Data Science Workshop Parkinson Classification And Prediction Using Machine Learning And Deep Learning With Python Gui
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DATA SCIENCE WORKSHOP: Parkinson Classification and Prediction Using Machine Learning and Deep Learning with Python GUI
In this data science workshop focused on Parkinson's disease classification and prediction, we begin by exploring the dataset containing features relevant to the disease. We perform data exploration to understand the structure of the dataset, check for missing values, and gain insights into the distribution of features. Visualizations are used to analyze the distribution of features and their relationship with the target variable, which is whether an individual has Parkinson's disease or not. After data exploration, we preprocess the dataset to prepare it for machine learning models. This involves handling missing values, scaling numerical features, and encoding categorical variables if necessary. We ensure that the dataset is split into training and testing sets to evaluate model performance effectively. With the preprocessed dataset, we move on to the classification task. Using various machine learning algorithms such as Logistic Regression, K-Nearest Neighbors, Decision Trees, Random Forests, Gradient Boosting, Naive Bayes, Adaboost, Extreme Gradient Boosting, Light Gradient Boosting, and Multi-Layer Perceptron (MLP), we train multiple models on the training data. To optimize the hyperparameters of these models, we utilize Grid Search, a technique to exhaustively search for the best combination of hyperparameters. For each machine learning model, we evaluate their performance on the test set using various metrics such as accuracy, precision, recall, and F1-score. These metrics help us understand the model's ability to correctly classify individuals with and without Parkinson's disease. Next, we delve into building an Artificial Neural Network (ANN) for Parkinson's disease prediction. The ANN architecture is designed with input, hidden, and output layers. We utilize the TensorFlow library to construct the neural network with appropriate activation functions, dropout layers, and optimizers. The ANN is trained on the preprocessed data for a fixed number of epochs, and we monitor its training and validation loss and accuracy to ensure proper training. After training the ANN, we evaluate its performance using the same metrics as the machine learning models, comparing its accuracy, precision, recall, and F1-score against the previous models. This comparison helps us understand the benefits and limitations of using deep learning for Parkinson's disease prediction. To provide a user-friendly interface for the classification and prediction process, we design a Python GUI using PyQt. The GUI allows users to load their own dataset, choose data preprocessing options, select machine learning classifiers, train models, and predict using the ANN. The GUI provides visualizations of the data distribution, model performance, and prediction results for better understanding and decision-making. In the GUI, users have the option to choose different data preprocessing techniques, such as raw data, normalization, and standardization, to observe how these techniques impact model performance. The choice of classifiers is also available, allowing users to compare different models and select the one that suits their needs best. Throughout the workshop, we emphasize the importance of proper evaluation metrics and the significance of choosing the right model for Parkinson's disease classification and prediction. We highlight the strengths and weaknesses of each model, enabling users to make informed decisions based on their specific requirements and data characteristics. Overall, this data science workshop provides participants with a comprehensive understanding of Parkinson's disease classification and prediction using machine learning and deep learning techniques. Participants gain hands-on experience in data preprocessing, model training, hyperparameter tuning, and designing a user-friendly GUI for efficient and effective data analysis and prediction.
