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Buchan, D. W.

Publications and source records attributed to Buchan, D. W..

2 recordsLinked to original sources

Hybrid Gated Fusion: A Multimodal Deep Learning Framework for Protein Function Annotation

Protein function annotation requires integrating diverse biological signals, yet existing multimodal methods often struggle with missing inputs and redundant information. We present Hybrid Gated Fusion, a multimodal architecture that combines intrinsic protein features, including sequence and structure, with extrinsic functional context from text and interaction networks. Rather than weighting all modalities equally, the model uses bilinear gating to assess both the informativeness of each modality and its agreement with the others, while auxiliary supervision reduces modality dominance and preserves useful signal in weaker modalities. On the CAFA3 benchmark, a single Hybrid Gated Fusion model achieves state-of-the-art performance in Biological Process (Fmax = 0.601) and Cellular Component (Fmax = 0.706), while remaining competitive in Molecular Function (Fmax = 0.702). Analysis of the learned gates shows that interaction networks and text often provide complementary functional signals, whereas structural features are down-weighted when redundant but remain valuable under sparse-input settings. These results establish Hybrid Gated Fusion as a robust and scalable framework for genome-scale protein function annotation. Availability and implementationSource code and reproduction scripts are freely available at https://github.com/psipred/PFP. Pre-computed embeddings, data splits, and model checkpoints are deposited at https://doi.org/10.5281/zenodo.19498341.

bioinformatics↗

Characterising Protein Search Drift using exhaustive protein search and Alphafold2

In this paper we present the first exhaustive analysis of iterative protein search drift and show how such results may impact downstream modelling. Assembling and extracting evolutionary information from families of related proteins is a core challenge in the studey of molecular evolution. For instance, iterative protein search is a common first step in a wide variety of bioinformatics tools and pipelines. And the output of such searches often form the inputs for modelling tools such as Alphafold2. Here we characterise profile drift; the tendency for some searches to become contaminated with sequences outside of the intended evolutionary family. We observe that drift occurs in nearly 15% of searches and can be observed to have measurable impacts on downstream predictive tasks such as structure prediction.

bioinformatics↗