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Dufault, C.

Publications and source records attributed to Dufault, C..

2 recordsLinked to original sources

Unsupervised Whole-Genome Representation Learning Captures Bacterial Phenotypes

Shifting from hand-crafted to learned representations of data has revolutionized fields like natural language processing and computer vision. Despite this, current approaches to bacterial phenotype prediction from the genome rely on training machine learning models on hand-crafted features, often binary indicators or counts of the presence of different conserved genomic elements and protein domains. Defining these shared elements and domains as our "genomic element vocabulary", we tokenize entire bacterial genomes as sequences of these conserved elements and take advantage of advances in long-context language modeling to perform self-supervised whole-genome representation learning (WGRL). Through multi-task pretraining on a phylogenetically diverse dataset of hundreds of thousands of bacterial genomes, we present a genomic language model which produces representations of input genomes with features predictive of a broad range of phenotypes. We assess the quality of the learned representations through k-nearest neighbours prediction of 25 bacterial phenotypes, finding our WGRL representations more predictive than standard protein domain presence/absence representations for 23/25 different phenotypes. We additionally find the WGRL representations are robust to both poor genome assembly quality and incompleteness. Through learning the relationships between evolutionarily conserved genomic elements with self-supervised long-context language modeling, we demonstrate the first approach for extracting general-purpose whole-genome representations while preserving gene order.

bioinformatics↗

Zero-shot segmentation using embeddings from a protein language model identifies functional regions in the human proteome

The biological function of a protein is often determined by its distinct functional units, such as folded domains and intrinsically disordered regions. Identifying and categorizing these protein segments from sequence has been a major focus in computational biology which has enabled the automatic annotation of folded protein domains. Here we show that embeddings from the unsupervised protein language model ProtT5 can be used to identify and categorize protein segments without relying on conserved patterns in primary amino acid sequence. We present Zero-shot Protein Segmentation (ZPS), where we use embeddings from ProtT5 to predict the boundaries of protein segments without training or fine-tuning any parameters. We find that ZPS boundary predictions for the human proteome are more consistent with reviewed annotations from UniProt than established bioinformatics tools and ProtT5 embeddings of ZPS segments can categorize folded domains, sub-domains, and intrinsically disordered regions. To explore ZPS predictions, we introduce a new way to visualize protein embeddings that closely resembles diagrams of distinct functional units in protein biology. Since ZPS and segment embeddings can be used without training or fine-tuning, the approach is not biased towards known annotations and can used to identify and categorize unannotated protein segments. We used the segment embeddings to identify unannotated mitochondrion targeting signals and SYGQ-rich prion-like domains, which are functional regions within intrinsically disordered regions. We expect the protein segment organization revealed here to lead to valuable information about protein function, including about intrinsically disordered regions and other less understood protein regions.

bioinformatics↗