Suppr超能文献

组织特异性富集分析,用于解码组织特异性。

deTS: tissue-specific enrichment analysis to decode tissue specificity.

机构信息

School of Biomedical Informatics, Center for Precision Health, The University of Texas Health Science Center at Houston, Houston, TX, USA.

Human Genetics Center, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX, USA.

出版信息

Bioinformatics. 2019 Oct 1;35(19):3842-3845. doi: 10.1093/bioinformatics/btz138.

Abstract

MOTIVATION

Diseases and traits are under dynamic tissue-specific regulation. However, heterogeneous tissues are often collected in biomedical studies, which reduce the power in the identification of disease-associated variants and gene expression profiles.

RESULTS

We present deTS, an R package, to conduct tissue-specific enrichment analysis with two built-in reference panels. Statistical methods are developed and implemented for detecting tissue-specific genes and for enrichment test of different forms of query data. Our applications using multi-trait genome-wide association studies data and cancer expression data showed that deTS could effectively identify the most relevant tissues for each query trait or sample, providing insights for future studies.

AVAILABILITY AND IMPLEMENTATION

https://github.com/bsml320/deTS and CRAN https://cran.r-project.org/web/packages/deTS/.

SUPPLEMENTARY INFORMATION

Supplementary data are available at Bioinformatics online.

摘要

动机

疾病和特征受到动态组织特异性调控。然而,生物医学研究中通常采集异质组织,这降低了鉴定与疾病相关变异和基因表达谱的能力。

结果

我们提出了 deTS,这是一个 R 包,可使用两个内置参考面板进行组织特异性富集分析。为检测组织特异性基因和不同形式查询数据的富集检验,开发并实现了统计方法。使用多性状全基因组关联研究数据和癌症表达数据的应用表明,deTS 可以有效地识别每个查询性状或样本最相关的组织,为未来的研究提供了思路。

可用性和实现

https://github.com/bsml320/deTS 和 CRAN https://cran.r-project.org/web/packages/deTS/。

补充信息

补充数据可在《生物信息学》在线获得。

相似文献

4
myTAI: evolutionary transcriptomics with R.我的TAI:使用R进行进化转录组学研究
Bioinformatics. 2018 May 1;34(9):1589-1590. doi: 10.1093/bioinformatics/btx835.
9
Varanto: variant enrichment analysis and annotation.瓦兰托(Varanto):变体富集分析和注释。
Bioinformatics. 2019 Sep 1;35(17):3154-3156. doi: 10.1093/bioinformatics/btz046.

引用本文的文献

7
Schizophrenia is associated with altered DNA methylation variance.精神分裂症与DNA甲基化变异的改变有关。
Mol Psychiatry. 2025 Apr;30(4):1383-1395. doi: 10.1038/s41380-024-02749-5. Epub 2024 Sep 13.

本文引用的文献

2
Genetic identification of brain cell types underlying schizophrenia.精神分裂症相关脑细胞类型的遗传鉴定。
Nat Genet. 2018 Jun;50(6):825-833. doi: 10.1038/s41588-018-0129-5. Epub 2018 May 21.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验