Effects of hardware heterogeneity on the performance of SVM Alzheimer's disease classifier

Fully automated machine learning methods based on structural magnetic resonance imaging (MRI) data can assist radiologists in the diagnosis of Alzheimer's disease (AD). These algorithms require large data sets to learn the separation of subjects with and without AD. Training and test data may c...

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Published inNeuroImage (Orlando, Fla.) Vol. 58; no. 3; pp. 785 - 792
Main Authors Abdulkadir, Ahmed, Mortamet, Bénédicte, Vemuri, Prashanthi, Jack, Clifford R., Krueger, Gunnar, Klöppel, Stefan
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.10.2011
Elsevier Limited
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Abstract Fully automated machine learning methods based on structural magnetic resonance imaging (MRI) data can assist radiologists in the diagnosis of Alzheimer's disease (AD). These algorithms require large data sets to learn the separation of subjects with and without AD. Training and test data may come from heterogeneous hardware settings, which can potentially affect the performance of disease classification. A total of 518 MRI sessions from 226 healthy controls and 191 individuals with probable AD from the multicenter Alzheimer's Disease Neuroimaging Initiative (ADNI) were used to investigate whether grouping data by acquisition hardware (i.e. vendor, field strength, coil system) is beneficial for the performance of a support vector machine (SVM) classifier, compared to the case where data from different hardware is mixed. We compared the change of the SVM decision value resulting from (a) changes in hardware against the effect of disease and (b) changes resulting simply from rescanning the same subject on the same machine. Maximum accuracy of 87% was obtained with a training set of all 417 subjects. Classifiers trained with 95 subjects in each diagnostic group and acquired with heterogeneous scanner settings had an empirical detection accuracy of 84.2±2.4% when tested on an independent set of the same size. These results mirror the accuracy reported in recent studies. Encouragingly, classifiers trained on images acquired with homogenous and heterogeneous hardware settings had equivalent cross-validation performances. Two scans of the same subject acquired on the same machine had very similar decision values and were generally classified into the same group. Higher variation was introduced when two acquisitions of the same subject were performed on two scanners with different field strengths. The variation was unbiased and similar for both diagnostic groups. The findings of the study encourage the pooling of data from different sites to increase the number of training samples and thereby improving performance of disease classifiers. Although small, a change in hardware could lead to a change of the decision value and thus diagnostic grouping. The findings of this study provide estimators for diagnostic accuracy of an automated disease diagnosis method involving scans acquired with different sets of hardware. Furthermore, we show that the level of confidence in the performance estimation significantly depends on the size of the training sample, and hence should be taken into account in a clinical setting. ► MRI data from multiple scanners was used to asses performance of disease classifier. ► Larger training sets led to higher performance and smaller confidence intervals. ► Scanning subjects on different systems introduced variance. ► No systematic effect due to change in field strength was found. ► For the presented setting, pooling of data was beneficial for the performance.
AbstractList Fully automated machine learning methods based on structural magnetic resonance imaging (MRI) data can assist radiologists in the diagnosis of Alzheimer's disease (AD). These algorithms require large data sets to learn the separation of subjects with and without AD. Training and test data may come from heterogeneous hardware settings, which can potentially affect the performance of disease classification. A total of 518 MRI sessions from 226 healthy controls and 191 individuals with probable AD from the multicenter Alzheimer's Disease Neuroimaging Initiative (ADNI) were used to investigate whether grouping data by acquisition hardware (i.e. vendor, field strength, coil system) is beneficial for the performance of a support vector machine (SVM) classifier, compared to the case where data from different hardware is mixed. We compared the change of the SVM decision value resulting from (a) changes in hardware against the effect of disease and (b) changes resulting simply from rescanning the same subject on the same machine. Maximum accuracy of 87% was obtained with a training set of all 417 subjects. Classifiers trained with 95 subjects in each diagnostic group and acquired with heterogeneous scanner settings had an empirical detection accuracy of 84.2±2.4% when tested on an independent set of the same size. These results mirror the accuracy reported in recent studies. Encouragingly, classifiers trained on images acquired with homogenous and heterogeneous hardware settings had equivalent cross-validation performances. Two scans of the same subject acquired on the same machine had very similar decision values and were generally classified into the same group. Higher variation was introduced when two acquisitions of the same subject were performed on two scanners with different field strengths. The variation was unbiased and similar for both diagnostic groups. The findings of the study encourage the pooling of data from different sites to increase the number of training samples and thereby improving performance of disease classifiers. Although small, a change in hardware could lead to a change of the decision value and thus diagnostic grouping. The findings of this study provide estimators for diagnostic accuracy of an automated disease diagnosis method involving scans acquired with different sets of hardware. Furthermore, we show that the level of confidence in the performance estimation significantly depends on the size of the training sample, and hence should be taken into account in a clinical setting. ► MRI data from multiple scanners was used to asses performance of disease classifier. ► Larger training sets led to higher performance and smaller confidence intervals. ► Scanning subjects on different systems introduced variance. ► No systematic effect due to change in field strength was found. ► For the presented setting, pooling of data was beneficial for the performance.
