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MAJIQlopedia:人类组织和癌症中 RNA 剪接变异的百科全书。

MAJIQlopedia: an encyclopedia of RNA splicing variations in human tissues and cancer.

机构信息

Department of Genetics, University of Pennsylvania, Philadelphia, PA 19104, USA.

Department of Biochemistry and Biophysics, University of Pennsylvania, Philadelphia, PA 19104, USA.

出版信息

Nucleic Acids Res. 2024 Jan 5;52(D1):D213-D221. doi: 10.1093/nar/gkad1043.

Abstract

Quantification of RNA splicing variations based on RNA-Sequencing can reveal tissue- and disease-specific splicing patterns. To study such splicing variations, we introduce MAJIQlopedia, an encyclopedia of splicing variations that encompasses 86 human tissues and 41 cancer datasets. MAJIQlopedia reports annotated and unannotated splicing events for a total of 486 175 alternative splice junctions in normal tissues and 338 317 alternative splice junctions in cancer. This database, available at https://majiq.biociphers.org/majiqlopedia/, includes a user-friendly interface that provides graphical representations of junction usage quantification for each junction across all tissue or cancer types. To demonstrate case usage of MAJIQlopedia, we review splicing variations in genes WT1, MAPT and BIN1, which all have known tissue or cancer-specific splicing variations. We also use MAJIQlopedia to highlight novel splicing variations in FDX1 and MEGF9 in normal tissues, and we uncover a novel exon inclusion event in RPS6KA6 that only occurs in two cancer types. Users can download the database, request the addition of data to the webtool, or install a MAJIQlopedia server to integrate proprietary data. MAJIQlopedia can serve as a reference database for researchers seeking to understand what splicing variations exist in genes of interest, and those looking to understand tissue- or cancer-specific splice isoform usage.

摘要

基于 RNA 测序的 RNA 剪接变异定量可以揭示组织和疾病特异性的剪接模式。为了研究这些剪接变异,我们引入了 MAJIQlopedia,这是一个涵盖 86 个人类组织和 41 个癌症数据集的剪接变异百科全书。MAJIQlopedia 报告了注释和未注释的剪接事件,总共包括正常组织中 486175 个替代剪接接头和癌症中 338317 个替代剪接接头。这个数据库可在 https://majiq.biociphers.org/majiqlopedia/ 上获取,包括一个用户友好的界面,提供了每个接头在所有组织或癌症类型中的接头使用定量的图形表示。为了演示 MAJIQlopedia 的案例使用,我们回顾了 WT1、MAPT 和 BIN1 基因的剪接变异,这些基因都有已知的组织或癌症特异性剪接变异。我们还使用 MAJIQlopedia 来突出正常组织中 FDX1 和 MEGF9 的新剪接变异,并揭示了 RPS6KA6 中仅在两种癌症类型中发生的新外显子包含事件。用户可以下载数据库,请求向网络工具添加数据,或安装 MAJIQlopedia 服务器以集成专有数据。MAJIQlopedia 可以作为研究人员的参考数据库,帮助他们了解感兴趣基因中存在哪些剪接变异,以及那些希望了解组织或癌症特异性剪接异构体使用情况的人。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ffb/10767883/f72b248e71a3/gkad1043figgra1.jpg

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