The high density, large capacity, and long-term stability of DNA molecules make them an emerging storage medium that is especially suitable for the long-term storage of large datasets. The DNA sequences used in storage need to consider relevant constraints to avoid nonspecific hybridization reactions, such as the No-runlength constraint, GC-content, and the Hamming distance. In this work, a new nonlinear control parameter strategy and a random opposition-based learning strategy were used to improve the Harris hawks optimization algorithm (for the improved algorithm NOL-HHO) in order to prevent it from falling into local optima. Experimental testing was performed on 23 widely used benchmark functions, and the proposed algorithm was used to obtain better coding lower bounds for DNA storage. The results show that our algorithm can better maintain a smooth transition between exploration and exploitation and has stronger global exploration capabilities as compared with other algorithms. At the same time, the improvement of the lower bound directly affects the storage capacity and code rate, which promotes the further development of DNA storage technology.

With the advent of the era of massive data, the increase of storage demand has far exceeded current storage capacity. DNA molecules provide a reliable solution for big data storage by virtue of their large capacity, high density, and long-term stability. To reduce errors in storing procedures, constructing a sufficient set of constraint encoding is critical for achieving DNA storage. A new version of the Marine Predator algorithm (called QRSS-MPA is proposed in this paper to increase the lower limit of the coding set while satisfying the specific combination of constraints. In order to demonstrate the effectiveness of the improvement, the classical CEC-05 test function is used to test and compare the mean, variance, scalability, and significance. In terms of storage, the lower limit of construction is compared with previous works, and the result is found to be significantly improved. In order to prevent the emergence of a secondary structure that leads to sequencing failure, we give a more stringent lower bound for the constraint coding set, which is of great significance for reducing the error rate of DNA storage amidst its rapid development.