Ultra-high resolution array painting facilitates breakpoint sequencing

被引:21
作者
Gribble, S. M.
Kalaitzopoulos, D.
Burford, D. C.
Prigmore, E.
Selzer, R. R.
Ng, B. L.
Matthews, N. S. W.
Porter, K. M.
Curley, R.
Lindsay, S. J.
Baptista, J.
Richmond, T. A.
Carter, N. P.
机构
[1] Wellcome Trust Sanger Inst, Cambridge CB10 1SA, England
[2] NimbleGen Syst, Madison, WI USA
[3] Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury, Wilts, England
基金
英国惠康基金;
关键词
D O I
10.1136/jmg.2006.044909
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objective: To describe a considerably advanced method of array painting, which allows the rapid, ultra-high resolution mapping of translocation breakpoints such that rearrangement junction fragments can be amplified directly and sequenced. Method: Ultra-high resolution array painting involves the hybridisation of probes generated by the amplification of small numbers of flow-sorted derivative chromosomes to oligonucleotide arrays designed to tile breakpoint regions at extremely high resolution. Results and discussion: How ultra-high resolution array painting of four balanced translocation cases rapidly and efficiently maps breakpoints to a point where junction fragments can be amplified easily and sequenced is demonstrated. With this new development, breakpoints can be mapped using just two array experiments: the first using whole-genome array painting to tiling resolution large insert clone arrays, the second using ultra-high-resolution oligonucleotide arrays targeted to the breakpoint regions. In this way, breakpoints can be mapped and then sequenced in a few weeks.
引用
收藏
页码:51 / 58
页数:8
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