BioVision: An application for the automated image analysis of histological sections

We describe a computer application, “BioVision”, that can be trained to quickly and effectively classify and quantify user definable histological objects (e.g., senile plaques, neurofibrillary tangles) within single or double-labeled immunocytochemically stained sections. For a given image populatio...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neurobiology of aging 2006-10, Vol.27 (10), p.1462-1476
Hauptverfasser: Chubb, Charles, Inagaki, Yoshiyuki, Sheu, Phillip, Cummings, Brian, Wasserman, Andrea, Head, Elizabeth, Cotman, Carl
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1476
container_issue 10
container_start_page 1462
container_title Neurobiology of aging
container_volume 27
creator Chubb, Charles
Inagaki, Yoshiyuki
Sheu, Phillip
Cummings, Brian
Wasserman, Andrea
Head, Elizabeth
Cotman, Carl
description We describe a computer application, “BioVision”, that can be trained to quickly and effectively classify and quantify user definable histological objects (e.g., senile plaques, neurofibrillary tangles) within single or double-labeled immunocytochemically stained sections. For a given image population, BioVision is interactively trained (in Independent User Mode) by an investigator to perform the desired classifications. This training yields a statistical model of the different types of objects occurring in the target image population. The resulting model can then be used (in Automated User Mode) to classify all objects in any image or images from the target population. BioVision simplifies the quantification of complex visual objects and improves inter-rater reliability. The program accomplishes classification in two major stages: pixel classification and blob classification. In pixel classification, each pixel is assigned to one of some number of substance classes, based on its chromatic properties and local context, reflecting basic histological distinctions of interest. In the blob classification phase, the image's pixels are first partitioned into “blobs”: maximal connected sets of pixels assigned to the same substance class. Then, based on its size, shape, textural and contextual properties, each blob is assigned to a histological object class. A Bayesian classifier is used in each of the pixel and blob classification stages. We report several tests of BioVision. First, we applied BioVision to classify senile plaques and neurofibrillary tangles in several test cases of Alzheimer's brain immunostained for beta-amyloid and PHF-tau and compared the results to those produced by experienced investigators. BioVision was trained to classify Plaque-type blobs as either plaques or plaque-type nonentities, and tangle-type blobs as either tangles or tangle-type nonentities. BioVision classified the objects with an accuracy comparable to the trained investigator. Next, we applied BioVision to the task of counting all the tangles in hippocampal images from 22 Alzheimer's disease (AD) cases selected to span a broad range of dementia levels from the tissue repository of UC Irvine's Center for the study of Brain Aging and Dementia. The tangle counts produced by BioVision proved to be significantly better predictors of the cases’ adjusted MMSE scores than any of tangle load, age at death, post mortem interval or the interval between the last MMSE score and death.
doi_str_mv 10.1016/j.neurobiolaging.2005.08.023
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68784601</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0197458005002277</els_id><sourcerecordid>68784601</sourcerecordid><originalsourceid>FETCH-LOGICAL-c415t-d9c9e13a473d48e32d07f7f9f2b60da544ea223c7497f52ee4eabb22a1b6b1b13</originalsourceid><addsrcrecordid>eNqNkE1r20AQhpeSUjtu_kLZQ8hN6uyHtFLpJTVxGjD0kDTXZbUaOWtkrbsrFfzvs8aG0FNzGl543hnmIeSaQc6AlV-3-YBT8I3zvdm4YZNzgCKHKgcuPpA5K4oqY7JWF2QOrFaZLCqYkcsYtwCgpCo_kRkruWIViDl5_OH8s4vOD9_o7UDNft87a8aUaecDHV-Qmmn0OzNiS93ObFIeTH-ILlLf0RcXR9_7Ter0NKI9FuNn8rEzfcSr81yQ36u7p-XPbP3r_mF5u86sZMWYtbWtkQkjlWhlhYK3oDrV1R1vSmhNISUazoVV6Zmu4IgpNw3nhjVlwxomFuTmtHcf_J8J46h3LlrsezOgn6IuK1XJEv4PslqASHYS-P0E2uBjDNjpfUhPh4NmoI_29Vb_a18f7WuodLKf6l_Od6Zmh-1b-aw7AasTgEnLX4dBR-twsNi6kOTp1rv3XXoF08af-Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19303000</pqid></control><display><type>article</type><title>BioVision: An application for the automated image analysis of histological sections</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Chubb, Charles ; Inagaki, Yoshiyuki ; Sheu, Phillip ; Cummings, Brian ; Wasserman, Andrea ; Head, Elizabeth ; Cotman, Carl</creator><creatorcontrib>Chubb, Charles ; Inagaki, Yoshiyuki ; Sheu, Phillip ; Cummings, Brian ; Wasserman, Andrea ; Head, Elizabeth ; Cotman, Carl</creatorcontrib><description>We describe a computer application, “BioVision”, that can be trained to quickly and effectively classify and quantify user definable histological objects (e.g., senile plaques, neurofibrillary tangles) within single or double-labeled immunocytochemically stained sections. For a given image population, BioVision is interactively trained (in Independent User Mode) by an investigator to perform the desired classifications. This training yields a statistical model of the different types of objects occurring in the target image population. The resulting model can then be used (in Automated User Mode) to classify all objects in any image or images from the target population. BioVision simplifies the quantification of complex visual objects and improves inter-rater reliability. The program accomplishes classification in two major stages: pixel classification and blob classification. In pixel classification, each pixel is assigned to one of some number of substance classes, based on its chromatic properties and local context, reflecting basic histological distinctions of interest. In the blob classification phase, the image's pixels are first partitioned into “blobs”: maximal connected sets of pixels assigned to the same substance class. Then, based on its size, shape, textural and contextual properties, each blob is assigned to a histological object class. A Bayesian classifier is used in each of the pixel and blob classification stages. We report several tests of BioVision. First, we applied BioVision to classify senile plaques and neurofibrillary tangles in several test cases of Alzheimer's brain immunostained for beta-amyloid and PHF-tau and compared the results to those produced by experienced investigators. BioVision was trained to classify Plaque-type blobs as either plaques or plaque-type nonentities, and tangle-type blobs as either tangles or tangle-type nonentities. BioVision classified the objects with an accuracy comparable to the trained investigator. Next, we applied BioVision to the task of counting all the tangles in hippocampal images from 22 Alzheimer's disease (AD) cases selected to span a broad range of dementia levels from the tissue repository of UC Irvine's Center for the study of Brain Aging and Dementia. The tangle counts produced by BioVision proved to be significantly better predictors of the cases’ adjusted MMSE scores than any of tangle load, age at death, post mortem interval or the interval between the last MMSE score and death.</description><identifier>ISSN: 0197-4580</identifier><identifier>EISSN: 1558-1497</identifier><identifier>DOI: 10.1016/j.neurobiolaging.2005.08.023</identifier><identifier>PMID: 16271803</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Alzheimer Disease - pathology ; Animals ; Artificial Intelligence ; Humans ; Image Enhancement - methods ; Image Interpretation, Computer-Assisted - methods ; Microscopy - methods ; Neurofibrillary Tangles - pathology ; Pattern Recognition, Automated - methods ; Plaque, Amyloid - pathology ; Software ; Trainable automated image analysis</subject><ispartof>Neurobiology of aging, 2006-10, Vol.27 (10), p.1462-1476</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-d9c9e13a473d48e32d07f7f9f2b60da544ea223c7497f52ee4eabb22a1b6b1b13</citedby><cites>FETCH-LOGICAL-c415t-d9c9e13a473d48e32d07f7f9f2b60da544ea223c7497f52ee4eabb22a1b6b1b13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.neurobiolaging.2005.08.023$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16271803$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chubb, Charles</creatorcontrib><creatorcontrib>Inagaki, Yoshiyuki</creatorcontrib><creatorcontrib>Sheu, Phillip</creatorcontrib><creatorcontrib>Cummings, Brian</creatorcontrib><creatorcontrib>Wasserman, Andrea</creatorcontrib><creatorcontrib>Head, Elizabeth</creatorcontrib><creatorcontrib>Cotman, Carl</creatorcontrib><title>BioVision: An application for the automated image analysis of histological sections</title><title>Neurobiology of aging</title><addtitle>Neurobiol Aging</addtitle><description>We describe a computer application, “BioVision”, that can be trained to quickly and effectively classify and quantify user definable histological objects (e.g., senile plaques, neurofibrillary tangles) within single or double-labeled immunocytochemically stained sections. For a given image population, BioVision is interactively trained (in Independent User Mode) by an investigator to perform the desired classifications. This training yields a statistical model of the different