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在基因组DNA中快速鉴定RNA基序。应用于酵母基因组中的tRNA搜索。

Very fast identification of RNA motifs in genomic DNA. Application to tRNA search in the yeast genome.

作者信息

el-Mabrouk N, Lisacek F

机构信息

Institut Gaspard Monge Université de Marne-la-Vallée, Noisy-le-Grand, France.

出版信息

J Mol Biol. 1996 Nov 22;264(1):46-55. doi: 10.1006/jmbi.1996.0622.

Abstract

A common strategy characterises the various methods independently defined to identify almost unambiguously different types of RNA molecules in DNA fragments. So far, the good quality of detection of RNA motif has been the prior motivation and effectively delayed the optimisation of programs. As an illustration of possible improvements, a modified version of tRNAscan is described. The previous algorithm was altered to run 500 times faster and to lower both rates of false positives and false negatives. The newly sequenced genome of Saccharomyces cerevisiae is scanned both ways in less than three minutes and results match annotations found in databanks with three exceptions, two of which being arguably not real tRNAs.

摘要

一种通用策略是各种独立定义的方法的特征,这些方法用于在DNA片段中几乎明确无误地识别不同类型的RNA分子。到目前为止,RNA基序检测的良好质量一直是首要动机,并有效地延迟了程序的优化。作为可能改进的一个例子,描述了tRNAscan的一个修改版本。以前的算法被修改后运行速度提高了500倍,同时降低了假阳性和假阴性率。新测序的酿酒酵母基因组用这两种方法扫描不到三分钟,结果与数据库中的注释相符,只有三个例外,其中两个可以说不是真正的tRNA。

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