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A new efficient method to detect genetic interactions for lung cancer GWAS

Luyapan, Jennifer (author)
Dartmouth College
Ji, Xuemei (author)
Dartmouth College
Li, Siting (author)
Dartmouth College
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Xiao, Xiangjun (author)
Baylor College of Medicine
Zhu, Dakai (author)
Dartmouth College,Baylor College of Medicine
Duell, Eric J. (author)
Catalan Institute of Oncology
Christiani, David C. (author)
Harvard University,Massachusetts General Hospital
Schabath, Matthew B. (author)
H. Lee Moffitt Cancer Center & Research Institute
Arnold, Susanne M. (author)
University of Kentucky
Zienolddiny, Shanbeh (author)
National Institute of Occupational Health, Norway
Brunnström, Hans (author)
Lund University,Lunds universitet,Förbättrad diagnostik och prognostik vid lungcancer och metastaser till lunga,Forskargrupper vid Lunds universitet,LUCC: Lunds universitets cancercentrum,Övriga starka forskningsmiljöer,Improved diagnostics and prognostics of lung cancer and metastases to the lungs,Lund University Research Groups,LUCC: Lund University Cancer Centre,Other Strong Research Environments
Melander, Olle (author)
Lund University,Lunds universitet,Kardiovaskulär forskning - hypertoni,Forskargrupper vid Lunds universitet,Cardiovascular Research - Hypertension,Lund University Research Groups
Thornquist, Mark D. (author)
Fred Hutchinson Cancer Research Center
MacKenzie, Todd A. (author)
Dartmouth College
Amos, Christopher I. (author)
Baylor College of Medicine,Dartmouth College
Gui, Jiang (author)
Dartmouth College
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 (creator_code:org_t)
2020-10-30
2020
English.
In: BMC Medical Genomics. - : Springer Science and Business Media LLC. - 1755-8794. ; 13:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: Genome-wide association studies (GWAS) have proven successful in predicting genetic risk of disease using single-locus models; however, identifying single nucleotide polymorphism (SNP) interactions at the genome-wide scale is limited due to computational and statistical challenges. We addressed the computational burden encountered when detecting SNP interactions for survival analysis, such as age of disease-onset. To confront this problem, we developed a novel algorithm, called the Efficient Survival Multifactor Dimensionality Reduction (ES-MDR) method, which used Martingale Residuals as the outcome parameter to estimate survival outcomes, and implemented the Quantitative Multifactor Dimensionality Reduction method to identify significant interactions associated with age of disease-onset. Methods: To demonstrate efficacy, we evaluated this method on two simulation data sets to estimate the type I error rate and power. Simulations showed that ES-MDR identified interactions using less computational workload and allowed for adjustment of covariates. We applied ES-MDR on the OncoArray-TRICL Consortium data with 14,935 cases and 12,787 controls for lung cancer (SNPs = 108,254) to search over all two-way interactions to identify genetic interactions associated with lung cancer age-of-onset. We tested the best model in an independent data set from the OncoArray-TRICL data. Results: Our experiment on the OncoArray-TRICL data identified many one-way and two-way models with a single-base deletion in the noncoding region of BRCA1 (HR 1.24, P = 3.15 × 10–15), as the top marker to predict age of lung cancer onset. Conclusions: From the results of our extensive simulations and analysis of a large GWAS study, we demonstrated that our method is an efficient algorithm that identified genetic interactions to include in our models to predict survival outcomes.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

Genetic interactions
Genome-wide association study
Lung cancer
Machine learning

Publication and Content Type

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