Evidence map›Paper›PMID 37502708›Full record

ArticleNAR genomics and bioinformatics2023

Single-cell reference mapping to construct and extend cell-type hierarchies.

Lieke Michielsen, Mohammad Lotfollahi, Daniel Strobl, Lisa Sikkema, Marcel J T Reinders, Fabian J Theis, Ahmed Mahfouz

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
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  5. bioRxiv : the preprint server for biology · 2026
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  9. Genome biology · 2025
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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.

Lieke MichielsenDepartment of Human Genetics, Leiden University Medical Center, 2333ZC Leiden, The Netherlands.ORCID https://orcid.org/0000-0003-4615-1309
Mohammad LotfollahiInstitute of Computational Biology, Helmholtz Zentrum München, Munich, Germany.
Daniel StroblInstitute of Computational Biology, Helmholtz Zentrum München, Munich, Germany.
Lisa SikkemaInstitute of Computational Biology, Helmholtz Zentrum München, Munich, Germany.
Marcel J T ReindersDepartment of Human Genetics, Leiden University Medical Center, 2333ZC Leiden, The Netherlands.ORCID https://orcid.org/0000-0002-1148-1562
Fabian J TheisInstitute of Computational Biology, Helmholtz Zentrum München, Munich, Germany.ORCID https://orcid.org/0000-0002-2419-1943
Ahmed MahfouzDepartment of Human Genetics, Leiden University Medical Center, 2333ZC Leiden, The Netherlands.ORCID https://orcid.org/0000-0001-8601-2149

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell genomics is now producing an ever-increasing amount of datasets that, when integrated, could provide large-scale reference atlases of tissue in health and disease. Such large-scale atlases increase the scale and generalizability of analyses and enable combining knowledge generated by individual studies. Specifically, individual studies often differ regarding cell annotation terminology and depth, with different groups specializing in different cell type compartments, often using distinct terminology. Understanding how these distinct sets of annotations are related and complement each other would mark a major step towards a consensus-based cell-type annotation reflecting the latest knowledge in the field. Whereas recent computational techniques, referred to as 'reference mapping' methods, facilitate the usage and expansion of existing reference atlases by mapping new datasets (i.e. queries) onto an atlas; a systematic approach towards harmonizing dataset-specific cell-type terminology and annotation depth is still lacking. Here, we present 'treeArches', a framework to automatically build and extend reference atlases while enriching them with an updatable hierarchy of cell-type annotations across different datasets. We demonstrate various use cases for treeArches, from automatically resolving relations between reference and query cell types to identifying unseen cell types absent in the reference, such as disease-associated cell states. We envision treeArches enabling data-driven construction of consensus atlas-level cell-type hierarchies and facilitating efficient usage of reference atlases.

Identifiers

PMID37502708
PMCPMC10370450

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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.