| Literature DB >> 22474181 |
Michael P Pound1, Andrew P French, Darren M Wells, Malcolm J Bennett, Tony P Pridmore.
Abstract
It is increasingly important in life sciences that many cell-scale and tissue-scale measurements are quantified from confocal microscope images. However, extracting and analyzing large-scale confocal image data sets represents a major bottleneck for researchers. To aid this process, CellSeT software has been developed, which utilizes tissue-scale structure to help segment individual cells. We provide examples of how the CellSeT software can be used to quantify fluorescence of hormone-responsive nuclear reporters, determine membrane protein polarity, extract cell and tissue geometry for use in later modeling, and take many additional biologically relevant measures using an extensible plug-in toolset. Application of CellSeT promises to remove subjectivity from the resulting data sets and facilitate higher-throughput, quantitative approaches to plant cell research.Mesh:
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Year: 2012 PMID: 22474181 PMCID: PMC3398551 DOI: 10.1105/tpc.112.096289
Source DB: PubMed Journal: Plant Cell ISSN: 1040-4651 Impact factor: 11.277