types of objects occurring in the target image population. The resulting model can then be used (in Automated User Mode) to classify all objects in any image or images from the target population. BioVision simplifies the quantification of complex visual objects and improves inter-rater reliability. The program accomplishes classification in two major stages: pixel classification and blob classification. In pixel classification, each pixel is assigned to one of some number of substance classes, based on its chromatic properties and local context, reflecting basic histological distinctions of interest. In the blob classification phase, the image's pixels are first partitioned into “blobs”: maximal connected sets of pixels assigned to the same substance class. Then, based on its size, shape, textural and contextual properties, each blob is assigned to a histological object class. A Bayesian classifier is used in each of the pixel and blob classification stages. We report several tests of BioVision. First, we applied BioVision to classify senile plaques and neurofibrillary tangles in several test cases of Alzheimer's brain immunostained for beta-amyloid and PHF-tau and compared the results to those produced by experienced investigators. BioVision was trained to classify Plaque-type blobs as either plaques or plaque-type nonentities, and tangle-type blobs as either tangles or tangle-type nonentities. BioVision classified the objects with an accuracy comparable to the trained investigator. Next, we applied BioVision to the task of counting all the tangles in hippocampal images from 22 Alzheimer's disease (AD) cases selected to span a broad range of dementia levels from the tissue repository of UC Irvine's Center for the study of Brain Aging and Dementia. The tangle counts produced by BioVision proved to be significantly better predictors of the cases’ adjusted MMSE scores than any of tangle load, age at death, post mortem interval or the interval between the last MMSE score and death.</description><subject>Alzheimer Disease - pathology</subject><subject>Animals</subject><subject>Artificial Intelligence</subject><subject>Humans</subject><subject>Image Enhancement - methods</subject><subject>Image Interpretation, Computer-Assisted - methods</subject><subject>Microscopy - methods</subject><subject>Neurofibrillary Tangles - pathology</subject><subject>Pattern Recognition, Automated - methods</subject><subject>Plaque, Amyloid - pathology</subject><subject>Software</subject><subject>Trainable automated image analysis</subject><issn>0197-4580</issn><issn>1558-1497</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1r20AQhpeSUjtu_kLZQ8hN6uyHtFLpJTVxGjD0kDTXZbUaOWtkrbsrFfzvs8aG0FNzGl543hnmIeSaQc6AlV-3-YBT8I3zvdm4YZNzgCKHKgcuPpA5K4oqY7JWF2QOrFaZLCqYkcsYtwCgpCo_kRkruWIViDl5_OH8s4vOD9_o7UDNft87a8aUaecDHV-Qmmn0OzNiS93ObFIeTH-ILlLf0RcXR9_7Ter0NKI9FuNn8rEzfcSr81yQ36u7p-XPbP3r_mF5u86sZMWYtbWtkQkjlWhlhYK3oDrV1R1vSmhNISUazoVV6Zmu4IgpNw3nhjVlwxomFuTmtHcf_J8J46h3LlrsezOgn6IuK1XJEv4PslqASHYS-P0E2uBjDNjpfUhPh4NmoI_29Vb_a18f7WuodLKf6l_Od6Zmh-1b-aw7AasTgEnLX4dBR-twsNi6kOTp1rv3XXoF08af-Q</recordid><startdate>20061001</startdate><enddate>20061001</enddate><creator>Chubb, Charles</creator><creator>Inagaki, Yoshiyuki</creator><creator>Sheu, Phillip</creator><creator>Cummings, Brian</creator><creator>Wasserman, Andrea</creator><creator>Head, Elizabeth</creator><creator>Cotman, Carl</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>20061001</creationdate><title>BioVision: An application for the automated image analysis of histological sections</title><author>Chubb, Charles ; Inagaki, Yoshiyuki ; Sheu, Phillip ; Cummings, Brian ; Wasserman, Andrea ; Head, Elizabeth ; Cotman, Carl</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-d9c9e13a473d48e32d07f7f9f2b60da544ea223c7497f52ee4eabb22a1b6b1b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Alzheimer Disease - pathology</topic><topic>Animals</topic><topic>Artificial Intelligence</topic><topic>Humans</topic><topic>Image Enhancement - methods</topic><topic>Image Interpretation, Computer-Assisted - methods</topic><topic>Microscopy - methods</topic><topic>Neurofibrillary Tangles - pathology</topic><topic>Pattern Recognition, Automated - methods</topic><topic>Plaque, Amyloid - pathology</topic><topic>Software</topic><topic>Trainable automated image analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chubb, Charles</creatorcontrib><creatorcontrib>Inagaki, Yoshiyuki</creatorcontrib><creatorcontrib>Sheu, Phillip</creatorcontrib><creatorcontrib>Cummings, Brian</creatorcontrib><creatorcontrib>Wasserman, Andrea</creatorcontrib><creatorcontrib>Head, Elizabeth</creatorcontrib><creatorcontrib>Cotman, Carl</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neurobiology