用分段训练的Elman递归神经网络滤除色谱数据中的噪声

分析了色谱信号噪声的分形特征,采用分段训练的Elman递归神经网络除噪.实验结果表明,此方法在滤除噪声时具有一般神经网络和中值滤波器所没有的优点,精度明显提高.     

模式滤波器在色谱信号除噪中的应用

提出一种模式滤波器方法,用于解决色谱信号中宽带噪声的除噪问题。模式滤波器的应用原理是基于色谱信号与宽带噪声之间的形态差异。工作过程：先采用模式匹配方法识别宽带噪声,再识别各种噪声的起始点与终止点,最后采用线性插值方法重构含噪声的色谱信号。方法具有实现简单、运算速度快、去除噪声能力强等特点。由实际采集的色谱信号经除噪处理后所得的结果表明：模式滤波器比一般滤波器具有更好的除噪效果。     

利用二进样条小波模极大方法消除毛细管电泳信号噪声的研究

根据毛细管电泳信号中噪声与真实信号的模极大值特性之间存在较大差异的特点，提出了一种利用二进样条小波模极大值法去噪的方法研究了信号的半峰宽、不同信噪比以及阈值的选取对去噪结果的影响，并对模拟含噪信号和含噪毛经电泳信号去噪前后的结果进行了比较，实验结果表明，该法能效地消除谱带较宽的毛细管电泳等信号中存在的噪声。     

自适应形态滤波器用于色谱信号的处理

建立了一种能自适应地调整尺度的形态滤波器对色谱信号中混杂的离散冲型噪声加以滤除的方法。结果表明,自适应形态滤波器在滤除脉冲型噪声进,比目前文献报道的中值滤波方法呈现出更好的效果,它能保存高度完整的信号信息,是处理色谱信号脉冲型噪声的有力工具。     

一种基于二进小波变换的自适应滤波方法

根据信号和噪声经小波变换后在不同尺度上有不同的特征，将相邻尺度二进小波变换值的相关量进行归一化处理并与小波变换值比较来判断信号与噪声，以噪声在各尺度的方差作为终止迭代的标准，提出了一种基于二进小波变换小波域选择噪声的自适应滤波方法。研究了模拟信号的去噪过程、半峰宽和信噪比对去噪结果的影响，并对模拟含噪信号和含噪毛细管电泳信号去噪前后的结果进行了比较。实验结果表明：由于该方法具有良好的自适应性和显著的滤波效果，必将得到广泛的应用。     

基于分形维数的分析信号自适应中值滤波

提出一种面向分析仪器谱图信号处理的分形维自适应中值波方法（AMeFFD）。该法延拓运用分形理论，定义了相对点盒维数概念，由此建立建立判定脉冲型噪声的特异性指标，从而可自动调节中值滤波窗口宽度，有效地滤除脉冲型噪声及其它类噪声。对仿真色谱信号及实测色谱图的处理结果表明：AMeFFD法克服了经典中值滤波算法的缺陷，无论在信号的均方根偏差还是谱峰差等指标上，均明显优于后者，能在确保谱峰不畸变的同时更有效地滤除脉冲型常见噪声，是处理化学谱图信号的有力工具。     

一种基于光谱信息计算解析的液相色谱滤噪新方法

提出一种基于光谱信息计算解析的高效液相色谱滤噪新方法.对于HPLC/DAD所获得的二维量测数据,取半峰高以上色谱数据点所对应的各列光谱数据进行计算处理,求得在检测波长下的单位标准光谱,并根据光谱维数据与单位标准光谱的关系,采用最小二乘法重构计算求出色谱维数据,从而去除色谱噪声.仿真实验和实测谱图的滤噪结果表明,该方法能有效滤除常见噪声,与中值滤波算法相比较,滤噪性能明显优于后者,是提高色谱定量分析准确度的有力工具.     

