4.5 Article

Benchmarking clustering algorithms on estimating the number of cell types from single-cell RNA-sequencing data

期刊

GENOME BIOLOGY
卷 23, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13059-022-02622-0

关键词

-

资金

  1. Australia National Health and Medical Research Council (NHMRC) [1173469]
  2. Postgraduate Research Excellence Award (PREA) Tuition Fee and Stipend Scholarship
  3. Research Training Program Tuition Fee Offset
  4. University of Sydney Postgraduate Award Stipend Scholarship
  5. National Health and Medical Research Council of Australia [1173469] Funding Source: NHMRC

向作者/读者索取更多资源

This study systematically benchmarks a range of clustering algorithms for single-cell RNA-seq data and summarizes the strengths and weaknesses of each method. The authors evaluate the performance of the algorithms using a large number of datasets and provide a multi-aspect recommendation to users.
Background: A key task in single-cell RNA-seq (scRNA-seq) data analysis is to accurately detect the number of cell types in the sample, which can be critical for downstream analyses such as cell type identification. Various scRNA-seq data clustering algorithms have been specifically designed to automatically estimate the number of cell types through optimising the number of clusters in a dataset. The lack of benchmark studies, however, complicates the choice of the methods. Results: We systematically benchmark a range of popular clustering algorithms on estimating the number of cell types in a variety of settings by sampling from the Tabula Muris data to create scRNA-seq datasets with a varying number of cell types, varying number of cells in each cell type, and different cell type proportions. The large number of datasets enables us to assess the performance of the algorithms, covering four broad categories of approaches, from various aspects using a panel of criteria. We further cross-compared the performance on datasets with high cell numbers using Tabula Muris and Tabula Sapiens data. Conclusions: We identify the strengths and weaknesses of each method on multiple criteria including the deviation of estimation from the true number of cell types, variability of estimation, clustering concordance of cells to their predefined cell types, and running time and peak memory usage. We then summarise these results into a multi-aspect recommendation to the users. The proposed stability-based approach for estimating the number of cell types is implemented in an R package and is freely available from (https://github.com/PYanaLab/scCCESS).

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据