$\require{mediawiki-texvc}$

연합인증

연합인증 가입 기관의 연구자들은 소속기관의 인증정보(ID와 암호)를 이용해 다른 대학, 연구기관, 서비스 공급자의 다양한 온라인 자원과 연구 데이터를 이용할 수 있습니다.

이는 여행자가 자국에서 발행 받은 여권으로 세계 각국을 자유롭게 여행할 수 있는 것과 같습니다.

연합인증으로 이용이 가능한 서비스는 NTIS, DataON, Edison, Kafe, Webinar 등이 있습니다.

한번의 인증절차만으로 연합인증 가입 서비스에 추가 로그인 없이 이용이 가능합니다.

다만, 연합인증을 위해서는 최초 1회만 인증 절차가 필요합니다. (회원이 아닐 경우 회원 가입이 필요합니다.)

연합인증 절차는 다음과 같습니다.

최초이용시에는
ScienceON에 로그인 → 연합인증 서비스 접속 → 로그인 (본인 확인 또는 회원가입) → 서비스 이용

그 이후에는
ScienceON 로그인 → 연합인증 서비스 접속 → 서비스 이용

연합인증을 활용하시면 KISTI가 제공하는 다양한 서비스를 편리하게 이용하실 수 있습니다.

Evaluation of Machine Learning Algorithm Utilization for Lung Cancer Classification Based on Gene Expression Levels 원문보기

Asian Pacific journal of cancer prevention : APJCP, v.17 no.2, 2016년, pp.835 - 838  

Podolsky, Maxim D (ITMO University) ,  Barchuk, Anton A (NN Petrov Research Institute of Oncology of the USSR Ministry of Health) ,  Kuznetcov, Vladimir I (KBST ITMO LLC) ,  Gusarova, Natalia F (ITMO University) ,  Gaidukov, Vadim S (ITMO University) ,  Tarakanov, Segrey A (ITMO University)

Abstract AI-Helper 아이콘AI-Helper

Background: Lung cancer remains one of the most common cancers in the world, both in terms of new cases (about 13% of total per year) and deaths (nearly one cancer death in five), because of the high case fatality. Errors in lung cancer type or malignant growth determination lead to degraded treatme...

주제어

AI 본문요약
AI-Helper 아이콘 AI-Helper

* AI 자동 식별 결과로 적합하지 않은 문장이 있을 수 있으니, 이용에 유의하시기 바랍니다.

제안 방법

  • Each sample is described by 12600 gene expression levels. Research task for this data set was to classify cancer types.
  • Each sample is presented by expression levels of 12,533 genes. The task is to make a binary classification of malignant pleural mesothelioma and adenocarcinoma.
  • Each sample is presented by expression levels of 7,129 genes. The task was to detect adenocarcinoma.
  • Each sample is presented by expression levels of 2,880 genes. The task was to detect recurrences.
  • At present it is optimal to use machine learning methods to ascertain a definite diagnosis. Their final aim is to obtain trained algorithms which compute type and developmental character of malignant growth by usage of one or several classification attributes. These algorithms can be used by clinicians as auxiliary tools to process huge amounts of patient data for establishing diagnosis (Sun et al.

대상 데이터

  • Samples were divided in two sets: training (sixteen samples of each cancer type) and testing (the remaining 149 samples). Each sample is presented by expression levels of 12,533 genes. The task is to make a binary classification of malignant pleural mesothelioma and adenocarcinoma.
  • , 2002); Consists of 96 samples: 86 -primary adenocarcinoma (where 67 -stage I, nineteen -stage III), ten -non-neoplastic tissue. Each sample is presented by expression levels of 7,129 genes. The task was to detect adenocarcinoma.
  • Samples of primary tumor and adjacent non-neoplastic tissue were taken during surgical intervention from May 1994 to June 2000 in the University of Michigan Hospital. Peripheral portions of resected lung carcinomas were sectioned, evaluated by a study pathologist and compared with routine H&E sections of the same tumors, and utilized for mRNA isolation.

이론/모형

  • At that, effectiveness of various algorithms differs depending on analyzed data sets. To evaluate effectiveness of the algorithms and compare them it is accepted to use Receiver Operating Characteristic curve (ROC curve) and Matthews Correlation Coefficient (MCC) as a measure of the quality of binary (two-class) as well as non-binary classifications (Baldi et al., 2000).
  • To train the algorithms using data sets of Dana-Farber Cancer Institute, University of Michigan and University of Toronto 10-fold cross validation was used. For Brigham and Women’s Hospital data set we have used training and testing samples that have been already prepared.
본문요약 정보가 도움이 되었나요?

