Publication:
Predicting the predisposition to colorectal cancer based on SNP profiles of immune phenotypes using supervised learning models.

dc.contributor.authorCakmak, Ali, Ayaz, Huzeyfe, Arıkan, Soykan, Ibrahimzada, Ali R, Demirkol, Şeyda, Sönmez, Dilara, Hakan, Mehmet T, Sürmen, Saime T, Horozoğlu, Cem, Doğan, Mehmet B, Küçükhüseyin, Özlem, Cacına, Canan, Kıran, Bayram, Zeybek, Ümit, Baysan, Mehmet, Yaylım, İlhan
dc.contributor.authorCakmak, A, Ayaz, H, Arikan, S, Ibrahimzada, AR, Demirkol, S, Sonmez, D, Hakan, MT, Surmen, ST, Horozoglu, C, Dogan, MB, Kucukhuseyin, O, Cacina, C, Kiran, B, Zeybek, U, Baysan, M, Yaylim, I
dc.date.accessioned2023-05-08T22:39:50Z
dc.date.available2023-05-08T22:39:50Z
dc.date.issued2022-11-11T00:00:00Z
dc.date.issued2023.01.01
dc.description.abstractThis study explores the machine learning-based assessment of predisposition to colorectal cancer based on single nucleotide polymorphisms (SNP). Such a computational approach may be used as a risk indicator and an auxiliary diagnosis method that complements the traditional methods such as biopsy and CT scan. Moreover, it may be used to develop a low-cost screening test for the early detection of colorectal cancers to improve public health. We employ several supervised classification algorithms. Besides, we apply data imputation to fill in the missing genotype values. The employed dataset includes SNPs observed in particular colorectal cancer-associated genomic loci that are located within DNA regions of 11 selected genes obtained from 115 individuals. We make the following observations: (i) random forest-based classifier using one-hot encoding and K-nearest neighbor (KNN)-based imputation performs the best among the studied classifiers with an F1 score of 89% and area under the curve (AUC) score of 0.96. (ii) One-hot encoding together with K-nearest neighbor-based data imputation increases the F1 scores by around 26% in comparison to the baseline approach which does not employ them. (iii) The proposed model outperforms a commonly employed state-of-the-art approach, ColonFlag, under all evaluated settings by up to 24% in terms of the AUC score. Based on the high accuracy of the constructed predictive models, the studied 11 genes may be considered a gene panel candidate for colon cancer risk screening.
dc.identifier.doi10.1007/s11517-022-02707-9
dc.identifier.eissn1741-0444
dc.identifier.endpage258
dc.identifier.issn0140-0118
dc.identifier.pubmed36357628
dc.identifier.scopus2-s2.0-85141696341
dc.identifier.startpage243
dc.identifier.urihttps://hdl.handle.net/20.500.12597/11719
dc.identifier.volume61
dc.identifier.wosWOS:000881669900001
dc.relation.ispartofMedical and Biological Engineering and Computing
dc.relation.ispartofMEDICAL & BIOLOGICAL ENGINEERING & COMPUTING
dc.rightsfalse
dc.subjectCancer screening
dc.titlePredicting the predisposition to colorectal cancer based on SNP profiles of immune phenotypes using supervised learning models.
dc.titlePredicting the predisposition to colorectal cancer based on SNP profiles of immune phenotypes using supervised learning models
dc.typeJournal Article
dspace.entity.typePublication
oaire.citation.issue1
oaire.citation.volume61
relation.isPubmedOfPublication76041a52-9cda-469b-b708-9417271d609b
relation.isPubmedOfPublication.latestForDiscovery76041a52-9cda-469b-b708-9417271d609b
relation.isScopusOfPublicationb132a2cd-1620-4317-bf27-fee40b887543
relation.isScopusOfPublication.latestForDiscoveryb132a2cd-1620-4317-bf27-fee40b887543
relation.isWosOfPublicationf5319b53-ead9-4d06-9ebb-c8edd8d07bbf
relation.isWosOfPublication.latestForDiscoveryf5319b53-ead9-4d06-9ebb-c8edd8d07bbf

Files

Collections