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Biology subjects

Shuai, R. W.

Publications and source records attributed to Shuai, R. W..

2 recordsLinked to original sources

Characterizing uncertainty in predictions of genomic sequence-to-activity models

Genomic sequence-to-activity models are increasingly utilized to understand gene regulatory syntax and probe the functional consequences of regulatory variation. Current models make accurate predictions of relative activity levels across the human reference genome, but their performance is more limited for predicting the effects of genetic variants, such as explaining gene expression variation across individuals. To better understand the causes of these shortcomings, we examine the uncertainty in predictions of genomic sequence-to-activity models using an ensemble of Basenji2 model replicates. We characterize prediction consistency on four types of sequences: reference genome sequences, reference genome sequences perturbed with TF motifs, eQTLs, and personal genome sequences. We observe that models tend to make high-confidence predictions on reference sequences, even when incorrect, and low-confidence predictions on sequences with variants. For eQTLs and personal genome sequences, we find that model replicates make inconsistent predictions in >50% of cases. Our findings suggest strategies to improve performance of these models.

genomics↗

Generative Language Modeling for Antibody Design

Discovery and optimization of monoclonal antibodies for therapeutic applications relies on large sequence libraries, but is hindered by developability issues such as low solubility, low thermal stability, high aggregation, and high immunogenicity. Generative language models, trained on millions of protein sequences, are a powerful tool for on-demand generation of realistic, diverse sequences. We present Immunoglobulin Language Model (IgLM), a deep generative language model for creating synthetic libraries by re-designing variable-length spans of antibody sequences. IgLM formulates antibody design as an autoregressive sequence generation task based on text-infilling in natural language. We trained IgLM on 558M antibody heavy- and light-chain variable sequences, conditioning on each sequences chain type and species-of-origin. We demonstrate that IgLM can generate full-length heavy and light chain sequences from a variety of species, as well as infilled CDR loop libraries with improved developability profiles. IgLM is a powerful tool for antibody design and should be useful in a variety of applications.

bioengineering↗