Authors
Bae, J., Jo, S., Kim, Y., Kim, D., Kim, K., Park, S., Park, S., Myung, S., Shin, H., Kim, M. H., Kang, M., Baek, M.
Abstract
Complementary all-atom structure predictors sample different solutions, but how to allocate a fixed sampling budget across them and select the best output remains unclear. Thal-Kak unifies five released predictors under shared upstream inputs and a common schema. Across FoldBench and CASP16, model mixing improves oracle sampling over single-model runs, but selection remains a bottleneck because confidence scores do not transfer across models and existing quality-assessment methods cannot resolve this gap.
Preprint server:
bioRxiv
The authors list and abstract were imported from bioRxiv on 25 Aug 2026.
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