Evidence map›Paper›PMID 40093094›Full record

ArticlebioRxiv : the preprint server for biology2025

Systematic evaluation of single-cell multimodal data integration for comprehensive human reference atlas.

Mario Acera-Mateos, Xian Adiconis, Jessica-Kanglin Li, Domenica Marchese, Ginevra Caratù, Chung-Chau Hon, Prabha Tiwari, Miki Kojima, Beate Vieth, Michael A Murphy and 17 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors.

Mario Acera-MateosJosep Carreras Leukemia Research Institute, Barcelona, Spain.ORCID 0000-0001-7032-2986
Xian AdiconisKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Jessica-Kanglin LiJosep Carreras Leukemia Research Institute, Barcelona, Spain.ORCID 0009-0002-7800-1348
Domenica MarcheseCentro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.ORCID 0000-0002-3036-4580
Ginevra CaratùCentro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.ORCID 0000-0003-1085-8062
Chung-Chau HonLaboratory for Regulatory Genomics, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa, Japan.
Prabha TiwariLaboratory for Transcriptome Technology, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa, Japan.
Miki KojimaLaboratory for Transcriptome Technology, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa, Japan.
Beate ViethAnthropology and Human Genomics, Faculty of Biology, Ludwig-Maximilians Universität München, 82152 Planegg, Germany.
Michael A MurphyDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Sean K SimmonsKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Thomas LefevreDepartment of Human Genetics, University of Leuven, KU Leuven, Leuven, Belgium.
Irene ClaesDepartment of Human Genetics, University of Leuven, KU Leuven, Leuven, Belgium.
Christopher L O'ConnorDivision of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Rajasree MenonDivision of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Edgar A OttoDivision of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Yoshinari AndoLaboratory for Transcriptome Technology, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa, Japan.
Katy VandereykenDepartment of Human Genetics, University of Leuven, KU Leuven, Leuven, Belgium.
Matthias KretzlerDivision of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Markus BitzerDivision of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Ernest FraenkelDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.ORCID 0000-0001-9249-8181
Thierry VoetDepartment of Human Genetics, University of Leuven, KU Leuven, Leuven, Belgium.ORCID 0000-0003-1204-9963
Wolfgang EnardAnthropology and Human Genomics, Faculty of Biology, Ludwig-Maximilians Universität München, 82152 Planegg, Germany.ORCID 0000-0002-4056-0550
Piero CarninciLaboratory for Transcriptome Technology, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa, Japan.
Holger HeynUniversity of Barcelona (UB), Barcelona, Spain.ORCID 0000-0002-3276-1889
Joshua Z LevinKlarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.ORCID 0000-0002-0170-3598
Elisabetta MereuJosep Carreras Leukemia Research Institute, Barcelona, Spain.ORCID 0000-0001-6101-8472

Funding

Epigenetic Pathology and Therapy in Huntington's DiseaseR01NS089076 · NINDS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI FRAENKEL, ERNEST, HOUSMAN, DAVID · 2015 to 2024
$4.9M
PREcision Medicine through IntErrogation of Rna in the kidnEy (PREMIERE)U01DK114907 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Nir Hacohen, Jeffrey Benton Hodgin · 2022 to 2026
$3.2M
NIDDK NIH HHS U01 DK114907NINDS NIH HHS R01 NS089076
6 · The paper itself

Abstract

The integration of multimodal single-cell data enables comprehensive organ reference atlases, yet its impact remains largely unexplored, particularly in complex tissues. We generated a benchmarking dataset for the renal cortex by integrating 3' and 5' scRNA-seq with joint snRNA-seq and snATAC-seq, profiling 119,744 high-quality nuclei/cells from 19 donors. To align cell identities and enable consistent comparisons, we developed the interpretable machine learning tool scOMM (single-cell Omics Multimodal Mapping) and systematically assessed integration strategies. "Horizontal" integration of scRNA and snRNA-seq improved cell-type identification, while "vertical" integration of snRNA-seq and snATAC-seq had an additive effect, enhancing resolution in homogeneous populations and difficult-to-identify states. Global integration was especially effective in identifying adaptive states and rare cell types, including WFDC2-expressing Thick Ascending Limb and Norn cells, previously undetected in kidney atlases. Our work establishes a robust framework for multimodal reference atlas generation, advancing single-cell analysis and extending its applicability to diverse tissues.

Identifiers

PMID40093094
PMCPMC11908249

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.