• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

FEATS:基于特征选择的单细胞 RNA-seq 数据聚类。

FEATS: feature selection-based clustering of single-cell RNA-seq data.

机构信息

University of the South Pacific and a Lecturer at Fiji National University.

Combinatics Inc., Tokyo, Japan.

出版信息

Brief Bioinform. 2021 Jul 20;22(4). doi: 10.1093/bib/bbaa306.

DOI:10.1093/bib/bbaa306
PMID:33285568
Abstract

MOTIVATION

Advances in next-generation sequencing have made it possible to carry out transcriptomic studies at single-cell resolution and generate vast amounts of single-cell RNA sequencing (RNA-seq) data rapidly. Thus, tools to analyze this data need to evolve as well as to improve accuracy and efficiency.

RESULTS

We present FEATS, a Python software package, that performs clustering on single-cell RNA-seq data. FEATS is capable of performing multiple tasks such as estimating the number of clusters, conducting outlier detection and integrating data from various experiments. We develop a univariate feature selection-based approach for clustering, which involves the selection of top informative features to improve clustering performance. This is motivated by the fact that cell types are often manually determined using the expression of only a few known marker genes. On a variety of single-cell RNA-seq datasets, FEATS gives superior performance compared with the current tools, in terms of adjusted Rand index and estimating the number of clusters. It achieves a 22% improvement in clustering and more accurately estimates the number of clusters when compared with other tools. In addition to cluster estimation, FEATS also performs outlier detection and data integration while giving an excellent computational performance. Thus, FEATS is a comprehensive clustering tool capable of addressing the challenges during the clustering of single-cell RNA-seq data.

AVAILABILITY

The installation instructions and documentation of FEATS is available at https://edwinv87.github.io/feats/.

SUPPLEMENTARY DATA

Supplementary data are available online at https://academic.oup.com/bib.

摘要

动机

下一代测序技术的进步使得在单细胞分辨率下进行转录组学研究并快速生成大量单细胞 RNA 测序(RNA-seq)数据成为可能。因此,分析这些数据的工具也需要不断发展,以提高准确性和效率。

结果

我们提出了 FEATS,这是一个用于分析单细胞 RNA-seq 数据的 Python 软件包。FEATS 能够执行多种任务,如估计聚类数、进行异常值检测和整合来自不同实验的数据。我们开发了一种基于单变量特征选择的聚类方法,该方法涉及选择信息量最大的特征来提高聚类性能。这是因为细胞类型通常是通过仅使用少数几个已知标记基因的表达来手动确定的。在各种单细胞 RNA-seq 数据集上,FEATS 在调整后的 Rand 指数和估计聚类数方面的性能优于当前工具。与其他工具相比,FEATS 在聚类方面的性能提高了 22%,并且更准确地估计了聚类数。除了聚类估计外,FEATS 还可以进行异常值检测和数据集成,同时提供出色的计算性能。因此,FEATS 是一种功能全面的聚类工具,能够解决单细胞 RNA-seq 数据聚类过程中的挑战。

