Cell Tracking in Microscopy Images Using a Rao-Blackwellized Particle Filter

Analysing migrating cells in microscopy time-lapse images has already helped the understanding of many biological processes and may be of importance in the development of new medical treatments. Today’s biological experiments tend to produce a huge amount of dynamic image data and tracking the indiv...

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Main Author: Lindmark, Sofia
Format: Others
Language:English
Published: Uppsala universitet, Avdelningen för visuell information och interaktion 2014
Subjects:
Online Access:http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-236769
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spelling ndltd-UPSALLA1-oai-DiVA.org-uu-2367692014-11-25T06:50:33ZCell Tracking in Microscopy Images Using a Rao-Blackwellized Particle FilterengLindmark, SofiaUppsala universitet, Avdelningen för visuell information och interaktion2014Cell trackingParticle filterRao-Blackwellized particle filterAnalysing migrating cells in microscopy time-lapse images has already helped the understanding of many biological processes and may be of importance in the development of new medical treatments. Today’s biological experiments tend to produce a huge amount of dynamic image data and tracking the individual cells by hand has become a bottleneck for the further analysis work. A number of cell tracking methods have therefore been developed over the past decades, but still many of the techniques have a limited performance. The aim of this Master Project is to develop a particle filter algorithm that automatically detects and tracks a large number of individual cells in an image sequence. The solution is based on a Rao-Blackwellized particle filter for multiple object tracking. The report also covers a review of existing automatic cell tracking techniques, a review of well-known filter techniques for single target tracking and how these techniques have been developed to handle multiple target tracking. The designed algorithm has been tested on real microscopy image data of neutrophils with 400 to 500 cells in each frame. The designed algorithm works well in areas of the images where no cells touch and can in these situations also correct for some segmentation mistakes. In areas where cells touch, the algorithm works well if the segmentation is correct, but often makes mistakes when it is not. A target effectiveness of 77 percent and a track purity of 80 percent are then achieved.  Student thesisinfo:eu-repo/semantics/bachelorThesistexthttp://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-236769UPTEC F, 1401-5757 ; 14048application/pdfinfo:eu-repo/semantics/openAccess
collection NDLTD
language English
format Others
sources NDLTD
topic Cell tracking
Particle filter
Rao-Blackwellized particle filter
spellingShingle Cell tracking
Particle filter
Rao-Blackwellized particle filter
Lindmark, Sofia
Cell Tracking in Microscopy Images Using a Rao-Blackwellized Particle Filter
description Analysing migrating cells in microscopy time-lapse images has already helped the understanding of many biological processes and may be of importance in the development of new medical treatments. Today’s biological experiments tend to produce a huge amount of dynamic image data and tracking the individual cells by hand has become a bottleneck for the further analysis work. A number of cell tracking methods have therefore been developed over the past decades, but still many of the techniques have a limited performance. The aim of this Master Project is to develop a particle filter algorithm that automatically detects and tracks a large number of individual cells in an image sequence. The solution is based on a Rao-Blackwellized particle filter for multiple object tracking. The report also covers a review of existing automatic cell tracking techniques, a review of well-known filter techniques for single target tracking and how these techniques have been developed to handle multiple target tracking. The designed algorithm has been tested on real microscopy image data of neutrophils with 400 to 500 cells in each frame. The designed algorithm works well in areas of the images where no cells touch and can in these situations also correct for some segmentation mistakes. In areas where cells touch, the algorithm works well if the segmentation is correct, but often makes mistakes when it is not. A target effectiveness of 77 percent and a track purity of 80 percent are then achieved. 
author Lindmark, Sofia
author_facet Lindmark, Sofia
author_sort Lindmark, Sofia
title Cell Tracking in Microscopy Images Using a Rao-Blackwellized Particle Filter
title_short Cell Tracking in Microscopy Images Using a Rao-Blackwellized Particle Filter
title_full Cell Tracking in Microscopy Images Using a Rao-Blackwellized Particle Filter
title_fullStr Cell Tracking in Microscopy Images Using a Rao-Blackwellized Particle Filter
title_full_unstemmed Cell Tracking in Microscopy Images Using a Rao-Blackwellized Particle Filter
title_sort cell tracking in microscopy images using a rao-blackwellized particle filter
publisher Uppsala universitet, Avdelningen för visuell information och interaktion
publishDate 2014
url http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-236769
work_keys_str_mv AT lindmarksofia celltrackinginmicroscopyimagesusingaraoblackwellizedparticlefilter
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