Fully automated machine learning methods based on structural magnetic resonance imaging (MRI) data can assist radiologists in the diagnosis of Alzheimer's disease (AD). These algorithms require large data sets to learn the separation of subjects with and without AD. Training and test data may come from heterogeneous hardware settings, which can potentially affect the performance of disease classification. A total of 518 MRI sessions from 226 healthy controls and 191 individuals with probable AD from the multicenter Alzheimer's Disease Neuroimaging Initiative (ADNI) were used to investigate whether grouping data by acquisition hardware (i.e. vendor, field strength, coil system) is beneficial for the performance of a support vector machine (SVM) classifier, compared to the case where data from different hardware is mixed. We compared the change of the SVM decision value resulting from (a) changes in hardware against the effect of disease and (b) changes resulting simply from rescanning the same subject on the same machine. Maximum accuracy of 87% was obtained with a training set of all 417 subjects. Classifiers trained with 95 subjects in each diagnostic group and acquired with heterogeneous scanner settings had an empirical detection accuracy of 84.2±2.4% when tested on an independent set of the same size. These results mirror the accuracy reported in recent studies. Encouragingly, classifiers trained on images acquired with homogenous and heterogeneous hardware settings had equivalent cross-validation performances. Two scans of the same subject acquired on the same machine had very similar decision values and were generally classified into the same group. Higher variation was introduced when two acquisitions of the same subject were performed on two scanners with different field strengths. The variation was unbiased and similar for both diagnostic groups. The findings of the study encourage the pooling of data from different sites to increase the number of training samples and thereby improving performance of disease classifiers. Although small, a change in hardware could lead to a change of the decision value and thus diagnostic grouping. The findings of this study provide estimators for diagnostic accuracy of an automated disease diagnosis method involving scans acquired with different sets of hardware. Furthermore, we show that the level of confidence in the performance estimation significantly depends on the size of the training sample, and hence should be taken into account in a clinical setting.
Fully automated machine learning methods based on structural magnetic resonance imaging (MRI) data can assist radiologists in the diagnosis of Alzheimer's disease (AD). These algorithms require large data sets to learn the separation of subjects with and without AD. Training and test data may come from heterogeneous hardware settings, which can potentially affect the performance of disease classification. A total of 518 MRI sessions from 226 healthy controls and 191 individuals with probable AD from the multicenter Alzheimer's Disease Neuroimaging Initiative (ADNI) were used to investigate whether grouping data by acquisition hardware (i.e. vendor, field strength, coil system) is beneficial for the performance of a support vector machine (SVM) classifier, compared to the case where data from different hardware is mixed. We compared the change of the SVM decision value resulting from (a) changes in hardware against the effect of disease and (b) changes resulting simply from rescanning the same subject on the same machine. Maximum accuracy of 87% was obtained with a training set of all 417 subjects. Classifiers trained with 95 subjects in each diagnostic group and acquired with heterogeneous scanner settings had an empirical detection accuracy of 84.2±2.4% when tested on an independent set of the same size. These results mirror the accuracy reported in recent studies. Encouragingly, classifiers trained on images acquired with homogenous and heterogeneous hardware settings had equivalent cross-validation performances. Two scans of the same subject acquired on the same machine had very similar decision values and were generally classified into the same group. Higher variation was introduced when two acquisitions of the same subject were performed on two scanners with different field strengths. The variation was unbiased and similar for both diagnostic groups. The findings of the study encourage the pooling of data from different sites to increase the number of training samples and thereby improving performance of disease classifiers. Although small, a change in hardware could lead to a change of the decision value and thus diagnostic grouping. The findings of this study provide estimators for diagnostic accuracy of an automated disease diagnosis method involving scans acquired with different sets of hardware. Furthermore, we show that the level of confidence in the performance estimation significantly depends on the size of the training sample, and hence should be taken into account in a clinical setting.Fully automated machine learning methods based on structural magnetic resonance imaging (MRI) data can assist radiologists in the diagnosis of Alzheimer's disease (AD). These algorithms require large data sets to learn the separation of subjects with and without AD. Training and test data may come from heterogeneous hardware settings, which can potentially affect the performance of disease classification. A total of 518 MRI sessions from 226 healthy controls and 191 individuals with probable AD from the multicenter Alzheimer's Disease Neuroimaging Initiative (ADNI) were used to investigate whether grouping data by acquisition hardware (i.e. vendor, field strength, coil system) is beneficial for the performance of a support vector machine (SVM) classifier, compared to the case where data from different hardware is mixed. We compared the change of the SVM decision value resulting from (a) changes in hardware against the effect of disease and (b) changes resulting simply from rescanning the same subject on the same machine. Maximum accuracy of 87% was obtained with a training set of all 417 subjects. Classifiers trained with 95 subjects in each diagnostic group and acquired with heterogeneous scanner settings had an empirical detection accuracy of 84.2±2.4% when tested on an independent set of the same size. These results mirror the accuracy reported in recent studies. Encouragingly, classifiers trained on images acquired with homogenous and heterogeneous hardware settings had equivalent cross-validation performances. Two scans of the same subject acquired on the same machine had very similar decision values and were generally classified into the same group. Higher variation was introduced when two acquisitions of the same subject were performed on two scanners with different field strengths. The variation was unbiased and similar for both diagnostic groups. The findings of the study encourage the pooling of data from different sites to increase the number of training samples and thereby improving performance of disease classifiers. Although small, a change in hardware could lead to a change of the decision value and thus diagnostic grouping. The findings of this study provide estimators for diagnostic accuracy of an automated disease diagnosis method involving scans acquired with different sets of hardware. Furthermore, we show that the level of confidence in the performance estimation significantly depends on the size of the training sample, and hence should be taken into account in a clinical setting.
