A spherical harmonics intensity model for 3D segmentation and 3D shape analysis of heterochromatin foci
•Model-based approach for automatic 3D segmentation of heterochromatin foci.•Novel 3D parametric intensity model based on a spherical harmonics expansion.•3D shape analysis of heterochromatin by exploiting the segmentation result.•Quantitative evaluation based on synthetic and real confocal microsco...
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Veröffentlicht in: | Medical image analysis 2016-08, Vol.32, p.18-31 |
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creator | Eck, Simon Wörz, Stefan Müller-Ott, Katharina Hahn, Matthias Biesdorf, Andreas Schotta, Gunnar Rippe, Karsten Rohr, Karl |
description | •Model-based approach for automatic 3D segmentation of heterochromatin foci.•Novel 3D parametric intensity model based on a spherical harmonics expansion.•3D shape analysis of heterochromatin by exploiting the segmentation result.•Quantitative evaluation based on synthetic and real confocal microscopy image data.•The approach copes well with high noise levels and various 3D shapes and sizes.
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The genome is partitioned into regions of euchromatin and heterochromatin. The organization of heterochromatin is important for the regulation of cellular processes such as chromosome segregation and gene silencing, and their misregulation is linked to cancer and other diseases. We present a model-based approach for automatic 3D segmentation and 3D shape analysis of heterochromatin foci from 3D confocal light microscopy images. Our approach employs a novel 3D intensity model based on spherical harmonics, which analytically describes the shape and intensities of the foci. The model parameters are determined by fitting the model to the image intensities using least-squares minimization. To characterize the 3D shape of the foci, we exploit the computed spherical harmonics coefficients and determine a shape descriptor. We applied our approach to 3D synthetic image data as well as real 3D static and real 3D time-lapse microscopy images, and compared the performance with that of previous approaches. It turned out that our approach yields accurate 3D segmentation results and performs better than previous approaches. We also show that our approach can be used for quantifying 3D shape differences of heterochromatin foci. |
doi_str_mv | 10.1016/j.media.2016.03.001 |
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[Display omitted]
The genome is partitioned into regions of euchromatin and heterochromatin. The organization of heterochromatin is important for the regulation of cellular processes such as chromosome segregation and gene silencing, and their misregulation is linked to cancer and other diseases. We present a model-based approach for automatic 3D segmentation and 3D shape analysis of heterochromatin foci from 3D confocal light microscopy images. Our approach employs a novel 3D intensity model based on spherical harmonics, which analytically describes the shape and intensities of the foci. The model parameters are determined by fitting the model to the image intensities using least-squares minimization. To characterize the 3D shape of the foci, we exploit the computed spherical harmonics coefficients and determine a shape descriptor. We applied our approach to 3D synthetic image data as well as real 3D static and real 3D time-lapse microscopy images, and compared the performance with that of previous approaches. It turned out that our approach yields accurate 3D segmentation results and performs better than previous approaches. We also show that our approach can be used for quantifying 3D shape differences of heterochromatin foci.</description><identifier>ISSN: 1361-8415</identifier><identifier>EISSN: 1361-8423</identifier><identifier>DOI: 10.1016/j.media.2016.03.001</identifier><identifier>PMID: 27037463</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>3D parametric intensity model ; Confocal light microscopy ; Heterochromatin - metabolism ; Humans ; Image Processing, Computer-Assisted - methods ; Imaging, Three-Dimensional - methods ; Least-Squares Analysis ; Microscopy, Confocal - methods ; Pericentric heterochromatin ; Spherical harmonics</subject><ispartof>Medical image analysis, 2016-08, Vol.32, p.18-31</ispartof><rights>2016 Elsevier B.V.</rights><rights>Copyright © 2016 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-9a5eced4dc2de3c0936b20d649333fa48fea325103a10d445e5150a8fcdab9513</citedby><cites>FETCH-LOGICAL-c425t-9a5eced4dc2de3c0936b20d649333fa48fea325103a10d445e5150a8fcdab9513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1361841516300019$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27037463$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eck, Simon</creatorcontrib><creatorcontrib>Wörz, Stefan</creatorcontrib><creatorcontrib>Müller-Ott, Katharina</creatorcontrib><creatorcontrib>Hahn, Matthias</creatorcontrib><creatorcontrib>Biesdorf, Andreas</creatorcontrib><creatorcontrib>Schotta, Gunnar</creatorcontrib><creatorcontrib>Rippe, Karsten</creatorcontrib><creatorcontrib>Rohr, Karl</creatorcontrib><title>A spherical harmonics intensity model for 3D segmentation and 3D shape analysis of heterochromatin foci</title><title>Medical image analysis</title><addtitle>Med Image Anal</addtitle><description>•Model-based approach for automatic 3D segmentation of heterochromatin foci.•Novel 3D parametric intensity model based on a spherical harmonics expansion.•3D shape analysis of heterochromatin by exploiting the segmentation result.•Quantitative evaluation based on synthetic and real confocal microscopy image data.•The approach copes well with high noise levels and various 3D shapes and sizes.
