The biggest challenge when using DNA as a storage medium is maintaining its stability. The relative occurrence of Guanine (G) and Cytosine (C) is essential for the longevity of DNA. In addition to that, reverse complementary base pairs should not be present in the code. These challenges are overcome by a proper choice of group homomorphisms. Algorithms for storage and retrieval of information in DNA stings are written by using kernel code. Complexities of these algorithms are less compared to the existing algorithms. Construction procedures followed in this paper are capable of constructing codes of required sizes and Reverse complement distance.
Due to the redundant nature of DNA synthesis and sequencing technologies, a basic model for a DNA storage system is a multi-draw "shuffling-sampling" channel. In this model, a random number of noisy copies of each sequence is observed at the channel output. Recent works have characterized the capacity of such a DNA storage channel under different noise and sequencing models, relying on sophisticated typicality-based approaches for the achievability. Here, we consider a multi-draw DNA storage channel in the setting of noise corruption by a binary erasure channel. We show that, in this setting, …
Error-correcting codes over sets, with applications to DNA storage, are studied. The DNA-storage channel receives a set of sequences, and produces a corrupted version of the set, including sequence loss, symbol substitution, symbol insertion/deletion, and limited-magnitude errors in symbols. Various parameter regimes are studied. New bounds on code parameters are provided, which improve upon known bounds. New codes are constructed, at times matching the bounds up to lower-or der terms or small constant factors.
Due to its longevity and enormous information density, DNA is an attractive medium for archival storage. In this work, we study the fundamental limits and trade-offs of DNA-based storage systems by introducing a new channel model, which we call the noisy shuffling-sampling channel. Motivated by current technological constraints on DNA synthesis and sequencing, this model captures three key distinctive aspects of DNA storage systems: (1) the data is written onto many short DNA molecules; (2) the molecules are corrupted by noise during synthesis and sequencing and (3) the data is read by randoml…
The process of DNA-based data storage (DNA storage for short) can be mathematically modelled as a communication channel, termed DNA storage channel, whose inputs and outputs are sets of unordered sequences. To design error correcting codes for DNA storage channel, a new metric, termed the sequence-subset distance, is introduced, which generalizes the Hamming distance to a distance function defined between any two sets of unordered vectors and helps to establish a uniform framework to design error correcting codes for DNA storage channel. We further introduce a family of error correcting codes,…
In the emerging field of DNA storage, data is encoded as DNA sequences and stored. The data is read out again by sequencing the stored DNA. Nanopore sequencing is a new sequencing technology that has many advantages over other methods; in particular, it is cheap, portable, and can support longer reads. While several practical coding schemes have been developed for DNA storage with nanopore sequencing, the theory is not well understood. Towards that end, we study a highly abstracted (deterministic) version of the nanopore sequencer, which highlights key features that make its analysis difficult…
Due to its longevity and enormous information density, DNA is an attractive medium for archival data storage. Thanks to rapid technological advances, DNA storage is becoming practically feasible, as demonstrated by a number of experimental storage systems, making it a promising solution for our society's increasing need of data storage. While in living things, DNA molecules can consist of millions of nucleotides, due to technological constraints, in practice, data is stored on many short DNA molecules, which are preserved in a DNA pool and cannot be spatially ordered. Moreover, imperfections i…
A method for encoding information in DNA sequences is described. The method is based on the precision-resolution framework, and is aimed to work in conjunction with a recently suggested terminator-free template independent DNA synthesis method. The suggested method optimizes the amount of information bits per synthesis time unit, namely, the writing rate. Additionally, the encoding scheme studied here takes into account the existence of multiple copies of the DNA sequence, which are independently distorted. Finally, quantizers for various run-length distributions are designed.
