Title :
An improved classification scheme for chromosomes with missing data
Author :
Poletti, Enea ; Ruggeri, Alfredo ; Grisan, Enrico
Author_Institution :
Dept. of Inf. Eng., Univ. of Padova, Padova, Italy
fDate :
Aug. 30 2011-Sept. 3 2011
Abstract :
Karyotyping, or the automatic classification of human chromosomes, is mostly based on the analysis of the chromosome specific banding pattern. Unfortunately, the most informative phases of the cell division cycle are composed of long chromosomes that easily overlap: the involved banding pattern information is corrupted, resulting in a drastic increase of the classification error. Assuming the availability of a probabilistic classifier, the improvement of the classification of chromosomes with corrupted data would require the additional estimation of the joint probability density of the observed and missing data for each chromosome class. Given the number of classes, the possible position and extension of the corrupted data within a chromosome, and the dimensionality of the feature space, a reliable estimation would need an impossible number of training samples. We chose to circumvent the estimation problem by developing a statistical generative model of the pattern of each class, so that the corrupted part can be substituted with a partial pattern synthetically generated from the model. This allows to obtain a Monte Carlo estimate of the maximum a posteriori probability for the class given the observation and the missing data, which reduces to a simple voting scheme if the a priori probability for each class is equal. Moreover, this Monte Carlo classification is superior to the voting scheme based on the simple imputation of the classes mean to the missing data.
Keywords :
Monte Carlo methods; cellular biophysics; image classification; probability; Monte Carlo classification; banding pattern information; cell division cycle; classification scheme; human chromosomes; missing data; posteriori probability; probabilistic classifier; probability density; statistical generative model; Biological cells; Conferences; Estimation; Humans; Monte Carlo methods; Training; Vectors; Algorithms; Artifacts; Chromosomes; Karyotyping; Pattern Recognition, Automated; Reproducibility of Results; Sample Size; Sensitivity and Specificity;
Conference_Titel :
Engineering in Medicine and Biology Society, EMBC, 2011 Annual International Conference of the IEEE
Conference_Location :
Boston, MA
Print_ISBN :
978-1-4244-4121-1
Electronic_ISBN :
1557-170X
DOI :
10.1109/IEMBS.2011.6091256