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Volumn 26, Issue 12, 2010, Pages

VARiD: A variation detection framework for color-space and letter-space platforms

Author keywords

[No Author keywords available]

Indexed keywords

ALGORITHM; ARTICLE; COMPUTER PROGRAM; DNA SEQUENCE; METHODOLOGY; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 77954202204     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btq184     Document Type: Article
Times cited : (9)

References (14)
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    • Flicek, P.1    Birney, E.2
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    • Evaluation of next generation sequencing platforms for population targeted sequencing studies
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    • Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
    • Langmead, B. et al. (2009) Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol., 10, R25+.
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  • 7
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    • Li, H.1    Durbin, R.2
  • 8
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    • Mapping short DNA sequencing reads and calling variants using mapping quality scores
    • Li, H. et al. (2008a) Mapping short DNA sequencing reads and calling variants using mapping quality scores. Genome res., 18, 1851-1858.
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  • 9
    • 40049104732 scopus 로고    scopus 로고
    • Soap: short oligonucleotide alignment program
    • Li, R. et al. (2008b) Soap: short oligonucleotide alignment program. Bioinformatics, 24, 713-714.
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