of aging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chubb, Charles</au><au>Inagaki, Yoshiyuki</au><au>Sheu, Phillip</au><au>Cummings, Brian</au><au>Wasserman, Andrea</au><au>Head, Elizabeth</au><au>Cotman, Carl</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>BioVision: An application for the automated image analysis of histological sections</atitle><jtitle>Neurobiology of aging</jtitle><addtitle>Neurobiol Aging</addtitle><date>2006-10-01</date><risdate>2006</risdate><volume>27</volume><issue>10</issue><spage>1462</spage><epage>1476</epage><pages>1462-1476</pages><issn>0197-4580</issn><eissn>1558-1497</eissn><abstract>We describe a computer application, “BioVision”, that can be trained to quickly and effectively classify and quantify user definable histological objects (e.g., senile plaques, neurofibrillary tangles) within single or double-labeled immunocytochemically stained sections. For a given image population, BioVision is interactively trained (in Independent User Mode) by an investigator to perform the desired classifications. This training yields a statistical model of the different types of objects occurring in the target image population. The resulting model can then be used (in Automated User Mode) to classify all objects in any image or images from the target population. BioVision simplifies the quantification of complex visual objects and improves inter-rater reliability. The program accomplishes classification in two major stages: pixel classification and blob classification. In pixel classification, each pixel is assigned to one of some number of substance classes, based on its chromatic properties and local context, reflecting basic histological distinctions of interest. In the blob classification phase, the image's pixels are first partitioned into “blobs”: maximal connected sets of pixels assigned to the same substance class. Then, based on its size, shape, textural and contextual properties, each blob is assigned to a histological object class. A Bayesian classifier is used in each of the pixel and blob classification stages. We report several tests of BioVision. First, we applied BioVision to classify senile plaques and neurofibrillary tangles in several test cases of Alzheimer's brain immunostained for beta-amyloid and PHF-tau and compared the results to those produced by experienced investigators. BioVision was trained to classify Plaque-type blobs as either plaques or plaque-type nonentities, and tangle-type blobs as either tangles or tangle-type nonentities. BioVision classified the objects with an accuracy comparable to the trained investigator. Next, we applied BioVision to the task of counting all the tangles in hippocampal images from 22 Alzheimer's disease (AD) cases selected to span a broad range of dementia levels from the tissue repository of UC Irvine's Center for the study of Brain Aging and Dementia. The tangle counts produced by BioVision proved to be significantly better predictors of the cases’ adjusted MMSE scores than any of tangle load, age at death, post mortem interval or the interval between the last MMSE score and death.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16271803</pmid><doi>10.1016/j.neurobiolaging.2005.08.023</doi><tpages>15</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0197-4580
ispartof Neurobiology of aging, 2006-10, Vol.27 (10), p.1462-1476
issn 0197-4580
1558-1497
language eng
recordid cdi_proquest_miscellaneous_68784601
source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Alzheimer Disease - pathology
Animals
Artificial Intelligence
Humans
Image Enhancement - methods
Image Interpretation, Computer-Assisted - methods
Microscopy - methods
Neurofibrillary Tangles - pathology
Pattern Recognition, Automated - methods
Plaque, Amyloid - pathology
Software
Trainable automated image analysis
title BioVision: An application for the automated image analysis of histological sections
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T02%3A20%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=BioVision:%20An%20application%20for%20the%20automated%20image%20analysis%20of%20histological%20sections&rft.jtitle=Neurobiology%20of%20aging&rft.au=Chubb,%20Charles&rft.date=2006-10-01&rft.volume=27&rft.issue=10&rft.spage=1462&rft.epage=1476&rft.pages=1462-1476&rft.issn=0197-4580&rft.eissn=1558-1497&rft_id=info:doi/10.1016/j.neurobiolaging.2005.08.023&rft_dat=%3Cproquest_cross%3E68784601%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=19303000&rft_id=info:pmid/16271803&rft_els_id=S0197458005002277&rfr_iscdi=true