{"title":"Denoising Piecewise Constant Nanopore Signals","authors":"Adrian Vidal;Emanuele Viterbo","doi":"10.1109/TSP.2025.3570417","DOIUrl":null,"url":null,"abstract":"Nanopore sequencing signals can be described as indirect noisy observations that reflect the instantaneous conductance of the nanopore channel as an analyte DNA molecule translocates through the pore in real time, with <inline-formula><tex-math>$\\delta$</tex-math></inline-formula> nucleotides (<inline-formula><tex-math>$\\delta$</tex-math></inline-formula>-mers) blocking the pore at any instant. The sequence of overlapping <inline-formula><tex-math>$\\delta$</tex-math></inline-formula>-mers along the ssDNA molecule are thus indirectly observed as a sequence of conductance levels (i.e., a <italic>signature</i>) that is used to characterize its DNA sequence. In this paper, we denoise piecewise constant nanopore signals drawn from the same Gaussian-output, left-to-right hidden Markov model (HMM) and recover the unknown signature that is used to parameterize the HMM. We place a Gaussian prior on the signature and use importance sampling to approximate the minimum mean-square error estimate (MMSE) of the signature given the signals. To circumvent the difficulty of sampling from the true posterior, we construct a proposal distribution from which the joint segmentation of the observed signals can be efficiently sampled in <inline-formula><tex-math>$O(Mn^{2}k)$</tex-math></inline-formula> time, where <inline-formula><tex-math>$ M $</tex-math></inline-formula> is the number of signals, <inline-formula><tex-math>$ n $</tex-math></inline-formula> is the average duration of each signal, and <inline-formula><tex-math>$ k $</tex-math></inline-formula> is the length of the signature. Finally, we evaluate the performance of the algorithm using both simulated and experimental nanopore signals generated by Oxford Nanopore Technologies’ (ONT) R10.4.1 nanopore. The proposed method can be effective in constructing accurate <inline-formula><tex-math>$\\delta$</tex-math></inline-formula>-mer tables used to fully characterize all the <inline-formula><tex-math>$4^{\\delta}$</tex-math></inline-formula> states of any nanopore sequencer.","PeriodicalId":13330,"journal":{"name":"IEEE Transactions on Signal Processing","volume":"73 ","pages":"1993-2007"},"PeriodicalIF":4.6000,"publicationDate":"2025-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE Transactions on Signal Processing","FirstCategoryId":"5","ListUrlMain":"https://ieeexplore.ieee.org/document/11004612/","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
引用次数: 0
Abstract
Nanopore sequencing signals can be described as indirect noisy observations that reflect the instantaneous conductance of the nanopore channel as an analyte DNA molecule translocates through the pore in real time, with $\delta$ nucleotides ($\delta$-mers) blocking the pore at any instant. The sequence of overlapping $\delta$-mers along the ssDNA molecule are thus indirectly observed as a sequence of conductance levels (i.e., a signature) that is used to characterize its DNA sequence. In this paper, we denoise piecewise constant nanopore signals drawn from the same Gaussian-output, left-to-right hidden Markov model (HMM) and recover the unknown signature that is used to parameterize the HMM. We place a Gaussian prior on the signature and use importance sampling to approximate the minimum mean-square error estimate (MMSE) of the signature given the signals. To circumvent the difficulty of sampling from the true posterior, we construct a proposal distribution from which the joint segmentation of the observed signals can be efficiently sampled in $O(Mn^{2}k)$ time, where $ M $ is the number of signals, $ n $ is the average duration of each signal, and $ k $ is the length of the signature. Finally, we evaluate the performance of the algorithm using both simulated and experimental nanopore signals generated by Oxford Nanopore Technologies’ (ONT) R10.4.1 nanopore. The proposed method can be effective in constructing accurate $\delta$-mer tables used to fully characterize all the $4^{\delta}$ states of any nanopore sequencer.
纳米孔测序信号可以被描述为间接的噪声观测,它反映了纳米孔通道的瞬时电导,因为分析物DNA分子实时通过孔易位,在任何时刻都有$\delta$-mers ($\delta$-mers)阻塞孔。因此,沿着ssDNA分子重叠的$\delta$-mers序列被间接观察到作为一个用于表征其DNA序列的电导水平序列(即一个特征)。在本文中,我们对从相同的高斯输出,从左到右隐马尔可夫模型(HMM)中提取的分段恒定纳米孔信号进行降噪,并恢复用于参数化HMM的未知签名。我们在签名上放置高斯先验,并使用重要性抽样来近似给定信号的签名的最小均方误差估计(MMSE)。为了避免从真实后验中采样的困难,我们构造了一个建议分布,从该分布中可以在$O(Mn^{2}k)$时间内有效地采样观察信号的联合分割,其中$ M $为信号的数量,$ n $为每个信号的平均持续时间,$ k $为签名的长度。最后,我们使用牛津纳米孔技术公司(ONT) R10.4.1纳米孔产生的模拟和实验纳米孔信号来评估算法的性能。所提出的方法可以有效地构建精确的$\delta$-mer表,用于充分表征任何纳米孔测序仪的所有$4^{\delta}$状态。
期刊介绍:
The IEEE Transactions on Signal Processing covers novel theory, algorithms, performance analyses and applications of techniques for the processing, understanding, learning, retrieval, mining, and extraction of information from signals. The term “signal” includes, among others, audio, video, speech, image, communication, geophysical, sonar, radar, medical and musical signals. Examples of topics of interest include, but are not limited to, information processing and the theory and application of filtering, coding, transmitting, estimating, detecting, analyzing, recognizing, synthesizing, recording, and reproducing signals.