Resolving the resolution of array CGH

被引:129
作者
Coe, Bradley P.
Ylstra, Bauke
Carvalho, Beatriz
Meijer, Gerrit A.
MacAulay, Calum
Lam, Wan L.
机构
[1] British Columbia Canc Res Ctr, Vancouver, BC V5Z 1L3, Canada
[2] Vrije Univ Amsterdam, Med Ctr, Amsterdam, Netherlands
关键词
nucleic acid hybridization; genomic hybridizations; DNA arrays; gene dosage; loss of heterozygosity; genetic techniques; technology assessment;
D O I
10.1016/j.ygeno.2006.12.012
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:647 / 653
页数:7
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