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Volumn 27, Issue 16, 2011, Pages 2300-2301

In-depth annotation of SNPs arising from resequencing projects using NGS-SNP

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; COMPUTER PROGRAM; GENOMICS; HIGH THROUGHPUT SEQUENCING; METHODOLOGY; MOLECULAR GENETICS; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 79961182320     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btr372     Document Type: Article
Times cited : (93)

References (11)
  • 1
    • 61449107734 scopus 로고    scopus 로고
    • SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms
    • Chelala,C. et al. (2009) SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms. Bioinformatics, 25, 655-661.
    • (2009) Bioinformatics , vol.25 , pp. 655-661
    • Chelala, C.1
  • 3
    • 57249114505 scopus 로고    scopus 로고
    • SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
    • Johnson,A.D. et al. (2008) SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics, 24, 2938-2939.
    • (2008) Bioinformatics , vol.24 , pp. 2938-2939
    • Johnson, A.D.1
  • 4
    • 75549090213 scopus 로고    scopus 로고
    • KEGG for representation and analysis of molecular networks involving diseases and drugs
    • Kanehisa,M. et al. (2010) KEGG for representation and analysis of molecular networks involving diseases and drugs. Nucleic Acids Res., 38, D355-D360.
    • (2010) Nucleic Acids Res. , vol.38
    • Kanehisa, M.1
  • 5
    • 55549097836 scopus 로고    scopus 로고
    • Mapping short DNA sequencing reads and calling variants using mapping quality scores
    • Li,H. et al. (2008) Mapping short DNA sequencing reads and calling variants using mapping quality scores. Genome Res., 18, 1851-1858.
    • (2008) Genome Res. , vol.18 , pp. 1851-1858
    • Li, H.1
  • 6
    • 68549104404 scopus 로고    scopus 로고
    • The Sequence Alignment/Map format and SAMtools
    • Li,H. et al. (2009) The Sequence Alignment/Map format and SAMtools. Bioinformatics, 25, 2078-2079.
    • (2009) Bioinformatics , vol.25 , pp. 2078-2079
    • Li, H.1
  • 7
    • 78651317908 scopus 로고    scopus 로고
    • Entrez Gene: gene-centered information at NCBI
    • Maglott,D. et al. (2011) Entrez Gene: gene-centered information at NCBI. Nucleic Acids Res., 39, D52-D57.
    • (2011) Nucleic Acids Res. , vol.39
    • Maglott, D.1
  • 8
    • 77951959817 scopus 로고    scopus 로고
    • CandiSNPer: a web tool for the identification of candidate SNPs for causal variants
    • Schmitt,A.O. et al. (2010) CandiSNPer: a web tool for the identification of candidate SNPs for causal variants. Bioinformatics, 26, 969-970.
    • (2010) Bioinformatics , vol.26 , pp. 969-970
    • Schmitt, A.O.1
  • 9
    • 77956640112 scopus 로고    scopus 로고
    • SeqAnt: a web service to rapidly identify and annotate DNA sequence variations
    • Shetty,A.C. et al. (2010) SeqAnt: a web service to rapidly identify and annotate DNA sequence variations. BMC Bioinformatics, 11, 471.
    • (2010) BMC Bioinformatics , vol.11 , pp. 471
    • Shetty, A.C.1
  • 10
    • 78651319979 scopus 로고    scopus 로고
    • Ongoing and future developments at the Universal Protein Resource
    • UniProt Consortium
    • UniProt Consortium. (2011) Ongoing and future developments at the Universal Protein Resource. Nucleic Acids Res., 39, D214-D219.
    • (2011) Nucleic Acids Res. , vol.39
  • 11
    • 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.