| Title: | LARGE-SCALE MULTIVARIATE SPARSE REGRESSION WITH APPLICATIONS TO UK BIOBANK. |
| Journal: | The Annals of Applied Statistics |
| Published: | 19 Jul 2022 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/36091495/ |
| DOI: | https://doi.org/10.1214/21-aoas1575 |
| URL: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454085 |
| Citations: | 6 (6 in last 2 years) as of 8 Aug 2024 |
Publication 7082
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Abstract
In high-dimensional regression problems, often a relatively small subset of the features are relevant for predicting the outcome, and methods that impose sparsity on the solution are popular. When multiple correlated outcomes are available (multitask), reduced rank regression is an effective way to borrow strength and capture latent structures that underlie the data. Our proposal is motivated by the UK Biobank population-based cohort study, where we are faced with large-scale, ultrahigh-dimensional features, and have access to a large number of outcomes (phenotypes)-lifestyle measures, biomarkers, and disease outcomes. We are hence led to fit sparse reduced-rank regression models, using computational strategies that allow us to scale to problems of this size. We use a scheme that alternates between solving the sparse regression problem and solving the reduced rank decomposition. For the sparse regression component we propose a scalable iterative algorithm based on adaptive screening that leverages the sparsity assumption and enables us to focus on solving much smaller subproblems. The full solution is reconstructed and tested via an optimality condition to make sure it is a valid solution for the original problem. We further extend the method to cope with practical issues, such as the inclusion of confounding variables and imputation of missing values among the phenotypes. Experiments on both synthetic data and the UK Biobank data demonstrate the effectiveness of the method and the algorithm. We present multiSnpnet package, available at http://github.com/junyangq/multiSnpnet that works on top of PLINK2 files, which we anticipate to be a valuable tool for generating polygenic risk scores from human genetic studies.6 Authors
- Junyang Qian
- Yosuke Tanigawa
- Ruilin Li
- Robert Tibshirani
- Manuel A Rivas
- Trevor Hastie
1 Application
| Application ID | Title |
|---|---|
| 24983 | Generating effective therapeutic hypotheses from genomic and hospital linkage data |
Enabling scientific discoveries that improve human health