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.
SYSNO ASEP 0392350 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title RepeatExplorer: 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, SAISource Title Bioinformatics. - : Oxford University Press - ISSN 1367-4803
Roč. 29, č. 6 (2013), s. 792-793Number of pages 2 s. Publication form Print - P Language eng - English Country GB - United Kingdom Keywords repetitiveDNA ; computational analysis ; next generation sequencing Subject RIV EB - Genetics ; Molecular Biology R&D Projects GBP501/12/G090 GA ČR - Czech Science Foundation (CSF) OC10037 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) Institutional support BC-A - RVO:60077344 UT WOS 000316270400017 DOI 10.1093/bioinformatics/btt054 Annotation Motivation: 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. Workplace Biology Centre (since 2006) Contact Dana Hypšová, eje@eje.cz, Tel.: 387 775 214 Year of Publishing 2014
Number of the records: 1