Evidence map›Paper›PMID 38646063›Full record

ArticleExpert systems with applications2024

DeepSeeded: Volumetric Segmentation of Dense Cell Populations with a Cascade of Deep Neural Networks in Bacterial Biofilm Applications.

Tanjin Taher Toma, Yibo Wang, Andreas Gahlmann, Scott T Acton

Abstract read
In one paragraph

Article in Expert systems with applications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

4 authors.

Tanjin Taher TomaDepartment of Electrical and Computer Engineering, University of Virginia, Charlottesville, 22904, Virginia, USA.
Yibo WangDepartment of Chemistry, University of Virginia, Charlottesville, 22904, Virginia, USA.
Andreas GahlmannDepartment of Chemistry, University of Virginia, Charlottesville, 22904, Virginia, USA.
Scott T ActonDepartment of Electrical and Computer Engineering, University of Virginia, Charlottesville, 22904, Virginia, USA.

Funding

Non-Invasive Single-Cell Morphometry and Tracking in Living Bacterial BiofilmsR01GM139002 · NIGMS · UNIVERSITY OF VIRGINIA · PI GAHLMANN, ANDREAS · 2020 to 2024
$1.5M
NIGMS NIH HHS R01 GM139002
6 · The paper itself

Abstract

Accurate and automatic segmentation of individual cell instances in microscopy images is a vital step for quantifying the cellular attributes, which can subsequently lead to new discoveries in biomedical research. In recent years, data-driven deep learning techniques have shown promising results in this task. Despite the success of these techniques, many fail to accurately segment cells in microscopy images with high cell density and low signal-to-noise ratio. In this paper, we propose a novel 3D cell segmentation approach DeepSeeded, a cascaded deep learning architecture that estimates seeds for a classical seeded watershed segmentation. The cascaded architecture enhances the cell interior and border information using Euclidean distance transforms and detects the cell seeds by performing voxel-wise classification. The data-driven seed estimation process proposed here allows segmenting touching cell instances from a dense, intensity-inhomogeneous microscopy image volume. We demonstrate the performance of the proposed method in segmenting 3D microscopy images of a particularly dense cell population called bacterial biofilms. Experimental results on synthetic and two real biofilm datasets suggest that the proposed method leads to superior segmentation results when compared to state-of-the-art deep learning methods and a classical method.

Indexed as

Bacterial biofilmsDeep learningDense cell segmentationMulti-scale structural similarity lossSeeded watershed

Identifiers

PMID38646063
PMCPMC11027476

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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.