An ensemble classification approach for melanoma diagnosis
Abstract Malignant melanoma is the deadliest form of skin cancer, and has, among cancer types, one of the most rapidly increasing incidence rates in the world. Early diagnosis is crucial, since if detected early, its cure is simple. In this paper, we present an effective approach to melanoma identif...
Ausführliche Beschreibung
Autor*in: |
Schaefer, Gerald [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2014 |
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Anmerkung: |
© Springer-Verlag Berlin Heidelberg 2014 |
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Übergeordnetes Werk: |
Enthalten in: Memetic computing - Berlin : Springer, 2009, 6(2014), 4 vom: 21. Okt., Seite 233-240 |
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Übergeordnetes Werk: |
volume:6 ; year:2014 ; number:4 ; day:21 ; month:10 ; pages:233-240 |
Links: |
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DOI / URN: |
10.1007/s12293-014-0144-8 |
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Katalog-ID: |
SPR024838543 |
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520 | |a Abstract Malignant melanoma is the deadliest form of skin cancer, and has, among cancer types, one of the most rapidly increasing incidence rates in the world. Early diagnosis is crucial, since if detected early, its cure is simple. In this paper, we present an effective approach to melanoma identification from dermoscopic images of skin lesions based on ensemble classification. First, we perform automatic border detection to segment the lesion from the background skin. Based on the extracted border, we extract a series of colour, texture and shape features. The derived features are then employed in a pattern classification stage for which we employ a novel, dedicated ensemble learning approach to address the class imbalance in the training data and to yield improved classification performance. Our classifier committee trains individual classifiers on balanced subspaces, removes redundant predictors based on a diversity measure and combines the remaining classifiers using a neural network fuser. Experimental results on a large dataset of dermoscopic skin lesion images show our approach to work well, to provide both high sensitivity and specificity, and our presented classifier ensemble to lead to statistically better recognition performance compared to other dedicated classification algorithms. | ||
650 | 4 | |a Medical imaging |7 (dpeaa)DE-He213 | |
650 | 4 | |a Skin lesion analysis |7 (dpeaa)DE-He213 | |
650 | 4 | |a Melanoma diagnosis |7 (dpeaa)DE-He213 | |
650 | 4 | |a Ensemble classification |7 (dpeaa)DE-He213 | |
650 | 4 | |a Imbalanced classification |7 (dpeaa)DE-He213 | |
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700 | 1 | |a Celebi, M. Emre |4 aut | |
700 | 1 | |a Iyatomi, Hitoshi |4 aut | |
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10.1007/s12293-014-0144-8 doi (DE-627)SPR024838543 (SPR)s12293-014-0144-8-e DE-627 ger DE-627 rakwb eng Schaefer, Gerald verfasserin aut An ensemble classification approach for melanoma diagnosis 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2014 Abstract Malignant melanoma is the deadliest form of skin cancer, and has, among cancer types, one of the most rapidly increasing incidence rates in the world. Early diagnosis is crucial, since if detected early, its cure is simple. In this paper, we present an effective approach to melanoma identification from dermoscopic images of skin lesions based on ensemble classification. First, we perform automatic border detection to segment the lesion from the background skin. Based on the extracted border, we extract a series of colour, texture and shape features. The derived features are then employed in a pattern classification stage for which we employ a novel, dedicated ensemble learning approach to address the class imbalance in the training data and to yield improved classification performance. Our classifier committee trains individual classifiers on balanced subspaces, removes redundant predictors based on a diversity measure and combines the remaining classifiers using a neural network fuser. Experimental results on a large dataset of dermoscopic skin lesion images show our approach to work well, to provide both high sensitivity and specificity, and our presented classifier ensemble to lead to statistically better recognition performance compared to other dedicated classification algorithms. Medical imaging (dpeaa)DE-He213 Skin lesion analysis (dpeaa)DE-He213 Melanoma diagnosis (dpeaa)DE-He213 Ensemble classification (dpeaa)DE-He213 Imbalanced classification (dpeaa)DE-He213 Krawczyk, Bartosz aut Celebi, M. Emre aut Iyatomi, Hitoshi aut Enthalten in Memetic computing Berlin : Springer, 2009 6(2014), 4 vom: 21. Okt., Seite 233-240 (DE-627)597545006 (DE-600)2489140-X 1865-9292 nnns volume:6 year:2014 number:4 day:21 month:10 pages:233-240 https://dx.doi.org/10.1007/s12293-014-0144-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 6 2014 4 21 10 233-240 |