可用性

FEATS 的安装说明和文档可在 https://edwinv87.github.io/feats/ 上获得。

补充数据

补充数据可在 https://academic.oup.com/bib/ 上在线获得。

相似文献

1
FEATS: feature selection-based clustering of single-cell RNA-seq data.FEATS:基于特征选择的单细胞 RNA-seq 数据聚类。
Brief Bioinform. 2021 Jul 20;22(4). doi: 10.1093/bib/bbaa306.
2
SAFE-clustering: Single-cell Aggregated (from Ensemble) clustering for single-cell RNA-seq data.SAFE-clustering:单细胞 RNA-seq 数据的单细胞聚集(来自集成)聚类。
Bioinformatics. 2019 Apr 15;35(8):1269-1277. doi: 10.1093/bioinformatics/bty793.
3
Autoencoder-based cluster ensembles for single-cell RNA-seq data analysis.基于自动编码器的单细胞 RNA-seq 数据分析聚类集成。
BMC Bioinformatics. 2019 Dec 24;20(Suppl 19):660. doi: 10.1186/s12859-019-3179-5.
4
Coupled co-clustering-based unsupervised transfer learning for the integrative analysis of single-cell genomic data.基于耦合协同聚类的无监督迁移学习在单细胞基因组数据综合分析中的应用。
Brief Bioinform. 2021 Jul 20;22(4). doi: 10.1093/bib/bbaa347.
5
An interpretable framework for clustering single-cell RNA-Seq datasets.用于聚类单细胞 RNA-Seq 数据集的可解释框架。
BMC Bioinformatics. 2018 Mar 9;19(1):93. doi: 10.1186/s12859-018-2092-7.
6
Joint learning dimension reduction and clustering of single-cell RNA-sequencing data.单细胞 RNA 测序数据的联合降维和聚类学习。
Bioinformatics. 2020 Jun 1;36(12):3825-3832. doi: 10.1093/bioinformatics/btaa231.
7
scGNN 2.0: a graph neural network tool for imputation and clustering of single-cell RNA-Seq data.scGNN 2.0:一种用于单细胞 RNA-Seq 数据插补和聚类的图神经网络工具。
Bioinformatics. 2022 Nov 30;38(23):5322-5325. doi: 10.1093/bioinformatics/btac684.
8
Improving Single-Cell RNA-seq Clustering by Integrating Pathways.通过整合途径来改善单细胞 RNA-seq 聚类。
Brief Bioinform. 2021 Nov 5;22(6). doi: 10.1093/bib/bbab147.
9
DIMM-SC: a Dirichlet mixture model for clustering droplet-based single cell transcriptomic data.DIMM-SC:一种基于 Dirichlet 混合模型的用于聚类基于液滴的单细胞转录组学数据的方法。
Bioinformatics. 2018 Jan 1;34(1):139-146. doi: 10.1093/bioinformatics/btx490.
10
coupleCoC+: An information-theoretic co-clustering-based transfer learning framework for the integrative analysis of single-cell genomic data.coupleCoC+:一种基于信息论的共聚类转移学习框架,用于单细胞基因组数据的综合分析。
PLoS Comput Biol. 2021 Jun 2;17(6):e1009064. doi: 10.1371/journal.pcbi.1009064. eCollection 2021 Jun.

引用本文的文献

1
On the use of QDE-SVM for gene feature selection and cell type classification from scRNA-seq data.基于 QDE-SVM 的 scRNA-seq 数据基因特征选择和细胞类型分类方法。
PLoS One. 2023 Oct 19;18(10):e0292961. doi: 10.1371/journal.pone.0292961. eCollection 2023.
2
CellBRF: a feature selection method for single-cell clustering using cell balance and random forest.CellBRF:一种基于细胞平衡和随机森林的单细胞聚类特征选择方法。
Bioinformatics. 2023 Jun 30;39(39 Suppl 1):i368-i376. doi: 10.1093/bioinformatics/btad216.
3
EnsMOD: A Software Program for Omics Sample Outlier Detection.
EnsMOD:一种用于组学样本离群值检测的软件程序。
J Comput Biol. 2023 Jun;30(6):726-735. doi: 10.1089/cmb.2022.0243. Epub 2023 Apr 12.
4
Cell Type Annotation Model Selection: General-Purpose vs. Pattern-Aware Feature Gene Selection in Single-Cell RNA-Seq Data.细胞类型注释模型选择:单细胞 RNA-Seq 数据中的通用型与模式感知特征基因选择
Genes (Basel). 2023 Feb 26;14(3):596. doi: 10.3390/genes14030596.
5
The Evolution of Single-Cell RNA Sequencing Technology and Application: Progress and Perspectives.单细胞 RNA 测序技术的发展与应用:进展与展望。
Int J Mol Sci. 2023 Feb 2;24(3):2943. doi: 10.3390/ijms24032943.
6
Self-supervised contrastive learning for integrative single cell RNA-seq data analysis.基于自监督对比学习的整合单细胞 RNA-seq 数据分析。
Brief Bioinform. 2022 Sep 20;23(5). doi: 10.1093/bib/bbac377.
7
LSH-GAN enables in-silico generation of cells for small sample high dimensional scRNA-seq data.LSH-GAN 可实现小样本高维 scRNA-seq 数据的计算机细胞生成。
Commun Biol. 2022 Jun 10;5(1):577. doi: 10.1038/s42003-022-03473-y.
8
Feature selection revisited in the single-cell era.单细胞时代的特征选择再探讨。
Genome Biol. 2021 Dec 1;22(1):321. doi: 10.1186/s13059-021-02544-3.
9
DeepFeature: feature selection in nonimage data using convolutional neural network.DeepFeature:使用卷积神经网络进行非图像数据的特征选择。
Brief Bioinform. 2021 Nov 5;22(6). doi: 10.1093/bib/bbab297.
10
Accurate feature selection improves single-cell RNA-seq cell clustering.准确的特征选择可提高单细胞 RNA-seq 细胞聚类。
Brief Bioinform. 2021 Sep 2;22(5). doi: 10.1093/bib/bbab034.