hdWGCNA identifies co-expression networks in high-dimensional transcriptomics data

被引:225
作者
Morabito, Samuel [1 ,2 ,3 ]
Reese, Fairlie [2 ,4 ]
Rahimzadeh, Negin [1 ,2 ,3 ]
Miyoshi, Emily [3 ,5 ]
Swarup, Vivek [2 ,3 ,5 ]
机构
[1] Univ Calif Irvine, Math Computat & Syst Biol MCSB Program, Irvine, CA USA
[2] Univ Calif Irvine, Ctr Complex Biol Syst CCBS, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Inst Memory Impairments & Neurol Disorders MIND, Irvine, CA 92697 USA
[4] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA USA
[5] Univ Calif Irvine, Dept Neurobiol & Behav, Irvine, CA 92697 USA
来源
CELL REPORTS METHODS | 2023年 / 3卷 / 06期
关键词
DE-NOVO MUTATIONS; ALZHEIMERS-DISEASE; SINGLE; MICROGLIA; PATTERNS; INSIGHTS;
D O I
10.1016/j.crmeth.2023.100498
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Biological systems are immensely complex, organized into a multi-scale hierarchy of functional units based on tightly regulated interactions between distinct molecules, cells, organs, and organisms. While experi-mental methods enable transcriptome-wide measurements across millions of cells, popular bioinformatic tools do not support systems-level analysis. Here we present hdWGCNA, a comprehensive framework for analyzing co-expression networks in high-dimensional transcriptomics data such as single-cell and spatial RNA sequencing (RNA-seq). hdWGCNA provides functions for network inference, gene module identifica-tion, gene enrichment analysis, statistical tests, and data visualization. Beyond conventional single-cell RNA-seq, hdWGCNA is capable of performing isoform-level network analysis using long-read single-cell data. We showcase hdWGCNA using data from autism spectrum disorder and Alzheimer's disease brain samples, identifying disease-relevant co-expression network modules. hdWGCNA is directly compatible with Seurat, a widely used R package for single-cell and spatial transcriptomics analysis, and we demon-strate the scalability of hdWGCNA by analyzing a dataset containing nearly 1 million cells.
引用
收藏
页数:27
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