Adversarial learning enables unbiased organism-wide cross-species alignment of single-cell RNA data

Samuel Cooper, Juan Javier Diaz-Mejia, Brendan Innes, Elias Williams, Dylan Mendonca, Octavian Focsa, Allison Nixon, Swechha Singh, Ronen Schuster, Boris Hinz, Matthew Buechler
{"title":"Adversarial learning enables unbiased organism-wide cross-species alignment of single-cell RNA data","authors":"Samuel Cooper, Juan Javier Diaz-Mejia, Brendan Innes, Elias Williams, Dylan Mendonca, Octavian Focsa, Allison Nixon, Swechha Singh, Ronen Schuster, Boris Hinz, Matthew Buechler","doi":"10.1101/2024.08.11.607498","DOIUrl":null,"url":null,"abstract":"Today's single-cell RNA (scRNA) datasets remain siloed, due to significant challenges associated with their integration at scale. Moreover, most scRNA analysis tools that operate at scale leverage supervised techniques that are insufficient for cell-type identification and discovery. Here we demonstrate that alignment of scRNA data using unsupervised models is accurate at both an organism wide scale and between species. To do this we show how adversarial training of a deep-learning model we term batch-adversarial single-cell variational inference (BA-scVI) can be employed to align standardized benchmark datasets that comprise dozens of scRNA studies and span tissues in both humans and mice. Analysis of the learnt cell-type space then enables us to identify evolutionarily conserved cell-types, including underappreciated complement expressing macrophage and fibroblast types, paving the way to larger phylogenetic analysis of cell-type evolution. Finally, we provide broad access to scREF, scREF-mu and the BA-scVI model via an online interface for atlas exploration and drag-and-drop alignment of new data.","PeriodicalId":501246,"journal":{"name":"bioRxiv - Genetics","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv - Genetics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.08.11.607498","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

Today's single-cell RNA (scRNA) datasets remain siloed, due to significant challenges associated with their integration at scale. Moreover, most scRNA analysis tools that operate at scale leverage supervised techniques that are insufficient for cell-type identification and discovery. Here we demonstrate that alignment of scRNA data using unsupervised models is accurate at both an organism wide scale and between species. To do this we show how adversarial training of a deep-learning model we term batch-adversarial single-cell variational inference (BA-scVI) can be employed to align standardized benchmark datasets that comprise dozens of scRNA studies and span tissues in both humans and mice. Analysis of the learnt cell-type space then enables us to identify evolutionarily conserved cell-types, including underappreciated complement expressing macrophage and fibroblast types, paving the way to larger phylogenetic analysis of cell-type evolution. Finally, we provide broad access to scREF, scREF-mu and the BA-scVI model via an online interface for atlas exploration and drag-and-drop alignment of new data.
逆向学习实现了单细胞 RNA 数据的无偏全生物体跨物种配准
当今的单细胞 RNA(scRNA)数据集仍然各自为政,这是因为大规模整合这些数据集面临巨大挑战。此外,大多数大规模运行的 scRNA 分析工具利用的是监督技术,而监督技术不足以进行细胞类型鉴定和发现。在这里,我们证明了使用无监督模型对scRNA数据进行配准在生物体范围内和物种之间都是准确的。为此,我们展示了如何利用我们称之为批量对抗性单细胞变异推理(BA-scVI)的深度学习模型的对抗性训练来对齐标准化的基准数据集,这些数据集由数十个 scRNA 研究组成,横跨人类和小鼠的组织。对所学细胞类型空间的分析使我们能够确定进化上保守的细胞类型,包括未得到充分重视的补体表达巨噬细胞和成纤维细胞类型,从而为细胞类型进化的大型系统发育分析铺平道路。最后,我们通过一个在线界面提供了对 scREF、scREF-mu 和 BA-scVI 模型的广泛访问,以便进行图谱探索和新数据的拖放比对。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信