Fully automated machine learning methods based on structural magnetic resonance imaging (MRI) data can assist radiologists in the diagnosis of Alzheimer’s disease (AD). These algorithms require large data sets to learn the separation of subjects with and without AD. Training and test data may come from heterogeneous hardware settings, which can potentially affect the performance of disease classification. A total of 518 MRI sessions from 226 healthy controls and 191 individuals with probable AD from the multicenter Alzheimer’s Disease Neuroimaging Initiative (ADNI) were used to investigate whether grouping data by acquisition hardware (i.e. vendor, field strength, coil system) is beneficial for the performance of a support vector machine (SVM) classifier, compared to the case where data from different hardware is mixed. We compared the change of the SVM decision value resulting from (a) changes in hardware against the effect of disease and (b) changes resulting simply from rescanning the same subject on the same machine. Maximum accuracy of 87% was obtained with a training set of all 417 subjects. Classifiers trained with 95 subjects in each diagnostic group and acquired with heterogeneous scanner settings had an empirical detection accuracy of 84.2±2.4% when tested on an independent set of the same size. These results mirror the accuracy reported in recent studies. Encouragingly, classifiers trained on images acquired with homogenous and heterogeneous hardware settings had equivalent cross-validation performances. Two scans of the same subject acquired on the same machine had very similar decision values and were generally classified into the same group. Higher variation was introduced when two acquisitions of the same subject were performed on two scanners with different field strengths. The variation was unbiased and similar for both diagnostic groups. The findings of the study encourage the pooling of data from different sites to increase the number of training samples and thereby improving performance of disease classifiers. Although small, a change in hardware could lead to a change of the decision value and thus diagnostic grouping. The findings of this study provide estimators for diagnostic accuracy of an automated disease diagnosis method involving scans acquired with different sets of hardware. Furthermore, we show that the level of confidence in the performance estimation significantly depends on the size of the training sample, and hence should be taken into account in a clinical setting.
Fully automated machine learning methods based on structural magnetic resonance imaging (MRI) data can assist radiologists in the diagnosis of Alzheimer's disease (AD). These algorithms require large data sets to learn the separation of subjects with and without AD. Training and test data may come from heterogeneous hardware settings, which can potentially affect the performance of disease classification. A total of 518 MRI sessions from 226 healthy controls and 191 individuals with probable AD from the multicenter Alzheimer's Disease Neuroimaging Initiative (ADNI) were used to investigate whether grouping data by acquisition hardware (i.e. vendor, field strength, coil system) is beneficial for the performance of a support vector machine (SVM) classifier, compared to the case where data from different hardware is mixed. We compared the change of the SVM decision value resulting from (a) changes in hardware against the effect of disease and (b) changes resulting simply from rescanning the same subject on the same machine. Maximum accuracy of 87% was obtained with a training set of all 417 subjects. Classifiers trained with 95 subjects in each diagnostic group and acquired with heterogeneous scanner settings had an empirical detection accuracy of 84.2 +/- 2.4% when tested on an independent set of the same size. These results mirror the accuracy reported in recent studies. Encouragingly, classifiers trained on images acquired with homogenous and heterogeneous hardware settings had equivalent cross-validation performances. Two scans of the same subject acquired on the same machine had very similar decision values and were generally classified into the same group. Higher variation was introduced when two acquisitions of the same subject were performed on two scanners with different field strengths. The variation was unbiased and similar for both diagnostic groups. The findings of the study encourage the pooling of data from different sites to increase the number of training samples and thereby improving performance of disease classifiers. Although small, a change in hardware could lead to a change of the decision value and thus diagnostic grouping. The findings of this study provide estimators for diagnostic accuracy of an automated disease diagnosis method involving scans acquired with different sets of hardware. Furthermore, we show that the level of confidence in the performance estimation significantly depends on the size of the training sample, and hence should be taken into account in a clinical setting.
