scFTAT: a novel cell annotation method integrating FFT and transformer.

IF 3.3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS BMC Bioinformatics Pub Date : 2025-02-25 DOI:10.1186/s12859-025-06061-z
Binhua Tang, Yiyao Chen
{"title":"scFTAT: a novel cell annotation method integrating FFT and transformer.","authors":"Binhua Tang, Yiyao Chen","doi":"10.1186/s12859-025-06061-z","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Advancements in high-throughput sequencing and deep learning have boosted single-cell RNA studies. However, current methods for annotating single-cell data face challenges due to high data sparsity and tedious manual annotation on large-scale data.</p><p><strong>Results: </strong>Thus, we proposed a novel annotation model integrating FFT (Fast Fourier Transform) and an enhanced Transformer, named scFTAT. Initially, it reduces data sparsity using LDA (Linear Discriminant Analysis). Subsequently, automatic cell annotation is achieved through a proposed module integrating FFT and an enhanced Transformer. Moreover, the model is fine-tuned to improve training performance by effectively incorporating such techniques as kernel approximation, position encoding enhancement, and attention enhancement modules. Compared to existing popular annotation tools, scFTAT maintains high accuracy and robustness on six typical datasets. Specifically, the model achieves an accuracy of 0.93 on the human kidney data, with an F1 score of 0.84, precision of 0.96, recall rate of 0.80, and Matthews correlation coefficient of 0.89. The highest accuracy of the compared methods is 0.92, with an F1 score of 0.71, precision of 0.75, recall rate of 0.73, and Matthews correlation coefficient of 0.85. The compiled codes and supplements are available at: https://github.com/gladex/scFTAT .</p><p><strong>Conclusion: </strong>In summary, the proposed scFTAT effectively integrates FFT and enhanced Transformer for automatic feature learning, addressing the challenges of high sparsity and tedious manual annotation in single-cell profiling data. Experiments on six typical scRNA-seq datasets from human and mouse tissues evaluate the model using five metrics as accuracy, F1 score, precision, recall, and Matthews correlation coefficient. Performance comparisons with existing methods further demonstrate the efficiency and robustness of our proposed method.</p>","PeriodicalId":8958,"journal":{"name":"BMC Bioinformatics","volume":"26 1","pages":"62"},"PeriodicalIF":3.3000,"publicationDate":"2025-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11853718/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Bioinformatics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12859-025-06061-z","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Advancements in high-throughput sequencing and deep learning have boosted single-cell RNA studies. However, current methods for annotating single-cell data face challenges due to high data sparsity and tedious manual annotation on large-scale data.

Results: Thus, we proposed a novel annotation model integrating FFT (Fast Fourier Transform) and an enhanced Transformer, named scFTAT. Initially, it reduces data sparsity using LDA (Linear Discriminant Analysis). Subsequently, automatic cell annotation is achieved through a proposed module integrating FFT and an enhanced Transformer. Moreover, the model is fine-tuned to improve training performance by effectively incorporating such techniques as kernel approximation, position encoding enhancement, and attention enhancement modules. Compared to existing popular annotation tools, scFTAT maintains high accuracy and robustness on six typical datasets. Specifically, the model achieves an accuracy of 0.93 on the human kidney data, with an F1 score of 0.84, precision of 0.96, recall rate of 0.80, and Matthews correlation coefficient of 0.89. The highest accuracy of the compared methods is 0.92, with an F1 score of 0.71, precision of 0.75, recall rate of 0.73, and Matthews correlation coefficient of 0.85. The compiled codes and supplements are available at: https://github.com/gladex/scFTAT .

Conclusion: In summary, the proposed scFTAT effectively integrates FFT and enhanced Transformer for automatic feature learning, addressing the challenges of high sparsity and tedious manual annotation in single-cell profiling data. Experiments on six typical scRNA-seq datasets from human and mouse tissues evaluate the model using five metrics as accuracy, F1 score, precision, recall, and Matthews correlation coefficient. Performance comparisons with existing methods further demonstrate the efficiency and robustness of our proposed method.

Abstract Image

Abstract Image

Abstract Image

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
scFTAT:一种结合FFT和变压器的单元注释新方法。
背景:高通量测序和深度学习的进步促进了单细胞RNA的研究。然而,目前的单细胞数据标注方法面临着数据稀疏性高和大规模数据手工标注繁琐的挑战。因此,我们提出了一种新的注释模型,将FFT(快速傅里叶变换)和增强的Transformer集成在一起,称为scFTAT。最初,它使用LDA(线性判别分析)降低数据稀疏性。随后,通过一个集成FFT和增强Transformer的模块实现自动单元注释。此外,通过有效地结合核逼近、位置编码增强和注意力增强模块等技术,对模型进行微调以提高训练性能。与现有流行的标注工具相比,scFTAT在6个典型数据集上保持了较高的准确性和鲁棒性。具体而言,该模型对人体肾脏数据的准确率为0.93,F1得分为0.84,准确率为0.96,召回率为0.80,马修斯相关系数为0.89。比较方法的最高准确率为0.92,F1得分为0.71,精密度为0.75,召回率为0.73,马修斯相关系数为0.85。结论:本文提出的scFTAT有效地集成了FFT和增强的Transformer用于自动特征学习,解决了单细胞分析数据的高稀疏性和繁琐的手动注释的挑战。在来自人类和小鼠组织的6个典型scRNA-seq数据集上进行实验,使用5个指标(准确性、F1评分、精度、召回率和马修斯相关系数)对模型进行评估。与现有方法的性能比较进一步证明了该方法的有效性和鲁棒性。
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
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.
期刊最新文献
Development of a comprehensive GWAS atlas for chicken breeds. scZiva: imputation method for single-cell RNA-seq data with zero-inflated variational autoencoder. Mke-resnet: a lightweight and interpretable deep learning framework for efficient RNA m6A site identification. SPICEY: an R package for quantifying tissue specificity from single cell multi-omics data. DAESC + : high-performance, integrated software for single-cell allele-specific expression data.
×
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