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10.1007/s12293-014-0144-8 doi (DE-627)SPR024838543 (SPR)s12293-014-0144-8-e DE-627 ger DE-627 rakwb eng Schaefer, Gerald verfasserin aut An ensemble classification approach for melanoma diagnosis 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2014 Abstract Malignant melanoma is the deadliest form of skin cancer, and has, among cancer types, one of the most rapidly increasing incidence rates in the world. Early diagnosis is crucial, since if detected early, its cure is simple. In this paper, we present an effective approach to melanoma identification from dermoscopic images of skin lesions based on ensemble classification. First, we perform automatic border detection to segment the lesion from the background skin. Based on the extracted border, we extract a series of colour, texture and shape features. The derived features are then employed in a pattern classification stage for which we employ a novel, dedicated ensemble learning approach to address the class imbalance in the training data and to yield improved classification performance. Our classifier committee trains individual classifiers on balanced subspaces, removes redundant predictors based on a diversity measure and combines the remaining classifiers using a neural network fuser. Experimental results on a large dataset of dermoscopic skin lesion images show our approach to work well, to provide both high sensitivity and specificity, and our presented classifier ensemble to lead to statistically better recognition performance compared to other dedicated classification algorithms. Medical imaging (dpeaa)DE-He213 Skin lesion analysis (dpeaa)DE-He213 Melanoma diagnosis (dpeaa)DE-He213 Ensemble classification (dpeaa)DE-He213 Imbalanced classification (dpeaa)DE-He213 Krawczyk, Bartosz aut Celebi, M. Emre aut Iyatomi, Hitoshi aut Enthalten in Memetic computing Berlin : Springer, 2009 6(2014), 4 vom: 21. Okt., Seite 233-240 (DE-627)597545006 (DE-600)2489140-X 1865-9292 nnns volume:6 year:2014 number:4 day:21 month:10 pages:233-240 https://dx.doi.org/10.1007/s12293-014-0144-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 6 2014 4 21 10 233-240 |
allfields_unstemmed |
10.1007/s12293-014-0144-8 doi (DE-627)SPR024838543 (SPR)s12293-014-0144-8-e DE-627 ger DE-627 rakwb eng Schaefer, Gerald verfasserin aut An ensemble classification approach for melanoma diagnosis 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2014 Abstract Malignant melanoma is the deadliest form of skin cancer, and has, among cancer types, one of the most rapidly increasing incidence rates in the world. Early diagnosis is crucial, since if detected early, its cure is simple. In this paper, we present an effective approach to melanoma identification from dermoscopic images of skin lesions based on ensemble classification. First, we perform automatic border detection to segment the lesion from the background skin. Based on the extracted border, we extract a series of colour, texture and shape features. The derived features are then employed in a pattern classification stage for which we employ a novel, dedicated ensemble learning approach to address the class imbalance in the training data and to yield improved classification performance. Our classifier committee trains individual classifiers on balanced subspaces, removes redundant predictors based on a diversity measure and combines the remaining classifiers using a neural network fuser. Experimental results on a large dataset of dermoscopic skin lesion images show our approach to work well, to provide both high sensitivity and specificity, and our presented classifier ensemble to lead to statistically better recognition performance compared to other dedicated classification algorithms. Medical imaging (dpeaa)DE-He213 Skin lesion analysis (dpeaa)DE-He213 Melanoma diagnosis (dpeaa)DE-He213 Ensemble classification (dpeaa)DE-He213 Imbalanced classification (dpeaa)DE-He213 Krawczyk, Bartosz aut Celebi, M. Emre aut Iyatomi, Hitoshi aut Enthalten in Memetic computing Berlin : Springer, 2009 6(2014), 4 vom: 21. Okt., Seite 233-240 (DE-627)597545006 (DE-600)2489140-X 1865-9292 nnns volume:6 year:2014 number:4 day:21 month:10 pages:233-240 https://dx.doi.org/10.1007/s12293-014-0144-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 6 2014 4 21 10 233-240 |
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10.1007/s12293-014-0144-8 doi (DE-627)SPR024838543 (SPR)s12293-014-0144-8-e DE-627 ger DE-627 rakwb eng Schaefer, Gerald verfasserin aut An ensemble classification approach for melanoma diagnosis 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag Berlin Heidelberg 2014 Abstract Malignant melanoma is the deadliest form of skin cancer, and has, among cancer types, one of the most rapidly increasing incidence rates in the world. Early diagnosis is crucial, since if detected early, its cure is simple. In this paper, we present an effective approach to melanoma identification from dermoscopic images of skin lesions based on ensemble classification. First, we perform automatic border detection to segment the lesion from the background