Mapping inherited and somatic variation in regulatory DNA: New roadmap for common disease clinical discoveries

Expert Review of Molecular Diagnostics

Volumn 13, Issue 6, 2013, Pages 519-522

  Roukos, Dimitrios H ^a   Baltogiannis, Giannis G ^a   Baltogiannis, George ^a  

^a UNIVERSITY OF IOANNINA   (Greece)

Author keywords

common disease; disease; genetic variation; genetics; genome mapping networks; genomics; noncoding sequence; regulatory DBA; somatic mutations; transcription factors

Indexed keywords

DNA; RNA POLYMERASE II; TRANSCRIPTION FACTOR;

ADVANCED CANCER; ASTHMA; BREAST CANCER; CHROMATIN IMMUNOPRECIPITATION; CLINICAL GENETICS; DNA METHYLATION; ELECTRON MICROSCOPY; ENHANCER REGION; ENVIRONMENTAL EXPOSURE; ENVIRONMENTAL FACTOR; EXOME; FAMILIAL CANCER; FAMILY HISTORY; GENE EXPRESSION; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; GENE FUNCTION; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC SUSCEPTIBILITY; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; GENOME; GENOTYPE ENVIRONMENT INTERACTION; HERITABILITY; HIGH THROUGHPUT SEQUENCING; HUMAN; INHERITANCE; LUNG CANCER; MUTATION; PATHOGENESIS; POINT MUTATION; PROMOTER REGION; REVIEW; SCHIZOPHRENIA; SOMATIC MUTATION; TRANSCRIPTION INITIATION SITE;

CHROMOSOME MAPPING; DNA; GENETIC DISEASES, INBORN; GENOME, HUMAN; HUMANS; MUTATION; REGULATORY SEQUENCES, NUCLEIC ACID;

EID: 84881101401     PISSN: 14737159     EISSN: 17448352     Source Type: Journal    
DOI: 10.1586/14737159.2013.811908     Document Type: Review

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