Author Klöppel, Stefan
Jack, Clifford R.
Vemuri, Prashanthi
Krueger, Gunnar
Mortamet, Bénédicte
Abdulkadir, Ahmed
AuthorAffiliation c Department of Radiology, Mayo Clinic, Rochester, MN, USA
a Department of Psychiatry and Psychotherapy, Section of Gerontopsychiatry and Neuropsychology, Freiburg Brain Imaging, University Medical Center Freiburg, Freiburg, Germany
b Advanced Clinical Imaging Technology, Siemens Suisse SA, Healthcare Sector IM&WS-Centre d’Imagerie Biomédicale (CIBM), Lausanne, Switzerland
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/21708272$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1006/nimg.2001.0848
10.1016/j.neuroimage.2007.07.007
10.1006/nimg.2000.0582
10.1385/JMN:17:2:101
10.1016/j.neuroimage.2007.09.073
10.1007/s00234-008-0463-x
10.1016/j.neuroimage.2010.01.005
10.1016/S0140-6736(96)05228-2
10.1212/WNL.42.1.183
10.1016/j.neuroimage.2009.11.046
10.1186/1471-2342-9-8
10.1016/j.nic.2005.09.008
10.1016/j.neuroimage.2007.10.051
10.1002/hbm.20599
10.1002/jmri.21049
10.1093/brain/awm112
10.1007/BF00308809
10.1212/WNL.34.7.939
10.1016/j.neuroimage.2005.02.018
10.1093/brain/awm319
10.1016/j.neuroimage.2010.06.013
10.1016/j.neuroimage.2009.10.066
10.1016/j.neuroimage.2007.09.066
10.1118/1.3116776
10.1016/j.neuroimage.2008.02.003
ContentType Journal Article
Copyright 2011 Elsevier Inc.
Copyright © 2011 Elsevier Inc. All rights reserved.
Copyright Elsevier Limited Oct 1, 2011
2011 Elsevier Inc. All rights reserved. 2011
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CorporateAuthor The Alzheimer's Disease Neuroimaging Initiative
Alzheimer's Disease Neuroimaging Initiative
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Research Support, N.I.H., Extramural
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Issue 3
Keywords Magnetic resonance imaging
MRI
Alzheimer's disease
Support vector machines (SVM)
Multi-site study
Language English
License Copyright © 2011 Elsevier Inc. All rights reserved.
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content type line 14
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These authors contributed equally to this work.
Data used in the preparation of this article were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database (http://www.loni.ucla.edu/ADNI). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. ADNI investigators include (complete listing available at: http://adni.loni.ucla.edu/wp-content/uploads/how_to_apply/ADNI_Authorship_List.pdf).
OpenAccessLink https://www.ncbi.nlm.nih.gov/pmc/articles/3258661
PMID 21708272
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References Ashburner (bb0010) 2007; 38
Braak, Braak (bb0035) 1991; 82
Gunter, Bernstein, Borowski, Ward, Britson, Felmlee, Schuff, Weiner, Jack (bb0060) 2009; 36
Huppertz, Kröll-Seger, Klöppel, Ganz, Kassubek (bb0065) 2010; 49
Mueller, Weiner, Thal, Petersen, Jack, Jagust, Trojanowski, Toga, Beckett (bb0115) 2005; 15
Vapnik (bb0135) 1998
Boser, Guyon, Vapnik (bb0030) 1992
Jack, Petersen, O'Brien, Tangalos (bb0070) 1992; 42
Shuter, Yeh, Graham, Au, Wang (bb0125) 2008; 41
McKhann, Drachman, Folstein, Katzman, Price, Stadlan (bb0100) 1984; 34
Acosta-Cabronero, Williams, Pereira, Pengas, Nestor (bb0005) 2008; 39
Klöppel, Stonnington, Chu, Draganski, Scahill, Rohrer, Fox, Jack, Ashburner, Frackowiak (bb0085) 2008; 131
Jack, Bernstein, Fox, Thompson, Alexander, Harvey, Borowski, Britson, Whitwell, Ward, Dale, Felmlee, Gunter, Hill, Killiany, Schuff, Fox-Bosetti, Lin, Studholme, DeCarli, Krueger, Ward, Metzger, Scott, Mallozzi, Blezek, Levy, Debbins, Fleisher, Albert, Green, Bartzokis, Glover, Mugler, Weiner (bb0075) 2008; 27
Klöppel, Stonnington, Chu, Draganski, Scahill, Rohrer, Fox, Ashburner, Frackowiak (bb0090) 2009; 132
Vemuri, Gunter, Senjem, Whitwell, Kantarci, Knopman, Boeve, Petersen, Jack (bb0140) 2008; 39
Klauschen, Goldman, Barra, Meyer-Lindenberg, Lundervold (bb0080) 2009; 30
Fox, Freeborough, Rossor (bb0050) 1996; 348
Ashburner, Friston (bb0015) 2000; 11
Moorhead, Gountouna, Job, McIntosh, Romaniuk, Lymer, Whalley, Waiter, Brennan, Ahearn, Cavanagh, Condon, Steele, Wardlaw, Lawrie (bb0105) 2009; 9
