Evidence map›Paper›PMID 39257757›Full record

ArticlebioRxiv : the preprint server for biology2024

Evaluation of a Deep Learning Based Approach to Computational Label Free Cell Viability Quantification.

Allison Reno, Jianan Tang, Madeline Sudbeck, Precious Fe Custodio, Brandi Baldus, Elizabeth McLaughlin, Fei Peng, Hai Xiao

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

8 authors.

Allison RenoDepartment of Bioengineering, Clemson University, Clemson, SC, USA.
Jianan TangHolcombe Department of Electrical and Computer Engineering, Clemson University, Clemson, SC, USA.
Madeline SudbeckDepartment of Biological Sciences, Clemson University, Clemson, SC, USA.
Precious Fe CustodioDepartment of Bioengineering, Clemson University, Clemson, SC, USA.
Brandi BaldusDepartment of Materials Science and Engineering, Clemson University, Clemson, SC, USA.
Elizabeth McLaughlinDepartment of Bioengineering, Clemson University, Clemson, SC, USA.
Fei PengDepartment of Materials Science and Engineering, Clemson University, Clemson, SC, USA.
Hai XiaoHolcombe Department of Electrical and Computer Engineering, Clemson University, Clemson, SC, USA.

Funding

Tissue Structural and Neural Remodeling in Human Sacroiliac JointP20GM121342 · NIGMS · CLEMSON UNIVERSITY · PI Hai Yao · 2018 to 2026
$24.7M
NIGMS NIH HHS P20 GM121342
6 · The paper itself

Abstract

One of the most common techniques found in a cell biology or tissue engineering lab is the cytotoxicity assay. This can be performed using a variety of different dyes and stains and various protocols to result in a clear indication of dead and live cells within a culture to quantify the viability of a culture and monitor for sudden drops or increases in viability by a drug, material, viral vector, etc introduced into the culture. This assay helps cell biologists determine the health of their culture and what toxicity added substances may add to the culture and whether they are appropriate and safe to use with human cells. However, many of the dyes and stains used for this process are eventually toxic to cells, rendering the cells useless after testing and preventing real time monitoring of the same culture over a period of hours or days. Computation biology is moving cell biology towards novel and innovative techniques such as in silico labeling and dye free labeling using deep learning algorithms. In this work, we investigate whether it is feasible to train a Resnet CNN model to detect morphological changes in human cells that indicate cell death in order to classify cells as live or dead without utilizing a stain or dye. This work also aims to train one CNN model to count all cells regardless of viability status to get a total cell count, and then one CNN model that specifically identifies and counts all of the dead cells for an accurate dead and live cell total by utilizing both pieces of data to determine a general viability percentage for the culture. Additionally, this work explores the use of various image enhancements to understand if this process helps or impedes the deep learning models in their detection of total cells and dead cells.

Identifiers

PMID39257757
PMCPMC11383692

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.