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Title: Abnormal cell detection using the Choquet integral
Author (s): Stanley, R. Joe
Keller, J.
Caldwell, C.W.
Gader, P.
Department/Lab Affiliations: Electrical and Computer Engineering
Image Processing Laboratory
Keywords: Choquet integral
Philadelphia chromosome
X chromosome
abnormal cell detection
automated Giemsa-banded chromosome image research
autosomal classes
cellular biophysics
classification schemes
data-driven homologue matching technique
dynamic programming
false positive rate
genetic abnormalities
genetics
homologous pairs
image recognition
integration
medical image processing
metaphase spreads
neural nets
neural networks
normal chromosome recognition
numerical aberrations
structural aberrations
Issue Date: 2001
Publisher: Institute of Electrical and Electronics Engineers
Citation: Stanley, R.; Keller, J.; Caldwell, C.W.; Gader, P., "Abnormal cell detection using the Choquet integral," Joint 9th IFSA World Congress and 20th NAFIPS International Conference, vol.2, pp.1134-1139, 25-28 July 2001
Abstract: Automated Giemsa-banded chromosome image research has been largely restricted to classification schemes associated with isolated chromosomes within metaphase spreads. In normal human metaphase spreads, there are 46 chromosomes occurring in homologous pairs for the autosomal classes 1-22 and the X chromosome for females. Many genetic abnormalities are directly linked to structural and/or numerical aberrations of chromosomes within metaphase spreads. Cells with the Philadelphia chromosome contain an abnormal chromosome for class 9 and for class 22, leaving a single normal chromosome for each class. A data-driven homologue matching technique is applied to recognizing normal chromosomes from classes 9 and 22. Homologue matching integrates neural networks, dynamic programming and the Choquet integral for chromosome recognition. The inability to locate matching homologous pairs for classes 9 and 22 provides an indication that the cell is abnormal, potentially containing the Philadelphia chromosome. Applying this technique to 50 normal and to 48 abnormal cells containing the Philadelphia chromosome yields 100.0% correct abnormal cell detection with a 24.0% false positive rate.
Type: Article - Conference proceedings
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titleAbnormal cell detection using the Choquet integral
contributor.authorStanley, R. Joe
contributor.authorKeller, J.
contributor.authorCaldwell, C.W.
contributor.authorGader, P.
contributor.deptlabElectrical and Computer Engineering
contributor.deptlabImage Processing Laboratory
subjectChoquet integral
subjectPhiladelphia chromosome
subjectX chromosome
subjectabnormal cell detection
subjectautomated Giemsa-banded chromosome image research
subjectautosomal classes
subjectcellular biophysics
subjectclassification schemes
subjectdata-driven homologue matching technique
subjectdynamic programming
subjectfalse positive rate
subjectgenetic abnormalities
subjectgenetics
subjecthomologous pairs
subjectimage recognition
subjectintegration
subjectmedical image processing
subjectmetaphase spreads
subjectneural nets
subjectneural networks
subjectnormal chromosome recognition
subjectnumerical aberrations
subjectstructural aberrations
date.issued2001
date.submitted2007
publisherInstitute of Electrical and Electronics Engineers
identifier.citationStanley, R.; Keller, J.; Caldwell, C.W.; Gader, P., "Abnormal cell detection using the Choquet integral," Joint 9th IFSA World Congress and 20th NAFIPS International Conference, vol.2, pp.1134-1139, 25-28 July 2001
identifier.pub.URI
http://ieeexplore.ieee.org/iel5/7506/20441/00944764.pdf?arnumber=94476
description.abstractAutomated Giemsa-banded chromosome image research has been largely restricted to classification schemes associated with isolated chromosomes within metaphase spreads. In normal human metaphase spreads, there are 46 chromosomes occurring in homologous pairs for the autosomal classes 1-22 and the X chromosome for females. Many genetic abnormalities are directly linked to structural and/or numerical aberrations of chromosomes within metaphase spreads. Cells with the Philadelphia chromosome contain an abnormal chromosome for class 9 and for class 22, leaving a single normal chromosome for each class. A data-driven homologue matching technique is applied to recognizing normal chromosomes from classes 9 and 22. Homologue matching integrates neural networks, dynamic programming and the Choquet integral for chromosome recognition. The inability to locate matching homologous pairs for classes 9 and 22 provides an indication that the cell is abnormal, potentially containing the Philadelphia chromosome. Applying this technique to 50 normal and to 48 abnormal cells containing the Philadelphia chromosome yields 100.0% correct abnormal cell detection with a 24.0% false positive rate.
typeArticle - Conference proceedings
type.DCMITypetext
type.statusFinal version
rightsThis material is presented to ensure timely dissemination of scholarly and technical work. Copyright and all rights therein are retained by authors or by other copyright holders. All persons copying this information are expected to adhere to the terms and constraints invoked by each author's copyright. In most cases, these works may not be reposted without the explicit permission of the copyright holder.
rights.URI
http://www.ieee.org/web/publications/rights/policies.html
date.accessioned2007-04-05T14:10:50Z
date.available2007-04-05T14:10:50Z
identifier.persist.URI
http://scholarsmine.mst.edu/post_prints/00944764_09007dcc8030c870.html
Full Text
00944764_09007dcc8030c875.pdf