Evidence map›Paper›PMID 40401216›Full record

ArticleNeurophotonics2025

Brain-wide 3D neuron detection and mapping with deep learning.

Yuanyang Liu, Ziyan Gao, Zhehao Xu, Chaoyue Yang, Pei Sun, Longhui Li, Hongbo Jia, Xiaowei Chen, Xiang Liao, Junxia Pan and 1 more

Abstract read
In one paragraph

Article in Neurophotonics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Yuanyang LiuChongqing University, School of Medicine, Center for Neurointelligence, Chongqing, China.
Ziyan GaoChongqing University, School of Medicine, Center for Neurointelligence, Chongqing, China.
Zhehao XuChongqing University, School of Medicine, Center for Neurointelligence, Chongqing, China.
Chaoyue YangThird Military Medical University, Brain Research Center, State Key Laboratory of Trauma and Chemical Poisoning, Chongqing, China.
Pei SunThird Military Medical University, Brain Research Center, State Key Laboratory of Trauma and Chemical Poisoning, Chongqing, China.
Longhui LiChongqing University, School of Medicine, Center for Neurointelligence, Chongqing, China.
Hongbo JiaChinese Academy of Sciences, Suzhou Institute of Biomedical Engineering and Technology, Brain Research Instrument Innovation Center, Suzhou, China.ORCID https://orcid.org/0000-0003-1585-2161
Xiaowei ChenThird Military Medical University, Brain Research Center, State Key Laboratory of Trauma and Chemical Poisoning, Chongqing, China.
Xiang LiaoChongqing University, School of Medicine, Center for Neurointelligence, Chongqing, China.ORCID https://orcid.org/0000-0001-6324-5206
Junxia PanThird Military Medical University, Brain Research Center, State Key Laboratory of Trauma and Chemical Poisoning, Chongqing, China.
Meng WangChongqing University, School of Medicine, Center for Neurointelligence, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Significance: Mapping the spatial distribution of specific neurons across the entire brain is essential for understanding the neural circuits associated with various brain functions, which in turn requires automated and reliable neuron detection and mapping techniques. Aim: To accurately identify somatic regions from 3D imaging data and generate reliable soma locations for mapping to diverse brain regions, we introduce NeuronMapper, a brain-wide 3D neuron detection and mapping approach that leverages the power of deep learning. Approach: NeuronMapper is implemented as a four-stage framework encompassing preprocessing, classification, detection, and mapping. Initially, whole-brain imaging data is divided into 3D sub-blocks during the preprocessing phase. A lightweight classification network then identifies the sub-blocks containing somata. Following this, a Video Swin Transformer-based segmentation network delineates the soma regions within the identified sub-blocks. Last, the locations of the somata are extracted and registered with the Allen Brain Atlas for comprehensive whole-brain neuron mapping. Results: Through the accurate detection and localization of somata, we achieved the mapping of somata at the one million level within the mouse brain. Comparative analyses with other soma detection techniques demonstrated that our method exhibits remarkably superior performance for whole-brain 3D soma detection. Conclusions: Our approach has demonstrated its effectiveness in detecting and mapping somata within whole-brain imaging data. This method can serve as a computational tool to facilitate a deeper understanding of the brain's complex networks and functions.

Indexed as

3D soma detectiondeep learningneuron mappingvideo swin transformerwhole-brain imaging

Identifiers

PMID40401216
PMCPMC12093273

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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.