Evidence map›Paper›PMID 38750526›Full record

ArticleBMC medical informatics and decision making2024

Optimizing deep learning-based segmentation of densely packed cells using cell surface markers.

Sunwoo Han, Khamsone Phasouk, Jia Zhu, Youyi Fong

Abstract read
In one paragraph

Article in BMC medical informatics and decision making, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Sunwoo HanVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, USA.
Khamsone PhasoukDepartment of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, United States.
Jia ZhuVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, USA. jzhu@fredhutch.org.
Youyi FongVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, USA. yfong@fredhutch.org.

Funding

Modeling of human HSV infection: development of immune-competent 3D skin-on-chip with vascular perfusionR01AI143773 · NIAID · UNIVERSITY OF WASHINGTON · PI ZHU, JIA · 2020 to 2024
$2.7M
High-Performance Compute Cluster for Comprehensive Cancer and Infectious Diseases ResearchS10OD028685 · OD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BRADLEY, PHILIP · 2020 to 2020
$2.0M
Biofabricated 3-D skin model for antiviral drug discovery against human HSV infectionU18TR003208 · NCATS · UNIVERSITY OF WASHINGTON · PI ZHU, JIA · 2020 to 2021
$1.0M
Fred Hutchinson Cancer Research Center Vaccine and Infectious Diseases Division Faculty Initiative FundNCATS NIH HHS U18 TR003208NIAID NIH HHS R01 AI143773NIH HHS AI143773, S10OD028685NIH HHS S10 OD028685
6 · The paper itself

Abstract

backgroundSpatial molecular profiling depends on accurate cell segmentation. Identification and quantitation of individual cells in dense tissues, e.g. highly inflamed tissue caused by viral infection or immune reaction, remains a challenge.

methodsWe first assess the performance of 18 deep learning-based cell segmentation models, either pre-trained or trained by us using two public image sets, on a set of immunofluorescence images stained with immune cell surface markers in skin tissue obtained during human herpes simplex virus (HSV) infection. We then further train eight of these models using up to 10,000+ training instances from the current image set. Finally, we seek to improve performance by tuning parameters of the most successful method from the previous step.

resultsThe best model before fine-tuning achieves a mean Average Precision (mAP) of 0.516. Prediction performance improves substantially after training. The best model is the cyto model from Cellpose. After training, it achieves an mAP of 0.694; with further parameter tuning, the mAP reaches 0.711.

conclusionSelecting the best model among the existing approaches and further training the model with images of interest produce the most gain in prediction performance. The performance of the resulting model compares favorably to human performance. The imperfection of the final model performance can be attributed to the moderate signal-to-noise ratio in the imageset.

Indexed as

Deep LearningBiomarkersHerpes SimplexHumansImage Processing, Computer-AssistedSkinBiomarkersCell segmentationComputer visionDeep learningHSV

Identifiers

PMID38750526
PMCPMC11094866

What OpenQuestion holds

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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 OpenQuestion graph.