SAGA (Simplified Association Genome-wide Analyses): a user-friendly Pipeline to Democratize Genome-Wide Association Studies

SAGA(简化的全基因组关联分析):一个用户友好的流程,旨在普及全基因组关联研究

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Abstract

Genome-wide association studies (GWAS) have enabled clinicians and researchers to identify genetic variants linked to complex traits and diseases(1-3). However, GWAS still face several challenges, particularly regarding accessibility and reproducibility (4-6). Conducting these analyses often requires substantial bioinformatics expertise for data preprocessing, software installation, and scripting(7-10). We then developed SAGA ("Simplified Association Genome-wide Analyses"), a BASH-based, open-source, fully automated pipeline that integrates three widely adopted tools-PLINK(11), GMMAT(12), and SAIGE(13)-for accessible, robust, and reproducible GWAS. After installation, users simply need to provide genotype and phenotype files in standard formats. The pipeline automates preprocessing, association testing, and visualization, outputting summary statistics, Manhattan plots, and quantile-quantile plots. SAGA enables robust GWAS for users without scripting experience, expanding access to complex genetic analyses.

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