The Applied Data Science Workshop On Medical Datasets Using Machine Learning and Deep Learning with Python GUI
Workshop 1: Heart Failure Analysis and Prediction Using Scikit-Learn, Keras, and TensorFlow with Python GUI Cardiovascular diseases (CVDs) are the number 1 cause of death globally taking an estimated 17.9 million lives each year, which accounts for 31% of all deaths worldwide. Heart failure is a common event caused by CVDs and this dataset contains 12 features that can be used to predict mortality by heart failure. People with cardiovascular disease or who are at high cardiovascular risk (due to the presence of one or more risk factors such as hypertension, diabetes, hyperlipidaemia or already established disease) need early detection and management wherein a machine learning models can be of great help. Dataset used in this project is from Davide Chicco, Giuseppe Jurman. Machine learning can predict survival of patients with heart failure from serum creatinine and ejection fraction alone. BMC Medical Informatics and Decision Making 20, 16 (2020). Attribute information in the dataset are as follows: age: Age; anaemia: Decrease of red blood cells or hemoglobin (boolean); creatinine_phosphokinase: Level of the CPK enzyme in the blood (mcg/L); diabetes: If the patient has diabetes (boolean); ejection_fraction: Percentage of blood leaving the heart at each contraction (percentage); high_blood_pressure: If the patient has hypertension (boolean); platelets: Platelets in the blood (kiloplatelets/mL); serum_creatinine: Level of serum creatinine in the blood (mg/dL); serum_sodium: Level of serum sodium in the blood (mEq/L); sex: Woman or man (binary); smoking: If the patient smokes or not (boolean); time: Follow-up period (days); and DEATH_EVENT: If the patient deceased during the follow-up period (boolean). The models used in this project are K-Nearest Neighbor, Random Forest, Naive Bayes, Logistic Regression, Decision Tree, Support Vector Machine, Adaboost, LGBM classifier, Gradient Boosting, XGB classifier, MLP classifier, and CNN 1D. Finally, you will develop a GUI using PyQt5 to plot boundary decision, ROC, distribution of features, feature importance, cross validation score, and predicted values versus true values, confusion matrix, learning curve, performace of the model, scalability of the model, training loss, and training accuracy. WORKSHOP 2: Cervical Cancer Classification and Prediction Using Machine Learning and Deep Learning with Python GUI About 11,000 new cases of invasive cervical cancer are diagnosed each year in the U.S. However, the number of new cervical cancer cases has been declining steadily over the past decades. Although it is the most preventable type of cancer, each year cervical cancer kills about 4,000 women in the U.S. and about 300,000 women worldwide. Numerous studies report that high poverty levels are linked with low screening rates. In addition, lack of health insurance, limited transportation, and language difficulties hinder a poor woman’s access to screening services. Human papilloma virus (HPV) is the main risk factor for cervical cancer. In adults, the most important risk factor for HPV is sexual activity with an infected person. Women most at risk for cervical cancer are those with a history of multiple sexual partners, sexual intercourse at age 17 years or younger, or both. A woman who has never been sexually active has a very low risk for developing cervical cancer. Sexual activity with multiple partners increases the likelihood of many other sexually transmitted infections (chlamydia, gonorrhea, syphilis). Studies have found an association between chlamydia and cervical cancer risk, including the possibility that chlamydia may prolong HPV infection. Therefore, early detection of cervical cancer using machine and deep learning models can be of great help. The dataset used in this project is obtained from UCI Repository and kindly acknowledged. This file contains a List of Risk Factors for Cervical Cancer leading to a Biopsy Examination. The models used in this project are K-Nearest Neighbor, Random Forest, Naive Bayes, Logistic Regression, Decision Tree, Support Vector Machine, Adaboost, LGBM classifier, Gradient Boosting, XGB classifier, MLP classifier, and CNN 1D. Finally, you will develop a GUI using PyQt5 to plot boundary decision, ROC, distribution of features, feature importance, cross validation score, and predicted values versus true values, confusion matrix, learning curve, performace of the model, scalability of the model, training loss, and training accuracy. WORKSHOP 3: Chronic Kidney Disease Classification and Prediction Using Machine Learning and Deep Learning with Python GUI Chronic kidney disease is the longstanding disease of the kidneys leading to renal failure. The kidneys filter waste and excess fluid from the blood. As kidneys fail, waste builds up. Symptoms develop slowly and aren't specific to the disease. Some