ERC 2.0 - evolutionary rate covariation update improves inference of functional interactions across large phylogenies.

Jordan Little, Guillermo Hoffmann Meyer, Aakash Grover, Alex Michael Francette, Raghavendran Partha, Karen M Arndt, Martin Smith, Nathan Clark, Maria Chikina
{"title":"ERC 2.0 - evolutionary rate covariation update improves inference of functional interactions across large phylogenies.","authors":"Jordan Little, Guillermo Hoffmann Meyer, Aakash Grover, Alex Michael Francette, Raghavendran Partha, Karen M Arndt, Martin Smith, Nathan Clark, Maria Chikina","doi":"10.1101/2025.02.24.639970","DOIUrl":null,"url":null,"abstract":"<p><p>Evolutionary Rate Covariation (ERC) is an established comparative genomics method that identifies sets of genes sharing patterns of sequence evolution, which suggests shared function. Whereas many functional predictions of ERC have been empirically validated, its predictive power has hitherto been limited by its inability to tackle the large numbers of species in contemporary comparative genomics datasets. This study introduces ERC2.0, an enhanced methodology for studying ERC across phylogenies with hundreds of species and tens of thousands of genes. ERC2.0 improves upon previous iterations of ERC in algorithm speed, normalizing for heteroskedasticity, and normalizing correlations via Fisher transformations. These improvements have resulted in greater statistical power to predict biological function. In exemplar yeast and mammalian datasets, we demonstrate that the predictive power of ERC2.0 is improved relative to the previous method, ERC1.0, and that further improvements are obtained by using larger yeast and mammalian phylogenies. We attribute the improvements to both the larger datasets and improved rate normalization. We demonstrate that ERC2.0 has high predictive accuracy for known annotations and can predict the functions of genes in non-model systems. Our findings underscore the potential for ERC2.0 to be used as a single-pass computational tool in candidate gene screening and functional predictions.</p>","PeriodicalId":519960,"journal":{"name":"bioRxiv : the preprint server for biology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11888306/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv : the preprint server for biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2025.02.24.639970","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Evolutionary Rate Covariation (ERC) is an established comparative genomics method that identifies sets of genes sharing patterns of sequence evolution, which suggests shared function. Whereas many functional predictions of ERC have been empirically validated, its predictive power has hitherto been limited by its inability to tackle the large numbers of species in contemporary comparative genomics datasets. This study introduces ERC2.0, an enhanced methodology for studying ERC across phylogenies with hundreds of species and tens of thousands of genes. ERC2.0 improves upon previous iterations of ERC in algorithm speed, normalizing for heteroskedasticity, and normalizing correlations via Fisher transformations. These improvements have resulted in greater statistical power to predict biological function. In exemplar yeast and mammalian datasets, we demonstrate that the predictive power of ERC2.0 is improved relative to the previous method, ERC1.0, and that further improvements are obtained by using larger yeast and mammalian phylogenies. We attribute the improvements to both the larger datasets and improved rate normalization. We demonstrate that ERC2.0 has high predictive accuracy for known annotations and can predict the functions of genes in non-model systems. Our findings underscore the potential for ERC2.0 to be used as a single-pass computational tool in candidate gene screening and functional predictions.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
ERC 2.0 -进化速率协变更新改进了跨大系统发生的功能相互作用推断。
进化速率协变(ERC)是一种成熟的比较基因组学方法,用于识别序列进化的基因共享模式,这表明共享功能。尽管ERC的许多功能预测已经得到了经验验证,但由于无法处理当代比较基因组学数据集中的大量物种,其预测能力迄今为止受到限制。本研究引入了ERC2.0,这是一种增强的方法,用于研究数百个物种和数万个基因的ERC跨系统发育。ERC2.0在算法速度、异方差归一化和通过Fisher变换归一化相关性方面改进了之前的ERC迭代。这些改进提高了预测生物功能的统计能力。在样本酵母和哺乳动物数据集中,我们证明了ERC2.0的预测能力相对于之前的方法ERC1.0有所提高,并且通过使用更大的酵母和哺乳动物系统发育得到了进一步的提高。我们将改进归功于更大的数据集和改进的率归一化。我们证明了ERC2.0对已知注释具有较高的预测精度,并且可以预测非模型系统中基因的功能。我们的发现强调了ERC2.0作为候选基因筛选和功能预测的单次计算工具的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Process for Standardizing and Assessing the Parameters Governing MS2 Virus-Like Particle Reassembly around Nucleic Acid Cargo. Next generation protein-corrole bio-assemblies provide effective tumoricidal treatment in a metastatic triple-negative breast cancer model. Rapid Histone Post-Translational Modification Analysis Using Alternative Proteases and Tandem Mass Tags. Negative-Valence Neurons in the Larval Zebrafish Pallium. Hookworm genomic diversity and population structure from accessible sample types: A validated approach to generate genome-wide polymorphism datasets from individual third-stage larvae.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1