Automatic Seedpoint Selection and Tracing of Microstructures in the Knife-Edge Scanning Microscope Mouse Brain Data Set

The Knife-Edge Scanning Microscope (KESM) enables imaging of an entire mouse brain at sub-micrometer resolution. By using the data sets from the KESM, we can trace the neuronal and vascular structures of the whole mouse brain. I investigated effective methods for automatic seedpoint selection on 3D...

Full description

Bibliographic Details
Main Author: Kim, Dongkun
Other Authors: Yoonsuck, Choe
Format: Others
Language:en_US
Published: 2011
Subjects:
Online Access:http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-10122
id ndltd-tamu.edu-oai-repository.tamu.edu-1969.1-ETD-TAMU-2011-08-10122
record_format oai_dc
spelling ndltd-tamu.edu-oai-repository.tamu.edu-1969.1-ETD-TAMU-2011-08-101222013-01-08T10:42:30ZAutomatic Seedpoint Selection and Tracing of Microstructures in the Knife-Edge Scanning Microscope Mouse Brain Data SetKim, DongkunKESMAutomatic seedpoint selectionTracing neuronal structureCounting somaThe Knife-Edge Scanning Microscope (KESM) enables imaging of an entire mouse brain at sub-micrometer resolution. By using the data sets from the KESM, we can trace the neuronal and vascular structures of the whole mouse brain. I investigated effective methods for automatic seedpoint selection on 3D data sets from the KESM. Furthermore, based on the detected seedpoints, I counted the total number of somata and traced the neuronal structures in the KESM data sets. In the first step, the acquired images from KESM were preprocessed as follows: inverting, noise filtering and contrast enhancement, merging, and stacking to create 3D volumes. Second, I used a morphological object detection algorithm to select seedpoints in the complex neuronal structures. Third, I used an interactive 3D seedpoint validation and a multi-scale approach to identify incorrectly detected somata due to the dense overlapping structures. Fourth, I counted the number of somata to investigate regional differences and morphological features of the mouse brain. Finally, I traced the neuronal structures using a local maximum intensity projection method that employs moving windows. The contributions of this work include reducing time required for setting seedpoints, decreasing the number of falsely detected somata, and improving 3D neuronal reconstruction and analysis performance.Yoonsuck, Choe2011-10-21T22:03:59Z2011-10-22T07:12:10Z2011-10-21T22:03:59Z2011-10-22T07:12:10Z2011-082011-10-21August 2011thesistextapplication/pdfhttp://hdl.handle.net/1969.1/ETD-TAMU-2011-08-10122en_US
collection NDLTD
language en_US
format Others
sources NDLTD
topic KESM
Automatic seedpoint selection
Tracing neuronal structure
Counting soma
spellingShingle KESM
Automatic seedpoint selection
Tracing neuronal structure
Counting soma
Kim, Dongkun
Automatic Seedpoint Selection and Tracing of Microstructures in the Knife-Edge Scanning Microscope Mouse Brain Data Set
description The Knife-Edge Scanning Microscope (KESM) enables imaging of an entire mouse brain at sub-micrometer resolution. By using the data sets from the KESM, we can trace the neuronal and vascular structures of the whole mouse brain. I investigated effective methods for automatic seedpoint selection on 3D data sets from the KESM. Furthermore, based on the detected seedpoints, I counted the total number of somata and traced the neuronal structures in the KESM data sets. In the first step, the acquired images from KESM were preprocessed as follows: inverting, noise filtering and contrast enhancement, merging, and stacking to create 3D volumes. Second, I used a morphological object detection algorithm to select seedpoints in the complex neuronal structures. Third, I used an interactive 3D seedpoint validation and a multi-scale approach to identify incorrectly detected somata due to the dense overlapping structures. Fourth, I counted the number of somata to investigate regional differences and morphological features of the mouse brain. Finally, I traced the neuronal structures using a local maximum intensity projection method that employs moving windows. The contributions of this work include reducing time required for setting seedpoints, decreasing the number of falsely detected somata, and improving 3D neuronal reconstruction and analysis performance.
author2 Yoonsuck, Choe
author_facet Yoonsuck, Choe
Kim, Dongkun
author Kim, Dongkun
author_sort Kim, Dongkun
title Automatic Seedpoint Selection and Tracing of Microstructures in the Knife-Edge Scanning Microscope Mouse Brain Data Set
title_short Automatic Seedpoint Selection and Tracing of Microstructures in the Knife-Edge Scanning Microscope Mouse Brain Data Set
title_full Automatic Seedpoint Selection and Tracing of Microstructures in the Knife-Edge Scanning Microscope Mouse Brain Data Set
title_fullStr Automatic Seedpoint Selection and Tracing of Microstructures in the Knife-Edge Scanning Microscope Mouse Brain Data Set
title_full_unstemmed Automatic Seedpoint Selection and Tracing of Microstructures in the Knife-Edge Scanning Microscope Mouse Brain Data Set
title_sort automatic seedpoint selection and tracing of microstructures in the knife-edge scanning microscope mouse brain data set
publishDate 2011
url http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-10122
work_keys_str_mv AT kimdongkun automaticseedpointselectionandtracingofmicrostructuresintheknifeedgescanningmicroscopemousebraindataset
_version_ 1716505229982171136