Detection of developmental dyslexia with machine learning using eye movement data
Raatikainen, P., Hautala, J., Loberg, O., Kärkkäinen, T., Leppänen, P., & Nieminen, P. (2021). Detection of developmental dyslexia with machine learning using eye movement data. Array, 12, Article 100087. https://doi.org/10.1016/j.array.2021.100087
Julkaistu sarjassa
ArrayTekijät
Päivämäärä
2021Tekijänoikeudet
© 2021 The Authors. Published by Elsevier Inc.
Dyslexia is a common neurocognitive learning disorder that can seriously hinder individuals’ aspirations if not detected and treated early. Instead of costly diagnostic assessment made by experts, in the near future dyslexia might be identified with ease by automated analysis of eye movements during reading provided by embedded eye tracking technology. However, the diagnostic machine learning methods need to be optimized first. Previous studies with machine learning have been quite successful in identifying dyslexic readers, however, using contrasting groups with large performance differences between diagnosed and good readers. A practical challenge is to identify also individuals with borderline skills. Here, machine learning methods were used to identify individuals with low performance of reading fluency (below 10 percentile from a normal distribution) using their eye movement recordings of reading. Random Forest was used to select most important eye movement features to be used as input to a Support Vector Machine classifier. This hybrid method was capable of reliably identifying dysfluent readers and it also provided insight into the data used. Our best model achieved accuracy of 89.7% with recall of 84.8%. Our results thus establish groundwork for automatic detection of dyslexia in a natural reading situation.
...
Julkaisija
ElsevierISSN Hae Julkaisufoorumista
2590-0056Asiasanat
Julkaisu tutkimustietojärjestelmässä
https://converis.jyu.fi/converis/portal/detail/Publication/100335752
Metadata
Näytä kaikki kuvailutiedotKokoelmat
Rahoittaja(t)
Suomen AkatemiaRahoitusohjelmat(t)
Profilointi, SA; Akatemiaohjelma, SALisätietoja rahoituksesta
This research was supported by the Academy of Finland , grants #274022, #311877, and #317030.Lisenssi
Samankaltainen aineisto
Näytetään aineistoja, joilla on samankaltainen nimeke tai asiasanat.
-
Automatic detection of developmental dyslexia from eye movement data
Raatikainen, Peter (2019)Lukemisen erityisvaikeus eli dysleksia on maailmanlaajuisesti yleisin neurologinen oppimisvaikeus. Se voi hoitamattomana merkittävästi haitata yksilön akateemista menestystä. Erityisvaikeuden tunnistaminen ja hoitaminen ... -
Aberrant brain functional networks in type 2 diabetes mellitus : A graph theoretical and support-vector machine approach
Lin, Lin; Zhang, Jindi; Liu, Yutong; Hao, Xinyu; Shen, Jing; Yu, Yang; Xu, Huashuai; Cong, Fengyu; Li, Huanjie; Wu, Jianlin (Frontiers Media SA, 2022)Objective: Type 2 diabetes mellitus (T2DM) is a high risk of cognitive decline and dementia, but the underlying mechanisms are not yet clearly understood. This study aimed to explore the functional connectivity (FC) and ... -
Comparing the forecasting performance of logistic regression and random forest models in criminal recidivism
Aaltonen, Olli-Pekka (2016)Rikosseuraamusalalla on viime vuosina kehitetty uusintarikollisuutta ennustavia malleja (Tyni, 2015), jotka perustuvat tyypillisesti rekisteripohjaisiin mittareihin, jotka mittaavat mm. tuomitun sukupuolta, ikää, rikostaustaa ... -
Developmental Dyslexia in Finnish
Lyytinen, Heikki; Richardson, Ulla; Aro, Mikko (Cambridge University Press, 2019) -
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia
Gialluisi, Alessandro; Andlauer, Till F. M.; Mirza-Schreiber, Nazanin; Moll, Kristina; Becker, Jessica; Hoffmann, Per; Ludwig, Kerstin U.; Czamara, Darina; Pourcain, Beate St; Honbolygó, Ferenc; Tóth, Dénes; Csépe, Valéria; Huguet, Guillaume; Chaix, Yves; Iannuzzi, Stephanie; Demonet, Jean-Francois; Morris, Andrew P.; Hulslander, Jacqueline; Willcutt, Erik G.; DeFries, John C.; Olson, Richard K.; Smith, Shelley D.; Pennington, Bruce F.; Vaessen, Anniek; Maurer, Urs; Lyytinen, Heikki; Peyrard-Janvid, Myriam; Leppänen, Paavo H. T.; Brandeis, Daniel; Bonte, Milene; Stein, John F.; Talcott, Joel B.; Fauchereau, Fabien; Wilcke, Arndt; Kirsten, Holger; Müller, Bent; Francks, Clyde; Bourgeron, Thomas; Monaco, Anthony P.; Ramus, Franck; Landerl, Karin; Kere, Juha; Scerri, Thomas S.; Paracchini, Silvia; Fisher, Simon E.; Schumacher, Johannes; Nöthen, Markus M.; Müller-Myhsok, Bertram; Schulte-Körne, Gerd (Nature Publishing Group, 2021)Developmental dyslexia (DD) is a learning disorder affecting the ability to read, with a heritability of 40–60%. A notable part of this heritability remains unexplained, and large genetic studies are warranted to identify ...
Ellei toisin mainittu, julkisesti saatavilla olevia JYX-metatietoja (poislukien tiivistelmät) saa vapaasti uudelleenkäyttää CC0-lisenssillä.