Cuingnet, Gérardin, Tessieras, Auzias, Lehéricy, Habert, Chupin, Benali, Colliot, Alzheimer's Disease Neuroimaging Initiative (bb0045) 2011; 56
Magnin, Mesrob, Kinkingnéhun, Pélégrini-Issac, Colliot, Sarazin, Dubois, Lehéricy, Benali (bb0095) 2009; 51
Ashburner, Friston (bb0020) 2005; 26
Cortes, Vapnik (bb0150) 1995; 20
Stonnington, Tan, Klöppel, Chu, Draganski, Jack, Chen, Ashburner, Frackowiak (bb0130) 2008; 39
Morris, Price (bb0110) 2001; 17
Chang, Lin (bb0040) 2001
Franke, Ziegler, Klöppel, Gaser, the Alzheimer's Disease Neuroimaging Initiative (bb0055) 2010; 50
Plant, Teipel, Oswald, Böhm, Meindl, Mourao-Miranda, Bokde, Hampel, Ewers (bb0120) 2010; 50
Whitwell, Przybelski, Weigand, Knopman, Boeve, Petersen, Jack (bb0145) 2007; 130
Baron, Chételat, Desgranges, Perchey, Landeau, de la Sayette, Eustache (bb0025) 2001; 14
Mueller (10.1016/j.neuroimage.2011.06.029_bb0115) 2005; 15
Vemuri (10.1016/j.neuroimage.2011.06.029_bb0140) 2008; 39
Ashburner (10.1016/j.neuroimage.2011.06.029_bb0015) 2000; 11
Shuter (10.1016/j.neuroimage.2011.06.029_bb0125) 2008; 41
Whitwell (10.1016/j.neuroimage.2011.06.029_bb0145) 2007; 130
Ashburner (10.1016/j.neuroimage.2011.06.029_bb0020) 2005; 26
Jack (10.1016/j.neuroimage.2011.06.029_bb0070) 1992; 42
Baron (10.1016/j.neuroimage.2011.06.029_bb0025) 2001; 14
Moorhead (10.1016/j.neuroimage.2011.06.029_bb0105) 2009; 9
Klauschen (10.1016/j.neuroimage.2011.06.029_bb0080) 2009; 30
McKhann (10.1016/j.neuroimage.2011.06.029_bb0100) 1984; 34
Huppertz (10.1016/j.neuroimage.2011.06.029_bb0065) 2010; 49
Plant (10.1016/j.neuroimage.2011.06.029_bb0120) 2010; 50
Cortes (10.1016/j.neuroimage.2011.06.029_bb0150) 1995; 20
Magnin (10.1016/j.neuroimage.2011.06.029_bb0095) 2009; 51
Boser (10.1016/j.neuroimage.2011.06.029_bb0030) 1992
Fox (10.1016/j.neuroimage.2011.06.029_bb0050) 1996; 348
Ashburner (10.1016/j.neuroimage.2011.06.029_bb0010) 2007; 38
Jack (10.1016/j.neuroimage.2011.06.029_bb0075) 2008; 27
Vapnik (10.1016/j.neuroimage.2011.06.029_bb0135) 1998
Cuingnet (10.1016/j.neuroimage.2011.06.029_bb0045) 2011; 56
Chang (10.1016/j.neuroimage.2011.06.029_bb0040)
Franke (10.1016/j.neuroimage.2011.06.029_bb0055) 2010; 50
Braak (10.1016/j.neuroimage.2011.06.029_bb0035) 1991; 82
Klöppel (10.1016/j.neuroimage.2011.06.029_bb0090) 2009; 132
Gunter (10.1016/j.neuroimage.2011.06.029_bb0060) 2009; 36
Morris (10.1016/j.neuroimage.2011.06.029_bb0110) 2001; 17
Klöppel (10.1016/j.neuroimage.2011.06.029_bb0085) 2008; 131
Acosta-Cabronero (10.1016/j.neuroimage.2011.06.029_bb0005) 2008; 39
Stonnington (10.1016/j.neuroimage.2011.06.029_bb0130) 2008; 39
References_xml – volume: 131
  start-page: 681
  year: 2008
  end-page: 689
  ident: bb0085
  article-title: Automatic classification of MR scans in Alzheimer's disease
  publication-title: Brain
– year: 2001
  ident: bb0040
  article-title: LIBSVM: a library for support vector machines
– volume: 50
  start-page: 162
  year: 2010
  end-page: 174
  ident: bb0120
  article-title: Automated detection of brain atrophy patterns based on MRI for the prediction of Alzheimer's disease
  publication-title: Neuroimage
– volume: 49
  start-page: 2216
  year: 2010
  end-page: 2224
  ident: bb0065
  article-title: Intra- and interscanner variability of automated voxel-based volumetry based on a 3D probabilistic atlas of human cerebral structures
  publication-title: Neuroimage
– volume: 51
  start-page: 73
  year: 2009
  end-page: 83
  ident: bb0095
  article-title: Support vector machine-based classification of Alzheimer's disease from whole-brain anatomical MRI
  publication-title: Neuroradiology
– volume: 26
  start-page: 839
  year: 2005
  end-page: 851
  ident: bb0020
  article-title: Unified segmentation
  publication-title: Neuroimage
– volume: 41
  start-page: 371
  year: 2008
  end-page: 379
  ident: bb0125
  article-title: Reproducibility of brain tissue volumes in longitudinal studies: effects of changes in signal-to-noise ratio and scanner software
  publication-title: Neuroimage
– volume: 11
  start-page: 805
  year: 2000
  end-page: 821
  ident: bb0015
  article-title: Voxel-based morphometry — the methods
  publication-title: Neuroimage
– volume: 132
  year: 2009
  ident: bb0090
