Designed for association studies in nested association mapping (NAM) panels, experimental and random panels. The method is described by Xavier et al. (2015) <doi:10.1093/bioinformatics/btv448>. It includes tools for genome-wide associations of multiple populations, marker quality control, population genetics analysis, genome-wide prediction, solving mixed models and finding variance components through likelihood and Bayesian methods.
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curl https://depscope.dev/api/check/conda/r-namFirst published · 2021-05-23 09:53:39.745000+00:00
Last updated · 2026-01-24 17:56:46.792000+00:00