Evidence map›Paper›PMID 21822463›Full record

ArticleProceedings. IEEE International Symposium on Biomedical Imaging2011

EXTRACTION AND ANALYSIS OF ACTIN NETWORKS BASED ON OPEN ACTIVE CONTOUR MODELS.

Ting Xu, Hongsheng Li, Tian Shen, Nikola Ojkic, Dimitrios Vavylonis, Xiaolei Huang

Abstract read
In one paragraph

Article in Proceedings. IEEE International Symposium on Biomedical Imaging, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.6field-weighted citation impact, top 6% of its field
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

13 citing papers in PubMed, 28 citations in OpenAlex.

  1. Automatic extraction of actin networks in plants.PLoS computational biology · 2023
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  4. Review
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  8. Quantitative analysis of F-actin redistribution in astrocytoma cells treated with candidate pharmaceuticals.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2014
    Article
  9. Article
  10. Article
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  12. A systems-biology approach to yeast actin cables.Advances in experimental medicine and biology · 2012
    Article
  13. Extraction of Individual Filaments from 2D Confocal Microscopy Images of Flat Cells.IEEE/ACM transactions on computational biology and bioinformatics
    Article
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

6 authors at 1 institution in 1 country.

Ting XuDepartment of Computer Science and Engineering, Lehigh University, Bethlehem, PA, USA.
Hongsheng Li
Tian Shen
Nikola Ojkic
Dimitrios Vavylonis
Xiaolei Huang
Lehigh University · US

Funding

Computational Analysis and Modeling of Contractile Ring AssemblyR21GM083928 · NIGMS · LEHIGH UNIVERSITY · PI HUANG, SHARON XIAOLEI, VAVYLONIS, DIMITRIOS · 2008 to 2009
$386k
NIGMS NIH HHS R21 GM083928
6 · The paper itself

Abstract

Network structures formed by actin filaments are present in many kinds of fluorescence microscopy images. In order to quantify the conformations and dynamics of such actin filaments, we propose a fully automated method to extract actin networks from images and analyze network topology. The method handles well intersecting filaments and, to some extent, overlapping filaments. First we automatically initialize a large number of Stretching Open Active Contours (SOACs) from ridge points detected by searching for plus-to-minus sign changes in the gradient map of the image. These initial SOACs then elongate simultaneously along the bright center-lines of filaments by minimizing an energy function. During their evolution, they may merge or stop growing, thus forming a network that represents the topology of the filament ensemble. We further detect junction points in the network and break the SOACs at junctions to obtain "SOAC segments". These segments are then re-grouped using a graph-cut spectral clustering method to represent the configuration of actin filaments. The proposed approach is generally applicable to extracting intersecting curvilinear structures in noisy images. We demonstrate its potential using two kinds of data: (1) actin filaments imaged by Total Internal Reflection Fluorescence Microscopy (TIRFM) in vitro; (2) actin cytoskeleton networks in fission yeast imaged by spinning disk confocal microscopy.

Identifiers

PMID21822463
PMCPMC3150558
OpenAlexW2155088535

What OpenQuestion holds

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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.