  article-title: A plea for confidence intervals and consideration of generalizability in diagnostic studies
  publication-title: Brain
– volume: 15
  start-page: 869
  year: 2005
  end-page: 877
  ident: bb0115
  article-title: The Alzheimer's disease neuroimaging initiative
  publication-title: Neuroimaging Clin. N. Am.
– start-page: 144
  year: 1992
  end-page: 152
  ident: bb0030
  article-title: A training algorithm for optimal margin classifiers
  publication-title: Fifth Annual Workshop on Computational Learning Theory, Pittsburgh. ACM
– volume: 39
  start-page: 1654
  year: 2008
  end-page: 1665
  ident: bb0005
  article-title: The impact of skull-stripping and radio-frequency bias correction on grey-matter segmentation for voxel-based morphometry
  publication-title: Neuroimage
– volume: 56
  start-page: 766
  year: 2011
  end-page: 781
  ident: bb0045
  article-title: Automatic classification of patients with Alzheimer's disease from structural MRI: a comparison of ten methods using the ADNI database
  publication-title: Neuroimage
– volume: 39
  start-page: 1186
  year: 2008
  end-page: 1197
  ident: bb0140
  article-title: Alzheimer's disease diagnosis in individual subjects using structural MR images: validation studies
  publication-title: Neuroimage
– volume: 34
  start-page: 939
  year: 1984
  end-page: 944
  ident: bb0100
  article-title: Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's disease
  publication-title: Neurology
– volume: 39
  start-page: 1180
  year: 2008
  end-page: 1185
  ident: bb0130
  article-title: Interpreting scan data acquired from multiple scanners: a study with Alzheimer's disease
  publication-title: Neuroimage
– volume: 82
  start-page: 239
  year: 1991
  end-page: 259
  ident: bb0035
  article-title: Neuropathological stageing of Alzheimer-related changes
  publication-title: Acta Neuropathol.
– year: 1998
  ident: bb0135
  article-title: Statistical Learning Theory
– volume: 27
  start-page: 685
  year: 2008
  end-page: 691
  ident: bb0075
  article-title: The Alzheimer's Disease Neuroimaging Initiative (ADNI): MRI methods
  publication-title: J. Magn. Reson. Imaging
– volume: 17
  start-page: 101
  year: 2001
  end-page: 118
  ident: bb0110
  article-title: Pathologic correlates of nondemented aging, mild cognitive impairment, and early-stage Alzheimer's disease
  publication-title: J. Mol. Neurosci.
– volume: 348
  start-page: 94
  year: 1996
  end-page: 97
  ident: bb0050
  article-title: Visualisation and quantification of rates of atrophy in Alzheimer's disease
  publication-title: Lancet
– volume: 30
  start-page: 1310
  year: 2009
  end-page: 1327
  ident: bb0080
  article-title: Evaluation of automated brain MR image segmentation and volumetry methods
  publication-title: Hum. Brain Mapp.
– volume: 50
  start-page: 883
  year: 2010
  end-page: 892
  ident: bb0055
  article-title: Estimating the age of healthy subjects from T1-weighted MRI scans using kernel methods: exploring the influence of various parameters
  publication-title: Neuroimage
– volume: 38
  start-page: 95
  year: 2007
  end-page: 113
  ident: bb0010
  article-title: A fast diffeomorphic image registration algorithm
  publication-title: Neuroimage
– volume: 42
  start-page: 183
  year: 1992
  end-page: 188
  ident: bb0070
  article-title: MR-based hippocampal volumetry in the diagnosis of Alzheimer's disease
  publication-title: Neurology
– volume: 14
  start-page: 298
  year: 2001
  end-page: 309
  ident: bb0025
  article-title: In vivo mapping of gray matter loss with voxel-based morphometry in mild Alzheimer's disease
  publication-title: Neuroimage
– volume: 20
  start-page: 273
  year: 1995
  end-page: 297
  ident: bb0150
  publication-title: Support-vector networks. Mach. Learn
– volume: 130
  start-page: 1777
  year: 2007
  end-page: 1786
  ident: bb0145
  article-title: 3D maps from multiple MRI illustrate changing atrophy patterns as subjects progress from mild cognitive impairment to Alzheimer's disease
  publication-title: Brain
– volume: 36
  start-page: 2193
  year: 2009
  end-page: 2205
  ident: bb0060
  article-title: Measurement of MRI scanner performance with the ADNI phantom
  publication-title: Med. Phys.
