Transcriptome size matters for single-cell RNA-seq normalization and bulk deconvolution

被引:0
|
作者
Lu, Songjian [1 ]
Yang, Jiyuan [1 ]
Yan, Lei [1 ]
Liu, Jingjing [1 ]
Wang, Judy Jiaru [1 ]
Jain, Rhea [1 ]
Yu, Jiyang [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Computat Biol, Memphis, TN 38105 USA
基金
美国国家卫生研究院;
关键词
RECONSTRUCTION;
D O I
10.1038/s41467-025-56623-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The variation of transcriptome size across cell types significantly impacts single-cell RNA sequencing (scRNA-seq) data normalization and bulk RNA-seq cellular deconvolution, yet this intrinsic feature is often overlooked. Here we introduce ReDeconv, a computational algorithm that incorporates transcriptome size into scRNA-seq normalization and bulk deconvolution. ReDeconv introduces a scRNA-seq normalization approach, Count based on Linearized Transcriptome Size (CLTS), which corrects differential expressed genes typically misidentified by standard count per 10 K normalization, as confirmed by orthogonal validations. By maintaining transcriptome size variation, CLTS-normalized scRNA-seq enhances the accuracy of bulk deconvolution. Additionally, ReDeconv mitigates gene length effects and models expression variances, thereby improving deconvolution outcomes, particularly for rare cell types. Evaluated with both synthetic and real datasets, ReDeconv surpasses existing methods in precision. ReDeconv alters the practice and provides a new standard for scRNA-seq analyses and bulk deconvolution. The software packages and a user-friendly web portal are available.
引用
收藏
页数:17
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