# Viability classification of unstained cells in microscopic images using deep learning

**Authors:** Tomoaki Kyoden, Shunsuke Akiguchi, Ryo Murakami, Tsugunobu Andoh, Noboru Yamada

PMC · DOI: 10.1186/s42649-026-00127-9 · 2026-03-20

## TL;DR

A deep learning algorithm was developed to classify live and dead cells in microscopic images without staining, offering a non-invasive alternative to traditional methods.

## Contribution

The novel contribution is a deep learning model that classifies unstained live and dead cells with high accuracy.

## Key findings

- The model achieved 0.931 accuracy in classifying live and dead cells from unstained images.
- The framework enabled estimation of spatial boundaries between live and dead cell populations.
- Performance was comparable to conventional stained-image analysis methods.

## Abstract

In research on cells conducted in vitro, cell viability is determined using staining techniques. However, interference with subsequent observation of live cell growth limits their applicability for real-time or continuous investigation. To address this limitation, we developed a deep learning–based algorithm capable of classifying live and dead cancer cells from microscopic images without staining. In this study, microscopic images were first captured prior to staining, and then the same regions were imaged again after staining to obtain live, dead, and other cell labels using a conventional staining method. The stained images served as ground truth data for supervised training with the corresponding pre-staining images. The proposed model achieved an accuracy of 0.931 after 99 training epochs in distinguishing live and dead cells from unstained images. This framework accurately differentiated live and dead cells directly from pre-staining images, demonstrating performance comparable to conventional stained-image analysis. Moreover, the approach enabled estimation of spatial boundaries between live and dead cell populations. These results demonstrate the potential of this approach as a non-invasive technique for assessing cell viability in in vitro studies.

## Full-text entities

- **Diseases:** necrobiosis (MESH:D017441), Necrosis (MESH:D009336), gastric cancer (MESH:D013274), breast cancer (MESH:D001943), cancer (MESH:D009369), skin cancer (MESH:D012878)
- **Chemicals:** trypan blue (MESH:D014343), CO2 (MESH:D002245), graphite (MESH:D006108), Evans blue (MESH:D005070), penicillin (MESH:D010406), Eagle's minimum essential medium (-), streptomycin (MESH:D013307)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** B16-BL6 — Mus musculus (Mouse), Mouse melanoma, Cancer cell line (CVCL_0157)

## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13003076/full.md

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Source: https://tomesphere.com/paper/PMC13003076