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TAPAS: tool for alternative polyadenylation site analysis

机译:塔皮斯:替代多腺苷酸分析的工具

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Motivation: The length of the 3' untranslated region (3' UTR) of an mRNA is essential for many biological activities such as mRNA stability, sub-cellular localization, protein translation, protein binding and translation efficiency. Moreover, correlation between diseases and the shortening (or lengthening) of 3' UTRs has been reported in the literature. This length is largely determined by the polyadenylation cleavage site in the mRNA. As alternative polyadenylation (APA) sites are common in mammalian genes, several tools have been published recently for detecting APA sites from RNA-Seq data or performing shortening/lengthening analysis. These tools consider either up to only two APA sites in a gene or only APA sites that occur in the last exon of a gene, although a gene may generally have more than two APA sites and an APA site may sometimes occur before the last exon. Furthermore, the tools are unable to integrate the analysis of shortening/lengthening events with APA site detection.
机译:动机:mRNA的3'未转换区域(3'UTR)的长度对于许多生物学活性,例如mRNA稳定性,亚细胞定位,蛋白质翻译,蛋白质结合和翻译效率是必不可少的。 此外,在文献中报道了疾病与3'UTR的缩短(或延长)之间的相关性。 该长度主要由mRNA中的聚腺苷酸切割位点确定。 作为允许的丙二醇基因常见的替代聚腺苷酸(APA)位点,最近已经公布了几种工具,用于检测来自RNA-SEQ数据的APA位点或进行缩短/加长分析。 这些工具认为在基因中只有两个APA位点或仅在基因的最后外显子中发生的APA位点,尽管基因通常具有超过两个APA位点,并且可能在最后的外显子之前可能发生APA位点。 此外,该工具无法与APA站点检测分析缩短/延长事件的分析。

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