Gene expression is regulated by transcription factors (TFs) that work together to read cis-regulatory DNA sequences. The "cis-regulatory code" -how cells interpret DNA sequences to determine when, where, and how much genes should be expressed -has proven to be exceedingly complex 1,2 . Recently, advances in the scale and resolution of functional genomics assays and Machine Learning (ML) have enabled significant progress towards deciphering this code 3-6 . However, the cis-regulatory code will likely never be solved if models are trained only on genomic sequences; regions of homology can easily lead to overestimation of predictive performance, and our genome is too short and has insufficient sequence diversity to learn all relevant parameters. Fortunately, randomly synthesized DNA sequences enable testing a far larger sequence space than exists in our genomes, and designed DNA sequences enable targeted queries to maximally improve the models. Since the same biochemical principles are used to interpret DNA regardless of its source, models trained on these synthetic data can predict genomic activity, often better than genome-trained models 7,8 . Here, we provide an outlook on the field, and propose a roadmap towards solving the cis-regulatory code by a combination of ML and massively parallel assays using synthetic DNA.
ContributionsCGD and JT conceptualized the paper. CGD produced the first draft, analyzed the data, and made the figures with advice from JT. CGD and JT edited the manuscript.