Evidence map›Paper›PMID 35288709›Full record

ArticleNature genetics2022

Systematic reconstruction of cellular trajectories across mouse embryogenesis.

Chengxiang Qiu, Junyue Cao, Beth K Martin, Tony Li, Ian C Welsh, Sanjay Srivatsan, Xingfan Huang, Diego Calderon, William Stafford Noble, Christine M Disteche and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Nature genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed
16.1field-weighted citation impact, top 1% of its field
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

119 citing papers in PubMed, 201 citations in OpenAlex.

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  7. bioRxiv : the preprint server for biology · 2026
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  8. bioRxiv : the preprint server for biology · 2026
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59 more citing papers are in PubMed but not listed here.

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

15 authors at 6 institutions in 2 countries.

Chengxiang QiuDepartment of Genome Sciences, University of Washington, Seattle, WA, USA. cxqiu@uw.edu.ORCID http://orcid.org/0000-0002-6346-8669
Junyue CaoThe Rockefeller University, New York, NY, USA.ORCID http://orcid.org/0000-0003-4097-489X
Beth K MartinDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Tony LiDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0003-3546-123X
Ian C WelshThe Jackson Laboratory, Bar Harbor, ME, USA.
Sanjay SrivatsanDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Xingfan HuangDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Diego CalderonDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-6990-9066
William Stafford NobleDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0001-7283-4715
Christine M DistecheDepartment of Pathology, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-5433-495X
Stephen A MurrayThe Jackson Laboratory, Bar Harbor, ME, USA.ORCID http://orcid.org/0000-0002-0594-1702
Malte SpielmannHuman Molecular Genomics Group, Max Planck Institute for Molecular Genetics, Berlin, Germany.
Cecilia B MoensDivision of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Cole TrapnellDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-8105-4347
Jay ShendureDepartment of Genome Sciences, University of Washington, Seattle, WA, USA. shendure@uw.edu.ORCID http://orcid.org/0000-0002-1516-1865
University of Washington · USJackson Laboratory · USFred Hutch Cancer Center · USHoward Hughes Medical Institute · USMax Planck Institute for Molecular Genetics · DERockefeller University · US

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
CARDIOVASCULAR RESEARCH TRAINING PROGRAMT32HL007828 · NHLBI · UNIVERSITY OF WASHINGTON · PI Francis Kim, Farid Moussavi-Harami · 1997 to 2026
$10.2M
Massively parallel characterization of variants and elements impacting transcriptional regulation in dynamic cellular systemsUM1HG011966 · NHGRI · UNIVERSITY OF WASHINGTON · PI Nadav Ahituv, Jay Ashok Shendure · 2021 to 2026
$9.7M
Versatile, exponentially scalable methods for single cell molecular profilingR01HG010632 · NHGRI · UNIVERSITY OF WASHINGTON · PI Jay Ashok Shendure, Bruce Colston Trapnell · 2019 to 2026
$5.9M
X chromosome regulation and role in aneuploidyR35GM131745 · NIGMS · UNIVERSITY OF WASHINGTON · PI Christine M. Disteche · 2019 to 2026
$4.1M
Topographic mapping by cranial motor neurons - Renewal - Resubmission - 1R01NS109425 · NINDS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Cecilia B Moens · 2018 to 2026
$2.9M
Howard Hughes Medical InstituteNHGRI NIH HHS R01 HG010632NHGRI NIH HHS UM1 HG011586NHGRI NIH HHS UM1 HG011966NHLBI NIH HHS T32 HL007828NIGMS NIH HHS R35 GM131745NINDS NIH HHS R01 NS109425
6 · The paper itself

Abstract

Mammalian embryogenesis is characterized by rapid cellular proliferation and diversification. Within a few weeks, a single-cell zygote gives rise to millions of cells expressing a panoply of molecular programs. Although intensively studied, a comprehensive delineation of the major cellular trajectories that comprise mammalian development in vivo remains elusive. Here, we set out to integrate several single-cell RNA-sequencing (scRNA-seq) datasets that collectively span mouse gastrulation and organogenesis, supplemented with new profiling of ~150,000 nuclei from approximately embryonic day 8.5 (E8.5) embryos staged in one-somite increments. Overall, we define cell states at each of 19 successive stages spanning E3.5 to E13.5 and heuristically connect them to their pseudoancestors and pseudodescendants. Although constructed through automated procedures, the resulting directed acyclic graph (TOME (trajectories of mammalian embryogenesis)) is largely consistent with our contemporary understanding of mammalian development. We leverage TOME to systematically nominate transcription factors (TFs) as candidate regulators of each cell type's specification, as well as 'cell-type homologs' across vertebrate evolution.

Indexed as

Embryonic DevelopmentOrganogenesisAnimalsEmbryo, MammalianGastrulationMammalsMice

Identifiers

PMID35288709
PMCPMC8920898
OpenAlexW4220985590

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.