Classification of Colorectal Cancer based on Gene Sequencing data with XGBoost Model: An application of Public Health Informatics


AKBULUT A. S., KÜÇÜKAKÇALI Z., ÇOLAK C.

CUKUROVA MEDICAL JOURNAL, vol.47, no.3, pp.1179-1186, 2022 (ESCI)

  • Publication Type: Article / Article
  • Volume: 47 Issue: 3
  • Publication Date: 2022
  • Doi Number: 10.17826/cumj.112853
  • Journal Name: CUKUROVA MEDICAL JOURNAL
  • Journal Indexes: Emerging Sources Citation Index (ESCI), Academic Search Premier, Directory of Open Access Journals, TR DİZİN (ULAKBİM)
  • Page Numbers: pp.1179-1186
  • Inonu University Affiliated: Yes

Abstract

Purpose: This study aims to classify open-access colorectal cancer gene data and identify essential genes with the XGBoost method, a machine learning method. Materials and Methods: The open-access colorectal cancer gene dataset was used in the study. The dataset included gene sequencing results of 10 mucosae from healthy controls and the colonic mucosa of 12 patients with colorectal cancer. XGboost, one of the machine learning methods, was used to classify the disease. Accuracy, balanced accuracy, sensitivity, selectivity, positive predictive value, and negative predictive value performance metrics were evaluated for model performance. Results: According to the variable selection method, 17 genes were selected, and modeling was performed with these input variables. Accuracy, balanced accuracy, sensitivity, specificity, positive predictive value, negative predictive value, and F1 score obtained from modeling results were 95.5%, 95.8%, 91.7%, 1%, 1%, and 90.9%, and 95.7%, respectively. According to the variable impotance acquired from the XGboost technique results, the CYR61, NR4A, FOSB, and NR4A2 genes can be employed as biomarkers for colorectal cancer. Conclusion: As a consequence of this research, genes that may be linked to colorectal cancer and genetic biomarkers for the illness were identified. In the future, the detected genes' reliability can be verified, therapeutic procedures can be established based on these genes, and their usefulness in clinical practice may be documented.