Current trend of annotating single nucleotide variation in humans - A case study on SNVrap

Methods

Volumn 79, Issue , 2015, Pages 32-40

  Li, Mulin Jun ^a,b   Wang, Junwen ^a,b  

^a UNIVERSITY OF HONG KONG   (Hong Kong)

^b UNIVERSITY OF HONG KONG   (China)

Author keywords

Functional annotation; Functional prediction; Next generation sequencing; Single nucleotide variation; Web server

Indexed keywords

MICRORNA; NUCLEOTIDE; RNA;

ALTERNATIVE RNA SPLICING; AMINO ACID SEQUENCE; ARTICLE; BINDING AFFINITY; CHROMATIN; CODON USAGE; DNA BINDING; ENHANCER REGION; EXON; FUNCTIONAL GENOMICS; GENE CONTROL; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC ASSOCIATION; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HISTONE MODIFICATION; HUMAN; HUMAN GENOME; POSTTRANSCRIPTIONAL GENE SILENCING; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; PROTEIN SECONDARY STRUCTURE; QUANTITATIVE TRAIT; SINGLE NUCLEOTIDE VARIATION; SOMATIC MUTATION; TRANSCRIPTION INITIATION; TRANSLATION INITIATION; UNTRANSLATED REGION; ALGORITHM; GENE EXPRESSION REGULATION; HIGH THROUGHPUT SEQUENCING; MOLECULAR GENETICS; PROCEDURES; SINGLE NUCLEOTIDE POLYMORPHISM; TRENDS;

ALGORITHMS; ALTERNATIVE SPLICING; GENE EXPRESSION REGULATION; GENETIC VARIATION; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MOLECULAR SEQUENCE ANNOTATION; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84929308758     PISSN: 10462023     EISSN: 10959130     Source Type: Journal    
DOI: 10.1016/j.ymeth.2014.10.003     Document Type: Article

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