Jeremy Mateos

Ramy Khabbaz, Jérémy Mateos, Marc Antonini et al.

The biochemical processes underlying DNA data storage, including synthesis, amplification, and sequencing, are inherently noisy. Consequently, base-level insertion, deletion, and substitution (IDS) errors, as well as sequence-level dropouts, occur and pose major challenges for reliable data retrieval. Here we introduce DNA-MGC+, a DNA storage codec designed to enable reliable and resource-efficient data retrieval under diverse operating conditions. We evaluate DNA-MGC+ across a wide range of in silico and in vitro settings, including experiments with both Illumina and Nanopore sequencing, and show that it consistently outperforms existing codecs. In particular, DNA-MGC+ achieves simultaneous gains in sequencing depth requirements, read cost, decoding time, storage density, and error-correction capability under explicit reliability constraints. Notable results include reliable decoding under IDS error rates of up to 24% in synthetic scenarios, and reliable retrieval at sequencing depths below 3x with read costs below 3.5 bits/nt under electrochemical synthesis for both Illumina and Nanopore sequencing.

Trung Hieu Le, Xavier Pic, Jeremy Mateos et al.

DNA exhibits remarkable potential as a data storage solution due to its impressive storage density and long-term stability, stemming from its inherent biomolecular structure. However, developing this novel medium comes with its own set of challenges, particularly in addressing errors arising from storage and biological manipulations. These challenges are further conditioned by the structural constraints of DNA sequences and cost considerations. In response to these limitations, we have pioneered a novel compression scheme and a cutting-edge Multiple Description Coding (MDC) technique utilizing neural networks for DNA data storage. Our MDC method introduces an innovative approach to encoding data into DNA, specifically designed to withstand errors effectively. Notably, our new compression scheme overperforms classic image compression methods for DNA-data storage. Furthermore, our approach exhibits superiority over conventional MDC methods reliant on auto-encoders. Its distinctive strengths lie in its ability to bypass the need for extensive model training and its enhanced adaptability for fine-tuning redundancy levels. Experimental results demonstrate that our solution competes favorably with the latest DNA data storage methods in the field, offering superior compression rates and robust noise resilience.