Fourier Tract Sampling (FouTS): A framework for improved inference of white matter tracts from diffusion MRI by explicitly modelling tract volume
Diffusion MRI tractography algorithm development is increasingly moving towards global techniques to incorporate “downstream” information and conditional probabilities between neighbouring tracts. Such approaches also enable white matter to be represented more tangibly than the abstract lines genera...
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description | Diffusion MRI tractography algorithm development is increasingly moving towards global techniques to incorporate “downstream” information and conditional probabilities between neighbouring tracts. Such approaches also enable white matter to be represented more tangibly than the abstract lines generated by the most common approaches to fibre tracking. However, previously proposed algorithms still use fibre-like models of white matter corresponding to thin strands of white matter tracts rather than the tracts themselves, and therefore require many components for accurate representations, which leads to poorly constrained inverse problems. We propose a novel tract-based model of white matter, the ‘Fourier tract’, which is able to represent rich tract shapes with a relatively low number of parameters, and explicitly decouples the spatial extent of the modelled tract from its ‘Apparent Connection Strength (ACS)’. The Fourier tract model is placed within a novel Bayesian framework, which relates the tract parameters directly to the observed signal, enabling a wide range of acquisition schemes to be used. The posterior distribution of the Bayesian framework is characterised via Markov-chain Monte-Carlo sampling to infer probable values of the ACS and spatial extent of the imaged white matter tracts, providing measures that can be directly applied to many research and clinical studies. The robustness of the proposed tractography algorithm is demonstrated on simulated basic tract configurations, such as curving, twisting, crossing and kissing tracts, and sections of more complex numerical phantoms. As an illustration of the approach in vivo, fibre tracking is performed on a central section of the brain in three subjects from 60 direction HARDI datasets.
•Infers spatial extent and approximate intra-axonal volume of white matter tracts•These measures are kept distinct from their probability (unlike prob. streamlines).•Incorporates downstream voxels and conditional probabilities of nearby tracts•Could be used on multi-shell acquisitions with appropriate signal model•Complex fibre regions are inferred more accurately than streamline methods. |
doi_str_mv | 10.1016/j.neuroimage.2015.05.090 |
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•Infers spatial extent and approximate intra-axonal volume of white matter tracts•These measures are kept distinct from their probability (unlike prob. streamlines).•Incorporates downstream voxels and conditional probabilities of nearby tracts•Could be used on multi-shell acquisitions with appropriate signal model•Complex fibre regions are inferred more accurately than streamline methods.</description><identifier>ISSN: 1053-8119</identifier><identifier>EISSN: 1095-9572</identifier><identifier>DOI: 10.1016/j.neuroimage.2015.05.090</identifier><identifier>PMID: 26070265</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Algorithms ; Diffusion ; Diffusion Magnetic Resonance Imaging - methods ; Fourier Analysis ; Humans ; Image Processing, Computer-Assisted - methods ; Models, Statistical ; Nerve Fibers, Myelinated ; Neural Pathways - anatomy & histology ; Probability ; White Matter - anatomy & histology</subject><ispartof>NeuroImage (Orlando, Fla.), 2015-10, Vol.120, p.412-427</ispartof><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Oct 15, 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c485t-53ea4d1ee203c4952129dbd33c54016a812c62ab3491e87e2f9ed59745e28d373</citedby><cites>FETCH-LOGICAL-c485t-53ea4d1ee203c4952129dbd33c54016a812c62ab3491e87e2f9ed59745e28d373</cites><orcidid>0000-0002-4160-2134</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1053811915005066$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26070265$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Close, Thomas G.</creatorcontrib><creatorcontrib>Tournier, Jacques-Donald</creatorcontrib><creatorcontrib>Johnston, Leigh A.