• 한국정보통신학회:학술대회논문집
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• 한국해양정보통신학회 2008년도 춘계종합학술대회 A
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• pp.776-779
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• 2008

DNA 기술의 발달로 얻어진 대량의 유전자 정보를 손쉽게 이상 값을 가진 유전자의 정확한 분류와 진단을 할 수 있는 방법인 Microarray 기술에 대한 기대가 커지고 있다. 정확한 분류를 하기 위해서는 추출된 유전자에 들어 있는 많은 잡음 즉 이상 값을 가진 유전자만을 추출할 필요가 있다. 따라서 본 논문에서는 세 가지 dataset에 대해 기존 연구방법의 여러 가지 유전자 추출 방법을 조사하고 Matlab으로 구현한 진화프로그램을 이용하여 새로운 데이터의 분류방법과 모델링 방법을 제안한다.

• 응용통계연구
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• 제18권2호
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• pp.355-369
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• 2005

마이크로어레이 실험에서는 유전자의 기능과 상호작용의 이해를 돕기 위한 방안으로 유전자발현자료의 시각화방법이 많이 사용되고 있다. 행렬도는 유전자와 샘플들을 동시에 그려볼 수 있어서, 유전자 또는 샘플의 군집이나 유전자-샘플간 연관작용을 알아보는데 더욱 유용하게 쓰일 수 있다. 본고에서는 마이크로어레이실험에서 행렬도를 이용하여 유전자의 군집 및 연관성을 알아보는 방법을 소개하고, 추가점기법을 이용하여 새로운 샘플을 분류하는 방법을 제안하였다. Golub et al.(1999)의 백혈병 데이터와 Alizadeh et al. (2000)의 림프구데이터, Ross et al.(2000)의 NCI60 종양조직데이터를 이용하여 유용성을 살펴보았으며, 계층적 군집분석 및 k-평균 군집분석 등 다른 기법을 이용한 결과와 비교하고 이러한 기법을 행렬도와 연계하는 방안을 살펴보았다.

• 한국생물정보학회:학술대회논문집
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• 한국생물정보시스템생물학회 2004년도 The 3rd Annual Conference for The Korean Society for Bioinformatics Association of Asian Societies for Bioinformatics 2004 Symposium
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• pp.107-116
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• 2004

The advent of microarray technologies gives an opportunity to moni tor the expression of ten thousands of genes, simultaneously. Such microarray data can be deteriorated by experimental errors and image artifacts, which generate non-negligible outliers that are estimated by 15% of typical microarray data. Thus, it is an important issue to detect and correct the se faulty probes prior to high-level data analysis such as classification or clustering. In this paper, we propose a systematic procedure for the detection of faulty probes and its proper correction in Genechip array based on multivariate statistical approaches. Principal component analysis (PCA), one of the most widely used multivariate statistical approaches, has been applied to construct a statistical correlation model with 20 pairs of probes for each gene. And, the faulty probes are identified by inspecting the squared prediction error (SPE) of each probe from the PCA model. Then, the outlying probes are reconstructed by the iterative optimization approach minimizing SPE. We used the public data presented from the gene chip project of human fibroblast cell. Through the application study, the proposed approach showed good performance for probe correction without removing faulty probes, which may be desirable in the viewpoint of the maximum use of data information.

• 전기학회논문지
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• 제58권7호
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• pp.1424-1434
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• 2009

DNA computing-inspired pattern classification based on the hypernetwork model is a novel approach to pattern classification problems. The hypernetwork model has been shown to be a powerful tool for multi-class data analysis. However, the ordinary hypernetwork model has limitations, such as operating sequentially only. In this paper, we propose a efficient implementing method of DNA computing-inspired pattern classifier using GPU. We show simulation results of multi-class pattern classification from hand-written digit data, DNA microarray data and 8 category scene data for performance evaluation. and we also compare of operation time of the proposed DNA computing-inspired pattern classifier on each operating environments such as CPU and GPU. Experiment results show competitive diagnosis results over other conventional machine learning algorithms. We could confirm the proposed DNA computing-inspired pattern classifier, designed on GPU using CUDA platform, which is suitable for multi-class data classification. And its operating speed is fast enough to comply point-of-care diagnostic purpose and real-time scene categorization and hand-written digit data classification.

• ETRI Journal
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• 제41권3호
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• pp.358-370
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• 2019

The main aim of this study is to select the optimal set of genes from microarray cancer datasets that contribute to the prediction of specific cancer types. This study proposes the enhancement of the feature selection filter algorithm based on Joe's normalized mutual information and its use for gene selection. The proposed algorithm is implemented and evaluated on seven benchmark microarray cancer datasets, namely, central nervous system, leukemia (binary), leukemia (3 class), leukemia (4 class), lymphoma, mixed lineage leukemia, and small round blue cell tumor, using five well-known classifiers, including the naive Bayes, radial basis function network, instance-based classifier, decision-based table, and decision tree. An average increase in the prediction accuracy of 5.1% is observed on all seven datasets averaged over all five classifiers. The average reduction in training time is 2.86 seconds. The performance of the proposed method is also compared with those of three other popular mutual information-based feature selection filters, namely, information gain, gain ratio, and symmetric uncertainty. The results are impressive when all five classifiers are used on all the datasets.

