Evidence map›Paper›PMID 39147977›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

A Hands-on Guide to AmoePy - a Python-Based Software Package to Analyze Cell Migration Data.

Ted Moldenhawer, Daniel Schindler, Matthias Holschneider, Wilhelm Huisinga, Carsten Beta

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Article in Methods in molecular biology (Clifton, N.J.), 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

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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.

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

5 authors.

Ted MoldenhawerInstitute of Physics and Astronomy, University of Potsdam, Potsdam, Germany.
Daniel SchindlerInstitute of Mathematics, University of Potsdam, Potsdam, Germany.
Matthias HolschneiderInstitute of Mathematics, University of Potsdam, Potsdam, Germany.
Wilhelm HuisingaInstitute of Mathematics, University of Potsdam, Potsdam, Germany.
Carsten BetaInstitute of Physics and Astronomy, University of Potsdam, Potsdam, Germany. beta@uni-potsdam.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amoeboid cell motility is fundamental for a multitude of biological processes such as embryogenesis, immune responses, wound healing, and cancer metastasis. It is characterized by specific cell shape changes: the extension and retraction of membrane protrusions, known as pseudopodia. A common approach to investigate the mechanisms underlying this type of cell motility is to study phenotypic differences in the locomotion of mutant cell lines. To characterize such differences, methods are required to quantify the contour dynamics of migrating cells. AmoePy is a Python-based software package that provides tools for cell segmentation, contour detection as well as analyzing and simulating contour dynamics. First, a digital representation of the cell contour as a chain of nodes is extracted from each frame of a time-lapse microscopy recording of a moving cell. Then, the dynamics of these nodes-referred to as virtual markers-are tracked as the cell contour evolves over time. From these data, various quantities can be calculated that characterize the contour dynamics, such as the displacement of the virtual markers or the local stretching rate of the marker chain. Their dynamics is typically visualized in space-time plots, the so-called kymographs, where the temporal evolution is displayed for the different locations along the cell contour. Using AmoePy, you can straightforwardly create kymograph plots and videos from stacks of experimental bright-field or fluorescent images of motile cells. A hands-on guide on how to install and use AmoePy is provided in this chapter.

Indexed as

Cell MovementSoftwareDictyosteliumImage Processing, Computer-AssistedKymographyPseudopodiaTime-Lapse ImagingCell migrationContour dynamicsData analysisD. discoideumKymograph

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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.