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Diagnostic Interpre...
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de Leeuw, Nicole
(author)
Diagnostic Interpretation of Array Data Using Public Databases and Internet Sources
- Article/chapterEnglish2012
Publisher, publication year, extent ...
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2012-05-07
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Hindawi Limited,2012
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printrdacarrier
Numbers
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LIBRIS-ID:oai:DiVA.org:uu-175597
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https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-175597URI
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https://doi.org/10.1002/humu.22049DOI
Supplementary language notes
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Language:English
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Summary in:English
Part of subdatabase
Classification
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
Notes
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The range of commercially available array platforms and analysis software packages is expanding and their utility is improving, making reliable detection of copy-number variants (CNVs) relatively straightforward. Reliable interpretation of CNV data, however, is often difficult and requires expertise. With our knowledge of the human genome growing rapidly, applications for array testing continuously broadening, and the resolution of CNV detection increasing, this leads to great complexity in interpreting what can be daunting data. Correct CNV interpretation and optimal use of the genotype information provided by single-nucleotide polymorphism probes on an array depends largely on knowledge present in various resources. In addition to the availability of host laboratories' own datasets and national registries, there are several public databases and Internet resources with genotype and phenotype information that can be used for array data interpretation. With so many resources now available, it is important to know which are fit-for-purpose in a diagnostic setting. We summarize the characteristics of the most commonly used Internet databases and resources, and propose a general data interpretation strategy that can be used for comparative hybridization, comparative intensity, and genotype-based array data.
Subject headings and genre
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array
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classification
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CNV
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database
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data interpretation
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diagnostic
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genome wide
Added entries (persons, corporate bodies, meetings, titles ...)
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Dijkhuizen, Trijnie
(author)
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Hehir-Kwa, Jayne Y.
(author)
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Carter, Nigel P.
(author)
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Feuk, LarsUppsala universitet,Genomik(Swepub:uu)larsfeuk
(author)
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Firth, Helen V.
(author)
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Kuhn, Robert M.
(author)
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Ledbetter, David H.
(author)
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Martin, Christa Lese
(author)
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van Ravenswaaij-Arts, Conny M. A.
(author)
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Scherer, Steven W.
(author)
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Shams, Soheil
(author)
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Van Vooren, Steven
(author)
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Sijmons, Rolf
(author)
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Swertz, Morris
(author)
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Hastings, Ros
(author)
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Uppsala universitetGenomik
(creator_code:org_t)
Related titles
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In:Human Mutation: Hindawi Limited33:6, s. 930-9401059-77941098-1004
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de Leeuw, Nicole
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Dijkhuizen, Trij ...
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Hehir-Kwa, Jayne ...
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Carter, Nigel P.
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Feuk, Lars
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Kuhn, Robert M.
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Ledbetter, David ...
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Scherer, Steven ...
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Van Vooren, Stev ...
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Sijmons, Rolf
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Hastings, Ros
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Human Mutation
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Uppsala University