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    <title>DSpace Collection:</title>
    <link>http://localhost:80/xmlui/handle/123456789/814</link>
    <description />
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        <rdf:li rdf:resource="http://localhost:80/xmlui/handle/123456789/1285" />
        <rdf:li rdf:resource="http://localhost:80/xmlui/handle/123456789/1284" />
        <rdf:li rdf:resource="http://localhost:80/xmlui/handle/123456789/1283" />
        <rdf:li rdf:resource="http://localhost:80/xmlui/handle/123456789/1282" />
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    <dc:date>2026-01-14T23:18:15Z</dc:date>
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  <item rdf:about="http://localhost:80/xmlui/handle/123456789/1285">
    <title>USING DIT-FFT ALGORITHM FOR IDENTIFICATION OF PROTEIN CODING REGION IN EUKARYOTIC GENE</title>
    <link>http://localhost:80/xmlui/handle/123456789/1285</link>
    <description>Title: USING DIT-FFT ALGORITHM FOR IDENTIFICATION OF PROTEIN CODING REGION IN EUKARYOTIC GENE
Authors: Subhajit Kar; Dr. Madhabi Ganguly; Saptarshi Das
Abstract: The new research platform on biomedical engineering by Digital Signal Processing (DSP) is playing a vital role in the prediction of protein coding regions (Exons) from genomic sequences with great accuracy. We can determine the protein coding area in DNA sequences with the help of period-3 property. It has been seen that in order to  find out the period-3 property, the DFT algorithm is mostly used but in this paper, we have tested FFT algorithm instead of DFT algorithm. DSP is basically concerned with processing numerical sequences. When digital signal processing used in DNA sequences analysis, it requires conversion of base characters sequence to the numerical version. The numerical representation of DNA sequences strongly impacts the biological properties mirrored through the numerical genre. In this work, the proposed technique based on DIT-FFT algorithm has been used to identify the exonic area with the help of integer value representation for transforming the DNA sequences. Digital  ̄lters are used to read out period 3 components from the output spectrum and to eliminate the unwanted high frequency noise from DNA sequences. To overcome background noise means to suppress the non-coding regions, i.e., Introns. Proposed algorithm is tested on four nucleotide sequences having single or multiple numbers of exons.</description>
    <dc:date>2018-12-13T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:80/xmlui/handle/123456789/1284">
    <title>Study of effectiveness of FIR and IIR filters in Exon identification: A comparative approach</title>
    <link>http://localhost:80/xmlui/handle/123456789/1284</link>
    <description>Title: Study of effectiveness of FIR and IIR filters in Exon identification: A comparative approach
Authors: Subhajit Kar; Dr. Madhabi Ganguly
Abstract: In recent years, DSP has been widely used in the area of DNA sequence analysis, detection of protein cod-ing and non-coding regions and also in finding abnormalities present in coding and non-coding regions. Using DSP tool, the detection of protein coding and non-coding regions has been executed with great accuracy and less complexity. In this paper, DNA nucleotide sequence is converted into corresponding EIIP sequence in the first step. In order to make a comparative study between different FIR and IIR filters, the sequence is passed through overall six FIR and IIR filters separately to extract the period three fre-quency components. Finally, Gaussian filter is used to suppress the high frequency noise present in the power spectrum. This study aims to find out most efficient FIR and IIR filters in predicting exons (coding regions) and introns (non-coding regions) based on different evaluating parameters as follows: (i) specificity-sensitivity values (ii) Matthews correlation coefficient (iii) Miss rate and wrong rate (iv)Discriminating factor (v) ROC.</description>
    <dc:date>2024-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:80/xmlui/handle/123456789/1283">
    <title>Application of genomic signal processing as a tool for high- performance classification of SARS-CoV-2 variants: a machine learning- based approach</title>
    <link>http://localhost:80/xmlui/handle/123456789/1283</link>
    <description>Title: Application of genomic signal processing as a tool for high- performance classification of SARS-CoV-2 variants: a machine learning- based approach
Authors: Subhajit Kar; Dr. Madhabi Ganguly
Abstract: From the beginning of COVID-19 pandemic, numerous mutants of SARS-CoV-2 have since been evolved owing to high transmissibility and virulence. Due to the limited effectiveness of previously imposed vaccines and preventive therapies, these strains are still causing concern. This paper proposes comparative evaluation of three novel genomic signal pro-cessing-based methods employing discrete wavelet decomposition with lifting (DWT), discrete Fourier transform (DFT), and singular value decomposition (SVD) for the classification of emerging SARS-CoV-2 variants utilizing feature extraction from collected SARS-CoV-2 variants acquired from the NCBI virus database. The efficiency and accuracy of the proposed alignment-free algorithms have been tested using three Coronavirus datasets including human Coronavirus (HCoV), SARS-CoV-2 variants (CoV-Variants and Omicron). The viral nucleotide sequences which are converted into numerical representation leveraging purine-pyrimidine mapping, DNA walk &amp; Z-curve are fed into DWT, SVD, &amp; DFT processors, respectively. In the approach with DWT, the second-generation wavelet transform employs two best wavelet&#xD;
bases Daubechies (Db) and Biorthogonal (Bior) based on the validation of the HCoV dataset for the feature extraction of the CoV-Variants dataset. Various machine learning algorithms, such as Support Vector Machine, K-nearest neighbors, and ensemble, are used to classify the virus strains and evaluate the efficacy of the algorithm. Finally, hyper-parametric tuning is done utilizing the Bayesian optimization technique to select the best fit model for KNN and SVM. The proposed algorithm has successfully classified the CoV-Variants dataset with an average accuracy of 98.76% utilizing the DWT, DFT, and SVD, while the best-achieved accuracy for this dataset is 98.9% using the DWT technique employing purine–pyrimidine mapping. The best-achieved accuracy rate for predicting Omicron is 99.8% using SVD-based technique. The best-obtained accuracy for HCoV dataset is 100% resulted in all three methods.</description>
    <dc:date>2023-12-10T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:80/xmlui/handle/123456789/1282">
    <title>Prediction of coding region and mutations in Human DNA by effective numerical coding and DSP technique</title>
    <link>http://localhost:80/xmlui/handle/123456789/1282</link>
    <description>Title: Prediction of coding region and mutations in Human DNA by effective numerical coding and DSP technique
Authors: Subhajit Kar; Dr. Madhabi Ganguly; Subhro Ghosal
Abstract: Proper numerical conversion of DNA sequences into digital signals unbolts the possibility to employ digital signal processing tools for analyzing genomic data. In this paper, a given DNA sequence is converted into numerical representation based on two bit binary representation of nucleotide bases Adenine (A), Cytosine (C), Guanine (G), and Thymine (T). The four bases A, C, T and G in a DNA primary sequence groupedintopurine{A,G}/pyrimidine{C,T}, amino{A,C}/keto{G,T} and weak-H bond{A,T} /strong- H bond{C,G}.Digital signal processing tools can be applied to the generated numerical sequence to predict the exons or coding regions in a gene, un-translated regions as well as any substitution mutation in coding region. Two staged digital filter comprises of a bandpass filter which essentially extracts the period three components from the sequence and secondly a low pass filter to eliminate high frequency noise present in the output spectra due to long range correlation of nucleotide bases are used. The locations of exons and untranslated regions found in the experiment conform to the original one as obtained from GenBank database.</description>
    <dc:date>2021-01-01T00:00:00Z</dc:date>
  </item>
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