Evidence map›Paper›PMID 39893178›Full record

ArticleNature communications2025

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

Songjian Lu, Jiyuan Yang, Lei Yan, Jingjing Liu, Judy Jiaru Wang, Rhea Jain, Jiyang Yu

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Songjian LuDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Jiyuan YangDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID http://orcid.org/0000-0003-0185-1133
Lei YanDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID http://orcid.org/0000-0001-5259-3379
Jingjing LiuDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID http://orcid.org/0000-0002-8184-8382
Judy Jiaru WangDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Rhea JainDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Jiyang YuDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA. Jiyang.Yu@stjude.org.ORCID http://orcid.org/0000-0003-3629-4330

Funding

Dissecting neuron-microglia-astrocyte interaction in AD pathogenesisRF1AG068581 · NIA · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI PENG, JUNMIN, ROSSOLL, WILFRIED · 2020 to 2023
$5.4M
Enabling immunotherapy for high-risk Group 3 medulloblastoma via systems immunologyU01CA281868 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Hongbo Chi, Jiyang Yu · 2023 to 2026
$3.2M
Clonal Therapy for Pediatric T-cell Acute Lymphoblastic LeukemiaU01CA264610 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI YANG, JUN J., YU, JIYANG · 2021 to 2025
$2.8M
Investigating the Molecular Determinants Driving Response and Resistance to HDAC6 Targeted Therapy in Breast CancerR01CA274251 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Jose M Silva, Jiyang Yu · 2024 to 2026
$1.7M
Intracellular and Intercellular Network Rewiring and Hidden Driver Inference from Single-Cell DataR01GM134382 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI YU, JIYANG · 2019 to 2023
$1.7M
Dissecting neuron-microglia-astrocyte interaction in AD pathogenesisR01AG068581 · NIA · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI PENG, JUNMIN, ROSSOLL, WILFRIED · 2024 to 2024
$1.2M
NCI NIH HHS R01 CA274251NCI NIH HHS U01 CA264610NCI NIH HHS U01 CA281868NIA NIH HHS R01 AG068581NIA NIH HHS RF1 AG068581NIGMS NIH HHS R01 GM134382U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) U01CA264610U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) U01CA281868U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM134382U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) RF1AG068581
6 · The paper itself

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.

Indexed as

Gene Expression ProfilingRNA-SeqSequence Analysis, RNASingle-Cell AnalysisTranscriptomeAlgorithmsAnimalsComputational BiologyHumansSingle-Cell Gene Expression AnalysisSoftware

Identifiers

PMID39893178
PMCPMC11787294

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.