小波系数区域相关阈值滤噪方法研究

报道了一种基于小波分析的新的滤噪方法小波系数区域相关阈值滤噪法的基本原理 ,并将其用于模拟信号与含噪色谱信号的滤噪研究。系统的描述了该方法的滤噪过程 ,讨论了相关运算区域大小、软硬阈值法、信号的频率、信噪比对滤噪结果的影响。对高效液相色谱信号的滤噪结果表明 ,该方法在保留信号的特征信息的同时能够有效地滤除信号中的噪音     

自适应拉曼光谱成像数据去噪及其在植物细胞壁光谱分析中的应用

拉曼光谱成像数据存在基线漂移与宇宙射线干扰峰两类噪声信号,无法直接用于光谱分析研究,必须去除。现有单光谱去噪方法处理结果不稳定、可重复性差。针对这一问题,本研究提出了一种自适应拉曼光谱成像数据新型去噪法,采用优化的自适应迭代惩罚最小二乘法( Adaptive iteratively reweighted penalized least-squares,airPLS)和基于主成分分析( PCA)的干扰峰消除算法修正光谱基线漂移和宇宙射线干扰峰,具有输入参数少、光谱失真小、处理速度快、去噪结果稳定等优点。利用本方法去除了芒草( Miscanthus sinensis)细胞壁拉曼光谱成像数据(9010条光谱)中的噪声信号,并对去噪后数据进行PCA和聚类分析(CA),成功区分非植物光谱与植物光谱,分类结果优于未去噪数据。预期本方法可应用于其它光谱成像数据去噪,为光谱的解译和定量分析提供可靠的研究基础。     

再现图像细节抑制散斑噪声技术研究

为了消除数字全息再现像产生的散斑噪声,一种基于边缘检测各向异性扩散方程的去噪算法被提出。在各向异性扩散方程(PM)基础上,通过将边缘检测算子结合梯度算子引导扩散过程,边缘检测算子对噪声具有低敏感度,可以更好地区分边缘信息,达到数字全息再现像去噪目的。通过去噪效果图对比和与中值滤波、均值滤波、小波变换滤波算法峰值信噪比(PNSR)的比较,表明本文提出的算法具有更好的去噪效果,在去除噪声的同时有效保护了图像的细节信息。     

Parametric studies of matched filters to enhance the signal-to-noise ratios of LC-MS-MS peaks

Chromatographic parameters of reference signals employed in matched filter methods have been studied using numerical experiments to improve the signal-to-noise (S/N) ratios of small liquid chromatography (LC) peaks obtained with electrospray tandem mass spectrometers (MS-MS). These parameters include the width, shape, and S/N ratios of chromatographic peaks used as the reference signal profiles. Our results show the effect of reference peak widths on improving the S/N ratio of chromatographic peaks; the influence of reference peak shapes is negligible. To verify simulation results, various reference signals, including analyte peaks of high concentration standards, internal standard peaks, and artificial Gaussian peaks of different widths, have been employed to enhance signal peaks on real liquid chromatography-tandem mass spectrometry (LC-MS-MS) chromatograms via matched filter methods. Our experimental results demonstrate that the S/N ratio enhancement of chromatographic peaks agree with the simulation predictions. These findings, therefore, suggest that regardless of peak shape, a well-smooth peak with a width close to that of the analyte peak is an adequate reference signal, when matched filter methods are used to improve LC-MS-MS chromatograms. Nevertheless, all methods processed LC-MS-MS peaks in this study do not achieve the ideal improvement ratios estimated with simulation results. We attribute this deficiency to spike-like noise, which have considerable low frequency components riding on LC-MS-MS chromatograms. Matched filtering, which works as a low-pass filter in the frequency domain, cannot effectively eliminate low frequency flicker noise contributed by these spikes. In addition, simple median filtering does not provide adequate improvement despite being able to smooth out most spikes in the chromatograms.     

Adaptive numerical morphological filter for identifying chromatographic signals.

