Evidence map›Paper›PMID 42423177›Full record

ArticleBiotechnology journal2026

Robust Cell Segmentation for Size Distribution Estimation via Synthetic-Data Training.

Han Bit Kim, Chaeeun Lee, Naeun Lee, Hyeongseok Han, Chanhun Park, Moo Sun Hong

Abstract read
In one paragraph

Article in Biotechnology journal, 2026. 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

6 authors.

Han Bit KimDepartment of Chemical and Biological Engineering, Seoul National University, Seoul, Republic of Korea.ORCID https://orcid.org/0009-0008-0711-0591
Chaeeun LeeDepartment of Chemical and Biological Engineering, Seoul National University, Seoul, Republic of Korea.ORCID https://orcid.org/0009-0009-3270-2836
Naeun LeeCJ BIO Research Institute, CJ CheilJedang, Suwon-Si, Gyeonggi-do, Republic of Korea.ORCID https://orcid.org/0009-0003-9035-8494
Hyeongseok HanCJ BIO Research Institute, CJ CheilJedang, Suwon-Si, Gyeonggi-do, Republic of Korea.ORCID https://orcid.org/0009-0005-5204-0754
Chanhun ParkCJ BIO Research Institute, CJ CheilJedang, Suwon-Si, Gyeonggi-do, Republic of Korea.ORCID https://orcid.org/0009-0004-7310-3155
Moo Sun HongDepartment of Chemical and Biological Engineering, Seoul National University, Seoul, Republic of Korea.ORCID https://orcid.org/0000-0003-2274-5030

Funding

Seoul National University
6 · The paper itself

Abstract

Polyhydroxyalkanoates (PHAs) are biodegradable and biocompatible plastics, yet large-scale production remains limited by costly batch operations and the lack of online analytical tools. Monitoring cell size distribution serves as a strong surrogate for intracellular PHA content, but training robust cell segmentation models for industrial bioprocesses requires extensive manual annotation, which is highly labor-intensive and impractical for densely populated microscopy images. To address this critical bottleneck, an annotation-free cell segmentation and size estimation pipeline tailored for real time monitoring is presented. Rather than relying on architectural modifications, this framework introduces a system-level automated training strategy: individual cells are automatically extracted from diluted-sample microscopy images using edge enhancement and rule-based binarization, then augmented and composited onto heterogeneous backgrounds to emulate the texture of undiluted, dense cultures. This fully synthetic data generation eliminates the need for manual labeling while enabling robust training of instance segmentation models. When implemented using a Mask R-CNN backbone, the proposed pipeline consistently tracks flow cytometry forward-scatter (FSC) distribution trends under diverse imaging conditions and achieves higher correlation with FSC data compared to Cellpose and CellSAM, representative foundation models for cell segmentation. This annotation-free methodology provides a practical and reliable automated online monitoring solution for intelligent PHA manufacturing.

Indexed as

Cell SizeImage Processing, Computer-AssistedPolyhydroxyalkanoatesFlow CytometryMicroscopyPolyhydroxyalkanoatesannotation‐freecell segmentationonline monitoringPHAsynthetic data

Identifiers

PMID42423177
PMCPMC13347755

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.