CodonBERT: Large Language Models for mRNA Design and Optimization
Sizhen Li, Saeed MoayedpouriD, Ruijiang LiiD, Michael BaileyiD, Saleh Riahi, Lorenzo Kogler-Anele, Milad MiladiiD, Jacob C. MineriD, Fabien Pertuy, Dinghai ZhengiD, Jun Wang, Akshay BalsubramaniiD, Khang TraniD, Minnie Zacharia, Monica Wu, Xiaobo Gu, Ryan W. ClintoniD, Carla Asquith, Joseph Skaleski, Lianne Boeglin, Sudha V. ChivukulaiD, Anusha P. Dias, Tod Strugnell, Fernando Ulloa Montoya, Vikram AgarwaliD, , Sven JägeriD
Abstract
AO_SCPLOWBSTRACTC_SCPLOWmRNA based vaccines and therapeutics are gaining popularity and usage across a wide range of conditions. One of the critical issues when designing such mRNAs is sequence optimization. Even small proteins or peptides can be encoded by an enormously large number of mRNAs. The actual mRNA sequence can have a large impact on several properties including expression, stability, immunogenicity, and more. To enable the selection of an optimal sequence, we developed CodonBERT, a large language model (LLM) for mRNAs. Unlike prior models, CodonBERT uses codons as inputs which enables it to learn better representations. CodonBERT was trained using more than 10 million mRNA sequences from a diverse set of organisms. The resulting model captures important biological concepts. CodonBERT can also be extended to perform prediction tasks for various mRNA properties. CodonBERT outperforms previous mRNA prediction methods including on a new flu vaccine dataset.
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