In this paper, we study error-correcting codes for the storage of data in synthetic deoxyribonucleic acid (DNA). We investigate a storage model where data is represented by an unordered set of $M$ sequences, each of length $L$. Errors within that model are losses of whole sequences and point errors inside the sequences, such as substitutions, insertions and deletions. We propose code constructions which can correct these errors with efficient encoders and decoders. By deriving upper bounds on the cardinalities of these codes using sphere packing arguments, we show that many of our codes are cl…
In this paper, we propose a strategy for making DNA-based data storage information-theoretically secure through the use of wiretap channel coding. This motivates us to extend the shuffling-sampling channel model of Shomorony and Heckel (2021) to include a wiretapper. Our main result is a characterization of the secure storage capacity of our DNA wiretap channel model, which is the maximum rate at which data can be stored within a pool of DNA molecules so as to be reliably retrieved by an authorized party (Bob), while ensuring that an unauthorized party (Eve) gets almost no information from her…
In this paper we study error-correcting codes for the storage of data in synthetic deoxyribonucleic acid (DNA). We investigate a storage model where a data set is represented by an unordered set of $M$ sequences, each of length $L$. Errors within that model are a loss of whole sequences and point errors inside the sequences, such as insertions, deletions and substitutions. We derive Gilbert-Varshamov lower bounds and sphere packing upper bounds on achievable cardinalities of error-correcting codes within this storage model. We further propose explicit code constructions than can correct errors…
Motivated by applications in DNA-based storage, we introduce the new problem of code design in the Damerau metric. The Damerau metric is a generalization of the Levenshtein distance which, in addition to deletions, insertions and substitution errors also accounts for adjacent transposition edits. We first provide constructions for codes that may correct either a single deletion or a single adjacent transposition and then proceed to extend these results to codes that can simultaneously correct a single deletion and multiple adjacent transpositions. We conclude with constructions for joint block…
In this paper, we study achievable rates of concatenated coding schemes over a deoxyribonucleic acid (DNA) storage channel. Our channel model incorporates the main features of DNA-based data storage. First, information is stored on many, short DNA strands. Second, the strands are stored in an unordered fashion inside the storage medium and each strand is replicated many times. Third, the data is accessed in an uncontrollable manner, i.e., random strands are drawn from the medium and received, possibly with errors. As one of our results, we show that there is a significant gap between the chann…
The DNA storage channel is considered, in which a codeword is comprised of $M$ unordered DNA molecules. At reading time, $N$ molecules are sampled with replacement, and then each molecule is sequenced. A coded-index concatenated-coding scheme is considered, in which the $m$th molecule of the codeword is restricted to a subset of all possible molecules (an inner code), which is unique for each $m$. The decoder has low-complexity, and is based on first decoding each molecule separately (the inner code), and then decoding the sequence of molecules (an outer code). Only mild assumptions are made o…
The DNA storage channel is considered, in which the $M$ Deoxyribonucleic acid (DNA) molecules comprising each codeword are stored without order, sampled $N$ times with replacement, and then sequenced over a discrete memoryless channel. For a constant coverage depth $M/N$ and molecule length scaling $Θ(\log M)$, lower (achievability) and upper (converse) bounds on the capacity of the channel, as well as a lower (achievability) bound on the reliability function of the channel are provided. Both the lower and upper bounds on the capacity generalize a bound which was previously known to hold only …
We propose coding techniques that limit the length of homopolymers runs, ensure the GC-content constraint, and are capable of correcting a single edit error in strands of nucleotides in DNA-based data storage systems. In particular, for given $\ell, ε > 0$, we propose simple and efficient encoders/decoders that transform binary sequences into DNA base sequences (codewords), namely sequences of the symbols A, T, C and G, that satisfy the following properties: (i) Runlength constraint: the maximum homopolymer run in each codeword is at most $\ell$, (ii) GC-content constraint: the GC-content of e…
The exponentially increasing demand for data storage has been facing more and more challenges during the past years. The energy costs that it represents are also increasing, and the availability of the storage hardware is not able to follow the storage demand's trend. The short lifespan of conventional storage media -- 10 to 20 years - forces the duplication of the hardware and worsens the situation. The majority of this storage demand concerns "cold" data, data very rarely accessed but that has to be kept for long periods of time. The coding abilities of synthetic DNA, and its long durability…
We describe properties and constructions of constraint-based codes for DNA-based data storage which account for the maximum repetition length and AT/GC balance. We present algorithms for computing the number of sequences with maximum repetition length and AT/GC balance constraint. We describe routines for translating binary runlength limited and/or balanced strings into DNA strands, and compute the efficiency of such routines. We show that the implementation of AT/GC-balanced codes is straightforward accomplished with binary balanced codes. We present codes that account for both the maximum re…