A morphological algorithm has been proposed to filter away impulsive noises confounded in the chromatographic signal. Compared with the conventional median filtering method, the results showed that the proposed method has the advantages of a better filtering effect and less distortion. In particular, the morphological filter with adaptive scale gives very good results.     

Optimal estimation of intensity of noisy peaks by matched filtering with application to chromatography : Part 1. General introduction and theoretical evaluations

The digital filter described provides optimal enhancement of the signal-to-noise ratio by using prior information about peak shape and type of noise. The filter, based onthe matched-filter principle, is applied to chromatographic data, but is also suitable for optimal processing of similar noisy signals. The current implementation of the filter permits the specific reduction of different types of noise. Several theoretical aspects concerning the interpretation and use of this advanced filter are discussed. Some calculations on peaks with Gaussian and Gamma distribution shape are given.     

Optimal estimation of intensity of noisy peaks by matched filtering with application to chromatography : Part 2. Program description and simulation experiments

The (digital) matched filter described in Part 1 is applied to chromatographic data files. Practical aspects concerning the use of this filter are discussed. A FORTRAN program for interactive application of the matched filter is described. This program was used for simulation experiments in order to assess the model errors. Results indicate only a weak dependence on the signal-to-noise ratio. Selection of a 1/f noise model is recommended when the type of the signal noise is unknown. The relation between the Gamma and Guassian functions used is shown.     

Selective Electrochemical Epinephrine Sensor Using Self‐Assembled Monomolecular Film of 1,8,15,22‐Tetraaminophthalocyanatonickel(II) on Gold Electrode

This article describes the highly sensitive and selective determination of epinephrine (EP) using self‐assembled monomolecular film (SAMF) of 1,8,15,22‐tetraamino‐phthalocyanatonickel(II) (4α‐Ni^IITAPc) on Au electrode. The 4α‐Ni^IITAPc SAMF modified electrode was prepared by spontaneous adsorption of 4α‐Ni^IITAPc from dimethylformamide solution. The modified electrode oxidizes EP at less over potential with enhanced current response in contrast to the bare Au electrode. The standard heterogeneous rate constant (k°) for the oxidation of EP at 4α‐Ni^IITAPc SAMF modified electrode was found to be 1.94×10^?2 cm s^?1 which was much higher than that at the bare Au electrode. Further, it was found that 4α‐Ni^IITAPc SAMF modified electrode separates the voltammetric signals of ascorbic acid (AA) and EP with a peak separation of 250 mV. Using amperometric method the lowest detection limit of 50 nM of EP was achieved at SAMF modified electrode. Simultaneous amperometric determination of AA and EP was also achieved at the SAMF modified electrode. Common physiological interferents such as uric acid, glucose, urea and NaCl do not interfere within the potential window of EP oxidation. The present 4α‐Ni^IITAPc SAMF modified electrode was also successfully applied to determine the concentration of EP in commercially available injection.     

Analysis of amino acid neurotransmitters by capillary electrophoresis and laser-induced fluorescence using a new fluorescein-derived label

A capillary electrophoresis laser-induced fluorescence detection method (CE-LIF) was developed for the separation of eight neurotransmitters tagged on their amino function with 6-oxy-(N-succinimidyl acetate)-9-(2′-methoxycarbonyl) fluorescein (SAMF), a new fluorescent reagent synthesized in our lab. Derivatization was performed in boric acid buffer (pH = 7.75) at 37 °C over 15 min. The pH-independent fluorescence of SAMF (pH 4–9) permits background buffers over a wide range of pH. It was demonstrated that an acidic running buffer offers a better resolution compared to basic medium in terms of resolution and peak shapes. Employing Cu²⁺ as the additive, the molecules were baseline-separated using a running buffer consisting of 40 mM sodium acetate and 2 mM Cu²⁺ (pH 6.0). The detection limits ranged from 1 to 2 × 10⁻¹⁰ M. The method has been validated for the characterization of lymphocyte samples. The results obtained illustrate the advantages of combining SAMF derivatization with CE-LIF for determining neurotransmitters.