatics; Genomics; High throughput DNA

Indexed keywords

ACCOUNTING; BIOINFORMATICS; GENOMICS; INTERMETHOD COMPARISON; MONITORING; NEXT GENERATION SEQUENCING; POSTMARKETING SURVEILLANCE; ALGORITHM; DIAGNOSTIC ERROR; DNA SEQUENCE; HIGH THROUGHPUT SEQUENCING; HUMAN; MOLECULAR DIAGNOSIS; NUCLEOTIDE SEQUENCE; SOFTWARE; STANDARDS;

EID: 85007236842     PISSN: 15240215     EISSN: 19434731     Source Type: Journal    
DOI: 10.7171/jbt.16-2704-002     Document Type: Article
Times cited : (59)

References (8)
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  • 2
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    • Langmead B, Salzberg SL. Fast gapped-read alignment with Bowtie 2. Nat Methods 2012;9:357-359.
    • (2012) Nat Methods , vol.9 , pp. 357-359
    • Langmead, B.1    Salzberg, S.L.2
  • 7
    • 52649157765 scopus 로고    scopus 로고
    • Substantial biases in ultra-short read data sets from high-throughput DNA sequencing
    • Dohm JC, Lottaz C, Borodina T, Himmelbauer H. Substantial biases in ultra-short read data sets from high-throughput DNA sequencing. Nucleic Acids Res 2008;36:e105.
    • (2008) Nucleic Acids Res , vol.36
    • Dohm, J.C.1    Lottaz, C.2    Borodina, T.3    Himmelbauer, H.4
  • 8
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    • A framework for variation discovery and genotyping using next-generation DNA sequencing data
    • DePristo MA, Banks E, Poplin R, et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet 2011;43:491-498.
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    • Depristo, M.A.1    Banks, E.2    Poplin, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.