– volume: 9
  start-page: 8
  year: 2009
  ident: bb0105
  article-title: Prospective multi-centre Voxel Based Morphometry study employing scanner specific segmentations: procedure development using CaliBrain structural MRI data
  publication-title: BMC Med. Imaging
– volume: 14
  start-page: 298
  year: 2001
  ident: 10.1016/j.neuroimage.2011.06.029_bb0025
  article-title: In vivo mapping of gray matter loss with voxel-based morphometry in mild Alzheimer's disease
  publication-title: Neuroimage
  doi: 10.1006/nimg.2001.0848
– volume: 132
  year: 2009
  ident: 10.1016/j.neuroimage.2011.06.029_bb0090
  article-title: A plea for confidence intervals and consideration of generalizability in diagnostic studies
  publication-title: Brain
– volume: 38
  start-page: 95
  year: 2007
  ident: 10.1016/j.neuroimage.2011.06.029_bb0010
  article-title: A fast diffeomorphic image registration algorithm
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2007.07.007
– volume: 11
  start-page: 805
  year: 2000
  ident: 10.1016/j.neuroimage.2011.06.029_bb0015
  article-title: Voxel-based morphometry — the methods
  publication-title: Neuroimage
  doi: 10.1006/nimg.2000.0582
– volume: 17
  start-page: 101
  year: 2001
  ident: 10.1016/j.neuroimage.2011.06.029_bb0110
  article-title: Pathologic correlates of nondemented aging, mild cognitive impairment, and early-stage Alzheimer's disease
  publication-title: J. Mol. Neurosci.
  doi: 10.1385/JMN:17:2:101
– year: 1998
  ident: 10.1016/j.neuroimage.2011.06.029_bb0135
– volume: 39
  start-page: 1186
  year: 2008
  ident: 10.1016/j.neuroimage.2011.06.029_bb0140
  article-title: Alzheimer's disease diagnosis in individual subjects using structural MR images: validation studies
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2007.09.073
– volume: 51
  start-page: 73
  year: 2009
  ident: 10.1016/j.neuroimage.2011.06.029_bb0095
  article-title: Support vector machine-based classification of Alzheimer's disease from whole-brain anatomical MRI
  publication-title: Neuroradiology
  doi: 10.1007/s00234-008-0463-x
– volume: 50
  start-page: 883
  year: 2010
  ident: 10.1016/j.neuroimage.2011.06.029_bb0055
  article-title: Estimating the age of healthy subjects from T1-weighted MRI scans using kernel methods: exploring the influence of various parameters
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2010.01.005
– volume: 348
  start-page: 94
  year: 1996
  ident: 10.1016/j.neuroimage.2011.06.029_bb0050
  article-title: Visualisation and quantification of rates of atrophy in Alzheimer's disease
  publication-title: Lancet
  doi: 10.1016/S0140-6736(96)05228-2
– volume: 42
  start-page: 183
  year: 1992
  ident: 10.1016/j.neuroimage.2011.06.029_bb0070
  article-title: MR-based hippocampal volumetry in the diagnosis of Alzheimer's disease
  publication-title: Neurology
  doi: 10.1212/WNL.42.1.183
– ident: 10.1016/j.neuroimage.2011.06.029_bb0040
– volume: 50
  start-page: 162
  year: 2010
  ident: 10.1016/j.neuroimage.2011.06.029_bb0120
  article-title: Automated detection of brain atrophy patterns based on MRI for the prediction of Alzheimer's disease
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2009.11.046
– volume: 9
  start-page: 8
  year: 2009
  ident: 10.1016/j.neuroimage.2011.06.029_bb0105
  article-title: Prospective multi-centre Voxel Based Morphometry study employing scanner specific segmentations: procedure development using CaliBrain structural MRI data
  publication-title: BMC Med. Imaging
  doi: 10.1186/1471-2342-9-8
– volume: 15
  start-page: 869
  year: 2005
  ident: 10.1016/j.neuroimage.2011.06.029_bb0115
  article-title: The Alzheimer's disease neuroimaging initiative
  publication-title: Neuroimaging Clin. N. Am.
