Mutations, structural variations, and genome-wide resequencing: Where to from here in our understanding of disease and evolution?

Human Mutation

Volumn 29, Issue 6, 2008, Pages 886-890

  Tabone, Tania ^a  

^a UNIVERSITY OF ADELAIDE   (Australia)

Author keywords

Bioinformatics; Databases; Mutation detection; Screening; SNP; Structural variation

Indexed keywords

QUANTUM DOT;

BIOINFORMATICS; CONFERENCE PAPER; DATA BASE; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; DIAGNOSTIC TEST; DNA MICROARRAY; FLUORESCENCE IN SITU HYBRIDIZATION; FLUORESCENCE RESONANCE ENERGY TRANSFER; GENE DELETION; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOME ANALYSIS; GENOTYPE; HIGH THROUGHPUT SCREENING; HUMAN; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROMOTER REGION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SINGLE NUCLEOTIDE POLYMORPHISM; SOMATIC MUTATION; SOUTHERN BLOTTING; TECHNOLOGY;

DIAGNOSIS; DISEASE; HUMANS; MUTATION; SEQUENCE ANALYSIS, DNA;

EID: 44849103482     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.20781     Document Type: Conference Paper

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