اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدWavelet Transform-Based Analysis of QRS complex in ECG Signals
123
0
0.0
(
0
)
نشر من قبل
Sabyasachi Mukhopadhyay
تاريخ النشر
2013
مجال البحث
الهندسة المعلوماتية
والبحث باللغة
English
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
In the present paper we have reported a wavelet based time-frequency multiresolution analysis of an ECG signal. The ECG (electrocardiogram), which records hearts electrical activity, is able to provide with useful information about the type of Cardiac disorders suffered by the patient depending upon the deviations from normal ECG signal pattern. We have plotted the coefficients of continuous wavelet transform using Morlet wavelet. We used different ECG signal available at MIT-BIH database and performed a comparative study. We demonstrated that the coefficient at a particular scale represents the presence of QRS signal very efficiently irrespective of the type or intensity of noise, presence of unusually high amplitude of peaks other than QRS peaks and Base line drift errors. We believe that the current studies can enlighten the path towards development of very lucid and time efficient algorithms for identifying and representing the QRS complexes that can be done with normal computers and processors.
قيم البحث
اقرأ أيضاً
We propose a signal analysis tool based on the sign (or the phase) of complex wavelet coefficients, which we call a signature. The signature is defined as the fine-scale limit of the signs of a signals complex wavelet coefficients. We show that the s
ignature equals zero at sufficiently regular points of a signal whereas at salient features, such as jumps or cusps, it is non-zero. At such feature points, the orientation of the signature in the complex plane can be interpreted as an indicator of local symmetry and antisymmetry. We establish that the signature rotates in the complex plane under fractional Hilbert transforms. We show that certain random signals, such as white Gaussian noise and Brownian motions, have a vanishing signature. We derive an appropriate discretization and show the applicability to signal analysis.
Recognizing fonts has become an important task in document analysis, due to the increasing number of available digital documents in different fonts and emphases. A generic font-recognition system independent of language, script and content is desirab
le for processing various types of documents. At the same time, categorizing calligraphy styles in handwritten manuscripts is important for palaeographic analysis, but has not been studied sufficiently in the literature. We address the font-recognition problem as analysis and categorization of textures. We extract features using complex wavelet transform and use support vector machines for classification. Extensive experimental evaluations on different datasets in four languages and comparisons with state-of-the-art studies show that our proposed method achieves higher recognition accuracy while being computationally simpler. Furthermore, on a new dataset generated from Ottoman manuscripts, we show that the proposed method can also be used for categorizing Ottoman calligraphy with high accuracy.
Since interactions in neural systems occur across multiple temporal scales, it is likely that information flow will exhibit a multiscale structure, thus requiring a multiscale generalization of classical temporal precedence causality analysis like Gr
angers approach. However, the computation of multiscale measures of information dynamics is complicated by theoretical and practical issues such as filtering and undersampling: to overcome these problems, we propose a wavelet-based approach for multiscale Granger causality (GC) analysis, which is characterized by the following properties: (i) only the candidate driver variable is wavelet transformed (ii) the decomposition is performed using the `a trous wavelet transform with cubic B-spline filter. We measure GC, at a given scale, by including the wavelet coefficients of the driver times series, at that scale, in the regression model of the target. To validate our method, we apply it to publicly available scalp EEG signals, and we find that the condition of closed eyes, at rest, is characterized by an enhanced GC among channels at slow scales w.r.t. eye open condition, whilst the standard Granger causality is not significantly different in the two conditions.
This paper addresses compressive sensing for multi-channel ECG. Compared to the traditional sparse signal recovery approach which decomposes the signal into the product of a dictionary and a sparse vector, the recently developed cosparse approach exp
loits sparsity of the product of an analysis matrix and the original signal. We apply the cosparse Greedy Analysis Pursuit (GAP) algorithm for compressive sensing of ECG signals. Moreover, to reduce processing time, classical signal-channel GAP is generalized to the multi-channel GAP algorithm, which simultaneously reconstructs multiple signals with similar support. Numerical experiments show that the proposed method outperforms the classical sparse multi-channel greedy algorithms in terms of accuracy and the single-channel cosparse approach in terms of processing speed.
Alignment-free sequence analysis approaches provide important alternatives over multiple sequence alignment (MSA) in biological sequence analysis because alignment-free approaches have low computation complexity and are not dependent on high level of
sequence identity, however, most of the existing alignment-free methods do not employ true full information content of sequences and thus can not accurately reveal similarities and differences among DNA sequences. We present a novel alignment-free computational method for sequence analysis based on Ramanujan-Fourier transform (RFT), in which complete information of DNA sequences is retained. We represent DNA sequences as four binary indicator sequences and apply RFT on the indicator sequences to convert them into frequency domain. The Euclidean distance of the complete RFT coefficients of DNA sequences are used as similarity measure. To address the different lengths in Euclidean space of RFT coefficients, we pad zeros to short DNA binary sequences so that the binary sequences equal the longest length in the comparison sequence data. Thus, the DNA sequences are compared in the same dimensional frequency space without information loss. We demonstrate the usefulness of the proposed method by presenting experimental results on hierarchical clustering of genes and genomes. The proposed method opens a new channel to biological sequence analysis, classification, and structural module identification.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
