# CSRefiner: a lightweight framework for fine-tuning cell segmentation models with small datasets

**Authors:** Can Shi, Yumei Li, Jing Guo, Qiuling Chen, Tingting Cao, Sha Liao, Ao Chen, Mei Li, Ying Zhang

PMC · DOI: 10.1093/bib/bbaf718 · Briefings in Bioinformatics · 2026-01-13

## TL;DR

CSRefiner is a lightweight framework that improves cell segmentation models using small datasets, enhancing accuracy for spatial transcriptomics.

## Contribution

CSRefiner introduces a versatile fine-tuning method that works with multiple models and requires minimal annotated data.

## Key findings

- CSRefiner achieves high accuracy with limited annotated data for cell segmentation.
- The framework is compatible with various mainstream segmentation models in spatial omics.
- It performs well across different staining types in whole-tissue analysis.

## Abstract

Recent advances in spatial omics technologies have enabled transcriptome profiling at subcellular resolution. By performing cell segmentation on nuclear or membrane staining images, researchers can acquire single cell level spatial gene expression data, which in turn enables subsequent biological interpretation. Although deep learning-based segmentation models achieve high overall accuracy, their performance remains suboptimal for whole-tissue analysis, particularly in ensuring consistent segmentation accuracy across diverse cell populations. Existing fine-tuning approaches often require extensive retraining or are tailored to specific model architectures, limiting their adaptability and scalability in practical settings. To address these challenges, we present CSRefiner, a lightweight and efficient fine-tuning framework for precise whole-tissue single-cell spatial expression analysis. Our approach incorporates support for fine-tuning widely used segmentation models in the field of spatial omics, while achieving high accuracy with very limited annotated data. This study demonstrates CSRefiner’s superior performance across various staining types and its compatibility with multiple mainstream models. Combining operational simplicity with robust accuracy, our framework offers a practical solution for real-world spatial transcriptomics applications.

## Full-text entities

- **Genes:** Dscaml1 (DS cell adhesion molecule like 1) [NCBI Gene 114873] {aka 4921507G06Rik, 4930435C18Rik, mKIAA1132}, Slit1 (slit guidance ligand 1) [NCBI Gene 20562] {aka Slil1, mKIAA0813}, Grin2a (glutamate receptor, ionotropic, NMDA2A (epsilon 1)) [NCBI Gene 14811] {aka GluN2A, GluRepsilon1, NMDAR2A, NR2A}, Gria1 (glutamate receptor, ionotropic, AMPA1 (alpha 1)) [NCBI Gene 14799] {aka 2900051M01Rik, Glr-1, Glr1, GluA1, GluR-A, GluRA}, Dscam (DS cell adhesion molecule) [NCBI Gene 13508] {aka 4932410A21Rik}, Cacna1e (calcium channel, voltage-dependent, R type, alpha 1E subunit) [NCBI Gene 12290] {aka A430040I15, BII, Cach6, Cacnl1a6, Cav2.3, Cchra1}, Kalrn (kalirin, RhoGEF kinase) [NCBI Gene 545156] {aka 2210407G14Rik, DUET, E530005C20Rik, Gm539, Hapip, TRAD}, Dlgap1 (DLG associated protein 1) [NCBI Gene 224997] {aka 4933422O14Rik, 9630002F18, D17Bwg0511e, GKAP/SAPAP, GKPA/SAPAP, Gkap}
- **Chemicals:** H&amp;E (MESH:D006371), paraformaldehyde (MESH:C003043), hematoxylin (MESH:D006416), paraffin (MESH:D010232), OCT (MESH:C051883), 4',6-diamidino-2-phenylindole (MESH:C007293), methanol (MESH:D000432), formalin (MESH:D005557), 0.1xSSC (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12796817/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12796817/full.md

## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12796817/full.md

---
Source: https://tomesphere.com/paper/PMC12796817