Macarons
Macarons selects subsets of single nucleotide polymorphisms (SNPs) to improve prediction of complex quantitative phenotypes in genome-wide association studies (GWAS).
Key Features:
- Feature selection: Selects small, complementary subsets of genomic variants for phenotype prediction in GWAS.
- High-dimensional handling: Operates when the number of screened loci substantially exceeds the number of samples.
- Linkage disequilibrium avoidance: Avoids selecting redundant pairs of SNPs that are likely to be in linkage disequilibrium.
- Parameter control: Employs two interpretable parameters to control the trade-off between computational time and predictive performance.
- Speed: Achieves runtimes at least two orders of magnitude faster than comparative selection methods.
- Predictive performance: Demonstrates similar or superior phenotype prediction compared to state-of-the-art selection methods.
- Scalability: Scales to genome-wide variant sets, processing on the order of 10^7 variants within minutes.
Scientific Applications:
- SNP selection for GWAS: Identifying SNP subsets associated with complex, quantitative phenotypes.
- Improved phenotype prediction: Enhancing prediction of quantitative traits by selecting complementary loci that jointly explain phenotypic variation.
- Large-scale genomic analyses: Applying feature selection to genome-scale datasets containing millions to tens of millions of variants.
Methodology:
Selects a small complementary subset of SNPs while avoiding redundant SNP pairs likely in linkage disequilibrium, with selection behavior governed by two interpretable parameters that trade off computational time and performance.
Topics
Details
- License:
- GPL-3.0
- Cost:
- Free of charge
- Tool Type:
- library
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- MATLAB, Python
- Added:
- 5/23/2022
- Last Updated:
- 5/23/2022
Operations
Publications
Yilmaz S, Fakhouri M, Koyutürk M, Çiçek AE, Tastan O. Uncovering complementary sets of variants for predicting quantitative phenotypes. Bioinformatics. 2021;38(4):908-917. doi:10.1093/bioinformatics/btab803. PMID:34864867.
PMID: 34864867