</creatorcontrib><creatorcontrib>Calamante, Fernando</creatorcontrib><creatorcontrib>Mareels, Iven</creatorcontrib><creatorcontrib>Connelly, Alan</creatorcontrib><title>Fourier Tract Sampling (FouTS): A framework for improved inference of white matter tracts from diffusion MRI by explicitly modelling tract volume</title><title>NeuroImage (Orlando, Fla.)</title><addtitle>Neuroimage</addtitle><description>Diffusion MRI tractography algorithm development is increasingly moving towards global techniques to incorporate “downstream” information and conditional probabilities between neighbouring tracts. Such approaches also enable white matter to be represented more tangibly than the abstract lines generated by the most common approaches to fibre tracking. However, previously proposed algorithms still use fibre-like models of white matter corresponding to thin strands of white matter tracts rather than the tracts themselves, and therefore require many components for accurate representations, which leads to poorly constrained inverse problems. We propose a novel tract-based model of white matter, the ‘Fourier tract’, which is able to represent rich tract shapes with a relatively low number of parameters, and explicitly decouples the spatial extent of the modelled tract from its ‘Apparent Connection Strength (ACS)’. The Fourier tract model is placed within a novel Bayesian framework, which relates the tract parameters directly to the observed signal, enabling a wide range of acquisition schemes to be used. The posterior distribution of the Bayesian framework is characterised via Markov-chain Monte-Carlo sampling to infer probable values of the ACS and spatial extent of the imaged white matter tracts, providing measures that can be directly applied to many research and clinical studies. The robustness of the proposed tractography algorithm is demonstrated on simulated basic tract configurations, such as curving, twisting, crossing and kissing tracts, and sections of more complex numerical phantoms. As an illustration of the approach in vivo, fibre tracking is performed on a central section of the brain in three subjects from 60 direction HARDI datasets.
•Infers spatial extent and approximate intra-axonal volume of white matter tracts•These measures are kept distinct from their probability (unlike prob. streamlines).•Incorporates downstream voxels and conditional probabilities of nearby tracts•Could be used on multi-shell acquisitions with appropriate signal model•Complex fibre regions are inferred more accurately than streamline methods.</description><subject>Algorithms</subject><subject>Diffusion</subject><subject>Diffusion Magnetic Resonance Imaging - methods</subject><subject>Fourier Analysis</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>Models, Statistical</subject><subject>Nerve Fibers, Myelinated</subject><subject>Neural Pathways - anatomy & histology</subject><subject>Probability</subject><subject>White Matter - anatomy & histology</subject><issn>1053-8119</issn><issn>1095-9572</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkcFu1DAQhiMEoqXwCsgSl3LI4nHixOZWqpZWKkKiy9ny2pPiJY4XO9l2H4M3xum2IHEByZIt6__nn5mvKAjQBVBo3q0XA04xOK9vcMEo8AXNR9InxSFQyUvJW_Z0fvOqFADyoHiR0ppSKqEWz4sD1tCWsoYfFj_PwxQdRrKM2ozkWvtN74Ybcpz_l9dv35MT0kXt8TbE76QLkTi_iWGLlrihw4iDQRI6cvvNjUi8HsdcapxLpewLnljXdVNyYSCfvlyS1Y7gXQ4wbux3xAeL_X3avYNsQz95fFk863Sf8NXDfVR8PT9bnl6UV58_Xp6eXJWmFnwseYW6toDIaGVqyRkwaVe2qgyv84q0AGYapldVLQFFi6yTaLlsa45M2Kqtjorjfd08z48J06i8SyY3pAcMU1LQcmBQN6L5DykI2ja5gyx985d0nRc85EEUCEFpzaERWSX2KhNDShE7tYkZZtwpoGomrNbqD2E1E1Y0H0mz9fVDwLTyaH8bH5FmwYe9APPythmtSsbNnKyLaEZlg_t3yi8XFbzU</recordid><startdate>20151015</startdate><enddate>20151015</enddate><creator>Close, Thomas G.</creator><creator>Tournier, Jacques-Donald</creator><creator>Johnston, Leigh A.</creator><creator>Calamante, Fernando</creator><creator>Mareels, Iven</creator><creator>Connelly, Alan</creator><general>Elsevier Inc</general><general>Elsevier Limited</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>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>7QO</scope><orcidid>https://orcid.org/0000-0002-4160-2134</orcidid></search><sort><creationdate>20151015</creationdate><title>Fourier Tract Sampling (FouTS): A framework for improved inference of white matter tracts from diffusion MRI by explicitly modelling tract volume</title><author>Close, Thomas G. ; Tournier, Jacques-Donald ; Johnston, Leigh A. ; Calamante, Fernando ; Mareels, Iven ; Connelly, Alan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c485t-53ea4d1ee203c4952129dbd33c54016a812c62ab3491e87e2f9ed59745e28d373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Algorithms</topic><topic>Diffusion</topic><topic>Diffusion Magnetic Resonance Imaging - methods</topic><topic>Fourier Analysis</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted - methods</topic><topic>Models, Statistical</topic><topic>Nerve Fibers, Myelinated</topic><topic>Neural Pathways - anatomy & histology</topic><topic>Probability</topic><topic>White Matter - anatomy & histology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Close, Thomas G.