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Volumn 28, Issue 5, 2012, Pages 724-725

Anntools: A comprehensive and versatile annotation toolkit for genomic variants

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; COMPUTER PROGRAM; COPY NUMBER VARIATION; GENETIC VARIABILITY; HUMAN; HUMAN GENOME; MOLECULAR GENETICS; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84857831329     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/bts032     Document Type: Article
Times cited : (36)

References (9)
  • 1
    • 0033539168 scopus 로고    scopus 로고
    • CpG islands as genomic footprints of promoters that are associated with replication origins
    • Antequera,F. and Bird,A. (1999) CpG islands as genomic footprints of promoters that are associated with replication origins. Curr. Biol., 9, R661-R667.
    • (1999) Curr. Biol. , vol.9
    • Antequera, F.1    Bird, A.2
  • 2
    • 77951943748 scopus 로고    scopus 로고
    • Ensembl variation resources
    • Chen,Y. et al. (2010) Ensembl variation resources. BMC Genomics, 11, 293-309.
    • (2010) BMC Genomics , vol.11 , pp. 293-309
    • Chen, Y.1
  • 3
    • 77950461601 scopus 로고    scopus 로고
    • Origins and functional impact of copy number variation in the human genome
    • Conrad,D.F. et al. (2010) Origins and functional impact of copy number variation in the human genome. Nature, 464, 704-712.
    • (2010) Nature , vol.464 , pp. 704-712
    • Conrad, D.F.1
  • 4
    • 79960405019 scopus 로고    scopus 로고
    • The variant call format and VCFtools
    • Danecek,P. et al. (2011) The variant call format and VCFtools. Bioinformatics, 27, 2156-2158.
    • (2011) Bioinformatics , vol.27 , pp. 2156-2158
    • Danecek, P.1
  • 5
    • 79960142070 scopus 로고    scopus 로고
    • SVA: software for annotating and visualizing sequenced human genomes
    • Ge,D. et al. (2011) SVA: software for annotating and visualizing sequenced human genomes. Bioinformatics, 27, 1998-2000.
    • (2011) Bioinformatics , vol.27 , pp. 1998-2000
    • Ge, D.1
  • 6
    • 60749104999 scopus 로고    scopus 로고
    • Next generation tools for the annotation of human SNPs
    • Karchin,R. (2009) Next generation tools for the annotation of human SNPs. Brief. Bioinform., 10, 35-52.
    • (2009) Brief. Bioinform. , vol.10 , pp. 35-52
    • Karchin, R.1
  • 7
    • 52949141845 scopus 로고    scopus 로고
    • Integrated detection and population-genetic analysis of SNPs and copy number variation
    • McCarroll,S.A. et al. (2008) Integrated detection and population-genetic analysis of SNPs and copy number variation. Nat. Genet., 40, 1166-1174.
    • (2008) Nat. Genet. , vol.40 , pp. 1166-1174
    • McCarroll, S.A.1
  • 8
    • 77956295988 scopus 로고    scopus 로고
    • The genome analysis toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data
    • McKenna,A. et al. (2010) The genome analysis toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res., 20, 1297-1303.
    • (2010) Genome Res , vol.20 , pp. 1297-1303
    • McKenna, A.1
  • 9
    • 77956534324 scopus 로고    scopus 로고
    • ANNOVAR: functional annotation of genetic variants from highthroughput sequencing data
    • Wang,K. et al. (2010) ANNOVAR: functional annotation of genetic variants from highthroughput sequencing data. Nucleic Acids Res., 38, e164.
    • (2010) Nucleic Acids Res , vol.38
    • Wang, K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.