Institute of Genomic Medicine/Zhejiang Provincial Key Laboratory of Medical Genetics, Wenzhou, China.
Nucleic Acids Res. 2010 Jul;38(Web Server issue):W392-7. doi: 10.1093/nar/gkq393. Epub 2010 May 16.
miRNAs are small, non-coding RNA that negatively regulate gene expression at post-transcriptional level, which play crucial roles in various physiological and pathological processes, such as development and tumorigenesis. Although deep sequencing technologies have been applied to investigate various small RNA transcriptomes, their computational methods are far away from maturation as compared to microarray-based approaches. In this study, a comprehensive web server mirTools was developed to allow researchers to comprehensively characterize small RNA transcriptome. With the aid of mirTools, users can: (i) filter low-quality reads and 3/5' adapters from raw sequenced data; (ii) align large-scale short reads to the reference genome and explore their length distribution; (iii) classify small RNA candidates into known categories, such as known miRNAs, non-coding RNA, genomic repeats and coding sequences; (iv) provide detailed annotation information for known miRNAs, such as miRNA/miRNA*, absolute/relative reads count and the most abundant tag; (v) predict novel miRNAs that have not been characterized before; and (vi) identify differentially expressed miRNAs between samples based on two different counting strategies: total read tag counts and the most abundant tag counts. We believe that the integration of multiple computational approaches in mirTools will greatly facilitate current microRNA researches in multiple ways. mirTools can be accessed at http://centre.bioinformatics.zj.cn/mirtools/ and http://59.79.168.90/mirtools.
miRNAs 是一种小的非编码 RNA,可在转录后水平上负调控基因表达,在发育和肿瘤发生等各种生理和病理过程中发挥关键作用。尽管深度测序技术已被应用于研究各种小 RNA 转录组,但与基于微阵列的方法相比,它们的计算方法还远未成熟。在这项研究中,开发了一个全面的 Web 服务器 mirTools,允许研究人员全面描述小 RNA 转录组。借助 mirTools,用户可以:(i)从原始测序数据中过滤低质量的读取和 3/5' 接头;(ii)将大规模短读取与参考基因组对齐,并探索它们的长度分布;(iii)将小 RNA 候选物分类为已知类别,如已知的 miRNAs、非编码 RNA、基因组重复和编码序列;(iv)为已知的 miRNAs 提供详细的注释信息,如 miRNA/miRNA*、绝对/相对读取计数和最丰富的标签;(v)预测以前未表征的新 miRNAs;以及(vi)基于两种不同的计数策略(总读取标签计数和最丰富标签计数)在样品之间识别差异表达的 miRNAs。我们相信,mirTools 中多种计算方法的集成将以多种方式极大地促进当前的 miRNA 研究。mirTools 可在 http://centre.bioinformatics.zj.cn/mirtools/ 和 http://59.79.168.90/mirtools 访问。