CNAplot - Software for visual inspection of chromosomal copy number alteration in cancer using juxtaposed sequencing read depth ratios and variant allele frequencies. | D2R Server publishing the DBLP Bibliography Database, hosted at L3S Research Center

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dc:creator	<https://dblp.l3s.de/d2r/resource/authors/Charlotte_G._Nyvold>
dc:creator	<https://dblp.l3s.de/d2r/resource/authors/Marcus_H._Hansen>
dc:creator	<https://dblp.l3s.de/d2r/resource/authors/Peter_Hokland>
foaf:homepage	<http://dx.doi.org/doi.org%2F10.1016%2Fj.softx.2020.100503>
foaf:homepage	<https://doi.org/10.1016/j.softx.2020.100503>
dc:identifier	DBLP journals/softx/HansenHN20 (xsd:string)
dc:identifier	DOI doi.org%2F10.1016%2Fj.softx.2020.100503 (xsd:string)
dcterms:issued	2020 (xsd:gYear)
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rdfs:label	CNAplot - Software for visual inspection of chromosomal copy number alteration in cancer using juxtaposed sequencing read depth ratios and variant allele frequencies. (xsd:string)
foaf:maker	<https://dblp.l3s.de/d2r/resource/authors/Charlotte_G._Nyvold>
foaf:maker	<https://dblp.l3s.de/d2r/resource/authors/Marcus_H._Hansen>
foaf:maker	<https://dblp.l3s.de/d2r/resource/authors/Peter_Hokland>
swrc:pages	100503 (xsd:string)
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rdfs:seeAlso	<http://dblp.uni-trier.de/db/journals/softx/softx11.html#HansenHN20>
rdfs:seeAlso	<https://doi.org/10.1016/j.softx.2020.100503>
dc:title	CNAplot - Software for visual inspection of chromosomal copy number alteration in cancer using juxtaposed sequencing read depth ratios and variant allele frequencies. (xsd:string)
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