Evidence map›Paper›PMID 40061870›Full record

ArticleBioinformatics advances2025

scLTNN: an innovative tool for automatically visualizing single-cell trajectories.

Cencan Xing, Zehua Zeng, Lei Hu, Jianing Kang, Shah Roshan, Yuanyan Xiong, Hongwu Du, Tongbiao Zhao

Abstract read
In one paragraph

Article in Bioinformatics advances, 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

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

8 authors.

Cencan XingDaxing Research Institute, School of Chemistry and Biological Engineering, University of Science and Technology, Beijing, Beijing 100083, China.ORCID https://orcid.org/0000-0002-0731-4809
Zehua ZengDaxing Research Institute, School of Chemistry and Biological Engineering, University of Science and Technology, Beijing, Beijing 100083, China.
Lei HuDaxing Research Institute, School of Chemistry and Biological Engineering, University of Science and Technology, Beijing, Beijing 100083, China.
Jianing KangDaxing Research Institute, School of Chemistry and Biological Engineering, University of Science and Technology, Beijing, Beijing 100083, China.
Shah RoshanDaxing Research Institute, School of Chemistry and Biological Engineering, University of Science and Technology, Beijing, Beijing 100083, China.
Yuanyan XiongKey Laboratory of Gene Engineering of the Ministry of Education, Institute of Healthy Aging Research, School of Life Sciences, Sun-Yat-sen University, Guangzhou 510006, China.ORCID https://orcid.org/0000-0002-3227-5215
Hongwu DuDaxing Research Institute, School of Chemistry and Biological Engineering, University of Science and Technology, Beijing, Beijing 100083, China.
Tongbiao ZhaoState Key Laboratory of Stem Cell and Reproductive Biology, Key Laboratory of Organ Regeneration and Reconstruction, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.ORCID https://orcid.org/0000-0003-1429-5818

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: Cellular state identification and trajectory inference enable the computational simulation of cell fate dynamics using single-cell RNA sequencing data. However, existing methods for constructing cell fate trajectories demand substantial computational resources or prior knowledge of the developmental process. Results: Here, based on the discovery of the consistent expression distribution of highly variable genes, we create a new tool named scRNA-seq latent time neural network (scLTNN) by combining an artificial neural network with a distribution model. This innovative tool is pre-trained and capable of automatically inferring the origin and terminal state of cells, and accurately illustrating the developmental trajectory of cells with minimal use of computational resources and time. We implement scLTNN on human bone marrow cells, mouse pancreatic endocrine lineage, and axial mesoderm lineage of zebrafish embryo, accurately reconstructing their cell fate trajectories, respectively. Our scLTNN tool provides a straightforward and efficient method for illustrating cell fate trajectories, applicable across various species without the need for prior knowledge of the biological process. Availability and implementation: https://github.com/Starlitnightly/scLTNN.

Identifiers

PMID40061870
PMCPMC11889453

What Socratic holds

Textmetadata
LicenceCC BY
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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.