An integrative variant analysis suite for whole exome next-generation sequencing data

BMC Bioinformatics

Volumn 13, Issue 1, 2012, Pages

  Challis, Danny ^a   Yu, Jin ^a   Evani, Uday S ^a   Jackson, Andrew R ^a   Paithankar, Sameer ^a   Coarfa, Cristian ^a   Milosavljevic, Aleksandar ^a   Gibbs, Richard A ^a   Yu, Fuli ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CODING REGION; FUNCTIONAL GENOMICS; GENOMIC DATABASE; HIGH SENSITIVITY; LOGISTIC REGRESSION MODELS; MAPPING ERROR; NEXT-GENERATION SEQUENCING; SEQUENCING METHOD;

REGRESSION ANALYSIS;

GENES;

ARTICLE; COMPUTER PROGRAM; EXOME; GENOMICS; HIGH THROUGHPUT SEQUENCING; HUMAN; HUMAN GENOME; INDEL MUTATION; OPEN READING FRAME; SINGLE NUCLEOTIDE POLYMORPHISM;

EXOME; GENOME, HUMAN; GENOMICS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; INDEL MUTATION; OPEN READING FRAMES; POLYMORPHISM, SINGLE NUCLEOTIDE; SOFTWARE;

EID: 84855593661     PISSN: None     EISSN: 14712105     Source Type: Journal    
DOI: 10.1186/1471-2105-13-8     Document Type: Article

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