Chromothripsis and human disease: piecing together the shattering process.

Chromothripsis and human disease: piecing together the shattering process.
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DOI:
10.1016/j.cell.2012.01.006
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发表时间:
2012-01-20
期刊:
影响因子:
64.5
通讯作者:
Wilson RK
Wilson RK
中科院分区:
生物学1区
文献类型:
--
作者:
Maher CA;Wilson RK

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高通量基因组学前所未有的分辨率使得最近发现了一种现象,即基因组的特定区域被粉碎,然后通过一个单一的破坏性事件缝合在一起,称为chromothripsis。管理这一过程的潜在机制现在正在出现,这对我们理解基因组重排在发育和疾病中的作用有影响。
The unprecedented resolution of high-throughput genomics has enabled the recent discovery of a phenomenon by which specific regions of the genome are shattered and then stitched together via a single devastating event, referred to as chromothripsis. Potential mechanisms governing this process are now emerging, with implications for our understanding of the role of genomic rearrangements in development and disease.
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