</creatorcontrib><creatorcontrib>Tournier, Jacques-Donald</creatorcontrib><creatorcontrib>Johnston, Leigh A.</creatorcontrib><creatorcontrib>Calamante, Fernando</creatorcontrib><creatorcontrib>Mareels, Iven</creatorcontrib><creatorcontrib>Connelly, Alan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><jtitle>NeuroImage (Orlando, Fla.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Close, Thomas G.</au><au>Tournier, Jacques-Donald</au><au>Johnston, Leigh A.</au><au>Calamante, Fernando</au><au>Mareels, Iven</au><au>Connelly, Alan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fourier Tract Sampling (FouTS): A framework for improved inference of white matter tracts from diffusion MRI by explicitly modelling tract volume</atitle><jtitle>NeuroImage (Orlando, Fla.)</jtitle><addtitle>Neuroimage</addtitle><date>2015-10-15</date><risdate>2015</risdate><volume>120</volume><spage>412</spage><epage>427</epage><pages>412-427</pages><issn>1053-8119</issn><eissn>1095-9572</eissn><abstract>Diffusion MRI tractography algorithm development is increasingly moving towards global techniques to incorporate “downstream” information and conditional probabilities between neighbouring tracts. Such approaches also enable white matter to be represented more tangibly than the abstract lines generated by the most common approaches to fibre tracking. However, previously proposed algorithms still use fibre-like models of white matter corresponding to thin strands of white matter tracts rather than the tracts themselves, and therefore require many components for accurate representations, which leads to poorly constrained inverse problems. We propose a novel tract-based model of white matter, the ‘Fourier tract’, which is able to represent rich tract shapes with a relatively low number of parameters, and explicitly decouples the spatial extent of the modelled tract from its ‘Apparent Connection Strength (ACS)’. The Fourier tract model is placed within a novel Bayesian framework, which relates the tract parameters directly to the observed signal, enabling a wide range of acquisition schemes to be used. The posterior distribution of the Bayesian framework is characterised via Markov-chain Monte-Carlo sampling to infer probable values of the ACS and spatial extent of the imaged white matter tracts, providing measures that can be directly applied to many research and clinical studies. The robustness of the proposed tractography algorithm is demonstrated on simulated basic tract configurations, such as curving, twisting, crossing and kissing tracts, and sections of more complex numerical phantoms. As an illustration of the approach in vivo, fibre tracking is performed on a central section of the brain in three subjects from 60 direction HARDI datasets.
•Infers spatial extent and approximate intra-axonal volume of white matter tracts•These measures are kept distinct from their probability (unlike prob. streamlines).•Incorporates downstream voxels and conditional probabilities of nearby tracts•Could be used on multi-shell acquisitions with appropriate signal model•Complex fibre regions are inferred more accurately than streamline methods.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26070265</pmid><doi>10.1016/j.neuroimage.2015.05.090</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-4160-2134</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Algorithms Diffusion Diffusion Magnetic Resonance Imaging - methods Fourier Analysis Humans Image Processing, Computer-Assisted - methods Models, Statistical Nerve Fibers, Myelinated Neural Pathways - anatomy & histology Probability White Matter - anatomy & histology |
title | Fourier Tract Sampling (FouTS): A framework for improved inference of white matter tracts from diffusion MRI by explicitly modelling tract volume |
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