Abstract

Background and objectiveImaging genetics has been widely used to help diagnose and treat mental illness, e.g., schizophrenia, by combining magnetic resonance imaging of the brain and genomic information for comprehensive and systematic analysis. As a result, utilizing the correlation between magnetic resonance imaging of the brain and genomic information is becoming an important challenge. MethodsIn this paper, the joint analysis of single nucleotide polymorphisms and functional magnetic resonance imaging is conducted for comprehensive study of schizophrenia. We developed a deep canonically correlated sparse autoencoder to classify schizophrenia patients from healthy controls, which can address the limitation of many existing methods such as canonical correlation analysis, deep canonical correlation analysis and sparse autoencoder. ResultsThe proposed deep canonically correlated sparse autoencoder can not only use complex nonlinear transformation and dimension reduction, but also achieve more accurate classifications. Our experiments showed the proposed method achieved an accuracy of 95.65% for SNP data sets and an accuracy of 80.53% for fMRI data sets. ConclusionsExperiments demonstrated higher accuracy of using the proposed method over other conventional models when classifying schizophrenia patients and healthy controls.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.