Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kobayashi, Takayoshi | en_US |
dc.contributor.author | Sundaram, Durga | en_US |
dc.contributor.author | Nakata, Kazuaki | en_US |
dc.contributor.author | Tsurui, Hiromichi | en_US |
dc.date.accessioned | 2019-04-03T06:36:00Z | - |
dc.date.available | 2019-04-03T06:36:00Z | - |
dc.date.issued | 2017-03-01 | en_US |
dc.identifier.issn | 1083-3668 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1117/1.JBO.22.3.036011 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/145294 | - |
dc.description.abstract | Qualifications of intracellular structure were performed for the first time using the gray-level co-occurrence matrix (GLCM) method for images of cells obtained by resolution-enhanced photothermal imaging. The GLCM method has been used to extract five parameters of texture features for five different types of cells in mouse brain; pyramidal neurons and glial cells in the basal nucleus (BGl), dentate gyrus granule cells, cerebellar Purkinje cells, and cerebellar granule cells. The parameters are correlation, contrast, angular second moment (ASM), inverse difference moment (IDM), and entropy for the images of cells of interest in a mouse brain. The parameters vary depending on the pixel distance taken in the analysis method. Based on the obtained results, we identified that the most suitable GLCM parameter is IDM for pyramidal neurons and BGl, granule cells in the dentate gyrus, Purkinje cells and granule cells in the cerebellum. It was also found that the ASM is the most appropriate for neurons in the basal nucleus. (C) The Authors. Published by SPIE under a Creative Commons Attribution 3.0 Unported License. | en_US |
dc.language.iso | en_US | en_US |
dc.subject | microscopy | en_US |
dc.subject | superresolution | en_US |
dc.subject | neurons | en_US |
dc.subject | cells | en_US |
dc.subject | cell analysis | en_US |
dc.subject | image analysis | en_US |
dc.title | Gray-level co-occurrence matrix analysis of several cell types in mouse brain using resolution-enhanced photothermal microscopy | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1117/1.JBO.22.3.036011 | en_US |
dc.identifier.journal | JOURNAL OF BIOMEDICAL OPTICS | en_US |
dc.citation.volume | 22 | en_US |
dc.citation.issue | 3 | en_US |
dc.citation.spage | 0 | en_US |
dc.citation.epage | 0 | en_US |
dc.contributor.department | 電子物理學系 | zh_TW |
dc.contributor.department | Department of Electrophysics | en_US |
dc.identifier.wosnumber | WOS:000397944900026 | en_US |
dc.citation.woscount | 2 | en_US |
Appears in Collections: | Articles |
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