Abstract:Analyzing microbial samples remains computationally challenging due to their diversity and complexity. The lack of robustde novoprotein function prediction methods exacerbates the difficulty in deriving functional insights from these samples. Traditional prediction methods, dependent on homology and sequence similarity, often fail to predict functions for novel proteins and proteins without known homologs. Moreover, most of these methods have been trained on largely eukaryotic data, and have not been evaluated… Show more
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