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GWAS Study

Machine Learning Study of SNPs in Noncoding Regions to Predict Non-small Cell Lung Cancer Susceptibility.

Huang Y, Bao T, Zhang T et al.

37689528 PubMed ID
GWAS Study Type
726 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HY
Huang Y
BT
Bao T
ZT
Zhang T
JG
Ji G
WY
Wang Y
LZ
Ling Z
LW
Li W
Chapter II

Abstract

Summary of the research findings

Non-small cell lung cancer (NSCLC) is the most common pathological subtype of lung cancer. Both environmental and genetic factors have been reported to impact the lung cancer susceptibility. We conducted a genome-wide association study (GWAS) of 287 NSCLC patients and 467 healthy controls in a Chinese population using the Illumina Genome-Wide Asian Screening Array Chip on 712,095 SNPs (single nucleotide polymorphisms). Using logistic regression modeling, GWAS identified 17 new noncoding region SNP loci associated with the NSCLC risk, and the top three (rs80040741, rs9568547, rs6010259) were under a stringent p-value (<3.02e-6). Notably, rs80040741 and rs6010259 were annotated from the intron regions of MUC3A and MLC1, respectively. Together with another five SNPs previously reported in Chinese NSCLC patients and another four covariates (e.g., smoking status, age, low dose CT screening, sex), a predictive model by machine learning methods can separate the NSCLC from healthy controls with an accuracy of 86%. This is the first time to apply machine learning method in predicting the NSCLC susceptibility using both genetic and clinical characteristics. Our findings will provide a promising method in NSCLC early diagnosis and improve our understanding of applying machine learning methods in precision medicine.

275 Han Chinese ancestry cases, 451 Han Chinese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

726
Total Participants
GWAS
Study Type
No
Replicated
East Asian
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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