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PD_NGSAtlas:一个整合精神疾病下一代测序表观基因组和转录组数据的参考数据库。

PD_NGSAtlas: a reference database combining next-generation sequencing epigenomic and transcriptomic data for psychiatric disorders.

作者信息

Zhao Zheng, Li Yongsheng, Chen Hong, Lu Jianping, Thompson Peter M, Chen Juan, Wang Zishan, Xu Juan, Xu Chun, Li Xia

机构信息

College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, 150081, China.

Southwest Brain Bank, Department of Psychiatry, UTHSCSA, San Antonio, TX, USA.

出版信息

BMC Med Genomics. 2014 Dec 31;7:71. doi: 10.1186/s12920-014-0071-z.

Abstract

BACKGROUND

Psychiatric disorders such as schizophrenia (SZ) and bipolar disorder (BP) are projected to lead the global disease burden within the next decade. Several lines of evidence suggest that epigenetic- or genetic-mediated dysfunction is frequently present in these disorders. To date, the inheritance patterns have been complicated by the problem of integrating epigenomic and transcriptomic factors that have yet to be elucidated. Therefore, there is a need to build a comprehensive database for storing epigenomic and transcriptomic data relating to psychiatric disorders.

DESCRIPTION

We have developed the PD_NGSAtlas, which focuses on the efficient storage of epigenomic and transcriptomic data based on next-generation sequencing and on the quantitative analyses of epigenetic and transcriptional alterations involved in psychiatric disorders. The current release of the PD_NGSAtlas contains 43 DNA methylation profiles and 37 transcription profiles detected by MeDIP-Seq and RNA-Seq, respectively, in two distinct brain regions and peripheral blood of SZ, BP and non-psychiatric controls. In addition to these data that were generated in-house, we have included, and will continue to include, published DNA methylation and gene expression data from other research groups, with a focus on psychiatric disorders. A flexible query engine has been developed for the acquisition of methylation profiles and transcription profiles for special genes or genomic regions of interest of the selected samples. Furthermore, the PD_NGSAtlas offers online tools for identifying aberrantly methylated and expressed events involved in psychiatric disorders. A genome browser has been developed to provide integrative and detailed views of multidimensional data in a given genomic context, which can help researchers understand molecular mechanisms from epigenetic and transcriptional perspectives. Moreover, users can download the methylation and transcription data for further analyses.

CONCLUSIONS

The PD_NGSAtlas aims to provide storage of epigenomic and transcriptomic data as well as quantitative analyses of epigenetic and transcriptional alterations involved in psychiatric disorders. The PD_NGSAtlas will be a valuable data resource and will enable researchers to investigate the pathophysiology and aetiology of disease in detail. The database is available at http://bioinfo.hrbmu.edu.cn/pd_ngsatlas/.

摘要

背景

精神分裂症(SZ)和双相情感障碍(BP)等精神疾病预计将在未来十年内成为全球疾病负担的主要原因。有几条证据表明,表观遗传或基因介导的功能障碍在这些疾病中经常出现。迄今为止,由于尚未阐明的表观基因组和转录组因素整合问题,遗传模式一直很复杂。因此,需要建立一个综合数据库来存储与精神疾病相关的表观基因组和转录组数据。

描述

我们开发了PD_NGSAtlas,它专注于基于下一代测序高效存储表观基因组和转录组数据,并对精神疾病中涉及的表观遗传和转录改变进行定量分析。当前版本的PD_NGSAtlas分别包含通过MeDIP-Seq和RNA-Seq在SZ、BP和非精神疾病对照的两个不同脑区和外周血中检测到的43个DNA甲基化谱和37个转录谱。除了这些内部生成的数据外,我们已经纳入并将继续纳入其他研究小组发表的DNA甲基化和基因表达数据,重点是精神疾病。我们开发了一个灵活的查询引擎,用于获取所选样本中特定基因或感兴趣基因组区域的甲基化谱和转录谱。此外,PD_NGSAtlas提供了在线工具,用于识别精神疾病中异常甲基化和表达的事件。我们开发了一个基因组浏览器,以在给定的基因组背景下提供多维数据的综合和详细视图,这有助于研究人员从表观遗传和转录角度理解分子机制。此外,用户可以下载甲基化和转录数据进行进一步分析。

结论

PD_NGSAtlas旨在存储表观基因组和转录组数据,并对精神疾病中涉及的表观遗传和转录改变进行定量分析。PD_NGSAtlas将是一个有价值的数据资源,并将使研究人员能够详细研究疾病的病理生理学和病因学。该数据库可在http://bioinfo.hrbmu.edu.cn/pd_ngsatlas/获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aa4/4308070/bea0e8bc5f9f/12920_2014_71_Fig1_HTML.jpg

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