참고문헌 (20)

  1. Baldi P, Brunak S, Chauvin Y, Andersen CAF, and Nielsen H (2000). Assessing the accuracy of prediction algorithms for classification: an overview. Bioinformatics, 16, 412-24. 

  2. Beer DG, Kardia SLR, Huang CC, et al (2002). Geneexpression profiles predict survival of patients with lung adenocarcinoma. Nature Medicine. 8, 816-24. 

  3. Bhattacharjee A, Richards WG, Staunton J, et al (2001). Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclasses. Proceedings of the National Academy of Sciences, 98, 13790-5. 

  4. Cai Z, Xu D, Zhang Q, et al (2015). Classification of lung cancer using ensemble-based feature selection and machine learning methods. Mol BioSyst, 11, 791-800. 

  5. Cheng P, Cheng Y, Li Y, et al (2012). Comparison of the gene expression profiles between smokers with and without lung cancer using RNA-Seq. Asian Pac J Cancer Prev, 13, 3605-9. 

  6. Cruz JA, and Wishart DS (2006). Applications of machine learning in cancer prediction and prognosis. Cancer Informatics, 2, 59-77. 

  7. Ferlay J, Soerjomataram I, Dikshit R, et al (2015). Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Intern J Cancer, 136, 359-86. 

  8. Gordon GJ, Jensen RV, Hsiao LL, et al (2002). Translation of microarray data into clinically relevant cancer diagnostic tests using gene expression ratios in lung cancer and mesothelioma. Cancer Research, 62, 4963-7. 

  9. Guo S, Yan F, Xu J, et al (2015). Identification and validation of the methylation biomarkers of non-small cell lung cancer (NSCLC). Clinical Epigenetics, 7, 3. 

  10. Han Y, Wang XB, Xiao N, and Liu ZD (2013). mRNA Expression and Clinical Significance of ERCC1, BRCA1, RRM1, TYMS and TUBB3 in postoperative patients with non-small cell lung cancer. Asian Pac J Cancer Prev, 14, 2987-90. 

  11. Hosseinzadeh F, Kayvan Joo AH, Ebrahimi M, Goliaei B (2013). Prediction of lung tumor types based on protein attributes by machine learning algorithms. Springer Plus, 2, 238. 

  12. Jung KW, Won YJ, Kong HJ, et al (2014). Cancer statistics in korea: incidence, mortality, survival, and prevalence in 2011. Cancer Res Treat, 46, 109-23. 

  13. Lei Win S, Htike ZZ, Yusof F, Noorbatcha AI (2014). Gene expression mining for predicting survivability of patients in earlystages of lung cancer. Int J Bioinformatics Biosciences, 4, 1-9. 

  14. Li J, Li D, Wei X, Su Y (2014). In silico comparative genomic analysis of two non-small cell lung cancer subtypes and their potentials for cancer classification. Cancer Genomics Proteomics, 11, 303-10. 

  15. Liu M, Pan H, Zhang F, et al (2013). Screening of differentially expressed genes among various TNM stages of lung adenocarcinoma by genomewide gene expression profile analysis. Asian Pac J Cancer Prev, 14, 6281-6. 

  16. Pass HI (2001). Malignant pleural mesothelioma: surgical roles and novel therapies. Clinical Lung Cancer, 3, 102-7. 

  17. Sun T, Wang J, Li X, et al (2013). Comparative evaluation of support vector machines for computer aided diagnosis of lung cancer in CT based on a multi-dimensional data set. Computer Methods Programs Biomedicine, 111, 519-24. 

  18. Wang JJ, Wu HF, Sun T, et al (2013). Prediction models for solitary pulmonary nodules based on curvelet textural features and clinical parameters. Asian Pac J Cancer Prev, 14, 6019-23. 

  19. Wigle DA, Jurisica I, Radulovich N, et al (2002). Molecular profiling of non-small cell lung cancer and correlation with disease-free survival. Cancer Res, 62, 3005-8. 

  20. Yu Z, Lu H, Si H, et al (2015). A highly efficient gene expression programming (GEP) model for auxiliary diagnosis of small cell lung cancer. PLoS ONE, 10, 125517. 

관련 콘텐츠

오픈액세스(OA) 유형

GOLD

오픈액세스 학술지에 출판된 논문

저작권 관리 안내
섹션별 컨텐츠 바로가기

AI-Helper ※ AI-Helper는 오픈소스 모델을 사용합니다.

AI-Helper 아이콘
AI-Helper
안녕하세요, AI-Helper입니다. 좌측 "선택된 텍스트"에서 텍스트를 선택하여 요약, 번역, 용어설명을 실행하세요.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.

선택된 텍스트

맨위로