A genomic foundation model for interpreting human genetic diversity
Interpreting human genomes requires models that recognize shared biological functions while accounting for variation underlying traits, disease susceptibility and adaptation. Here we present hEVO, a genomic foundation model trained on 4.784 billion distinct haplotype sequences reconstructed from whole genome sequencing (WGS) data for 63,809 individuals selected from 550,237 samples across eight…
We haven't written up this one. bioRxiv has the full story — the link below goes straight to it.
