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dcterms:bibliographicCitation <http://dblp.uni-trier.de/rec/bibtex/journals/bioinformatics/EmdeSWSVKHR12>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Anne-Katrin_Emde>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/David_Weese>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Knut_Reinert>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Marcel_H._Schulz>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Martin_Vingron>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Ruping_Sun>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Stefan_A._Haas>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Vera_M._Kalscheuer>
foaf:homepage <http://dx.doi.org/doi.org%2F10.1093%2Fbioinformatics%2Fbts019>
foaf:homepage <https://doi.org/10.1093/bioinformatics/bts019>
dc:identifier DBLP journals/bioinformatics/EmdeSWSVKHR12 (xsd:string)
dc:identifier DOI doi.org%2F10.1093%2Fbioinformatics%2Fbts019 (xsd:string)
dcterms:issued 2012 (xsd:gYear)
swrc:journal <https://dblp.l3s.de/d2r/resource/journals/bioinformatics>
rdfs:label Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS. (xsd:string)
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Anne-Katrin_Emde>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/David_Weese>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Knut_Reinert>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Marcel_H._Schulz>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Martin_Vingron>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Ruping_Sun>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Stefan_A._Haas>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Vera_M._Kalscheuer>
swrc:number 5 (xsd:string)
swrc:pages 619-627 (xsd:string)
owl:sameAs <http://bibsonomy.org/uri/bibtexkey/journals/bioinformatics/EmdeSWSVKHR12/dblp>
owl:sameAs <http://dblp.rkbexplorer.com/id/journals/bioinformatics/EmdeSWSVKHR12>
rdfs:seeAlso <http://dblp.uni-trier.de/db/journals/bioinformatics/bioinformatics28.html#EmdeSWSVKHR12>
rdfs:seeAlso <https://doi.org/10.1093/bioinformatics/bts019>
dc:title Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS. (xsd:string)
dc:type <http://purl.org/dc/dcmitype/Text>
rdf:type swrc:Article
rdf:type foaf:Document
swrc:volume 28 (xsd:string)