Prediction of functional regulatory SNPs in monogenic and complex disease

Human Mutation

Volumn 32, Issue 10, 2011, Pages 1183-1190

  Zhao, Yiqiang ^a,b   Clark, Wyatt T ^c   Mort, Matthew ^d   Cooper, David N ^d   Radivojac, Predrag ^c   Mooney, Sean D ^a,b  

^a BUCK INSTITUTE FOR RESEARCH ON AGING   (United States)

^b INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c INDIANA UNIVERSITY   (United States)

^d CARDIFF UNIVERSITY   (United Kingdom)

Author keywords

Complex disease; Machine learning; Monogenic disease; Regulatory mutations; Single nucleotide polymorphisms; SNP

Indexed keywords

DNA;

ARTICLE; GENE EXPRESSION; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC ASSOCIATION; GENOME ANALYSIS; HUMAN; HUMAN GENOME; MONOGENIC DISORDER; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ALLELES; CHEMOKINE CCL5; DATABASES, GENETIC; GENE EXPRESSION REGULATION; GENETIC DISEASES, INBORN; GENOME-WIDE ASSOCIATION STUDY; HUMANS; MODELS, THEORETICAL; POLYMORPHISM, SINGLE NUCLEOTIDE; REGULATORY SEQUENCES, NUCLEIC ACID; SENSITIVITY AND SPECIFICITY;

EID: 80053040393     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.21559     Document Type: Article

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