TY - JOUR
T1 - Explaining the unique nature of individual gait patterns with deep learning
AU - Horst, Fabian
AU - Lapuschkin, Sebastian
AU - Samek, Wojciech
AU - Müller, Klaus Robert
AU - Schöllhorn, Wolfgang I.
N1 - Funding Information:
The authors thank all the participating subjects for their time and patience as well as Christin Rupprecht and Eva Klein for her encouragement and support during the data collection. No benefits in any form have been received or will be received from a commercial party related directly or indirectly to the subject of this article. This work was supported by the Institute of Information & Communications Technology Planning & Evaluation (IITP) grant funded by the Korea government (No. 2017-0-00451). This work was also supported by the grant DFG (MU 987/17-1) and by the German Ministry for Education and Research as Berlin Big Data Centre (BBDC) (01IS14013A) and Berlin Center for Machine Learning under Grant 01IS18037I. This publication only reflects the authors views. Funding agencies are not liable for any use that may be made of the information contained herein.
Publisher Copyright:
© 2019, The Author(s).
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Machine learning (ML) techniques such as (deep) artificial neural networks (DNN) are solving very successfully a plethora of tasks and provide new predictive models for complex physical, chemical, biological and social systems. However, in most cases this comes with the disadvantage of acting as a black box, rarely providing information about what made them arrive at a particular prediction. This black box aspect of ML techniques can be problematic especially in medical diagnoses, so far hampering a clinical acceptance. The present paper studies the uniqueness of individual gait patterns in clinical biomechanics using DNNs. By attributing portions of the model predictions back to the input variables (ground reaction forces and full-body joint angles), the Layer-Wise Relevance Propagation (LRP) technique reliably demonstrates which variables at what time windows of the gait cycle are most relevant for the characterisation of gait patterns from a certain individual. By measuring the time-resolved contribution of each input variable to the prediction of ML techniques such as DNNs, our method describes the first general framework that enables to understand and interpret non-linear ML methods in (biomechanical) gait analysis and thereby supplies a powerful tool for analysis, diagnosis and treatment of human gait.
AB - Machine learning (ML) techniques such as (deep) artificial neural networks (DNN) are solving very successfully a plethora of tasks and provide new predictive models for complex physical, chemical, biological and social systems. However, in most cases this comes with the disadvantage of acting as a black box, rarely providing information about what made them arrive at a particular prediction. This black box aspect of ML techniques can be problematic especially in medical diagnoses, so far hampering a clinical acceptance. The present paper studies the uniqueness of individual gait patterns in clinical biomechanics using DNNs. By attributing portions of the model predictions back to the input variables (ground reaction forces and full-body joint angles), the Layer-Wise Relevance Propagation (LRP) technique reliably demonstrates which variables at what time windows of the gait cycle are most relevant for the characterisation of gait patterns from a certain individual. By measuring the time-resolved contribution of each input variable to the prediction of ML techniques such as DNNs, our method describes the first general framework that enables to understand and interpret non-linear ML methods in (biomechanical) gait analysis and thereby supplies a powerful tool for analysis, diagnosis and treatment of human gait.
UR - http://www.scopus.com/inward/record.url?scp=85061838354&partnerID=8YFLogxK
U2 - 10.1038/s41598-019-38748-8
DO - 10.1038/s41598-019-38748-8
M3 - Article
C2 - 30787319
AN - SCOPUS:85061838354
SN - 2045-2322
VL - 9
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 2391
ER -