skin. Based on the extracted border, we extract a series of colour, texture and shape features. The derived features are then employed in a pattern classification stage for which we employ a novel, dedicated ensemble learning approach to address the class imbalance in the training data and to yield improved classification performance. Our classifier committee trains individual classifiers on balanced subspaces, removes redundant predictors based on a diversity measure and combines the remaining classifiers using a neural network fuser. Experimental results on a large dataset of dermoscopic skin lesion images show our approach to work well, to provide both high sensitivity and specificity, and our presented classifier ensemble to lead to statistically better recognition performance compared to other dedicated classification algorithms. Medical imaging (dpeaa)DE-He213 Skin lesion analysis (dpeaa)DE-He213 Melanoma diagnosis (dpeaa)DE-He213 Ensemble classification (dpeaa)DE-He213 Imbalanced classification (dpeaa)DE-He213 Krawczyk, Bartosz aut Celebi, M. Emre aut Iyatomi, Hitoshi aut Enthalten in Memetic computing Berlin : Springer, 2009 6(2014), 4 vom: 21. Okt., Seite 233-240 (DE-627)597545006 (DE-600)2489140-X 1865-9292 nnns volume:6 year:2014 number:4 day:21 month:10 pages:233-240 https://dx.doi.org/10.1007/s12293-014-0144-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 6 2014 4 21 10 233-240 |
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Schaefer, Gerald @@aut@@ Krawczyk, Bartosz @@aut@@ Celebi, M. Emre @@aut@@ Iyatomi, Hitoshi @@aut@@ |
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Schaefer, Gerald |
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Schaefer, Gerald misc Medical imaging misc Skin lesion analysis misc Melanoma diagnosis misc Ensemble classification misc Imbalanced classification An ensemble classification approach for melanoma diagnosis |
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An ensemble classification approach for melanoma diagnosis Medical imaging (dpeaa)DE-He213 Skin lesion analysis (dpeaa)DE-He213 Melanoma diagnosis (dpeaa)DE-He213 Ensemble classification (dpeaa)DE-He213 Imbalanced classification (dpeaa)DE-He213 |
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ensemble classification approach for melanoma diagnosis |
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An ensemble classification approach for melanoma diagnosis |
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Abstract Malignant melanoma is the deadliest form of skin cancer, and has, among cancer types, one of the most rapidly increasing incidence rates in the world. Early diagnosis is crucial, since if detected early, its cure is simple. In this paper, we present an effective approach to melanoma identification from dermoscopic images of skin lesions based on ensemble classification. First, we perform automatic border detection to segment the lesion from the background skin. Based on the extracted border, we extract a series of colour, texture and shape features. The derived features are then employed in a pattern classification stage for which we employ a novel, dedicated ensemble learning approach to address the class imbalance in the training data and to yield improved classification performance. Our classifier committee trains individual classifiers on balanced subspaces, removes redundant predictors based on a diversity measure and combines the remaining classifiers using a neural network fuser. Experimental results on a large dataset of dermoscopic skin lesion images show our approach to work well, to provide both high sensitivity and specificity, and our presented classifier ensemble to lead to statistically better recognition performance compared to other dedicated classification algorithms. © Springer-Verlag Berlin Heidelberg 2014 |
abstractGer |
Abstract Malignant melanoma is the deadliest form of skin cancer, and has, among cancer types, one of the most rapidly increasing incidence rates in the world. Early diagnosis is crucial, since if detected early, its cure is simple. In this paper, we present an effective approach to melanoma identification from dermoscopic images of skin lesions based on ensemble classification. First, we perform automatic border detection to segment the lesion from the background skin. Based on the extracted border, we extract a series of colour, texture and shape features. The derived features are then employed in a pattern classification stage for which we employ a novel, dedicated ensemble learning approach to address the class imbalance in the training data and to yield improved classification performance. Our classifier committee trains individual classifiers on balanced subspaces, removes redundant predictors based on a diversity measure and combines the remaining classifiers using a neural network fuser. Experimental results on a large dataset of dermoscopic skin lesion images show our approach to work well, to provide both high sensitivity and specificity, and our presented classifier ensemble to lead to statistically better recognition performance compared to other dedicated classification algorithms. © Springer-Verlag Berlin Heidelberg 2014 |
