METHOD: Here, we propose a simple two-stage procedure for sharing information between related high-dimensional prediction or classification problems. In both stages, we perform sparse regression separately for each problem. While this is done without prior information in the first stage, we use the coefficients from the first stage as prior information for the second stage. Specifically, we designed feature-specific and sign-specific adaptive weights to share information on feature selection, effect directions, and effect sizes between different problems. RESULTS: The proposed approach is applicable to multi-task learning as well as transfer learning. It provides sparse models (i.e. with few non-zero coefficients for each problem) that are easy to interpret. We show by simulation and application that it tends to select fewer features while achieving a similar predictive performance as compared to available methods. AVAILABILITY AND IMPLEMENTATION: An implementation is available in the R package "sparselink" (https://github.com/rauschenberger/sparselink, https://cran.r-project.org/package=sparselink).

SUMMARY: We developed BIODICA, an integrated computational environment for application of independent component analysis (ICA) to bulk and single-cell molecular profiles, interpretation of the results in terms of biological functions and correlation with metadata. The computational core is the novel Python package stabilized-ica which provides interface to several ICA algorithms, a stabilization procedure, meta-analysis and component interpretation tools. BIODICA is equipped with a user-friendly graphical user interface, allowing non-experienced users to perform the ICA-based omics data analysis. The results are provided in interactive ways, thus facilitating communication with biology experts. AVAILABILITY AND IMPLEMENTATION: BIODICA is implemented in Java, Python and JavaScript. The source code is freely available on GitHub under the MIT and the GNU LGPL licenses. BIODICA is supported on all major operating systems. URL: https://sysbio-curie.github.io/biodica-environment/.

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MOTIVATION: The application of information encoded in molecular networks for prognostic purposes is a crucial objective of systems biomedicine. This approach has not been widely investigated in the cardiovascular research area. Within this area, the prediction of clinical outcomes after suffering a heart attack would represent a significant step forward. We developed a new quantitative prediction-based method for this prognostic problem based on the discovery of clinically relevant transcriptional association networks. This method integrates regression trees and clinical class-specific networks, and can be applied to other clinical domains. RESULTS: Before analyzing our cardiovascular disease dataset, we tested the usefulness of our approach on a benchmark dataset with control and disease patients. We also compared it to several algorithms to infer transcriptional association networks and classification models. Comparative results provided evidence of the prediction power of our approach. Next, we discovered new models for predicting good and bad outcomes after myocardial infarction. Using blood-derived gene expression data, our models reported areas under the receiver operating characteristic curve above 0.70. Our model could also outperform different techniques based on co-expressed gene modules. We also predicted processes that may represent novel therapeutic targets for heart disease, such as the synthesis of leucine and isoleucine. AVAILABILITY: The SATuRNo software is freely available at http://www.lsi.us.es/isanepo/toolsSaturno/.