people have no symptoms at all and are diagnosed by a lab test. Medication helps manage symptoms. In later stages, filtering the blood with a machine (dialysis) or a transplant may be required The dataset used in this project was taken over a 2-month period in India with 25 features (eg, red blood cell count, white blood cell count, etc). The target is the 'classification', which is either 'ckd' or 'notckd' - ckd=chronic kidney disease. It contains measures of 24 features for 400 people. Quite a lot of features for just 400 samples. There are 14 categorical features, while 10 are numerical. The dataset needs cleaning: in that it has NaNs and the numeric features need to be forced to floats. Attribute Information: Age(numerical) age in years; Blood Pressure(numerical) bp in mm/Hg; Specific Gravity(categorical) sg - (1.005,1.010,1.015,1.020,1.025); Albumin(categorical) al - (0,1,2,3,4,5); Sugar(categorical) su - (0,1,2,3,4,5); Red Blood Cells(categorical) rbc - (normal,abnormal); Pus Cell (categorical) pc - (normal,abnormal); Pus Cell clumps(categorical) pcc - (present, notpresent); Bacteria(categorical) ba - (present,notpresent); Blood Glucose Random(numerical) bgr in mgs/dl; Blood Urea(numerical) bu in mgs/dl; Serum Creatinine(numerical) sc in mgs/dl; Sodium(numerical) sod in mEq/L; Potassium(numerical) pot in mEq/L; Hemoglobin(numerical) hemo in gms; Packed Cell Volume(numerical); White Blood Cell Count(numerical) wc in cells/cumm; Red Blood Cell Count(numerical) rc in millions/cmm; Hypertension(categorical) htn - (yes,no); Diabetes Mellitus(categorical) dm - (yes,no); Coronary Artery Disease(categorical) cad - (yes,no); Appetite(categorical) appet - (good,poor); Pedal Edema(categorical) pe - (yes,no); Anemia(categorical) ane - (yes,no); and Class (categorical) class - (ckd,notckd). The models used in this project are K-Nearest Neighbor, Random Forest, Naive Bayes, Logistic Regression, Decision Tree, Support Vector Machine, Adaboost, LGBM classifier, Gradient Boosting, XGB classifier, MLP classifier, and CNN 1D. Finally, you will develop a GUI using PyQt5 to plot boundary decision, ROC, distribution of features, feature importance, cross validation score, and predicted values versus true values, confusion matrix, learning curve, performace of the model, scalability of the model, training loss, and training accuracy. WORKSHOP 4: Lung Cancer Classification and Prediction Using Machine Learning and Deep Learning with Python GUI The effectiveness of cancer prediction system helps the people to know their cancer risk with low cost and it also helps the people to take the appropriate decision based on their cancer risk status. The data is collected from the website online lung cancer prediction system. Total number of attributes in the dataset is 16, while number of instances is 309. Following are attribute information of dataset: Gender: M(male), F(female); Age: Age of the patient; Smoking: YES=2 , NO=1; Yellow fingers: YES=2 , NO=1; Anxiety: YES=2 , NO=1; Peer_pressure: YES=2 , NO=1; Chronic Disease: YES=2 , NO=1; Fatigue: YES=2 , NO=1; Allergy: YES=2 , NO=1; Wheezing: YES=2 , NO=1; Alcohol: YES=2 , NO=1; Coughing: YES=2 , NO=1; Shortness of Breath: YES=2 , NO=1; Swallowing Difficulty: YES=2 , NO=1; Chest pain: YES=2 , NO=1; and Lung Cancer: YES , NO. The models used in this project are K-Nearest Neighbor, Random Forest, Naive Bayes, Logistic Regression, Decision Tree, Support Vector Machine, Adaboost, LGBM classifier, Gradient Boosting, XGB classifier, MLP classifier, and CNN 1D. Finally, you will develop a GUI using PyQt5 to plot boundary decision, ROC, distribution of features, feature importance, cross validation score, and predicted values versus true values, confusion matrix, learning curve, performace of the model, scalability of the model, training loss, and training accuracy. WORKSHOP 5: Alzheimer’s Disease Classification and Prediction Using Machine Learning and Deep Learning with Python GUI Alzheimer's is a type of dementia that causes problems with memory, thinking and behavior. Symptoms usually develop slowly and get worse over time, becoming severe enough to interfere with daily tasks. Alzheimer's is not a normal part of aging. The greatest known risk factor is increasing age, and the majority of people with Alzheimer's are 65 and older. But Alzheimer's is not just a disease of old age. Approximately 200,000 Americans under the age of 65 have younger-onset Alzheimer’s disease (also known as early-onset Alzheimer’s). The dataset consists of a longitudinal MRI data of 374 subjects aged 60 to 96. Each subject was scanned at least once. Everyone is right-handed. 206 of the subjects were grouped as 'Nondemented' throughout the study. 107 of the subjects were grouped as 'Demented' at the time of their initial visits and remained so throughout the study. 