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

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.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2025-02-01
DOI
https://doi.org/10.1038/s41467-025-56623-1
Citations
9
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
6.45

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

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

Songjian Lu, Jiyuan Yang, Jingjing Liu, J. Wang et al.
9 citations
Nature Communications
Single-cell and spatial transcriptomics
6.45
article

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

Songjian Lu, Jiyuan Yang, Jingjing Liu, J. Wang, Ruchit Jain, Lei Yan, Jiyang Yu
article en
9 citations

Abstract

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.

Nature CommunicationsVol. 16(1)
St. Jude Children's Research Hospital (US)
American Lebanese Syrian Associated Charities, National Institutes of Health, National Institute on Aging, National Cancer Institute, National Institute of General Medical Sciences
Openalex Percentile: Top 3%
Single-cell and spatial transcriptomics
6.45
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.