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准确识别人类 Alu 与非 Alu RNA 编辑位点。

Accurate identification of human Alu and non-Alu RNA editing sites.

机构信息

Department of Genetics, Stanford University, California, USA.

出版信息

Nat Methods. 2012 Jun;9(6):579-81. doi: 10.1038/nmeth.1982. Epub 2012 Apr 4.

DOI:10.1038/nmeth.1982
PMID:22484847
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3662811/
Abstract

We developed a computational framework to robustly identify RNA editing sites using transcriptome and genome deep-sequencing data from the same individual. As compared with previous methods, our approach identified a large number of Alu and non-Alu RNA editing sites with high specificity. We also found that editing of non-Alu sites appears to be dependent on nearby edited Alu sites, possibly through the locally formed double-stranded RNA structure.

摘要

我们开发了一种计算框架,使用来自同一个体的转录组和基因组深度测序数据,稳健地识别 RNA 编辑位点。与以前的方法相比,我们的方法以高特异性识别出大量的 Alu 和非 Alu RNA 编辑位点。我们还发现,非 Alu 位点的编辑似乎依赖于附近编辑的 Alu 位点,可能是通过局部形成的双链 RNA 结构。

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Transcriptome-wide sequencing reveals numerous APOBEC1 mRNA-editing targets in transcript 3' UTRs.转录组测序揭示了大量 APOBEC1 mRNA 编辑靶标在转录本 3'UTR 中。
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