mulea: An R package for enrichment analysis using multiple ontologies and empirical false discovery rate.

IF 2.9 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS BMC Bioinformatics Pub Date : 2024-10-18 DOI:10.1186/s12859-024-05948-7
Cezary Turek, Márton Ölbei, Tamás Stirling, Gergely Fekete, Ervin Tasnádi, Leila Gul, Balázs Bohár, Balázs Papp, Wiktor Jurkowski, Eszter Ari
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Abstract

Traditional gene set enrichment analyses are typically limited to a few ontologies and do not account for the interdependence of gene sets or terms, resulting in overcorrected p-values. To address these challenges, we introduce mulea, an R package offering comprehensive overrepresentation and functional enrichment analysis. mulea employs a progressive empirical false discovery rate (eFDR) method, specifically designed for interconnected biological data, to accurately identify significant terms within diverse ontologies. mulea expands beyond traditional tools by incorporating a wide range of ontologies, encompassing Gene Ontology, pathways, regulatory elements, genomic locations, and protein domains. This flexibility enables researchers to tailor enrichment analysis to their specific questions, such as identifying enriched transcriptional regulators in gene expression data or overrepresented protein domains in protein sets. To facilitate seamless analysis, mulea provides gene sets (in standardised GMT format) for 27 model organisms, covering 22 ontology types from 16 databases and various identifiers resulting in almost 900 files. Additionally, the muleaData ExperimentData Bioconductor package simplifies access to these pre-defined ontologies. Finally, mulea's architecture allows for easy integration of user-defined ontologies, or GMT files from external sources (e.g., MSigDB or Enrichr), expanding its applicability across diverse research areas. mulea is distributed as a CRAN R package downloadable from https://cran.r-project.org/web/packages/mulea/ and https://github.com/ELTEbioinformatics/mulea . It offers researchers a powerful and flexible toolkit for functional enrichment analysis, addressing limitations of traditional tools with its progressive eFDR and by supporting a variety of ontologies. Overall, mulea fosters the exploration of diverse biological questions across various model organisms.

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mulea:使用多本体和经验错误发现率进行富集分析的 R 软件包。
传统的基因组富集分析通常仅限于少数几个本体,而且不考虑基因组或术语之间的相互依赖关系,从而导致过校正 p 值。mulea 采用一种渐进式经验错误发现率 (eFDR) 方法,专为相互关联的生物数据而设计,可准确识别不同本体中的重要术语。mulea 的功能超越了传统工具,纳入了广泛的本体,包括基因本体、通路、调控元件、基因组位置和蛋白质域。这种灵活性使研究人员能够针对具体问题进行富集分析,例如在基因表达数据中识别富集的转录调控因子,或在蛋白质组中识别代表性过高的蛋白质域。为便于进行无缝分析,mulea 提供了 27 种模式生物的基因集(标准化 GMT 格式),涵盖来自 16 个数据库的 22 种本体类型和各种标识符,形成近 900 个文件。此外,muleaData ExperimentData Bioconductor 软件包简化了对这些预定义本体的访问。最后,mulea 的架构允许轻松集成用户定义的本体或来自外部资源(如 MSigDB 或 Enrichr)的 GMT 文件,从而扩大了其在不同研究领域的适用性。mulea 以 CRAN R 软件包的形式发布,可从 https://cran.r-project.org/web/packages/mulea/ 和 https://github.com/ELTEbioinformatics/mulea 下载。它为研究人员提供了一个强大而灵活的功能富集分析工具包,通过渐进式 eFDR 和支持各种本体解决了传统工具的局限性。总之,mulea 有助于探索各种模式生物的各种生物学问题。
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来源期刊
BMC Bioinformatics
BMC Bioinformatics 生物-生化研究方法
CiteScore
5.70
自引率
3.30%
发文量
506
审稿时长
4.3 months
期刊介绍: BMC Bioinformatics is an open access, peer-reviewed journal that considers articles on all aspects of the development, testing and novel application of computational and statistical methods for the modeling and analysis of all kinds of biological data, as well as other areas of computational biology. BMC Bioinformatics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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