RESUMO
Parkinson's Disease is a disorder with diagnostic symptoms that include a change to a walking gait. The disease is problematic to diagnose. An objective method of monitoring the gait of a patient is required to ensure the effectiveness of diagnosis and treatments. We examine the suitability of Extreme Gradient Boosting (XGBoost) and Artificial Neural Network (ANN) Models compared to Symbolic Regression (SR) using genetic programming that was demonstrated to be successful in previous works on gait. The XGBoost and ANN models are found to out-perform SR, but the SR model is more human explainable.
Assuntos
Transtornos Neurológicos da Marcha , Doença de Parkinson , Marcha , Transtornos Neurológicos da Marcha/diagnóstico , Transtornos Neurológicos da Marcha/genética , Humanos , Redes Neurais de Computação , Doença de Parkinson/diagnóstico , Doença de Parkinson/genética , CaminhadaRESUMO
DNA error correcting codes over the edit metric consist of embeddable markers for sequencing projects that are tolerant of sequencing errors. When a genetic library has multiple sources for its sequences, use of embedded markers permit tracking of sequence origin. This study compares different methods for synthesizing DNA error correcting codes. A new code-finding technique called the salmon algorithm is introduced and used to improve the size of best known codes in five difficult cases of the problem, including the most studied case: length six, distance three codes. An updated table of the best known code sizes with 36 improved values, resulting from three different algorithms, is presented. Mathematical background results for the problem from multiple sources are summarized. A discussion of practical details that arise in application, including biological design and decoding, is also given in this study.