Applications: Difference between revisions
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Several image processing pipelines have already been developed in MiToBo. <br/> | Several image processing pipelines have already been developed in MiToBo. <br/> | ||
Below you can find selected example applications, some of them have been published already. | Below you can find selected example applications, some of them have been published already. | ||
* [[Applications/MTBCellCounter | MTB Cell Counter]] (since MiToBo 1.5), <br/> a tool for semi-automatic labeling and counting of spot-like structures like, e.g., plastides, stress granules or p-bodies | |||
* [[Applications/MiCa | MiCA - MiToBo Cell Image Analyzer]]<br/> for segmenting cell boundaries and sub-cellular particles in fluorescent microscopy images | * [[Applications/MiCa | MiCA - MiToBo Cell Image Analyzer]]<br/> for segmenting cell boundaries and sub-cellular particles in fluorescent microscopy images | ||
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* [[Applications/ActinAnalyzer2D | Actin Analyzer 2D]] (since MiToBo 1.4) <br/> for quantifying and comparing actin microfilament structures | * [[Applications/ActinAnalyzer2D | Actin Analyzer 2D]] (since MiToBo 1.4) <br/> for quantifying and comparing actin microfilament structures | ||
Revision as of 16:48, 17 June 2015
Several image processing pipelines have already been developed in MiToBo.
Below you can find selected example applications, some of them have been published already.
- MTB Cell Counter (since MiToBo 1.5),
a tool for semi-automatic labeling and counting of spot-like structures like, e.g., plastides, stress granules or p-bodies
- MiCA - MiToBo Cell Image Analyzer
for segmenting cell boundaries and sub-cellular particles in fluorescent microscopy images
- Neuron Analyzer 2D
for segmenting the area of neurites and quantify protein concentrations within these neurites
- Scratch Assay Analyzer
for analysis of collective cell migration based on scratch/ wound closure assay images
- Cell Migration Analyzer
for migration analysis based on single cell tracking
- Actin Analyzer 2D (since MiToBo 1.4)
for quantifying and comparing actin microfilament structures
