Quantifying deleterious effects of regulatory variants

Nucleic Acids Research

Volumn 45, Issue 5, 2017, Pages 2307-2317

  Li, Shan ^a   Alvarez, Roberto Vera ^a   Sharan, Roded ^b   Landsman, David ^a   Ovcharenko, Ivan ^a  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b TEL AVIV UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYRIBONUCLEASE I; TRANSCRIPTION FACTOR; PROTEIN BINDING;

ACCURACY; ARTICLE; BINDING AFFINITY; CHROMATIN; CONTROLLED STUDY; GENE EXPRESSION; GENE FREQUENCY; GENE INACTIVATION; GENE MUTATION; GENETIC VARIABILITY; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE PHENOTYPE CORRELATION; HUMAN; PRIORITY JOURNAL; QUANTITATIVE TRAIT LOCUS; REGULATORY SEQUENCE; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; SUPPORT VECTOR MACHINE; VALIDATION PROCESS; ANTIBODY SPECIFICITY; B LYMPHOCYTE; CYTOLOGY; ENHANCER REGION; GENETIC ASSOCIATION STUDY; GENETIC TRANSCRIPTION; GENETICS; HIGH THROUGHPUT SEQUENCING; HUMAN GENOME; MACHINE LEARNING; METABOLISM; NUCLEOTIDE SEQUENCE; STATISTICAL MODEL;

B-LYMPHOCYTES; BASE SEQUENCE; DEOXYRIBONUCLEASE I; ENHANCER ELEMENTS, GENETIC; GENETIC ASSOCIATION STUDIES; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; LIKELIHOOD FUNCTIONS; MACHINE LEARNING; ORGAN SPECIFICITY; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN BINDING; QUANTITATIVE TRAIT LOCI; TRANSCRIPTION FACTORS; TRANSCRIPTION, GENETIC;

EID: 85018257444     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkw1263     Document Type: Article

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