| Title: | Fast numerical optimization for genome sequencing data in population biobanks |
| Journal: | Bioinformatics |
| Published: | 19 Jun 2021 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/34146108/ |
| DOI: | https://doi.org/10.1093/bioinformatics/btab452 |
| URL: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206591 |
| Citations: | 12 (7 in last 2 years) as of 8 Aug 2024 |
Publication 9757
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Abstract
MOTIVATION: Large-scale and high-dimensional genome sequencing data poses computational challenges. General-purpose optimization tools are usually not optimal in terms of computational and memory performance for genetic data.</p>
RESULTS: We develop two efficient solvers for optimization problems arising from large-scale regularized regressions on millions of genetic variants sequenced from hundreds of thousands of individuals. These genetic variants are encoded by the values in the set {0,1,2,NA}. We take advantage of this fact and use two bits to represent each entry in a genetic matrix, which reduces memory requirement by a factor of 32 compared to a double precision floating point representation. Using this representation, we implemented an iteratively reweighted least square algorithm to solve Lasso regressions on genetic matrices, which we name snpnet-2.0. When the dataset contains many rare variants, the predictors can be encoded in a sparse matrix. We utilize the sparsity in the predictor matrix to further reduce memory requirement and computational speed. Our sparse genetic matrix implementation uses both the compact two-bit representation and a simplified version of compressed sparse block format so that matrix-vector multiplications can be effectively parallelized on multiple CPU cores. To demonstrate the effectiveness of this representation, we implement an accelerated proximal gradient method to solve group Lasso on these sparse genetic matrices. This solver is named sparse-snpnet, and will also be included as part of snpnet R package. Our implementation is able to solve Lasso and group Lasso, linear, logistic and Cox regression problems on sparse genetic matrices that contain 1 000 000 variants and almost 100 000 individuals within 10 min and using less than 32GB of memory.</p>
AVAILABILITY AND IMPLEMENTATION: https://github.com/rivas-lab/snpnet/tree/compact.</p>
7 Authors
- Ruilin Li
- Christopher Chang
- Yosuke Tanigawa
- Balasubramanian Narasimhan
- Trevor Hastie
- Robert Tibshirani
- Manuel A Rivas
1 Application
| Application ID | Title |
|---|---|
| 24983 | Generating effective therapeutic hypotheses from genomic and hospital linkage data |
Enabling scientific discoveries that improve human health