Back

permGWAS2: Enhanced and Accelerated Permutation-based Genome-Wide Association Studies

John, M.; Korte, A.; Grimm, D. G.

2023-11-29 bioinformatics
10.1101/2023.11.28.569016 bioRxiv
Show abstract

MotivationPermutation-based significance thresholds have been shown to be a robust alternative to Bonferroni-based significance thresholds in genome-wide association studies (GWAS). However, the implementation of permutation-based thresholds is computationally demanding. The recently published method permGWAS introduced a batch-wise approach using 4D tensors to efficiently compute permutation-based GWAS. However, running multiple univariate tests in parallel leads to many repetitive computations and increased computational resources. More importantly, the previous version of permGWAS does not take into account the population structure when permuting the phenotype. ResultsWe propose permGWAS2, an improved and accelerated version that uses a block matrix decomposition to optimize computations, thereby reducing redundant computations. It also introduces an alternative permutation strategy that takes into account the population structure during permutation. We show that this improved framework provides a more streamlined approach to performing permutation-based GWAS with a lower false discovery rate compared to the previous version and the traditional Bonferroni correction. AvailabilitypermGWAS2 is open-source and publicly available on GitHub for download: https://github.com/grimmlab/permGWAS.

Matching journals

The top 3 journals account for 50% of the predicted probability mass.

50% of probability mass above

"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.