Disease gene discovery through integrative genomics

Annual Review of Genomics and Human Genetics

Volumn 6, Issue , 2005, Pages 381-406

  Giallourakis, Cosmas ^a,b   Henson, Charlotte ^a   Reich, Michael ^a   Xie, Xiaohui ^a   Mootha, Vamsi K ^a,b,c  

^a BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^b MASSACHUSETTS GENERAL HOSPITAL   (United States)

^c HARVARD MEDICAL SCHOOL   (United States)

Author keywords

Functional genomics; Human genetics; Machine learning; Positional cloning

Indexed keywords

COMPLEMENTARY DNA; CYTOCHROME C OXIDASE; DNA; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; MESSENGER RNA; PROTEIN; RNA; TRANSMEMBRANE CONDUCTANCE REGULATOR; TUMOR NECROSIS FACTOR RELATED APOPTOSIS INDUCING LIGAND;

ALGORITHM; CLONING; CPG ISLAND; DNA SEQUENCE; FUNCTIONAL GENOMICS; GENE; GENE EXPRESSION; GENE FUNCTION; GENE SEQUENCE; GENE STRUCTURE; GENETIC VARIABILITY; GENOMICS; GENOTYPE; HIGH THROUGHPUT SCREENING; HUMAN; HUMAN GENETICS; IN SITU HYBRIDIZATION; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PHENOTYPE; PROTEIN INTERACTION; PROTEOMICS; REVIEW; UNTRANSLATED REGION;

DATABASES, GENETIC; GENE EXPRESSION PROFILING; GENETIC DISEASES, INBORN; GENOME, HUMAN; GENOMICS; HUMANS; MODELS, GENETIC; PHENOTYPE; PROTEOMICS;

EID: 25844439570     PISSN: 15278204     EISSN: None     Source Type: Book Series    
DOI: 10.1146/annurev.genom.6.080604.162234     Document Type: Review

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