Number of the records: 1  

RepeatExplorer: a Galaxy-based web server for genome-wide characterization of eukaryotic repetitive elements from next-generation sequence reads

  1. 1.
    SYSNO ASEP0392350
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleRepeatExplorer: a Galaxy-based web server for genome-wide characterization of eukaryotic repetitive elements from next-generation sequence reads
    Author(s) Novák, Petr (BC-A) RID, ORCID
    Neumann, Pavel (BC-A) RID, ORCID
    Pech, Jiří (BC-A)
    Steinhaisl, J. (CZ)
    Macas, Jiří (BC-A) RID, ORCID, SAI
    Source TitleBioinformatics. - : Oxford University Press - ISSN 1367-4803
    Roč. 29, č. 6 (2013), s. 792-793
    Number of pages2 s.
    Publication formPrint - P
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsrepetitiveDNA ; computational analysis ; next generation sequencing
    Subject RIVEB - Genetics ; Molecular Biology
    R&D ProjectsGBP501/12/G090 GA ČR - Czech Science Foundation (CSF)
    OC10037 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Institutional supportBC-A - RVO:60077344
    UT WOS000316270400017
    DOI10.1093/bioinformatics/btt054
    AnnotationMotivation: Repetitive DNA makes up large portions of plant and animal nuclear genomes, yet it remains the least-characterized genome component in most species studied so far. Although the recent availability of high-throughput sequencing data provides necessary resources for in-depth investigation of genomic repeats, its utility is hampered by the lack of specialized bioinformatics tools and appropriate computational resources that would enable large-scale repeat analysis to be run by biologically oriented researchers. Results: Here we present RepeatExplorer, a collection of software tools for characterization of repetitive elements, which is accessible via web interface. A key component of the server is the computational pipeline using a graph-based sequence clustering algorithm to facilitate de novo repeat identification without the need for reference databases of known elements. Because the algorithm uses short sequences randomly sampled from the genome as input, it is ideal for analyzing next-generation sequence reads.
    WorkplaceBiology Centre (since 2006)
    ContactDana Hypšová, eje@eje.cz, Tel.: 387 775 214
    Year of Publishing2014
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.