14 subjects were grouped as 'Nondemented' at the time of their initial visit and were subsequently characterized as 'Demented' at a later visit. These fall under the 'Converted' category. Following are some important features in the dataset: EDUC:Years of Education; SES: Socioeconomic Status; MMSE: Mini Mental State Examination; CDR: Clinical Dementia Rating; eTIV: Estimated Total Intracranial Volume; nWBV: Normalize Whole Brain Volume; and ASF: Atlas Scaling Factor. The models used in this project are K-Nearest Neighbor, Random Forest, Naive Bayes, Logistic Regression, Decision Tree, Support Vector Machine, Adaboost, LGBM classifier, Gradient Boosting, XGB classifier, MLP classifier, and CNN 1D. Finally, you will develop a GUI using PyQt5 to plot boundary decision, ROC, distribution of features, feature importance, cross validation score, and predicted values versus true values, confusion matrix, learning curve, performance of the model, scalability of the model, training loss, and training accuracy. WORKSHOP 6: Parkinson Classification and Prediction Using Machine Learning and Deep Learning with Python GUI The dataset was created by Max Little of the University of Oxford, in collaboration with the National Centre for Voice and Speech, Denver, Colorado, who recorded the speech signals. The original study published the feature extraction methods for general voice disorders. This dataset is composed of a range of biomedical voice measurements from 31 people, 23 with Parkinson's disease (PD). Each column in the table is a particular voice measure, and each row corresponds one of 195 voice recording from these individuals ("name" column). The main aim of the data is to discriminate healthy people from those with PD, according to "status" column which is set to 0 for healthy and 1 for PD. The data is in ASCII CSV format. The rows of the CSV file contain an instance corresponding to one voice recording. There are around six recordings per patient, the name of the patient is identified in the first column. Attribute information of this dataset are as follows: name - ASCII subject name and recording number; MDVP:Fo(Hz) - Average vocal fundamental frequency; MDVP:Fhi(Hz) - Maximum vocal fundamental frequency; MDVP:Flo(Hz) - Minimum vocal fundamental frequency; MDVP:Jitter(%); MDVP:Jitter(Abs); MDVP:RAP; MDVP:PPQ; Jitter:DDP – Several measures of variation in fundamental frequency; MDVP:Shimmer; MDVP:Shimmer(dB); Shimmer:APQ3; Shimmer:APQ5; MDVP:APQ; Shimmer:DDA - Several measures of variation in amplitude; NHR; HNR - Two measures of ratio of noise to tonal components in the voice; status - Health status of the subject (one) - Parkinson's, (zero) – healthy; RPDE,D2 - Two nonlinear dynamical complexity measures; DFA - Signal fractal scaling exponent; and spread1,spread2,PPE - Three nonlinear measures of fundamental frequency variation. The models used in this project are K-Nearest Neighbor, Random Forest, Naive Bayes, Logistic Regression, Decision Tree, Support Vector Machine, Adaboost, LGBM classifier, Gradient Boosting, XGB classifier, MLP classifier, and CNN 1D. Finally, you will develop a GUI using PyQt5 to plot boundary decision, ROC, distribution of features, feature importance, cross validation score, and predicted values versus true values, confusion matrix, learning curve, performance of the model, scalability of the model, training loss, and training accuracy. WORKSHOP 7: Liver Disease Classification and Prediction Using Machine Learning and Deep Learning with Python GUI Patients with Liver disease have been continuously increasing because of excessive consumption of alcohol, inhale of harmful gases, intake of contaminated food, pickles and drugs. This dataset was used to evaluate prediction algorithms in an effort to reduce burden on doctors. This dataset contains 416 liver patient records and 167 non liver patient records collected from North East of Andhra Pradesh, India. The "Dataset" column is a class label used to divide groups into liver patient (liver disease) or not (no disease). This data set contains 441 male patient records and 142 female patient records. Any patient whose age exceeded 89 is listed as being of age "90". Columns in the dataset: Age of the patient; Gender of the patient; Total Bilirubin; Direct Bilirubin; Alkaline Phosphotase; Alamine Aminotransferase; Aspartate Aminotransferase; Total Protiens; Albumin; Albumin and Globulin Ratio; and Dataset: field used to split the data into two sets (patient with liver disease, or no disease). The models used in this project are K-Nearest Neighbor, Random Forest, Naive Bayes, Logistic Regression, Decision Tree, Support Vector Machine, Adaboost, LGBM classifier, Gradient Boosting, XGB classifier, MLP classifier, and CNN 1D. Finally, you will develop a GUI using PyQt5 to plot boundary decision, ROC, distribution of features, feature importance, cross validation score, and predicted values versus true values, confusion matrix, learning curve, performance of the model, scalability of the model, training loss, and training accuracy.
