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Evaluation of deep learning-based feature selection for single-cell RNA sequencing data analysis
被引:4
|作者:
Huang, Hao
[1
,2
,3
]
Liu, Chunlei
[1
,3
]
Wagle, Manoj M.
[1
,2
,3
]
Yang, Pengyi
[1
,2
,3
,4
]
机构:
[1] Univ Sydney, Childrens Med Res Inst, Fac Med & Hlth, Computat Syst Biol Unit, Westmead, NSW 2145, Australia
[2] Univ Sydney, Fac Sci, Sch Math & Stat, Camperdown, NSW 2006, Australia
[3] Univ Sydney, Sydney Precis Data Sci Ctr, Camperdown, NSW 2006, Australia
[4] Univ Sydney, Charles Perkins Ctr, Camperdown, NSW 2006, Australia
基金:
英国医学研究理事会;
关键词:
IDENTITY;
D O I:
10.1186/s13059-023-03100-x
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
BackgroundFeature selection is an essential task in single-cell RNA-seq (scRNA-seq) data analysis and can be critical for gene dimension reduction and downstream analyses, such as gene marker identification and cell type classification. Most popular methods for feature selection from scRNA-seq data are based on the concept of differential distribution wherein a statistical model is used to detect changes in gene expression among cell types. Recent development of deep learning-based feature selection methods provides an alternative approach compared to traditional differential distribution-based methods in that the importance of a gene is determined by neural networks.ResultsIn this work, we explore the utility of various deep learning-based feature selection methods for scRNA-seq data analysis. We sample from Tabula Muris and Tabula Sapiens atlases to create scRNA-seq datasets with a range of data properties and evaluate the performance of traditional and deep learning-based feature selection methods for cell type classification, feature selection reproducibility and diversity, and computational time.ConclusionsOur study provides a reference for future development and application of deep learning-based feature selection methods for single-cell omics data analyses.
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页数:20
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