[Display omitted]
The genome is partitioned into regions of euchromatin and heterochromatin. The organization of heterochromatin is important for the regulation of cellular processes such as chromosome segregation and gene silencing, and their misregulation is linked to cancer and other diseases. We present a model-based approach for automatic 3D segmentation and 3D shape analysis of heterochromatin foci from 3D confocal light microscopy images. Our approach employs a novel 3D intensity model based on spherical harmonics, which analytically describes the shape and intensities of the foci. The model parameters are determined by fitting the model to the image intensities using least-squares minimization. To characterize the 3D shape of the foci, we exploit the computed spherical harmonics coefficients and determine a shape descriptor. We applied our approach to 3D synthetic image data as well as real 3D static and real 3D time-lapse microscopy images, and compared the performance with that of previous approaches. It turned out that our approach yields accurate 3D segmentation results and performs better than previous approaches. We also show that our approach can be used for quantifying 3D shape differences of heterochromatin foci.</description><subject>3D parametric intensity model</subject><subject>Confocal light microscopy</subject><subject>Heterochromatin - metabolism</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>Imaging, Three-Dimensional - methods</subject><subject>Least-Squares Analysis</subject><subject>Microscopy, Confocal - methods</subject><subject>Pericentric heterochromatin</subject><subject>Spherical harmonics</subject><issn>1361-8415</issn><issn>1361-8423</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1PAyEQhonR-P0LTAxHL12Hr2334MH4nZh40TOhMOvS7EKFrUn_vdSqR08w8LwzmYeQMwYVA1ZfLqoBnTcVL0UFogJgO-SQiZpNZpKL3b87UwfkKOcFAEylhH1ywKcgprIWh-T9muZlh8lb09POpCEGbzP1YcSQ_bimQ3TY0zYmKm5pxvcBw2hGHwM1wX2_dWaJpTD9OvtMY0s7HDFF26U4FDKUsPUnZK81fcbTn_OYvN3fvd48Tp5fHp5urp8nVnI1Thqj0KKTznKHwkIj6jkHV8tGCNEaOWvRCK4YCMPASalQMQVm1lpn5o1i4phcbPsuU_xYYR714LPFvjcB4yprNm1qLmvV8IKKLWpTzDlhq5fJDyatNQO9MawX-tuw3hjWIHQxXFLnPwNW8_L7l_lVWoCrLYBlzU-PSWfrMZStfEI7ahf9vwO-AFamjiA</recordid><startdate>201608</startdate><enddate>201608</enddate><creator>Eck, Simon</creator><creator>Wörz, Stefan</creator><creator>Müller-Ott, Katharina</creator><creator>Hahn, Matthias</creator><creator>Biesdorf, Andreas</creator><creator>Schotta, Gunnar</creator><creator>Rippe, Karsten</creator><creator>Rohr, Karl</creator><general>Elsevier B.V</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>7X8</scope></search><sort><creationdate>201608</creationdate><title>A spherical harmonics intensity model for 3D segmentation and 3D shape analysis of heterochromatin foci</title><author>Eck, Simon ; Wörz, Stefan ; Müller-Ott, Katharina ; Hahn, Matthias ; Biesdorf, Andreas ; Schotta, Gunnar ; Rippe, Karsten ; Rohr, Karl</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-9a5eced4dc2de3c0936b20d649333fa48fea325103a10d445e5150a8fcdab9513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>3D parametric intensity model</topic><topic>Confocal light microscopy</topic><topic>Heterochromatin - metabolism</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted - methods</topic><topic>Imaging, Three-Dimensional - methods</topic><topic>Least-Squares Analysis</topic><topic>Microscopy, Confocal - methods</topic><topic>Pericentric