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      Error-Correcting Output Codes in Classification of Human Induced Pluripotent Stem Cell Colony Images

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          Abstract

          The purpose of this paper is to examine how well the human induced pluripotent stem cell (hiPSC) colony images can be classified using error-correcting output codes (ECOC). Our image dataset includes hiPSC colony images from three classes (bad, semigood, and good) which makes our classification task a multiclass problem. ECOC is a general framework to model multiclass classification problems. We focus on four different coding designs of ECOC and apply to each one of them k-Nearest Neighbor ( k-NN) searching, naïve Bayes, classification tree, and discriminant analysis variants classifiers. We use Scaled Invariant Feature Transformation (SIFT) based features in classification. The best accuracy (62.4%) is obtained with ternary complete ECOC coding design and k-NN classifier (standardized Euclidean distance measure and inverse weighting). The best result is comparable with our earlier research. The quality identification of hiPSC colony images is an essential problem to be solved before hiPSCs can be used in practice in large-scale. ECOC methods examined are promising techniques for solving this challenging problem.

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          Most cited references29

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          An Introduction to Statistical Learning

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            Naive (Bayes) at forty: The independence assumption in information retrieval

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              Is Open Access

              Model for long QT syndrome type 2 using human iPS cells demonstrates arrhythmogenic characteristics in cell culture

              SUMMARY Long QT syndrome (LQTS) is caused by functional alterations in cardiac ion channels and is associated with prolonged cardiac repolarization time and increased risk of ventricular arrhythmias. Inherited type 2 LQTS (LQT2) and drug-induced LQTS both result from altered function of the hERG channel. We investigated whether the electrophysiological characteristics of LQT2 can be recapitulated in vitro using induced pluripotent stem cell (iPSC) technology. Spontaneously beating cardiomyocytes were differentiated from two iPSC lines derived from an individual with LQT2 carrying the R176W mutation in the KCNH2 (HERG) gene. The individual had been asymptomatic except for occasional palpitations, but his sister and father had died suddenly at an early age. Electrophysiological properties of LQT2-specific cardiomyocytes were studied using microelectrode array and patch-clamp, and were compared with those of cardiomyocytes derived from control cells. The action potential duration of LQT2-specific cardiomyocytes was significantly longer than that of control cardiomyocytes, and the rapid delayed potassium channel (IKr) density of the LQT2 cardiomyocytes was significantly reduced. Additionally, LQT2-derived cardiac cells were more sensitive than controls to potentially arrhythmogenic drugs, including sotalol, and demonstrated arrhythmogenic electrical activity. Consistent with clinical observations, the LQT2 cardiomyocytes demonstrated a more pronounced inverse correlation between the beating rate and repolarization time compared with control cells. Prolonged action potential is present in LQT2-specific cardiomyocytes derived from a mutation carrier and arrhythmias can be triggered by a commonly used drug. Thus, the iPSC-derived, disease-specific cardiomyocytes could serve as an important platform to study pathophysiological mechanisms and drug sensitivity in LQT2.
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                Author and article information

                Journal
                Biomed Res Int
                Biomed Res Int
                BMRI
                BioMed Research International
                Hindawi Publishing Corporation
                2314-6133
                2314-6141
                2016
                26 October 2016
                : 2016
                : 3025057
                Affiliations
                1School of Information Sciences, University of Tampere, Kanslerinrinne 1, 33014 Tampere, Finland
                2BioMediTech, University of Tampere, Biokatu 12, 33520 Tampere, Finland
                3School of Medicine, University of Tampere, Biokatu 12, 33520 Tampere, Finland
                Author notes

                Academic Editor: Hong-Lin Su

                Author information
                http://orcid.org/0000-0001-6341-7055
                http://orcid.org/0000-0003-0334-2172
                http://orcid.org/0000-0003-2298-9553
                Article
                10.1155/2016/3025057
                5101360
                966b7380-39a6-4991-87d6-d68b948bd388
                Copyright © 2016 Henry Joutsijoki et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 25 July 2016
                : 14 September 2016
                Funding
                Funded by: Ella and Georg Ehrnrooth Foundation
                Funded by: Finnish Cultural Foundation Pirkanmaa Regional Fund
                Categories
                Research Article

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