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GeneTrail:一个用于高通量谱分析的框架。

GeneTrail: A Framework for the Analysis of High-Throughput Profiles.

作者信息

Gerstner Nico, Kehl Tim, Lenhof Kerstin, Eckhart Lea, Schneider Lara, Stöckel Daniel, Backes Christina, Meese Eckart, Keller Andreas, Lenhof Hans-Peter

机构信息

Center for Bioinformatics, Saarland Informatics Campus, Saarbrücken, Germany.

Healthcare Digital & Data, Merck Healthcare KGaA, Darmstadt, Germany.

出版信息

Front Mol Biosci. 2021 Sep 16;8:716544. doi: 10.3389/fmolb.2021.716544. eCollection 2021.

DOI:10.3389/fmolb.2021.716544
PMID:34604304
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8481803/
Abstract

Experimental high-throughput techniques, like next-generation sequencing or microarrays, are nowadays routinely applied to create detailed molecular profiles of cells. In general, these platforms generate high-dimensional and noisy data sets. For their analysis, powerful bioinformatics tools are required to gain novel insights into the biological processes under investigation. Here, we present an overview of the GeneTrail tool suite that offers rich functionality for the analysis and visualization of (epi-)genomic, transcriptomic, miRNomic, and proteomic profiles. Our framework enables the analysis of standard bulk, time-series, and single-cell measurements and includes various state-of-the-art methods to identify potentially deregulated biological processes and to detect driving factors within those deregulated processes. We highlight the capabilities of our web service with an analysis of a single-cell COVID-19 data set that demonstrates its potential for uncovering complex molecular mechanisms. GeneTrail can be accessed freely and without login requirements at http://genetrail.bioinf.uni-sb.de.

摘要

如今,实验性高通量技术,如下一代测序或微阵列,通常用于创建细胞的详细分子图谱。一般来说,这些平台会生成高维且有噪声的数据集。为了对其进行分析,需要强大的生物信息学工具来深入了解所研究的生物过程。在此,我们概述了GeneTrail工具套件,它为(表观)基因组、转录组、miRNA组和蛋白质组图谱的分析和可视化提供了丰富的功能。我们的框架能够分析标准的批量、时间序列和单细胞测量数据,并包括各种先进方法,以识别潜在失调的生物过程,并检测这些失调过程中的驱动因素。我们通过对一个单细胞COVID-19数据集的分析突出了我们网络服务的功能,该分析展示了其揭示复杂分子机制的潜力。可通过http://genetrail.bioinf.uni-sb.de免费且无需登录访问GeneTrail。

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Natl Sci Rev. 2020 Jun;7(6):998-1002. doi: 10.1093/nsr/nwaa041. Epub 2020 Mar 13.
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Integrated analysis of multimodal single-cell data.多模态单细胞数据的综合分析。
Cell. 2021 Jun 24;184(13):3573-3587.e29. doi: 10.1016/j.cell.2021.04.048. Epub 2021 May 31.
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Targeting Runt-Related Transcription Factor 1 Prevents Pulmonary Fibrosis and Reduces Expression of Severe Acute Respiratory Syndrome Coronavirus 2 Host Mediators.
靶向 runt 相关转录因子 1 可预防肺纤维化并降低严重急性呼吸综合征冠状病毒 2 宿主介质的表达。
Am J Pathol. 2021 Jul;191(7):1193-1208. doi: 10.1016/j.ajpath.2021.04.006. Epub 2021 Apr 21.
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Population-Predicted MHC Class II Epitope Presentation of SARS-CoV-2 Structural Proteins Correlates to the Case Fatality Rates of COVID-19 in Different Countries.人群预测的 SARS-CoV-2 结构蛋白 MHC II 表位呈递与不同国家 COVID-19 的病死率相关。
Int J Mol Sci. 2021 Mar 5;22(5):2630. doi: 10.3390/ijms22052630.
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Mining of high throughput screening database reveals AP-1 and autophagy pathways as potential targets for COVID-19 therapeutics.高通量筛选数据库的挖掘揭示了 AP-1 和自噬途径可能成为 COVID-19 治疗的靶点。
Sci Rep. 2021 Mar 24;11(1):6725. doi: 10.1038/s41598-021-86110-8.
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J Infect Dis. 2021 Apr 23;223(8):1322-1333. doi: 10.1093/infdis/jiab065.
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Dysregulation of Cell Signaling by SARS-CoV-2.新冠病毒对细胞信号的失调调控。
Trends Microbiol. 2021 Mar;29(3):224-237. doi: 10.1016/j.tim.2020.12.007. Epub 2020 Dec 19.
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Entropy (Basel). 2020 Apr 10;22(4):427. doi: 10.3390/e22040427.
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