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Statistical performance analysis of signal variance-based dipole models for MEG/EEG source localization and detection
A set of dipole fitting algorithms that incorporate different assumptions about the variability of the signal component into their mathematical models is presented and analyzed. Dipole fitting is performed by minimizing the squared error between the selected data model and available data. Dipole mod...
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Published in: | IEEE transactions on biomedical engineering 2003-02, Vol.50 (2), p.137-149 |
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description | A set of dipole fitting algorithms that incorporate different assumptions about the variability of the signal component into their mathematical models is presented and analyzed. Dipole fitting is performed by minimizing the squared error between the selected data model and available data. Dipole models based on moments that have 1) constant amplitude and orientation, 2) variable amplitude and fixed known orientation, 3) variable amplitude and fixed unknown orientation, and 4) variable amplitude and variable orientation are considered. The presence of a dipolar source is determined by comparing the fractional energy explained by the dipole model to a threshold. Source localization is accomplished by searching to find the location that explains the largest fractional signal energy using a dipole model. Expressions for the probability of a false positive decision and probability of correct detection are derived and used to evaluate the effect of variability in the dipole on performance and to address the effects of model mismatch and location errors. Simulated and measured data experiments are presented to illustrate the performance of both detection and localization methods. The results indicate that models which account for variance outperform the constant orientation and magnitude model even when the number of observations is relatively small and the signal of interest contains a very modest variance component. |
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Dipole fitting is performed by minimizing the squared error between the selected data model and available data. Dipole models based on moments that have 1) constant amplitude and orientation, 2) variable amplitude and fixed known orientation, 3) variable amplitude and fixed unknown orientation, and 4) variable amplitude and variable orientation are considered. The presence of a dipolar source is determined by comparing the fractional energy explained by the dipole model to a threshold. Source localization is accomplished by searching to find the location that explains the largest fractional signal energy using a dipole model. Expressions for the probability of a false positive decision and probability of correct detection are derived and used to evaluate the effect of variability in the dipole on performance and to address the effects of model mismatch and location errors. Simulated and measured data experiments are presented to illustrate the performance of both detection and localization methods. The results indicate that models which account for variance outperform the constant orientation and magnitude model even when the number of observations is relatively small and the signal of interest contains a very modest variance component.</description><identifier>ISSN: 0018-9294</identifier><identifier>EISSN: 1558-2531</identifier><identifier>DOI: 10.1109/TBME.2002.807661</identifier><identifier>PMID: 12665027</identifier><identifier>CODEN: IEBEAX</identifier><language>eng</language><publisher>New York, NY: IEEE</publisher><subject>Action Potentials - physiology ; Algorithm design and analysis ; Algorithms ; Biological and medical sciences ; Brain Mapping - methods ; Brain modeling ; Computer Simulation ; Delay ; Electroencephalography ; Electroencephalography - methods ; Electromagnetic Fields ; Epilepsy ; Epilepsy - physiopathology ; False Positive Reactions ; Humans ; Magnetoencephalography - methods ; Mathematical model ; Mathematical models ; Medical sciences ; Models, Neurological ; Models, Statistical ; Morphology ; Neurons - physiology ; Performance analysis ; Quality Control ; Reproducibility of Results ; Sensitivity and Specificity ; Signal analysis ; Signal detection ; Stochastic Processes</subject><ispartof>IEEE transactions on biomedical engineering, 2003-02, Vol.50 (2), p.137-149</ispartof><rights>2003 