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ASpedia:人类选择性剪接的综合百科全书。

ASpedia: a comprehensive encyclopedia of human alternative splicing.

机构信息

Research Institute, National Cancer Center, 323 Ilsan-ro, Goyang-si, Kyeonggi-do 10408, Republic of Korea.

Department of Computer Engineering, Dong-A University, 37 Nakdong-daero 550 Beon-gil, Saha-gu, Busan 49315, Republic of Korea.

出版信息

Nucleic Acids Res. 2018 Jan 4;46(D1):D58-D63. doi: 10.1093/nar/gkx1014.

Abstract

Alternative splicing confers the human genome complexity by increasing the diversity of expressed mRNAs. Hundreds or thousands of splicing regions have been identified through differential alternative splicing analysis of high-throughput datasets. However, it is hard to explain the functional impact of each splicing event. Protein domain formation and nonsense-mediated decay are considered the main functional features of splicing. However, other functional features such as miRNA target sites, phosphorylation sites and single-nucleotide variations are directly affected by alternative splicing and affect downstream function. Hence, we established ASpedia: a comprehensive database for human alternative splicing annotation, which encompasses a range of functions, from genomic annotation to isoform-specific function (ASpedia, http://combio.snu.ac.kr/aspedia). The database provides three features: (i) genomic annotation extracted from DNA, RNA and proteins; (ii) transcription and regulation elements analyzed from next-generation sequencing datasets; and (iii) isoform-specific functions collected from known and published datasets. The ASpedia web application includes three components: an annotation database, a retrieval system and a browser specialized in the identification of human alternative splicing events. The retrieval system supports multiple AS event searches resulting from high-throughput analysis and the AS browser comprises genome tracks. Thus, ASpedia facilitates the systemic annotation of the functional impacts of multiple AS events.

摘要

可变剪接通过增加表达 mRNA 的多样性赋予人类基因组复杂性。通过对高通量数据集的差异可变剪接分析,已经鉴定了数百个或数千个剪接区域。然而,很难解释每个剪接事件的功能影响。蛋白质结构域形成和无意义介导的衰变被认为是剪接的主要功能特征。然而,其他功能特征,如 miRNA 靶位、磷酸化位点和单核苷酸变异,直接受到可变剪接的影响,并影响下游功能。因此,我们建立了 ASpedia:一个用于人类可变剪接注释的综合数据库,涵盖了从基因组注释到异构体特异性功能(ASpedia,http://combio.snu.ac.kr/aspedia)的各种功能。该数据库提供了三个功能:(i)从 DNA、RNA 和蛋白质中提取的基因组注释;(ii)从下一代测序数据集中分析的转录和调控元件;(iii)从已知和已发表的数据集收集的异构体特异性功能。ASpedia 网络应用程序包括三个组件:注释数据库、检索系统和专门用于识别人类可变剪接事件的浏览器。检索系统支持基于高通量分析的多个 AS 事件搜索,AS 浏览器包括基因组轨道。因此,ASpedia 促进了多个 AS 事件的功能影响的系统注释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb8c/5753336/cf2a65c69419/gkx1014fig1.jpg

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