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Volumn 28, Issue 7, 2012, Pages 1024-1025

Breakpointer: Using local mapping artifacts to support sequence breakpoint discovery from single-end reads

Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; ARTICLE; ARTIFACT; BIOLOGY; DNA SEQUENCE; GENETIC VARIABILITY; HUMAN; METHODOLOGY;

EID: 84859254885     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/bts064     Document Type: Article
Times cited : (17)

References (12)
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    • DePristo, M.A.1
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    • Mapping and sequencing of structural variation from eight human genomes
    • Kidd, J.M. et al. (2008) Mapping and sequencing of structural variation from eight human genomes. Nature, 453, 56-64.
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    • Kidd, J.M.1
  • 5
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    • The Sequence Alignment/Map format and SAMtools
    • Li, H. et al. (2009) The Sequence Alignment/Map format and SAMtools. Bioinformatics, 25, 2078-2079.
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    • Computational methods for discovering structural variation with next-generation sequencing
    • Medvedev, P. et al. (2009) Computational methods for discovering structural variation with next-generation sequencing. Nat. Methods, 6, S13-S20.
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    • Medvedev, P.1
  • 8
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    • An initial map of insertion and deletion (INDEL) variation in the human genome
    • Mills, R.E. et al. (2006) An initial map of insertion and deletion (INDEL) variation in the human genome. Genome Res., 16, 1182-1190.
    • (2006) Genome Res , vol.16 , pp. 1182-1190
    • Mills, R.E.1
  • 9
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    • Mapping copy number variation by population-scale genome sequencing
    • Mills, R.E. et al. (2011a) Mapping copy number variation by population-scale genome sequencing. Nature, 470, 59-65.
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    • Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.