[RDF data]
Home | Example Publications
PropertyValue
dcterms:bibliographicCitation <http://dblp.uni-trier.de/rec/bibtex/conf/bibm/ZengSLCBJ20>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Kristin_Bilyeu>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/M%E2%88%9A%C2%B0ria_Skrabisov%E2%88%9A%C2%B0>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Shuai_Zeng>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Trupti_Joshi>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Yen_On_Chan>
dc:creator <https://dblp.l3s.de/d2r/resource/authors/Zhen_Lyu>
foaf:homepage <http://dx.doi.org/doi.org%2F10.1109%2FBIBM49941.2020.9313539>
foaf:homepage <https://doi.org/10.1109/BIBM49941.2020.9313539>
dc:identifier DBLP conf/bibm/ZengSLCBJ20 (xsd:string)
dc:identifier DOI doi.org%2F10.1109%2FBIBM49941.2020.9313539 (xsd:string)
dcterms:issued 2020 (xsd:gYear)
rdfs:label SNPViz v2.0: A web-based tool for enhanced haplotype analysis using large scale resequencing datasets and discovery of phenotypes causative gene using allelic variations. (xsd:string)
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Kristin_Bilyeu>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/M%E2%88%9A%C2%B0ria_Skrabisov%E2%88%9A%C2%B0>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Shuai_Zeng>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Trupti_Joshi>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Yen_On_Chan>
foaf:maker <https://dblp.l3s.de/d2r/resource/authors/Zhen_Lyu>
swrc:pages 1408-1415 (xsd:string)
dcterms:partOf <https://dblp.l3s.de/d2r/resource/publications/conf/bibm/2020>
owl:sameAs <http://bibsonomy.org/uri/bibtexkey/conf/bibm/ZengSLCBJ20/dblp>
owl:sameAs <http://dblp.rkbexplorer.com/id/conf/bibm/ZengSLCBJ20>
rdfs:seeAlso <http://dblp.uni-trier.de/db/conf/bibm/bibm2020.html#ZengSLCBJ20>
rdfs:seeAlso <https://doi.org/10.1109/BIBM49941.2020.9313539>
swrc:series <https://dblp.l3s.de/d2r/resource/conferences/bibm>
dc:title SNPViz v2.0: A web-based tool for enhanced haplotype analysis using large scale resequencing datasets and discovery of phenotypes causative gene using allelic variations. (xsd:string)
dc:type <http://purl.org/dc/dcmitype/Text>
rdf:type swrc:InProceedings
rdf:type foaf:Document