LAUSR

Abstract Interpreting protein function from sequence data is a fundamental goal of bioinformatics. However, our current understanding of protein diversity is bottlenecked by the fact that most proteins have only been functionally validated in model organisms, limiting our understanding of how function varies with gene sequence diversity. Thus, accuracy of inferences in clades without model representatives is questionable. Unsupervised learning may help to ameliorate this bias by identifying highly complex patterns and structure from large data sets without external labels. Here, we present DeepSeqProt, an unsupervised deep learning program for exploring large protein sequence data sets. DeepSeqProt is a clustering tool capable of distinguishing between broad classes of proteins while learning local and global structure of functional space. DeepSeqProt is capable of learning salient biological features from unaligned, unannotated sequences. DeepSeqProt is more likely to capture complete protein families and statistically significant shared ontologies within proteomes than other clustering methods. We hope this framework will prove of use to researchers and provide a preliminary step in further developing unsupervised deep learning in molecular biology.