SNP discovery performance of two second-generation sequencing platforms in the NOD2 gene region

Human Mutation

Volumn 31, Issue 7, 2010, Pages 875-885

  Melum, Espen ^a,b   May, Sandra ^a   Schilhabel, Markus B ^a   Thomsen, Ingo ^a   Karlsen, Tom H ^b   Rosenstiel, Philip ^a   Schreiber, Stefan ^a,c   Franke, Andre ^a  

^a UNIVERSITY OF KIEL   (Germany)

^b OSLO UNIVERSITY HOSPITAL   (Norway)

^c UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

Author keywords

454 FLX; Benchmarking; Coverage simulation; NOD2; Rare variants; Second generation sequencing; SNP discovery; SOLiD

Indexed keywords

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; CROHN DISEASE; GENE; GENE LOCUS; GENE SEQUENCE; GENOME ANALYSIS; HAPLOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; NOD2 GENE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SIMULATION; SINGLE NUCLEOTIDE POLYMORPHISM; DNA SEQUENCE; GENETIC PREDISPOSITION; GENETICS; PROCEDURES; REPRODUCIBILITY;

CASPASE RECRUITMENT DOMAIN PROTEIN 15; NOD2 PROTEIN, HUMAN;

CROHN DISEASE; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; NOD2 SIGNALING ADAPTOR PROTEIN; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; REPRODUCIBILITY OF RESULTS; SEQUENCE ANALYSIS, DNA;

EID: 77954121752     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.21276     Document Type: Article

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