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Detecting and Comparing Non-Coding RNAs in the High-Throughput Era

机译:在高通量时代检测和比较非编码RNA

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In recent years there has been a growing interest in the field of non-coding RNA. This surge is a direct consequence of the discovery of a huge number of new non-coding genes and of the finding that many of these transcripts are involved in key cellular functions. In this context, accurately detecting and comparing RNA sequences has become important. Aligning nucleotide sequences is a key requisite when searching for homologous genes. Accurate alignments reveal evolutionary relationships, conserved regions and more generally any biologically relevant pattern. Comparing RNA molecules is, however, a challenging task. The nucleotide alphabet is simpler and therefore less informative than that of amino-acids. Moreover for many non-coding RNAs, evolution is likely to be mostly constrained at the structural level and not at the sequence level. This results in very poor sequence conservation impeding comparison of these molecules. These difficulties define a context where new methods are urgently needed in order to exploit experimental results to their full potential. This review focuses on the comparative genomics of non-coding RNAs in the context of new sequencing technologies and especially dealing with two extremely important and timely research aspects: the development of new methods to align RNAs and the analysis of high-throughput data.
机译:近年来,对非编码RNA领域的兴趣日益浓厚。这种激增是发现大量新的非编码基因以及发现许多这些转录本参与关键细胞功能的直接结果。在这种情况下,准确地检测和比较RNA序列已变得很重要。搜索同源基因时,比对核苷酸序列是关键条件。准确的比对揭示了进化关系,保守区域以及更普遍的任何生物学相关模式。然而,比较RNA分子是一项艰巨的任务。核苷酸字母比氨基酸字母更简单,因此提供的信息更少。此外,对于许多非编码RNA,进化可能主要受制于结构水平而不是序列水平。这导致非常差的序列保守性,阻碍了这些分子的比较。这些困难定义了一个迫切需要新方法以便充分利用实验结果的环境。这篇综述的重点是在新测序技术背景下的非编码RNA的比较基因组学,尤其是涉及两个极为重要和及时的研究方面:开发比对RNA的新方法和高通量数据的分析。

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