ScanIndel: A hybrid framework for indel detection via gapped alignment, split reads and de novo assembly

Genome Medicine

Volumn 7, Issue 1, 2015, Pages

  Yang, Rendong ^a   Nelson, Andrew C ^b   Henzler, Christine ^a   Thyagarajan, Bharat ^b   Silverstein, Kevin A T ^a  

^a UNIVERSITY OF MINNESOTA   (United States)

^b UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMPLICON; ARTICLE; GENE DELETION; GENE IDENTIFICATION; GENE INSERTION; GENETIC ANALYSIS; GENETIC ANALYZER; GENOME; HUMAN; MEASUREMENT ACCURACY; PRIORITY JOURNAL; SENSITIVITY AND SPECIFICITY; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS; SIMULATION; SOFT CLIPPING ANALYZER FOR INDELS; ALGORITHM; BIOLOGY; CHROMOSOMAL MAPPING; DNA SEQUENCE; GENOMICS; HUMAN GENOME; INDEL MUTATION; PROCEDURES;

ALGORITHMS; CHROMOSOME MAPPING; COMPUTATIONAL BIOLOGY; GENOME, HUMAN; GENOMICS; HUMANS; INDEL MUTATION; SENSITIVITY AND SPECIFICITY; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, DNA;

EID: 84949201877     PISSN: None     EISSN: 1756994X     Source Type: Journal    
DOI: 10.1186/s13073-015-0251-2     Document Type: Article

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