Massively parallel sequencing approaches for characterization of structural variation

Methods in Molecular Biology

Volumn 838, Issue , 2012, Pages 369-384

  Koboldt, Daniel C ^a   Larson, David E ^a   Chen, Ken ^a   Ding, Li ^a   Wilson, Richard K ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

454, Illumina; Abi solid; Copy number variants; Deletions; Duplications; Indels; Insertions; Inversions; Next generation sequencing; Paired end sequencing; Solexa; Translocations

Indexed keywords

ALGORITHM; AMINO ACID SEQUENCE; ARTICLE; BASE PAIRING; COMPUTER PROGRAM; DNA SEQUENCE; GENE DELETION; GENE DUPLICATION; GENE LIBRARY; GENE TRANSLOCATION; GENETIC DATABASE; HIGH THROUGHPUT SEQUENCING; HUMAN; HUMAN GENOME; METHODOLOGY; MOLECULAR GENETICS; REPRODUCIBILITY; SINGLE NUCLEOTIDE POLYMORPHISM;

ALGORITHMS; AMINO ACID SEQUENCE; BASE PAIRING; DATABASES, GENETIC; GENE DELETION; GENE DUPLICATION; GENE LIBRARY; GENOME, HUMAN; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MOLECULAR SEQUENCE DATA; POLYMORPHISM, SINGLE NUCLEOTIDE; REPRODUCIBILITY OF RESULTS; SEQUENCE ANALYSIS, DNA; SOFTWARE; TRANSLOCATION, GENETIC;

EID: 84863037350     PISSN: 10643745     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-61779-507-7_18     Document Type: Article

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