메뉴 건너뛰기




Volumn 31, Issue 24, 2015, Pages 3994-3996

Svviz: A read viewer for validating structural variants

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; COMPUTER PROGRAM; GENETIC VARIATION; GENOMICS; PROCEDURES; SEQUENCE ALIGNMENT;

EID: 84950238284     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btv478     Document Type: Article
Times cited : (40)

References (8)
  • 1
    • 55549089660 scopus 로고    scopus 로고
    • Accurate whole human genome sequencing using reversible terminator chemistry
    • Bentley, D.R. et al. (2008) Accurate whole human genome sequencing using reversible terminator chemistry. Nature, 456, 53-59.
    • (2008) Nature , vol.456 , pp. 53-59
    • Bentley, D.R.1
  • 2
    • 79952596594 scopus 로고    scopus 로고
    • Bambino: A variant detector and alignment viewer for next-generation sequencing data in the SAM/BAM format
    • Edmonson, M.N. et al. (2011) Bambino: a variant detector and alignment viewer for next-generation sequencing data in the SAM/BAM format. Bioinformatics, 27, 865-866.
    • (2011) Bioinformatics , vol.27 , pp. 865-866
    • Edmonson, M.N.1
  • 3
    • 58149234737 scopus 로고    scopus 로고
    • Real-time DNA sequencing from single polymerase molecules
    • Eid, J. et al. (2009) Real-time DNA sequencing from single polymerase molecules. Science, 323, 133-138.
    • (2009) Science , vol.323 , pp. 133-138
    • Eid, J.1
  • 4
    • 84925550089 scopus 로고    scopus 로고
    • PyBamView: A browser-based application for viewing short read alignments
    • Gymrek, M. (2014) PyBamView: a browser-based application for viewing short read alignments. Bioinformatics, 30, 3405-3407.
    • (2014) Bioinformatics , vol.30 , pp. 3405-3407
    • Gymrek, M.1
  • 5
    • 84901308393 scopus 로고    scopus 로고
    • Visualization and probability-based scoring of structural variants within repetitive sequences
    • Halper-Stromberg, E. et al. (2014) Visualization and probability-based scoring of structural variants within repetitive sequences. Bioinformatics, 30, 1514-1521.
    • (2014) Bioinformatics , vol.30 , pp. 1514-1521
    • Halper-Stromberg, E.1
  • 6
    • 78651271733 scopus 로고    scopus 로고
    • Integrative genomics viewer
    • Robinson, J.T. et al. (2011) Integrative genomics viewer. Nat. Biotechnol., 29, 24-26.
    • (2011) Nat. Biotechnol. , vol.29 , pp. 24-26
    • Robinson, J.T.1
  • 7
    • 84891755297 scopus 로고    scopus 로고
    • SSW library: An SIMD Smith-Waterman C/C++ library for use in genomic applications
    • Zhao, M. et al. (2013) SSW library: an SIMD Smith-Waterman C/C++ library for use in genomic applications. PLoS One, 8, e82138.
    • (2013) PLoS One , vol.8 , pp. e82138
    • Zhao, M.1
  • 8
    • 84897387657 scopus 로고    scopus 로고
    • Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
    • Zook, J.M. et al. (2014) Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls. Nat. Biotechnol., 32, 246-251.
    • (2014) Nat. Biotechnol. , vol.32 , pp. 246-251
    • Zook, J.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.