Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/29687
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dc.contributor.authorWang, Maxen
dc.contributor.authorGe, Wenboen
dc.contributor.authorApthorp, Deborahen
dc.contributor.authorSuominen, Hannaen
dc.date.accessioned2020-11-24T23:11:50Z-
dc.date.available2020-11-24T23:11:50Z-
dc.date.issued2020-07-27-
dc.identifier.citationJMIR Biomedical Engineering, 5(1), p. 1-13en
dc.identifier.issn2561-3278en
dc.identifier.urihttps://hdl.handle.net/1959.11/29687-
dc.description.abstract<b>Background</b><br/>Parkinson disease (PD) is a common neurodegenerative disorder that affects between 7 and 10 million people worldwide. No objective test for PD currently exists, and studies suggest misdiagnosis rates of up to 34%. Machine learning (ML) presents an opportunity to improve diagnosis; however, the size and nature of data sets make it difficult to generalize the performance of ML models to real-world applications.<br/><b>Objective</b><br/>This study aims to consolidate prior work and introduce new techniques in feature engineering and ML for diagnosis based on vowel phonation. Additional features and ML techniques were introduced, showing major performance improvements on the large mPower vocal phonation data set.<br/><b>Methods</b><br/>We used 1600 randomly selected /aa/ phonation samples from the entire data set to derive rules for filtering out faulty samples from the data set. The application of these rules, along with a joint age-gender balancing filter, results in a data set of 511 PD patients and 511 controls. We calculated features on a 1.5-second window of audio, beginning at the 1-second mark, for a support vector machine. This was evaluated with 10-fold cross-validation (CV), with stratification for balancing the number of patients and controls for each CV fold.<br/><b>Results</b><br/>We showed that the features used in prior literature do not perform well when extrapolated to the much larger mPower data set. Owing to the natural variation in speech, the separation of patients and controls is not as simple as previously believed. We presented significant performance improvements using additional novel features (with 88.6% certainty, derived from a Bayesian correlated t test) in separating patients and controls, with accuracy exceeding 58%.<br/><b>Conclusions</b><br/>The results are promising, showing the potential for ML in detecting symptoms imperceptible to a neurologist.en
dc.languageenen
dc.publisherJMIR Publications, Incen
dc.relation.ispartofJMIR Biomedical Engineeringen
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleRobust Feature Engineering for Parkinson Disease Diagnosis: New Machine Learning Techniquesen
dc.typeJournal Articleen
dc.identifier.doi10.2196/13611en
dcterms.accessRightsUNE Greenen
local.contributor.firstnameMaxen
local.contributor.firstnameWenboen
local.contributor.firstnameDeborahen
local.contributor.firstnameHannaen
local.subject.for2008110904 Neurology and Neuromuscular Diseasesen
local.subject.for2008170203 Knowledge Representation and Machine Learningen
local.subject.seo2008920112 Neurodegenerative Disorders Related to Ageingen
local.profile.schoolSchool of Psychologyen
local.profile.emaildapthorp@une.edu.auen
local.output.categoryC1en
local.record.placeauen
local.record.institutionUniversity of New Englanden
local.publisher.placeCanadaen
local.identifier.runningnumbere13611en
local.format.startpage1en
local.format.endpage13en
local.peerreviewedYesen
local.identifier.volume5en
local.identifier.issue1en
local.title.subtitleNew Machine Learning Techniquesen
local.access.fulltextYesen
local.contributor.lastnameWangen
local.contributor.lastnameGeen
local.contributor.lastnameApthorpen
local.contributor.lastnameSuominenen
dc.identifier.staffune-id:dapthorpen
local.profile.orcid0000-0001-5785-024Xen
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.identifier.unepublicationidune:1959.11/29687en
dc.identifier.academiclevelStudenten
dc.identifier.academiclevelStudenten
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
local.title.maintitleRobust Feature Engineering for Parkinson Disease Diagnosisen
local.relation.fundingsourcenoteThis research was supported by the Australian Government Research Training Program Scholarship and delivered in partnership with Our Health in Our Hands, a strategic initiative of the Australian National University, which aims to transform health care by developing new personalized health technologies and solutions in collaboration with patients, clinicians, and health care providers.en
local.output.categorydescriptionC1 Refereed Article in a Scholarly Journalen
local.search.authorWang, Maxen
local.search.authorGe, Wenboen
local.search.authorApthorp, Deborahen
local.search.authorSuominen, Hannaen
local.open.fileurlhttps://rune.une.edu.au/web/retrieve/76fb6a07-125e-48d9-842e-91b093434e33en
local.uneassociationYesen
local.atsiresearchNoen
local.sensitive.culturalNoen
local.year.published2020en
local.fileurl.openhttps://rune.une.edu.au/web/retrieve/76fb6a07-125e-48d9-842e-91b093434e33en
local.fileurl.openpublishedhttps://rune.une.edu.au/web/retrieve/76fb6a07-125e-48d9-842e-91b093434e33en
local.subject.for2020320905 Neurology and neuromuscular diseasesen
local.subject.for2020461105 Reinforcement learningen
local.subject.for2020461106 Semi- and unsupervised learningen
local.subject.seo2020200101 Diagnosis of human diseases and conditionsen
dc.notification.tokena0c2477a-b6ad-4c42-8927-077e69393ab1en
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School of Psychology
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