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PMID: 17276656 Published · ppublish English Evaluation Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Resolving the resolution of array CGH.

Genomics ·Vol. 89 ·No. 5 ·2007-05-00 ·Pages 647-53

Coe BP, Ylstra B, Carvalho B, Meijer GA, Macaulay C, Lam WL

Abstract

Many recent technologies have been designed to supplant conventional metaphase CGH technology with the goal of refining the description of segmental copy number status throughout the genome. However, the emergence of new technologies has led to confusion as to how to describe adequately the capabilities of each array platform. The design of a CGH array can incorporate a uniform or a highly variable element distribution. This can lead to bias in the reporting of average or median resolutions, making it difficult to provide a fair comparison of platforms. In this report, we propose a new definition of resolution for array CGH technology, termed "functional resolution," that incorporates the uniformity of element spacing on the array, as well as the sensitivity of each platform to single-copy alterations. Calculation of these metrics is automated through the development of a Java-based application, "ResCalc," which is applicable to any array CGH platform.

MeSH Terms
Gene Dosage Genome, Human Humans Loss of Heterozygosity Nucleic Acid Hybridization/methods Oligonucleotide Array Sequence Analysis/methods Sensitivity and Specificity Technology Assessment, Biomedical/methods
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Coe Bradley P
British Columbia Cancer Research Centre, 675 West 10th Avenue, Vancouver, BC, Canada V5Z 1L3. bcoe@bccrc.ca
Ylstra Bauke
Carvalho Beatriz
Meijer Gerrit A
Macaulay Calum
Lam Wan L
Article Info
Journal
Genomics
Abbr.
Genomics
ISSN
0888-7543
Published
2007-05-00
Epub
2007-00-02
Pages
647-53
Language
English
Region
United States
NLM ID
8800135
Subset
IM
Grants
NIDCR NIH HHS · R01 DE015965 · United States
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