Evidence map›Paper›PMID 40268962›Full record

ArticleScientific data2025

Single Molecule Localization Super-resolution Dataset for Deep Learning with Paired Low-resolution Images.

Xian'ao Zhao, Tianjie Yang, Tianying Pan, Lusheng Gu, Tao Xu, Wei Ji

Abstract readDataset
In one paragraph

Article in Scientific data, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

6 authors.

Xian'ao Zhao *National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Tianjie Yang *National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Tianying Pan *National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Lusheng GuNational Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Tao XuNational Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China. xutao@ibp.ac.cn.
Wei JiNational Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China. jiwei@ibp.ac.cn.

Funding

National Natural Science Foundation of China (National Science Foundation of China) 2022YFC3400602National Natural Science Foundation of China (National Science Foundation of China) 32027901National Natural Science Foundation of China (National Science Foundation of China) 32322050, 32170704National Natural Science Foundation of China (National Science Foundation of China) T2225020, 92254306
6 · The paper itself

Abstract

Deep learning super-resolution microscopy has advanced rapidly in recent years. Super-resolution images acquired by single molecule localization microscopy (SMLM) are ideal sources for high-quality datasets. However, the scarcity of public datasets limits the development of deep learning methods. Here, we describe a biological image dataset, DL-SMLM, which provides paired low-resolution fluorescence images and super-resolution SMLM data for training super-resolution models. DL-SMLM consists of six different subcellular structures, including microtubules, lumen and membrane of endoplasmic reticulum (ER), Clathrin coated pits (CCPs), outer membrane of mitochondria (OMM) and inner membrane of mitochondria (IMM). There are 188 sets of raw SMLM data and 100 signal levels for each low-resolution image. This allows software developers to generate thousands of training pairs through data segmentation. The performance of the imaging system was further evaluated using DNA origami samples. Finally, we demonstrated examples of super-resolution models trained using data from DL-SMLM, highlighting the effectiveness of DL-SMLM for developing deep learning super-resolution microscopy.

Indexed as

Deep LearningSingle Molecule ImagingEndoplasmic ReticulumImage Processing, Computer-AssistedMicroscopy, Fluorescence

Identifiers

PMID40268962
PMCPMC12019355

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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.