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The concept of DNA storage was first suggested in 1959 by Richard Feynman who shared his vision regarding nanotechnology in the talk “There is plenty of room at the bottom”. Later, towards the end of the 20-th century, the interest in storage solutions based on DNA molecules was increased as a result of the human genome project which in turn led to a significant progress in sequencing and assembly methods. DNA storage enjoys major advantages over the well-established magnetic and optical storage solutions. As opposed to magnetic solutions, DNA storage does not require electrical supply to maintain data integrity and is superior to other storage solutions in both density and durability. Given the trends in cost decreases of DNA synthesis and sequencing, it is now acknowledged that within the next 10-15 years DNA storage may become a highly competitive archiving technology and probably later the main such technology. With that said, the current implementations of DNA based storage systems are very limited and are not fully optimized to address the unique pattern of errors which characterize the synthesis and sequencing processes. In this work, we propose a robust, efficient and scalable solution to implement DNA-based storage systems. Our method deploys Deep Neural Networks (DNN) which reconstruct a sequence of letters based on imperfect cluster of copies generated by the synthesis and sequencing processes. A tailor-made Error-Correcting Code (ECC) is utilized to combat patterns of errors which occur during this process. Since our reconstruction method is adapted to imperfect clusters, our method overcomes the time bottleneck of the noisy DNA copies clustering process by allowing the use of a rapid and scalable pseudo-clustering instead. Our architecture combines between convolutions and transformers blocks and is trained using synthetic data modelled after real data statistics.

We address the challenge of optimizing the capacity-achieving input distribution for a multinomial channel under the constraint of limited input support size, which is a crucial aspect in the design of DNA storage systems. We propose an algorithm that further elaborates the Multidimensional Dynamic Assignment Blahut-Arimoto (M-DAB) algorithm. Our proposed algorithm integrates variational autoencoder for determining the optimal locations of input distribution, into the alternating optimization of the input distribution locations and weights.

Recent advancements in DNA storage show that composite DNA letters can significantly enhance storage capacity. We model this process as a multinomial channel and propose an optimization algorithm to determine its capacity-achieving input distribution (CAID) for an arbitrary number of output reads. Our empirical results match a scaling law that determines that the support size grows exponentially with capacity. In addition, we introduce a limited-support optimization algorithm that optimizes the input distribution under a restricted support size, making it more feasible for real-world DNA storage systems. We also extend our model to account for noise and study its effect on capacity and input design.

Code release for the paper: “Input Optimization in the Composite DNA Storage Channel” by Adir Kobovich and Nir Weinberger.