🤖 AI Summary
This study addresses the significant rate penalty imposed by deterministic GC-content constraints in composite DNA storage by proposing an ε-probabilistic constraint framework. Methodologically, the authors integrate combinatorial type analysis with finite-state Markov chain modeling to derive capacity bounds for the composite DNA channel, and further design a multi-type enumerative encoder capable of achieving this capacity. By overcoming the limitations of conventional deterministic models, this work establishes capacity achievability under both global and local sliding-window constraints, thereby substantially enhancing the efficiency of DNA data storage systems.
📝 Abstract
This paper addresses the challenge of encoding biochemical GC-content constraints in composite DNA-based data storage. Previous deterministic models impose high rate penalties by avoiding any possibility for a strand to fall outside the allowed range. To account for the stochastic nature of composite DNA, we introduce an $ε$-probabilistic constraint framework, and derive capacity bounds for global constraints using composition types and for local sliding-window constraints via finite-state Markov chains. Furthermore, we propose a capacity-achieving multi-type enumerative encoder.