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用于访问来自高资源和低资源环境的健康孕妇的基因和模块水平血液转录组谱的数据分析浏览应用程序。

A data browsing application for accessing gene and module-level blood transcriptome profiles of healthy pregnant women from high- and low-resource settings.

机构信息

Research Branch, Sidra Medicine, Al Gharrafa St, Doha 26999, Qatar.

Department of Infectious Diseases, St Jude's Children Research Hospital, 262 Danny Thomas Pl, Memphis, TN 38105, USA.

出版信息

Database (Oxford). 2024 Apr 2;2024. doi: 10.1093/database/baae021.

Abstract

Transcriptome profiling data, generated via RNA sequencing, are commonly deposited in public repositories. However, these data may not be easily accessible or usable by many researchers. To enhance data reuse, we present well-annotated, partially analyzed data via a user-friendly web application. This project involved transcriptome profiling of blood samples from 15 healthy pregnant women in a low-resource setting, taken at 6 consecutive time points beginning from the first trimester. Additional blood transcriptome profiles were retrieved from the National Center for Biotechnology Information (NCBI) Gene Expression Omnibus (GEO) public repository, representing a cohort of healthy pregnant women from a high-resource setting. We analyzed these datasets using the fixed BloodGen3 module repertoire. We deployed a web application, accessible at https://thejacksonlaboratory.shinyapps.io/BloodGen3_Pregnancy/which displays the module-level analysis results from both original and public pregnancy blood transcriptome datasets. Users can create custom fingerprint grid and heatmap representations via various navigation options, useful for reports and manuscript preparation. The web application serves as a standalone resource for exploring blood transcript abundance changes during pregnancy. Alternatively, users can integrate it with similar applications developed for earlier publications to analyze transcript abundance changes of a given BloodGen3 signature across a range of disease cohorts. Database URL: https://thejacksonlaboratory.shinyapps.io/BloodGen3_Pregnancy/.

摘要

转录组谱数据是通过 RNA 测序生成的,通常被存储在公共数据库中。然而,这些数据可能不容易被许多研究人员获取或使用。为了增强数据的可重用性,我们通过用户友好的网络应用程序提供了经过良好注释、部分分析的数据。该项目涉及在资源有限的环境中对 15 名健康孕妇的血液样本进行转录组谱分析,从妊娠早期开始连续 6 个时间点采集样本。从国家生物技术信息中心(NCBI)基因表达综合数据库(GEO)公共数据库中检索到了额外的血液转录组谱数据,这些数据代表了来自资源丰富环境的健康孕妇队列。我们使用固定的 BloodGen3 模块库对这些数据集进行了分析。我们部署了一个网络应用程序,可在 https://thejacksonlaboratory.shinyapps.io/BloodGen3_Pregnancy/ 上访问,该应用程序显示了原始和公共妊娠血液转录组数据集的模块级分析结果。用户可以通过各种导航选项创建自定义指纹网格和热图表示,这对于报告和手稿准备非常有用。该网络应用程序是探索妊娠期间血液转录丰度变化的独立资源。或者,用户可以将其与为早期出版物开发的类似应用程序集成,以分析给定 BloodGen3 特征在一系列疾病队列中的转录丰度变化。数据库 URL:https://thejacksonlaboratory.shinyapps.io/BloodGen3_Pregnancy/。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e61/10986794/206089d13bf8/baae021f1.jpg

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