abstract_unstemmed |
Abstract Malignant melanoma is the deadliest form of skin cancer, and has, among cancer types, one of the most rapidly increasing incidence rates in the world. Early diagnosis is crucial, since if detected early, its cure is simple. In this paper, we present an effective approach to melanoma identification from dermoscopic images of skin lesions based on ensemble classification. First, we perform automatic border detection to segment the lesion from the background skin. Based on the extracted border, we extract a series of colour, texture and shape features. The derived features are then employed in a pattern classification stage for which we employ a novel, dedicated ensemble learning approach to address the class imbalance in the training data and to yield improved classification performance. Our classifier committee trains individual classifiers on balanced subspaces, removes redundant predictors based on a diversity measure and combines the remaining classifiers using a neural network fuser. Experimental results on a large dataset of dermoscopic skin lesion images show our approach to work well, to provide both high sensitivity and specificity, and our presented classifier ensemble to lead to statistically better recognition performance compared to other dedicated classification algorithms. © Springer-Verlag Berlin Heidelberg 2014 |
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An ensemble classification approach for melanoma diagnosis |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR024838543</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230403080922.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201007s2014 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s12293-014-0144-8</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR024838543</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s12293-014-0144-8-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Schaefer, Gerald</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="3"><subfield code="a">An ensemble classification approach for melanoma diagnosis</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2014</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Springer-Verlag Berlin Heidelberg 2014</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Malignant melanoma is the deadliest form of skin cancer, and has, among cancer types, one of the most rapidly increasing incidence rates in the world. Early diagnosis is crucial, since if detected early, its cure is simple. In this paper, we present an effective approach to melanoma identification from dermoscopic images of skin lesions based on ensemble classification. First, we perform automatic border detection to segment the lesion from the background skin. Based on the extracted border, we extract a series of colour, texture and shape features. The derived features are then employed in a pattern classification stage for which we employ a novel, dedicated ensemble learning approach to address the class imbalance in the training data and to yield improved classification performance. Our classifier committee trains individual classifiers on balanced subspaces, removes redundant predictors based on a diversity measure and combines the remaining classifiers using a neural network fuser. Experimental results on a large dataset of dermoscopic skin lesion images show our approach to work well, to provide both high sensitivity and specificity, and our presented classifier ensemble to lead to statistically better recognition performance compared to other dedicated classification algorithms.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Medical imaging</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Skin lesion analysis</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Melanoma diagnosis</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Ensemble classification</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Imbalanced classification</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Krawczyk, Bartosz</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Celebi, M. Emre</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Iyatomi, Hitoshi</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Memetic computing</subfield><subfield code="d">Berlin : Springer, 2009</subfield><subfield code="g">6(2014), 4 vom: 21. Okt., Seite 233-240</subfield><subfield code="w">(DE-627)597545006</subfield><subfield code="w">(DE-600)2489140-X</subfield><subfield code="x">1865-9292</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:6</subfield><subfield code="g">year:2014</subfield><subfield code="g">number:4</subfield><subfield code="g">day:21</subfield><subfield code="g">month:10</subfield><subfield code="g">pages:233-240</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://dx.doi.org/10.1007/s12293-014-0144-8</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_SPRINGER</subfield></datafield><datafield tag="912" 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