augix/SNPBag
Towards a universal foundation model for biobank-scale human genome variation
SNPBag helps biomedical researchers and geneticists analyze large-scale human genomic data. It takes raw whole-genome SNP data as input and can perform tasks like inferring missing genotypes, determining ancestry, or assessing genetic relatedness between individuals. This tool is designed for those working with biobank-scale genetic datasets.
Use this if you need to perform tasks like genotype imputation, haplotype phasing, ancestry inference, or relatedness inference on large human whole-genome SNP datasets.
Not ideal if you are working with non-human genomic data or need to perform custom genetic analyses beyond the five pre-trained tasks.
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Jupyter Notebook
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Last pushed
Dec 17, 2025
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