Scholarlink

Background <p>Compositional data analysis (CoDA) is an emerging statistical framework and has been extended to microbiome, bulk RNA-seq, and cell type proportions in single-cell RNA-seq (scRNA-seq), which typically has 50–200 components. Here, we explore the high-dimensional application of CoDA (CoDA-hd) and its various log-ratio (LR) transformations to raw count matrix of scRNA-seq which has over 20,000 components (e.g., protein coding genes). scRNA-seq matrices are typically sparse and high-dimensional. Common approaches of normalization such as log-normalization may lead to suspicious findings as previously shown for trajectory inference. Although RNA-seq is compositional data by nature, the geometry of CoDA in high-dimensional simplex is not compatible with most downstream analyses of scRNA-seq which are based on Euclidean space. In this study, we attempted to explore: (1) CoDA adaptability to scRNA-seq; (2) handling of zero data: prior-log-normalization, imputation or with specific count addition scheme; (3) transformation to Euclidean space and compatibility with downstream analyses.</p> Results <p>Our results suggest that (1) the innovative count addition schemes (e.g., SGM) enable the application of CoDA to high dimensional sparse data (i.e., scRNA-seq); (2) log-normalized data could be transformed to CoDA LR representation; (3) CoDA LR transformations such as count-added centered-log-ratio (CLR) had some advantages in dimension reduction visualization, clustering, and trajectory inference in the tested real and simulated datasets. CLR provided more distinct and well-separated clusters in dimension reductions, improved the Slingshot trajectory inference, and eliminated the suspicious trajectory that was probably caused by the dropouts.</p> Conclusions <p>We therefore conclude that CoDA may be a preferred scale-free model to handle scRNA-seq data for these downstream tasks. Additionally, an R package ‘CoDAhd’ was developed for conducting CoDA LR transformations for high dimensional scRNA-seq data. The code for implementing CoDA-hd, along with some example datasets, are available at <a href="https://github.com/GO3295/CoDAhd">https://github.com/GO3295/CoDAhd</a>.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Compositional data modeling of high-dimensional single cell RNA-seq (CoDA-hd): its advantages over commonly used normalization approaches

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年10月21日

查看全文
  • Jinghan Huang,
  • Sheung Chi Phillip Yam,
  • K. S. Leung,
  • Minghua Deng,
  • Nelson L. S. Tang

摘要

Background

Compositional data analysis (CoDA) is an emerging statistical framework and has been extended to microbiome, bulk RNA-seq, and cell type proportions in single-cell RNA-seq (scRNA-seq), which typically has 50–200 components. Here, we explore the high-dimensional application of CoDA (CoDA-hd) and its various log-ratio (LR) transformations to raw count matrix of scRNA-seq which has over 20,000 components (e.g., protein coding genes). scRNA-seq matrices are typically sparse and high-dimensional. Common approaches of normalization such as log-normalization may lead to suspicious findings as previously shown for trajectory inference. Although RNA-seq is compositional data by nature, the geometry of CoDA in high-dimensional simplex is not compatible with most downstream analyses of scRNA-seq which are based on Euclidean space. In this study, we attempted to explore: (1) CoDA adaptability to scRNA-seq; (2) handling of zero data: prior-log-normalization, imputation or with specific count addition scheme; (3) transformation to Euclidean space and compatibility with downstream analyses.

Results

Our results suggest that (1) the innovative count addition schemes (e.g., SGM) enable the application of CoDA to high dimensional sparse data (i.e., scRNA-seq); (2) log-normalized data could be transformed to CoDA LR representation; (3) CoDA LR transformations such as count-added centered-log-ratio (CLR) had some advantages in dimension reduction visualization, clustering, and trajectory inference in the tested real and simulated datasets. CLR provided more distinct and well-separated clusters in dimension reductions, improved the Slingshot trajectory inference, and eliminated the suspicious trajectory that was probably caused by the dropouts.

Conclusions

We therefore conclude that CoDA may be a preferred scale-free model to handle scRNA-seq data for these downstream tasks. Additionally, an R package ‘CoDAhd’ was developed for conducting CoDA LR transformations for high dimensional scRNA-seq data. The code for implementing CoDA-hd, along with some example datasets, are available at https://github.com/GO3295/CoDAhd.