Department of Biomedicine and Health Sciences, Graduate School, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Precision Medicine Research Center, IRCGP, College of Medicine, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
BMC Bioinformatics. 2022 May 2;23(1):155. doi: 10.1186/s12859-022-04691-1.
Recent deep sequencing technologies have proven to be valuable resources to gain insights into the expression profiles of diverse tRNAs. However, despite these technologies, the association of tRNAs with diverse diseases has not been explored in depth because analytical tools are lacking.
We developed a user-friendly tool, tRNA Expression Analysis Software Utilizing R for Easy use (tReasure), to analyze differentially expressed tRNAs (DEtRNAs) from deep sequencing data of small RNAs using R packages. tReasure can quantify individual mature tRNAs, isodecoders, and isoacceptors. By adopting stringent mapping strategies, tReasure supports the precise measurement of mature tRNA read counts. The whole analysis workflow for determining DEtRNAs (uploading FASTQ files, removing adapter sequences and poor-quality reads, mapping and quantifying tRNAs, filtering out low count tRNAs, determining DEtRNAs, and visualizing statistical analysis) can be performed with the tReasure package.
tReasure is an open-source software available for download at https://treasure.pmrc.re.kr and will be indispensable for users who have little experience with command-line software to explore the biological implication of tRNA expression.
最近的深度测序技术已被证明是一种有价值的资源,可以深入了解各种 tRNA 的表达谱。然而,尽管有了这些技术,由于缺乏分析工具,tRNA 与各种疾病的关联仍未得到深入探索。
我们开发了一个用户友好的工具,即利用 R 进行简易分析的 tRNA 表达分析软件(tReasure),该软件使用 R 包分析来自小 RNA 深度测序数据的差异表达 tRNA(DEtRNA)。tReasure 可以定量个体成熟 tRNA、同解码和同工受体。通过采用严格的映射策略,tReasure 支持成熟 tRNA 读数的精确测量。确定 DETRNA 的整个分析工作流程(上传 FASTQ 文件、去除接头序列和低质量读数、映射和定量 tRNA、过滤低计数 tRNA、确定 DETRNA 和可视化统计分析)可以使用 tReasure 包完成。
tReasure 是一个开源软件,可在 https://treasure.pmrc.re.kr 下载,对于那些对命令行软件没有经验的用户来说,它将是探索 tRNA 表达生物学意义不可或缺的工具。