scholarly journals chemmodlab: a cheminformatics modeling laboratory R package for fitting and assessing machine learning models

2018 ◽  
Vol 10 (1) ◽  
Author(s):  
Jeremy R. Ash ◽  
Jacqueline M. Hughes-Oliver
2019 ◽  
Author(s):  
Javier de Velasco Oriol ◽  
Antonio Martinez-Torteya ◽  
Victor Trevino ◽  
Israel Alanis ◽  
Edgar E. Vallejo ◽  
...  

AbstractBackgroundMachine learning models have proven to be useful tools for the analysis of genetic data. However, with the availability of a wide variety of such methods, model selection has become increasingly difficult, both from the human and computational perspective.ResultsWe present the R package FRESA.CAD Binary Classification Benchmarking that performs systematic comparisons between a collection of representative machine learning methods for solving binary classification problems on genetic datasets.ConclusionsFRESA.CAD Binary Benchmarking demonstrates to be a useful tool over a variety of binary classification problems comprising the analysis of genetic data showing both quantitative and qualitative advantages over similar packages.


2022 ◽  
Author(s):  
Albane Ruaud ◽  
Niklas A Pfister ◽  
Ruth E Ley ◽  
Nicholas D Youngblut

Background: Tree ensemble machine learning models are increasingly used in microbiome science as they are compatible with the compositional, high-dimensional, and sparse structure of sequence-based microbiome data. While such models are often good at predicting phenotypes based on microbiome data, they only yield limited insights into how microbial taxa or genomic content may be associated. Results: We developed endoR, a method to interpret a fitted tree ensemble model. First, endoR simplifies the fitted model into a decision ensemble from which it then extracts information on the importance of individual features and their pairwise interactions and also visualizes these data as an interpretable network. Both the network and importance scores derived from endoR provide insights into how features, and interactions between them, contribute to the predictive performance of the fitted model. Adjustable regularization and bootstrapping help reduce the complexity and ensure that only essential parts of the model are retained. We assessed the performance of endoR on both simulated and real metagenomic data. We found endoR to infer true associations with more or comparable accuracy than other commonly used approaches while easing and enhancing model interpretation. Using endoR, we also confirmed published results on gut microbiome differences between cirrhotic and healthy individuals. Finally, we utilized endoR to gain insights into components of the microbiome that predict the presence of human gut methanogens, as these hydrogen-consumers are expected to interact with fermenting bacteria in a complex syntrophic network. Specifically, we analyzed a global metagenome dataset of 2203 individuals and confirmed the previously reported association between Methanobacteriaceae and Christensenellales. Additionally, we observed that Methanobacteriaceae are associated with a network of hydrogen-producing bacteria. Conclusion: Our method accurately captures how tree ensembles use features and interactions between them to predict a response. As demonstrated by our applications, the resultant visualizations and summary outputs facilitate model interpretation and enable the generation of novel hypotheses about complex systems. An implementation of endoR is available as an open-source R-package on GitHub (https://github.com/leylabmpi/endoR).


Sensors ◽  
2021 ◽  
Vol 21 (8) ◽  
pp. 2726
Author(s):  
Ryan Moore ◽  
Kristin R. Archer ◽  
Leena Choi

Accelerometers are increasingly being used in biomedical research, but the analysis of accelerometry data is often complicated by both the massive size of the datasets and the collection of unwanted data from the process of delivery to study participants. Current methods for removing delivery data involve arduous manual review of dense datasets. We aimed to develop models for the classification of days in accelerometry data as activity from human wear or the delivery process. These models can be used to automate the cleaning of accelerometry datasets that are adulterated with activity from delivery. We developed statistical and machine learning models for the classification of accelerometry data in a supervised learning context using a large human activity and delivery labeled accelerometry dataset. Model performances were assessed and compared using Monte Carlo cross-validation. We found that a hybrid convolutional recurrent neural network performed best in the classification task with an F1 score of 0.960 but simpler models such as logistic regression and random forest also had excellent performance with F1 scores of 0.951 and 0.957, respectively. The best performing models and related data processing techniques are made publicly available in the R package, Physical Activity.


2020 ◽  
Vol 2 (1) ◽  
pp. 3-6
Author(s):  
Eric Holloway

Imagination Sampling is the usage of a person as an oracle for generating or improving machine learning models. Previous work demonstrated a general system for using Imagination Sampling for obtaining multibox models. Here, the possibility of importing such models as the starting point for further automatic enhancement is explored.


2021 ◽  
Author(s):  
Norberto Sánchez-Cruz ◽  
Jose L. Medina-Franco

<p>Epigenetic targets are a significant focus for drug discovery research, as demonstrated by the eight approved epigenetic drugs for treatment of cancer and the increasing availability of chemogenomic data related to epigenetics. This data represents a large amount of structure-activity relationships that has not been exploited thus far for the development of predictive models to support medicinal chemistry efforts. Herein, we report the first large-scale study of 26318 compounds with a quantitative measure of biological activity for 55 protein targets with epigenetic activity. Through a systematic comparison of machine learning models trained on molecular fingerprints of different design, we built predictive models with high accuracy for the epigenetic target profiling of small molecules. The models were thoroughly validated showing mean precisions up to 0.952 for the epigenetic target prediction task. Our results indicate that the herein reported models have considerable potential to identify small molecules with epigenetic activity. Therefore, our results were implemented as freely accessible and easy-to-use web application.</p>


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