The paper introduces Evolutionary Curriculum Learning (ECL), which trains biological VAEs by progressively expanding the evolutionary distance of sequences exposed around sampled anchors, using a power-law schedule. Across two VAE architectures and two domains, ECL improves protein variant-effect prediction with EVE and RNA generation with RfamGen. For p53, mean ClinVar AUROC increases from 0.981 to 0.989; for PTEN, ECL reaches 1.000 in every seed versus an unstable baseline averaging 0.905. RNA covariance-model bit scores improve across three tested families, but the family-level evidence remains limited.
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