INIST-CNRS</rights><rights>Copyright The Institute of Electrical and Electronics Engineers, Inc. (IEEE) 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-b7c3b833b1111bbd8147aba5626eeb65859ca18f25e2a5cee5fa341e942054533</citedby><cites>FETCH-LOGICAL-c479t-b7c3b833b1111bbd8147aba5626eeb65859ca18f25e2a5cee5fa341e942054533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://ieeexplore.ieee.org/document/1185137$$EHTML$$P50$$Gieee$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,54796</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14603476$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12665027$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rodriguez-Rivera, A.</creatorcontrib><creatorcontrib>Van Veen, B.D.</creatorcontrib><creatorcontrib>Wakai, R.T.</creatorcontrib><title>Statistical performance analysis of signal variance-based dipole models for MEG/EEG source localization and detection</title><title>IEEE transactions on biomedical engineering</title><addtitle>TBME</addtitle><addtitle>IEEE Trans Biomed Eng</addtitle><description>A set of dipole fitting algorithms that incorporate different assumptions about the variability of the signal component into their mathematical models is presented and analyzed. Dipole fitting is performed by minimizing the squared error between the selected data model and available data. Dipole models based on moments that have 1) constant amplitude and orientation, 2) variable amplitude and fixed known orientation, 3) variable amplitude and fixed unknown orientation, and 4) variable amplitude and variable orientation are considered. The presence of a dipolar source is determined by comparing the fractional energy explained by the dipole model to a threshold. Source localization is accomplished by searching to find the location that explains the largest fractional signal energy using a dipole model. Expressions for the probability of a false positive decision and probability of correct detection are derived and used to evaluate the effect of variability in the dipole on performance and to address the effects of model mismatch and location errors. Simulated and measured data experiments are presented to illustrate the performance of both detection and localization methods. The results indicate that models which account for variance outperform the constant orientation and magnitude model even when the number of observations is relatively small and the signal of interest contains a very modest variance component.</description><subject>Action Potentials - physiology</subject><subject>Algorithm design and analysis</subject><subject>Algorithms</subject><subject>Biological and medical sciences</subject><subject>Brain Mapping - methods</subject><subject>Brain modeling</subject><subject>Computer Simulation</subject><subject>Delay</subject><subject>Electroencephalography</subject><subject>Electroencephalography - methods</subject><subject>Electromagnetic Fields</subject><subject>Epilepsy</subject><subject>Epilepsy - physiopathology</subject><subject>False Positive Reactions</subject><subject>Humans</subject><subject>Magnetoencephalography - methods</subject><subject>Mathematical model</subject><subject>Mathematical models</subject><subject>Medical sciences</subject><subject>Models, Neurological</subject><subject>Models, Statistical</subject><subject>Morphology</subject><subject>Neurons - physiology</subject><subject>Performance analysis</subject><subject>Quality Control</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Signal analysis</subject><subject>Signal detection</subject><subject>Stochastic Processes</subject><issn>0018-9294</issn><issn>1558-2531</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqFkc-L1DAYhoMo7rh6FwQJgnrqbH4nPepSR2EXD67nkqZfJUs7GZNWWP96vzIDAx40l_CR530D30PIS862nLP66u7jbbMVjImtY9YY_ohsuNauElryx2TDGHdVLWp1QZ6Vco-jcso8JRdcGKOZsBuyfJv9HMscgx_pAfKQ8uT3Aajf-_GhxELTQEv8gRP95XNc36rOF-hpHw9pBDqlHsZCMUhvm91V0-xoSUvGijFhafyN_WmPfZiAGcI6PSdPBj8WeHG6L8n3T83d9efq5uvuy_WHmyooW89VZ4PsnJQdx9N1vePK-s5rIwxAZ7TTdfDcDUKD8DoA6MFLxaFWgmmlpbwk74-9h5x-LlDmdoolwDj6PaSltM5JppR1Csl3_yStxN1ZJf8LCmeEkNwi-OYv8B7Xgntcv1VSW8E5QuwIhZxKyTC0hxwnnx9aztpVcbsqblfF7VExRl6fepdugv4cODlF4O0J8AUFDBmdxXLmlGFSWYPcqyMXAeD8zJ3m0so_nCu25Q</recordid><startdate>20030201</startdate><enddate>20030201</enddate><creator>Rodriguez-Rivera, A.</creator><creator>Van Veen, B.D.</creator><creator>Wakai, R.T.</creator><general>IEEE</general><general>Institute of Electrical and Electronics Engineers</general><general>The Institute of Electrical and Electronics Engineers, Inc. 