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A Bayesian Gene-Based Genome-Wide Association Study Analysis of Osteosarcoma Trio Data Using a Hierarchically Structured Prior

机译:基于贝叶斯基因的全基因组全基因组关联研究使用分层结构先验分析

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摘要

Osteosarcoma is considered to be the most common primary malignant bone cancer among children and young adults. Previous studies suggest growth spurts and height to be risk factors for osteosarcoma. However, studies on the genetic cause are still limited given the rare occurrence of the disease. In this study, we investigated in a family trio data set that is composed of 209 patients and their unaffected parents and conducted a genome-wide association study (GWAS) to identify genetic risk factors for osteosarcoma. We performed a Bayesian gene-based GWAS based on the single-nucleotide polymorphism (SNP)-level summary statistics obtained from a likelihood ratio test of the trio data, which uses a hierarchically structured prior that incorporates the SNP-gene hierarchical structure. The Bayesian approach has higher power than SNP-level GWAS analysis due to the reduced number of tests and is robust by accounting for the correlations between SNPs so that it borrows information across SNPs within a gene. We identified 217 genes that achieved genome-wide significance. Ingenuity pathway analysis of the gene set indicated that osteosarcoma is potentially related to TP53, estrogen receptor signaling, xenobiotic metabolism signaling, and RANK signaling in osteoclasts.
机译:骨肉瘤被认为是儿童和年轻人中最常见的原发性恶性骨癌。先前的研究表明,生长突增和身高是骨肉瘤的危险因素。但是,鉴于这种疾病的罕见发生,对遗传原因的研究仍然很有限。在这项研究中,我们调查了由209名患者及其未受影响的父母组成的家庭三重数据集,并进行了全基因组关联研究(GWAS),以识别骨肉瘤的遗传危险因素。我们基于从三重奏数据的似然比测试获得的单核苷酸多态性(SNP)级汇总统计数据,基于贝叶斯基因进行了GWAS,该统计使用了包含SNP基因分级结构的分级结构。由于减少了测试数量,贝叶斯方法比SNP级GWAS分析具有更高的功效,并且通过考虑SNP之间的相关性而变得健壮,因此它可以借用基因中SNP之间的信息。我们确定了217个基因,在全基因组范围内具有重要意义。基因集的独创性途径分析表明,骨肉瘤可能与破骨细胞中的TP53,雌激素受体信号传导,异种代谢信号和RANK信号有关。

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