THE APPLIED DATA SCIENCE WORKSHOP: Prostate Cancer Classification and Recognition Using Machine Learning and Deep Learning with Python GUI
The Applied Data Science Workshop on Prostate Cancer Classification and Recognition using Machine Learning and Deep Learning with Python GUI involved several steps and components. The project aimed to analyze prostate cancer data, explore the features, develop machine learning models, and create a graphical user interface (GUI) using PyQt5. The project began with data exploration, where the prostate cancer dataset was examined to understand its structure and content. Various statistical techniques were employed to gain insights into the data, such as checking the dimensions, identifying missing values, and examining the distribution of the target variable. The next step involved exploring the distribution of features in the dataset. Visualizations were created to analyze the characteristics and relationships between different features. Histograms, scatter plots, and correlation matrices were used to uncover patterns and identify potential variables that may contribute to the classification of prostate cancer. Machine learning models were then developed to classify prostate cancer based on the available features. Several algorithms, including Logistic Regression, K-Nearest Neighbors, Decision Trees, Random Forests, Gradient Boosting, Naive Bayes, Adaboost, Extreme Gradient Boosting, Light Gradient Boosting, and Multi-Layer Perceptron (MLP), were implemented. Each model was trained and evaluated using appropriate techniques such as cross-validation and grid search for hyperparameter tuning. The performance of each machine learning model was assessed using evaluation metrics such as accuracy, precision, recall, and F1-score. These metrics provided insights into the effectiveness of the models in accurately classifying prostate cancer cases. Model comparison and selection were based on their performance and the specific requirements of the project. In addition to the machine learning models, a deep learning model based on an Artificial Neural Network (ANN) was implemented. The ANN architecture consisted of multiple layers, including input, hidden, and output layers. The ANN model was trained using the dataset, and its performance was evaluated using accuracy and loss metrics. To provide a user-friendly interface for the project, a GUI was designed using PyQt, a Python library for creating desktop applications. The GUI allowed users to interact with the machine learning models and perform tasks such as selecting the prediction method, loading data, training models, and displaying results. The GUI included various graphical components such as buttons, combo boxes, input fields, and plot windows. These components were designed to facilitate data loading, model training, and result visualization. Users could choose the prediction method, view accuracy scores, classification reports, and confusion matrices, and explore the predicted values compared to the actual values. The GUI also incorporated interactive features such as real-time updates of prediction results based on user selections and dynamic plot generation for visualizing model performance. Users could switch between different prediction methods, observe changes in accuracy, and examine the history of training loss and accuracy through plotted graphs. Data preprocessing techniques, such as standardization and normalization, were applied to ensure the consistency and reliability of the machine learning and deep learning models. The dataset was divided into training and testing sets to assess model performance on unseen data and detect overfitting or underfitting. Model persistence was implemented to save the trained machine learning and deep learning models to disk, allowing for easy retrieval and future use. The saved models could be loaded and utilized within the GUI for prediction tasks without the need for retraining. Overall, the Applied Data Science Workshop on Prostate Cancer Classification and Recognition provided a comprehensive framework for analyzing prostate cancer data, developing machine learning and deep learning models, and creating an interactive GUI. The project aimed to assist in the accurate classification and recognition of prostate cancer cases, facilitating informed decision-making and potentially contributing to improved patient outcomes.