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physiology</topic><topic>Algorithm design and analysis</topic><topic>Algorithms</topic><topic>Biological and medical sciences</topic><topic>Brain Mapping - methods</topic><topic>Brain modeling</topic><topic>Computer Simulation</topic><topic>Delay</topic><topic>Electroencephalography</topic><topic>Electroencephalography - methods</topic><topic>Electromagnetic Fields</topic><topic>Epilepsy</topic><topic>Epilepsy - physiopathology</topic><topic>False Positive Reactions</topic><topic>Humans</topic><topic>Magnetoencephalography - methods</topic><topic>Mathematical model</topic><topic>Mathematical models</topic><topic>Medical sciences</topic><topic>Models, Neurological</topic><topic>Models, Statistical</topic><topic>Morphology</topic><topic>Neurons - physiology</topic><topic>Performance analysis</topic><topic>Quality Control</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Signal analysis</topic><topic>Signal detection</topic><topic>Stochastic Processes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rodriguez-Rivera, A.</creatorcontrib><creatorcontrib>Van Veen, B.D.</creatorcontrib><creatorcontrib>Wakai, R.T.</creatorcontrib><collection>IEEE All-Society Periodicals Package (ASPP) 1998-Present</collection><collection>IEEE Xplore (Online service)</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts – Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><jtitle>IEEE transactions on biomedical engineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rodriguez-Rivera, A.</au><au>Van Veen, B.D.</au><au>Wakai, R.T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Statistical performance analysis of signal variance-based dipole models for MEG/EEG source localization and detection</atitle><jtitle>IEEE transactions on biomedical engineering</jtitle><stitle>TBME</stitle><addtitle>IEEE Trans Biomed Eng</addtitle><date>2003-02-01</date><risdate>2003</risdate><volume>50</volume><issue>2</issue><spage>137</spage><epage>149</epage><pages>137-149</pages><issn>0018-9294</issn><eissn>1558-2531</eissn><coden>IEBEAX</coden><abstract>A set of dipole fitting algorithms that incorporate different assumptions about the variability of the signal component into their mathematical models is presented and analyzed. Dipole fitting is performed by minimizing the squared error between the selected data model and available data. Dipole models based on moments that have 1) constant amplitude and orientation, 2) variable amplitude and fixed known orientation, 3) variable amplitude and fixed unknown orientation, and 4) variable amplitude and variable orientation are considered. The presence of a dipolar source is determined by comparing the fractional energy explained by the dipole model to a threshold. Source localization is accomplished by searching to find the location that explains the largest fractional signal energy using a dipole model. Expressions for the probability of a false positive decision and probability of correct detection are derived and used to evaluate the effect of variability in the dipole on performance and to address the effects of model mismatch and location errors. Simulated and measured data experiments are presented to illustrate the performance of both detection and localization methods. The results indicate that models which account for variance outperform the constant orientation and magnitude model even when the number of observations is relatively small and the signal of interest contains a very modest variance component.</abstract><cop>New York, NY</cop><pub>IEEE</pub><pmid>12665027</pmid><doi>10.1109/TBME.2002.807661</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Action Potentials - physiology Algorithm design and analysis Algorithms Biological and medical sciences Brain Mapping - methods Brain modeling Computer Simulation Delay Electroencephalography Electroencephalography - methods Electromagnetic Fields Epilepsy Epilepsy - physiopathology False Positive Reactions Humans Magnetoencephalography - methods Mathematical model Mathematical models Medical sciences Models, Neurological Models, Statistical Morphology Neurons - physiology Performance analysis Quality Control Reproducibility of Results Sensitivity and Specificity Signal analysis Signal detection Stochastic Processes |
title | Statistical performance analysis of signal variance-based dipole models for MEG/EEG source localization and detection |
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