  doi: 10.1016/j.nic.2005.09.008
– volume: 39
  start-page: 1654
  year: 2008
  ident: 10.1016/j.neuroimage.2011.06.029_bb0005
  article-title: The impact of skull-stripping and radio-frequency bias correction on grey-matter segmentation for voxel-based morphometry
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2007.10.051
– volume: 30
  start-page: 1310
  year: 2009
  ident: 10.1016/j.neuroimage.2011.06.029_bb0080
  article-title: Evaluation of automated brain MR image segmentation and volumetry methods
  publication-title: Hum. Brain Mapp.
  doi: 10.1002/hbm.20599
– volume: 27
  start-page: 685
  year: 2008
  ident: 10.1016/j.neuroimage.2011.06.029_bb0075
  article-title: The Alzheimer's Disease Neuroimaging Initiative (ADNI): MRI methods
  publication-title: J. Magn. Reson. Imaging
  doi: 10.1002/jmri.21049
– volume: 130
  start-page: 1777
  year: 2007
  ident: 10.1016/j.neuroimage.2011.06.029_bb0145
  article-title: 3D maps from multiple MRI illustrate changing atrophy patterns as subjects progress from mild cognitive impairment to Alzheimer's disease
  publication-title: Brain
  doi: 10.1093/brain/awm112
– volume: 82
  start-page: 239
  year: 1991
  ident: 10.1016/j.neuroimage.2011.06.029_bb0035
  article-title: Neuropathological stageing of Alzheimer-related changes
  publication-title: Acta Neuropathol.
  doi: 10.1007/BF00308809
– volume: 34
  start-page: 939
  year: 1984
  ident: 10.1016/j.neuroimage.2011.06.029_bb0100
  article-title: Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's disease
  publication-title: Neurology
  doi: 10.1212/WNL.34.7.939
– volume: 26
  start-page: 839
  year: 2005
  ident: 10.1016/j.neuroimage.2011.06.029_bb0020
  article-title: Unified segmentation
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2005.02.018
– volume: 20
  start-page: 273
  year: 1995
  ident: 10.1016/j.neuroimage.2011.06.029_bb0150
  publication-title: Support-vector networks. Mach. Learn
– volume: 131
  start-page: 681
  year: 2008
  ident: 10.1016/j.neuroimage.2011.06.029_bb0085
  article-title: Automatic classification of MR scans in Alzheimer's disease
  publication-title: Brain
  doi: 10.1093/brain/awm319
– volume: 56
  start-page: 766
  year: 2011
  ident: 10.1016/j.neuroimage.2011.06.029_bb0045
  article-title: Automatic classification of patients with Alzheimer's disease from structural MRI: a comparison of ten methods using the ADNI database
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2010.06.013
– volume: 49
  start-page: 2216
  year: 2010
  ident: 10.1016/j.neuroimage.2011.06.029_bb0065
  article-title: Intra- and interscanner variability of automated voxel-based volumetry based on a 3D probabilistic atlas of human cerebral structures
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2009.10.066
– volume: 39
  start-page: 1180
  year: 2008
  ident: 10.1016/j.neuroimage.2011.06.029_bb0130
  article-title: Interpreting scan data acquired from multiple scanners: a study with Alzheimer's disease
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2007.09.066
– start-page: 144
  year: 1992
  ident: 10.1016/j.neuroimage.2011.06.029_bb0030
  article-title: A training algorithm for optimal margin classifiers
– volume: 36
  start-page: 2193
  year: 2009
  ident: 10.1016/j.neuroimage.2011.06.029_bb0060
  article-title: Measurement of MRI scanner performance with the ADNI phantom
  publication-title: Med. Phys.
  doi: 10.1118/1.3116776
– volume: 41
  start-page: 371
  year: 2008
  ident: 10.1016/j.neuroimage.2011.06.029_bb0125
  article-title: Reproducibility of brain tissue volumes in longitudinal studies: effects of changes in signal-to-noise ratio and scanner software
  publication-title: Neuroimage
  doi: 10.1016/j.neuroimage.2008.02.003
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Snippet Fully automated machine learning methods based on structural magnetic resonance imaging (MRI) data can assist radiologists in the diagnosis of Alzheimer's...
Fully automated machine learning methods based on structural magnetic resonance imaging (MRI) data can assist radiologists in the diagnosis of Alzheimer’s...
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SubjectTerms Accuracy
Alzheimer Disease - classification
Alzheimer Disease - diagnosis
Alzheimer's disease
Artificial Intelligence
Automation
Classifiers
Computers
Diagnostic systems
Field strength
Hardware
Humans
Image Interpretation, Computer-Assisted - instrumentation
Magnetic Resonance Imaging
MRI
Multi-site study
Scanners
Standard deviation
Studies
Support Vector Machine
Support vector machines
Support vector machines (SVM)
Training
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Title Effects of hardware heterogeneity on the performance of SVM Alzheimer's disease classifier
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Volume 58
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