dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs

Human Mutation

Volumn 37, Issue 3, 2016, Pages 235-241

  Liu, Xiaoming ^a   Wu, Chunlei ^b   Li, Chang ^a   Boerwinkle, Eric ^a,c  

^a UNIVERSITY OF TEXAS SCHOOL OF PUBLIC HEALTH   (United States)

^b SCRIPPS RESEARCH INSTITUTE   (United States)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

Database; DbNSFP; DbscSNV; Functional prediction; Nonsynonymous mutation; Splice site mutation

Indexed keywords

ARTICLE; CHROMOSOME; COMPARATIVE STUDY; CONTROLLED STUDY; GENE FREQUENCY; GENETIC DATABASE; HUMAN; NONSYNONYMOUS SINGLE NUCLEOTIDE VARIATION; PHYLOGENETIC TREE; PREDICTION; PRIORITY JOURNAL; SCORING SYSTEM; SINGLE NUCLEOTIDE POLYMORPHISM; SPLICE SITE VARIATION; SPLICING DEFECT; BIOLOGY; EXOME; GENETICS; MOLECULAR GENETICS; PROCEDURES; RNA SPLICING;

COMPUTATIONAL BIOLOGY; EXOME; GENE FREQUENCY; HUMANS; MOLECULAR SEQUENCE ANNOTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; RNA SPLICING;

EID: 84957942283     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.22932     Document Type: Article

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