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分类依据与纠错

AI 根据所提供的论文材料归类:摘要中的网络是细胞内基因网络,未提供微观经济网络、社会互动或干扰效应的研究依据。

反馈分类问题

Heterogeneous Gene Network Estimation for Single-Cell Transcriptomic Data via a Joint Regularized Deep Neural Network

通过联合正则化深度神经网络估计单细胞异质基因网络

正在核对关联版本…

代码、数据与补充材料

正在核对对应版本的资源…

关注这篇论文的作者
Jingyuan Yang
Tao Li
Tianyi Wang
Shuangge Ma
Mengyun Wu

通过联合正则化深度神经网络估计单细胞异质基因网络

研究问题
如何从单细胞转录组数据中同时估计不同细胞亚群的基因网络,并处理未知异质性、零膨胀和非线性基因关系?
方法与思路
作者结合联合正则化深度神经网络与基于 Mahalanobis 距离的 K-means,利用选择层及共享、亚群特有神经元构建网络。
材料陈述的贡献
摘要称方法在多组织、多物种数据中提高网络估计与细胞分组表现,并识别具有生物学意义的枢纽基因及富集模块。
阅读关注点
应核对聚类与网络估计如何衔接、零膨胀处理机制、选择层对应的边定义,以及准确性和生物学解释性的评价依据。
阅读边界
仅据所给 OpenAlex 摘要,不推断刊本变化;摘要未说明网络关系的因果含义、比较指标与验证设计,不能将估计边解释为因果调控。

原文摘要

Estimation of intracellular gene networks has been a critical component of single-cell transcriptomic data analysis, which can provide crucial insights into the complex interplay between genes, facilitating the discovery of the biological basis of human life at single-cell resolution. Despite notable achievements, existing methodologies often falter in their practicality, primarily due to their narrow focus on simplistic linear relationships and inadequate handling of cellular heterogeneity. To bridge these gaps, we propose a joint regularized deep neural network method incorporating Mahalanobis distance-based K-means clustering (JRDNN-KM) to estimate multiple networks for various cell subgroups simultaneously, accounting for both unknown cellular heterogeneity and zero inflation, and, more importantly, complex nonlinear relationships among genes. We introduce an innovative selection layer for network construction, along with hidden layers that include both shared and subgroup-specific neurons, to capture common patterns and subgroup-specific variations across networks. Applied to real single-cell transcriptomic data from multiple tissues and species, JRDNN-KM demonstrates higher accuracy and biological interpretability in network estimation, and more accurately identifies cell subgroups compared to current state-of-the-art methods. Building on network construction, we further find hub genes with important biological implications and modules with statistical enrichment of biological processes.

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