heterochromatin</topic><topic>Spherical harmonics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eck, Simon</creatorcontrib><creatorcontrib>Wörz, Stefan</creatorcontrib><creatorcontrib>Müller-Ott, Katharina</creatorcontrib><creatorcontrib>Hahn, Matthias</creatorcontrib><creatorcontrib>Biesdorf, Andreas</creatorcontrib><creatorcontrib>Schotta, Gunnar</creatorcontrib><creatorcontrib>Rippe, Karsten</creatorcontrib><creatorcontrib>Rohr, Karl</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Medical image analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eck, Simon</au><au>Wörz, Stefan</au><au>Müller-Ott, Katharina</au><au>Hahn, Matthias</au><au>Biesdorf, Andreas</au><au>Schotta, Gunnar</au><au>Rippe, Karsten</au><au>Rohr, Karl</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A spherical harmonics intensity model for 3D segmentation and 3D shape analysis of heterochromatin foci</atitle><jtitle>Medical image analysis</jtitle><addtitle>Med Image Anal</addtitle><date>2016-08</date><risdate>2016</risdate><volume>32</volume><spage>18</spage><epage>31</epage><pages>18-31</pages><issn>1361-8415</issn><eissn>1361-8423</eissn><abstract>•Model-based approach for automatic 3D segmentation of heterochromatin foci.•Novel 3D parametric intensity model based on a spherical harmonics expansion.•3D shape analysis of heterochromatin by exploiting the segmentation result.•Quantitative evaluation based on synthetic and real confocal microscopy image data.•The approach copes well with high noise levels and various 3D shapes and sizes.
[Display omitted]
The genome is partitioned into regions of euchromatin and heterochromatin. The organization of heterochromatin is important for the regulation of cellular processes such as chromosome segregation and gene silencing, and their misregulation is linked to cancer and other diseases. We present a model-based approach for automatic 3D segmentation and 3D shape analysis of heterochromatin foci from 3D confocal light microscopy images. Our approach employs a novel 3D intensity model based on spherical harmonics, which analytically describes the shape and intensities of the foci. The model parameters are determined by fitting the model to the image intensities using least-squares minimization. To characterize the 3D shape of the foci, we exploit the computed spherical harmonics coefficients and determine a shape descriptor. We applied our approach to 3D synthetic image data as well as real 3D static and real 3D time-lapse microscopy images, and compared the performance with that of previous approaches. It turned out that our approach yields accurate 3D segmentation results and performs better than previous approaches. We also show that our approach can be used for quantifying 3D shape differences of heterochromatin foci.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27037463</pmid><doi>10.1016/j.media.2016.03.001</doi><tpages>14</tpages></addata></record> |
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subjects | 3D parametric intensity model Confocal light microscopy Heterochromatin - metabolism Humans Image Processing, Computer-Assisted - methods Imaging, Three-Dimensional - methods Least-Squares Analysis Microscopy, Confocal - methods Pericentric heterochromatin Spherical harmonics |
title | A spherical harmonics intensity model for 3D segmentation and 3D shape analysis of heterochromatin foci |
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