Evidence map›Paper›PMID 40012008›Full record

ArticleGenome biology2025

Cross-species imputation and comparison of single-cell transcriptomic profiles.

Ran Zhang, Mu Yang, Jacob Schreiber, Diana R O'Day, James M A Turner, Jay Shendure, William Stafford Noble, Christine M Disteche, Xinxian Deng

Abstract readComparative Study
In one paragraph

Article in Genome biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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  3. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Ran Zhang *Department of Genome Sciences, University of Washington, Seattle, USA.
Mu Yang *Department of Biomedical Informatics and Medical Education, University of Washington, Seattle, USA.
Jacob SchreiberDepartment of Genetics, Stanford University, Stanford, USA.
Diana R O'DayBrotman Baty Institute for Precision Medicine, University of Washington, Seattle, USA.
James M A TurnerSex Chromosome Biology Laboratory, The Francis Crick Institute, London, UK.
Jay ShendureDepartment of Genome Sciences, University of Washington, Seattle, USA.
William Stafford NobleDepartment of Genome Sciences, University of Washington, Seattle, USA. wnoble@uw.edu.ORCID http://orcid.org/0000-0001-7283-4715
Christine M DistecheDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, USA. cdisteche@uw.edu.
Xinxian DengDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, USA. dengx2@uw.edu.

Funding

UW 4-Dimensional Genomic Organization of Mammalian Embryogenesis CenterUM1HG011586 · NHGRI · UNIVERSITY OF WASHINGTON · PI DISTECHE, CHRISTINE M., NOBLE, WILLIAM STAFFORD · 2020 to 2024
$10.3M
X chromosome regulation and role in aneuploidyR35GM131745 · NIGMS · UNIVERSITY OF WASHINGTON · PI Christine M. Disteche · 2019 to 2026
$4.1M
Gene-by-gene studies of dosage regulation pathways of the mammalian active X chromosomeR01GM127327 · NIGMS · UNIVERSITY OF WASHINGTON · PI DENG, XINXIAN · 2018 to 2019
$622k
NHGRI NIH HHS UM1 HG011531NHGRI NIH HHS UM1 HG011586NIGMS NIH HHS R01 GM127327NIGMS NIH HHS R35 GM131745NIGMS NIH HHS R35GM131745
6 · The paper itself

Abstract

Cross-species comparison and prediction of gene expression profiles are important to understand regulatory changes during evolution and to transfer knowledge learned from model organisms to humans. Single-cell RNA-seq (scRNA-seq) profiles enable us to capture gene expression profiles with respect to variations among individual cells; however, cross-species comparison of scRNA-seq profiles is challenging because of data sparsity, batch effects, and the lack of one-to-one cell matching across species. Moreover, single-cell profiles are challenging to obtain in certain biological contexts, limiting the scope of hypothesis generation. Here we developed Icebear, a neural network framework that decomposes single-cell measurements into factors representing cell identity, species, and batch factors. Icebear enables accurate prediction of single-cell gene expression profiles across species, thereby providing high-resolution cell type and disease profiles in under-characterized contexts. Icebear also facilitates direct cross-species comparison of single-cell expression profiles for conserved genes that are located on the X chromosome in eutherian mammals but on autosomes in chicken. This comparison, for the first time, revealed evolutionary and diverse adaptations of X-chromosome upregulation in mammals.

Indexed as

Gene Expression ProfilingSingle-Cell AnalysisTranscriptomeAnimalsChickensHumansMiceRNA-SeqSpecies Specificity

Identifiers

PMID40012008
PMCPMC11863430

What Socratic holds

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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 Socratic graph.