stana: an R package for metagenotyping analysis and interactive application based on clinical data.

IF 4 Q1 GENETICS & HEREDITY NAR Genomics and Bioinformatics Pub Date : 2025-01-08 eCollection Date: 2025-03-01 DOI:10.1093/nargab/lqae191
Noriaki Sato, Kotoe Katayama, Daichi Miyaoka, Miho Uematsu, Ayumu Saito, Kosuke Fujimoto, Satoshi Uematsu, Seiya Imoto
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Abstract

Metagenotyping of metagenomic data has recently attracted increasing attention as it resolves intraspecies diversity by identifying single nucleotide variants. Furthermore, gene copy number analysis within species provides a deeper understanding of metabolic functions in microbial communities. However, a platform for examining metagenotyping results based on relevant grouping data is lacking. Here, we have developed the R package, stana, for the processing and analysis of metagenotyping results. The package consists of modules for preprocessing, statistical analysis, functional analysis and visualization. An interactive analysis environment for exploring the metagenotyping results was also developed and publicly released with over 1000 publicly available metagenome samples related to human diseases. Three examples exploring the relationship between the metagenotypes of the gut microbiome and human diseases are presented-end-stage renal disease, Crohn's disease and Parkinson's disease. The results suggest that stana facilitated the confirmation of the original study's findings and the generation of a new hypothesis. The GitHub repository for the package is available at https://github.com/noriakis/stana.

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stana:一个基于临床数据的元基因型分析和交互式应用程序的R包。
元基因组数据的元基因组分型最近引起了越来越多的关注,因为它通过识别单核苷酸变异来解决种内多样性。此外,物种内基因拷贝数分析提供了对微生物群落代谢功能的更深入了解。然而,一个基于相关分组数据检验元基因型结果的平台是缺乏的。在这里,我们开发了R包,stana,用于处理和分析元基因分型结果。该软件包由预处理、统计分析、功能分析和可视化模块组成。还开发并公开发布了用于探索宏基因组分型结果的交互式分析环境,其中包含1000多个与人类疾病相关的公开可获得的宏基因组样本。三个例子探讨了肠道微生物群的宏基因型与人类疾病之间的关系——终末期肾病、克罗恩病和帕金森病。结果表明,stana促进了原始研究结果的确认和新假设的产生。该包的GitHub存储库可从https://github.com/noriakis/stana获得。
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来源期刊
CiteScore
8.00
自引率
2.20%
发文量
95
审稿时长
15 weeks
期刊最新文献
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