• Asian Pacific Journal of Cancer Prevention
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• 제17권5호
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• pp.2375-2382
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• 2016

Cancer is a major health problem in Oman. It is reported that cancer incidence in Oman is the second highest after Saudi Arabia among Gulf Cooperation Council countries. Based on GLOBOCAN estimates, Oman is predicted to face an almost two-fold increase in cancer incidence in the period 2008-2020. However, cancer research in Oman is still in its infancy. This is due to the fact that medical institutions and infrastructure that play central roles in data collection and analysis are relatively new developments in Oman. We believe the country requires an organized plan and efforts to promote local cancer research. In this paper, we discuss current research progress in cancer diagnosis using machine learning techniques to optimize computer aided cancer detection and classification (CAD). We specifically discuss CAD using two major medical data, i.e., medical imaging and microarray gene expression profiling, because medical imaging like mammography, MRI, and PET have been widely used in Oman for assisting radiologists in early cancer diagnosis and microarray data have been proven to be a reliable source for differential diagnosis. We also discuss future cancer research directions and benefits to Oman economy for entering the cancer research and treatment business as it is a multi-billion dollar industry worldwide.

• 응용통계연구
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• 제24권1호
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• pp.137-143
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• 2011

The classification of subjects with unknown distribution in a small sample size often involves order-restricted constraints in multivariate parameter setups. Those problems make the optimality of a conventional likelihood ratio based statistical inferences not feasible. Fortunately, Roy (1953) introduced union-intersection principle(UIP) which provides an alternative avenue. Multivariate linear rank statistics along with that principle, yield a considerably appropriate robust testing procedure. Furthermore, conditionally distribution-free test based upon exact permutation theory is used to generate p-values, even in a small sample. Applications of this method are illustrated in a real microarray data example (Lobenhofer et al., 2002).

• 정보처리학회논문지D
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• 제16D권5호
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• pp.643-650
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• 2009

생명정보 대량 획득기술의 하나인 마이크로어레이(microarray)는 DNA와 각종 유전자 연구에 사용되는 도구로 확립되면서, 생명정보학(Bioinformatics)분야의 발전에 크게 기여하였다. 그러나 마이크로어레이는 생명정보학분야의 핵심기술 중 하나로 발전하였음에도 불구하고 실험으로 생성되는 데이터는 형태가 다양하고 매우 복잡한 형태를 갖기 때문에 데이터의 공유나 저장에서 많은 어려움을 겪고 있다. 본 논문에서는 마이크로어레이 데이터의 관리를 원활하게 하기위한 XML 기반의 표준 포맷인 MAGE-ML스키마에서 구조적으로 유사한 엘리먼트가 반복적으로 나타나는 특징과 대다수의 엘리먼트들이 특정 엘리먼트의 자식으로만 온다는 구조적 특징을 이용하여, MAGE-ML의 스키마를 단순화 하고 저장구조를 효율적으로 설계하는 방법을 제안한다. 이 방법에서 인라인 기법(Inlining Technique)을 이용한 스키마의 단순화와 새롭게 제시하는 엘리먼트의 구조적 형태를 기준으로 분류하는 기법을 이용한다. 이를 통하여 데이터베이스 스키마는 간략화 되며 테이블조인의 횟수가 줄어들고 성능은 향상된다.

• Journal of the Korean Data and Information Science Society
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• 제20권2호
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• pp.311-319
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• 2009

군집과 분류분석에서 L1 데이터 뎁스를 이용한 DDclust와 DDclass라고 불리는 로버스트한 방법이 Jornsten (2004)에 의하여 제안되었다. SVM-기반방법이 많이 사용되나 이상치가 있는 경우에는 약간의 문제가 있다. 유전자 자료에서는 유전자 수가 많기 때문에 적절한 유전자 선택과정이 필요하다. 따라서 적절한 유전자 또는 유전자 군집을 선택하여 분류에 이용하면 분류의 성능을 향상시킬 수 있다. 이러한 관점에서 뎁스 기반 분류방법과 SVM-기반 분류방법을 비교 연구하여 그 성능을 비교 하였다.

• Asian Pacific Journal of Cancer Prevention
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• 제17권1호
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• pp.95-100
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• 2016

Background: Survival time of lymphoma patients can be estimated with the help of microarray technology. In this study, with the use of iterative Bayesian Model Averaging (BMA) method, survival time of Mantle Cell Lymphoma patients (MCL) was estimated and in reference to the findings, patients were divided into two high-risk and low-risk groups. Materials and Methods: In this study, gene expression data of MCL patients were used in order to select a subset of genes for survival analysis with microarray data, using the iterative BMA method. To evaluate the performance of the method, patients were divided into high-risk and low-risk based on their scores. Performance prediction was investigated using the log-rank test. The bioconductor package "iterativeBMAsurv" was applied with R statistical software for classification and survival analysis. Results: In this study, 25 genes associated with survival for MCL patients were identified across 132 selected models. The maximum likelihood estimate coefficients of the selected genes and the posterior probabilities of the selected models were obtained from training data. Using this method, patients could be separated into high-risk and low-risk groups with high significance (p<0.001). Conclusions: The iterative BMA algorithm has high precision and ability for survival analysis. This method is capable of identifying a few predictive variables associated with survival, among many variables in a set of microarray data. Therefore, it can be used as a low-cost diagnostic tool in clinical research.