Evidence map›Paper›PMID 39974978›Full record

ArticlebioRxiv : the preprint server for biology2025

SAMCell: Generalized Label-Free Biological Cell Segmentation with Segment Anything.

Alexandra D VandeLoo, Nathan J Malta, Emilio Aponte, Caitlin van Zyl, Danfei Xu, Craig R Forest

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

5 · Who and what money

Authors and funding

6 authors.

Alexandra D VandeLooSchool of Biological Sciences, Georgia Institute of Technology, Atlanta, Georgia, USA.ORCID 0009-0001-3035-3427
Nathan J MaltaSchool of Computer Science, Georgia Institute of Technology, Atlanta, Georgia, USA.
Emilio AponteSchool of Computer Science, Georgia Institute of Technology, Atlanta, Georgia, USA.
Caitlin van ZylDepartment of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia, USA.
Danfei XuSchool of Interactive Computing, Georgia Institute of Technology, Atlanta, Georgia, USA.
Craig R ForestSchool of Computer Science, Georgia Institute of Technology, Atlanta, Georgia, USA.

Funding

Novel Platforms for Systematic Optical Control of Complex Neural Circuits In VivoR01DA029639 · NIDA · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYDEN, EDWARD S. · 2010 to 2023
$6.7M
High-throughput robotic analysis of integrated neuronal phenotypesR01EY023173 · NEI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYDEN, EDWARD S., FOREST, CRAIG · 2012 to 2016
$4.3M
Automated cell-type-specific electrophysiology for understanding circuit dysregulation in Alzheimer's DiseaseRF1AG079269 · NIA · EMORY UNIVERSITY · PI FOREST, CRAIG, ROWAN, MATTHEW J.M. · 2022 to 2024
$2.4M
Scalable Cell- and Circuit-Targeted ElectrophysiologyR01NS102727 · NINDS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BOYDEN, EDWARD S., FOREST, CRAIG · 2017 to 2020
$2.2M
In-vivo circuit activity measurement at single cell, sub-threshold resolutionU01MH106027 · NIMH · GEORGIA INSTITUTE OF TECHNOLOGY · PI FOREST, CRAIG, STANLEY, GARRETT B. · 2014 to 2016
$1.5M
NEI NIH HHS R01 EY023173NIA NIH HHS RF1 AG079269NIDA NIH HHS R01 DA029639NIMH NIH HHS U01 MH106027NINDS NIH HHS R01 NS102727
6 · The paper itself

Abstract

Background: When analyzing cells in culture, assessing cell morphology (shape), confluency (density), and growth patterns are necessary for understanding cell health. These parameters are generally obtained by a skilled biologist inspecting light microscope images, but this can become very laborious for high throughput applications. One way to speed up this process is by automating cell segmentation. Cell segmentation is the task of drawing a separate boundary around each individual cell in a microscope image. This task is made difficult by vague cell boundaries and the transparent nature of cells. Many techniques for automatic cell segmentation exist, but these methods often require annotated datasets, model retraining, and associated technical expertise. Results: We present SAMCell, a modified version of Meta's Segment Anything Model (SAM) trained on an existing large-scale dataset of microscopy images containing varying cell types and confluency. We find that our approach works on a wide range of microscopy images, including cell types not seen in training and on images taken by a different microscope. We also present a user-friendly UI that reduces the technical expertise needed to use this automated microscopy technique. Conclusions: Using SAMCell, biologists can quickly and automatically obtain cell segmentation results of higher quality than previous methods. Further, these results can be obtained through our custom GUI without expertise in Machine Learning, thus decreasing the human labor required in cell culturing.

Indexed as

Cell SegmentationMachine LearningSegment Anything Model

Identifiers

PMID39974978
PMCPMC11839016

What OpenQuestion holds

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Registered trials

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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.