Evidence map›Paper›PMID 30334766›Full record

ArticleIEEE/ACM transactions on computational biology and bioinformatics

Automated Cell Tracking Using Motion Prediction-Based Matching and Event Handling.

Fatima Boukari, Sokratis Makrogiannis

Abstract read
In one paragraph

Article in IEEE/ACM transactions on computational biology and bioinformatics. 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.

  1. Article
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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

2 authors.

Fatima Boukari
Sokratis Makrogiannis

Funding

QUANTITATIVE IMAGE ANALYSIS TECHNIQUES FOR STUDIES OF AGING PHENOTYPES AND AGE-RELATED DISEASESSC3GM113754 · NIGMS · DELAWARE STATE UNIVERSITY · PI MAKROGIANNIS, SOKRATIS · 2015 to 2024
$686k
NIGMS NIH HHS SC3 GM113754
6 · The paper itself

Abstract

Automated cell segmentation and tracking enables the quantification of static and dynamic cell characteristics and is significant for disease diagnosis, treatment, drug development, and other biomedical applications. This paper introduces a method for fully automated cell tracking, lineage construction, and quantification. Cell detection is performed in the joint spatio-temporal domain by a motion diffusion-based Partial Differential Equation (PDE) combined with energy minimizing active contours. In the tracking stage, we adopt a variational joint local-global optical flow technique to determine the motion vector field. We utilize the predicted cell motion jointly with spatial cell features to define a maximum likelihood criterion to find inter-frame cell correspondences assuming Markov dependency. We formulate cell tracking and cell event detection as a graph partitioning problem. We propose a solution obtained by minimization of a global cost function defined over the set of all cell tracks. We construct a cell lineage tree that represents the cell tracks and cell events. Finally, we compute morphological, motility, and diffusivity measures and validate cell tracking against manually generated reference standards. The automated tracking method applied to reference segmentation maps produces an average tracking accuracy score ( TRA) of 99 percent, and the fully automated segmentation and tracking system produces an average TRA of 89 percent.

Indexed as

AlgorithmsCell MovementCell TrackingHeLa CellsHumansImage Processing, Computer-AssistedImaging, Three-DimensionalSingle-Cell Analysis

Identifiers

PMID30334766
PMCPMC6832744

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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.