Learning deep features and topological structure of cells for clustering of scRNA-sequencing data

可解释性 计算机科学 人工智能 子空间拓扑 深度学习 聚类分析 图形 自编码 又称作 机器学习 特征(语言学) 模式识别(心理学) 算法 理论计算机科学 哲学 语言学 图书馆学
作者
Haiyue Wang,Xiaoke Ma
出处
期刊:Briefings in Bioinformatics [Oxford University Press]
卷期号:23 (3) 被引量:8
标识
DOI:10.1093/bib/bbac068
摘要

Single-cell RNA sequencing (scRNA-seq) measures gene transcriptome at the cell level, paving the way for the identification of cell subpopulations. Although deep learning has been successfully applied to scRNA-seq data, these algorithms are criticized for the undesirable performance and interpretability of patterns because of the noises, high-dimensionality and extraordinary sparsity of scRNA-seq data. To address these issues, a novel deep learning subspace clustering algorithm (aka scGDC) for cell types in scRNA-seq data is proposed, which simultaneously learns the deep features and topological structure of cells. Specifically, scGDC extends auto-encoder by introducing a self-representation layer to extract deep features of cells, and learns affinity graph of cells, which provide a better and more comprehensive strategy to characterize structure of cell types. To address heterogeneity of scRNA-seq data, scGDC projects cells of various types onto different subspaces, where types, particularly rare cell types, are well discriminated by utilizing generative adversarial learning. Furthermore, scGDC joins deep feature extraction, structural learning and cell type discovery, where features of cells are extracted under the guidance of cell types, thereby improving performance of algorithms. A total of 15 scRNA-seq datasets from various tissues and organisms with the number of cells ranging from 56 to 63 103 are adopted to validate performance of algorithms, and experimental results demonstrate that scGDC significantly outperforms 14 state-of-the-art methods in terms of various measurements (on average 25.51% by improvement), where (rare) cell types are significantly associated with topology of affinity graph of cells. The proposed model and algorithm provide an effective strategy for the analysis of scRNA-seq data (The software is coded using python, and is freely available for academic https://github.com/xkmaxidian/scGDC).

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
看看不要钱完成签到,获得积分10
刚刚
Icanfly完成签到 ,获得积分10
刚刚
科研通AI6.4应助安详凡松采纳,获得20
刚刚
lili发布了新的文献求助10
刚刚
居家家发布了新的文献求助10
刚刚
刚刚
2秒前
乐观的小馒头完成签到,获得积分10
3秒前
4秒前
心想柿橙完成签到,获得积分10
5秒前
清爽的飞瑶完成签到,获得积分10
5秒前
yue发布了新的文献求助10
6秒前
wjw发布了新的文献求助10
6秒前
Zoey完成签到 ,获得积分20
7秒前
li完成签到,获得积分10
8秒前
勤奋幻露应助xxqiao采纳,获得10
8秒前
arniu2008发布了新的文献求助10
8秒前
居家家完成签到,获得积分10
8秒前
aaron_hill发布了新的文献求助10
9秒前
开心橙完成签到,获得积分10
10秒前
李健的小迷弟应助诸军则采纳,获得10
11秒前
明理映阳发布了新的文献求助30
11秒前
严究生完成签到,获得积分10
13秒前
充电宝应助叶落采纳,获得10
15秒前
aaron_hill完成签到,获得积分10
15秒前
斯文败类应助sdl采纳,获得10
16秒前
SciGPT应助龙龙冲采纳,获得10
16秒前
17秒前
yuanyingge完成签到,获得积分10
18秒前
夏雪儿完成签到,获得积分10
19秒前
飞奔的水煮蛋完成签到,获得积分10
20秒前
英俊的铭应助无何化有采纳,获得10
20秒前
20秒前
布布完成签到,获得积分10
20秒前
22秒前
JasonChan发布了新的文献求助10
22秒前
xchmnvpy完成签到,获得积分10
24秒前
foreverlessness应助304anchi采纳,获得10
24秒前
诚心凤灵完成签到 ,获得积分10
25秒前
CHEN完成签到 ,获得积分10
25秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1314
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Navigating Normative Orders. Interdisciplinary Perspectives 800
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
Organizational Behavior 510
Management and the Arts 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7746019
求助须知:如何正确求助?哪些是违规求助? 9293900
关于积分的说明 20222699
捐赠科研通 7325709
什么是DOI,文献DOI怎么找? 3308041
关于科研通互助平台的介绍 2459990
邀请新用户注册赠送积分活动 2319478