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pubmed-article:18992251pubmed:abstractTextThis paper presents automated methods to quantify dynamic phenomena such as cell-cell interactions and cell migration patterns from time-lapse series of multi-channel three-dimensional image stacks of living specimens. Various 5-dimensional (x, y, z, t, lambda) images containing dendritic cells (DC), and T-cells or thymocytes in the developing mouse thymic cortex and lymph node were acquired by two-photon laser scanning microscopy (TPLSM). The cells were delineated automatically using a mean-shift clustering algorithm. This enables morphological measurements to be computed. A robust multiple-hypothesis tracking algorithm was used to track thymocytes (the DC were stationary). The tracking data enable dynamic measurements to be computed, including migratory patterns of thymocytes, and duration of thymocyte-DC contacts. Software was developed for efficient inspection, corrective editing, and validation of the automated analysis results. Our software-generated results agreed with manually generated measurements to within 8%.lld:pubmed
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pubmed-article:18992251pubmed:authorpubmed-author:LangH DHDlld:pubmed
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pubmed-article:18992251pubmed:dateRevised2011-9-26lld:pubmed
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pubmed-article:18992251pubmed:articleTitleAutomated 5-D analysis of cell migration and interaction in the thymic cortex from time-lapse sequences of 3-D multi-channel multi-photon images.lld:pubmed
pubmed-article:18992251pubmed:affiliationDepartment of Electrical, Computer, and System Engineering, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.lld:pubmed
pubmed-article:18992251pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:18992251pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
pubmed-article:18992251pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed
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