Â鶹´«Ã½AV

This paper studies achievable rates of nanopore-based DNA storage when nanopore signals are decoded using a tractable channel model that does not rely on a basecalling algorithm. Specifically, the noisy nanopore channel (NNC) with the Scrappie pore model generates average output levels via i.i.d. geometric sample duplications corrupted by i.i.d. Gaussian noise (NNC-Scrappie). Simplified message passing algorithms are derived for efficient soft decoding of nanopore signals using NNC-Scrappie.

In this paper, we consider a recent channel model of a nanopore sequencer proposed by McBain, Viterbo, and Saunderson (2024), termed the noisy nanopore channel (NNC). In essence, an NNC is a duplication channel with structured, Markov inputs, that is corrupted by memoryless noise. We first discuss a (tight) lower bound on the capacity of the NNC in the absence of random noise. Next, we present lower and upper bounds on the channel capacity of general noisy nanopore channels.

The central problem in sequence reconstruction is to find the minimum number of distinct channel outputs required to uniquely reconstruct the transmitted sequence. According to Levenshtein’s work in 2001, this number is determined by the size of the maximum intersection between the error balls of any two distinct input sequences of the channel. In this work, we study the sequence reconstruction problem for the q-ary single-deletion single-substitution channel for any fixed integer q≥2.

In DNA sequencing, we often need to infer an unknown sequence from a collection of its corrupted copies. Each copy cannot faithfully tell the truth due to DNA fragmentation, point mutations, and measurement errors. The theoretical guarantee of unique reconstruction is thus of concern. This motivated the study of sequence reconstruction problems three decades ago. Recently, synthetic DNA has been regarded as an ultra-dense data storage medium. Sequence reconstruction is a crucial step in achieving reliable and efficient data readout.