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      Novelty detection for metabolic dynamics established on breast cancer tissue using 2D NMR TOCSY spectra

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          Highlights

          • Automatic novelty detection of metabolites of 2D-TOCSY NMR spectra.

          • Metabolic profiling of the dynamics changes in Breast cancer tissue sample.

          • Accurate and fast automatic multicomponent peak assignment of 2D NMR spectrum.

          • One- and multi- novelty detection of metabolites.

          Abstract

          Most metabolic profiling approaches focus only on identifying pre-known metabolites on NMR TOCSY spectrum using configured parameters. However, there is a lack of tasks dealing with automating the detection of new metabolites that might appear during the dynamic evolution of biological cells. Novelty detection is a category of machine learning that is used to identify data that emerge during the test phase and were not considered during the training phase. We propose a novelty detection system for detecting novel metabolites in the 2D NMR TOCSY spectrum of a breast cancer-tissue sample. We build one- and multi-class recognition systems using different classifiers such as, Kernel Null Foley-Sammon Transform, Kernel Density Estimation, and Support Vector Data Description. The training models were constructed based on different sizes of training data and are used in the novelty detection procedure. Multiple evaluation measures were applied to test the performance of the novelty detection methods. Depending on the training data size, all classifiers were able to achieve 0% false positive rates and total misclassification error in addition to 100% true positive rates. The median total time for the novelty detection process varies between 1.5 and 20 seconds, depending on the classifier and the amount of training data. The results of our novel metabolic profiling method demonstrate its suitability, robustness and speed in automated metabolic research.

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          A survey on Image Data Augmentation for Deep Learning

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            Receiver operating characteristic curve in diagnostic test assessment.

            The performance of a diagnostic test in the case of a binary predictor can be evaluated using the measures of sensitivity and specificity. However, in many instances, we encounter predictors that are measured on a continuous or ordinal scale. In such cases, it is desirable to assess performance of a diagnostic test over the range of possible cutpoints for the predictor variable. This is achieved by a receiver operating characteristic (ROC) curve that includes all the possible decision thresholds from a diagnostic test result. In this brief report, we discuss the salient features of the ROC curve, as well as discuss and interpret the area under the ROC curve, and its utility in comparing two different tests or predictor variables of interest.
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              HMDB: the Human Metabolome Database

              The Human Metabolome Database (HMDB) is currently the most complete and comprehensive curated collection of human metabolite and human metabolism data in the world. It contains records for more than 2180 endogenous metabolites with information gathered from thousands of books, journal articles and electronic databases. In addition to its comprehensive literature-derived data, the HMDB also contains an extensive collection of experimental metabolite concentration data compiled from hundreds of mass spectra (MS) and Nuclear Magnetic resonance (NMR) metabolomic analyses performed on urine, blood and cerebrospinal fluid samples. This is further supplemented with thousands of NMR and MS spectra collected on purified, reference metabolites. Each metabolite entry in the HMDB contains an average of 90 separate data fields including a comprehensive compound description, names and synonyms, structural information, physico-chemical data, reference NMR and MS spectra, biofluid concentrations, disease associations, pathway information, enzyme data, gene sequence data, SNP and mutation data as well as extensive links to images, references and other public databases. Extensive searching, relational querying and data browsing tools are also provided. The HMDB is designed to address the broad needs of biochemists, clinical chemists, physicians, medical geneticists, nutritionists and members of the metabolomics community. The HMDB is available at:
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                Author and article information

                Contributors
                Journal
                Comput Struct Biotechnol J
                Comput Struct Biotechnol J
                Computational and Structural Biotechnology Journal
                Research Network of Computational and Structural Biotechnology
                2001-0370
                01 June 2022
                2022
                01 June 2022
                : 20
                : 2965-2977
                Affiliations
                [a ]Leibniz-Institut für Analytische Wissenschaften - ISAS - e.V, 44139 Dortmund, Germany
                [b ]Image Analysis Group, TU Dortmund, 44227 Dortmund, Germany
                Author notes
                [* ]Corresponding author. lubaba.migdadi@ 123456isas.de
                Article
                S2001-0370(22)00206-9
                10.1016/j.csbj.2022.05.050
                9213235
                35782733
                2528a775-6e83-4a1a-b91b-7128a2d36ed5
                © 2022 Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 17 March 2022
                : 26 May 2022
                : 26 May 2022
                Categories
                Research Article

                tocsy, total correlation spectroscopy,knfst, kernel null foley–sammon transform,svdd, support vector data description,kde, kernel density estimation,nmr, nuclear magnetic resonance,atp, adenosine triphosphate,bmrb, biological magnetic resonance data bank,hmdb, human metabolome database,roc, receiver operating characteristic,auc, area under curve,novelty detection,machine learning,classification,2d nmr tocsy,metabolic profiling,breast cancer,chemometrics,metabolomics

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