About: Human 2.1M Whole-Genome CGH Tiling Array v2.0

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About: Human 2.1M Whole-Genome CGH Tiling Array v2.0 Goto Sponge NotDistinct Permalink

An Entity of Type : owl:Class, within Data Space : wasabi.inria.fr associated with source document(s)

Attributes	Values
type	Class
label	Human 2.1M Whole-Genome CGH Tiling Array v2.0
subClassOf	tiling microarray nodeID://b665192694 nodeID://b665216991 nodeID://b665815513 nodeID://b665839810 nodeID://b665872025 nodeID://b665896322 nodeID://b665920619 nodeID://b665944916 nodeID://b669080738 nodeID://b669104923
described by	proxy:entity/http/purl.obolibrary.org/obo/obi.owl
term editor	PERSON: Venkat Malladi, Chris Stoeckert, Jie Zheng, Alan Ruttenberg
example of usage	Filges, Isabel, et al. "Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel–Giedion syndrome." Journal of medical genetics 48.2 (2011): 117-122. PMID:21037274
definition	A tiling array which is manufactured by the Nimblegen corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for human DNA against 2.1 million features. A tiling array which is manufactured by the Nimblegen corporation. Built to analyze DNA sequence copy number by comparative genomic hybridization for human DNA against 2.1 million features.
definition source	http://www.nimblegen.com/downloads/support/05434483001_NG_CGHLOH_UGuide_v9p1.pdf
alternative label	Nimblegen Human 2.1M Whole-Genome CGH Tiling Array v2.0
editor preferred term	Human 2.1M Whole-Genome CGH Tiling Array v2.0
has curation status	metadata complete
is topic of	Ontology for Biomedical Investigations

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