全基因组关联研究
乳腺癌
生物
遗传关联
转录组
候选基因
基因
遗传学
计算生物学
癌症
单核苷酸多态性
基因型
基因表达
作者
Guimin Gao,Peter N. Fiorica,Julian McClellan,Alvaro N. Barbeira,James L. Li,Olufunmilayo I. Olopade,Hae Kyung Im,Dezheng Huo
出处
期刊:Cold Spring Harbor Laboratory - medRxiv
日期:2022-10-01
被引量:1
标识
DOI:10.1101/2022.09.30.22280575
摘要
Abstract Genome-wide association studies (GWAS) have identified more than 200 genomic loci for breast cancer risk, but specific causal genes in most of these loci have not been identified. In fact, transcriptome-wide association studies (TWAS) of breast cancer performed using gene expression prediction models trained in breast tissue have yet to clearly identify most target genes. To identify novel candidate genes, we performed a joint TWAS analysis that combined TWAS signals from multiple tissues. We used expression prediction models trained in 47 tissues from the Genotype-Tissue Expression data using a multivariate adaptive shrinkage method along with association summary statistics from the Breast Cancer Association Consortium and UK Biobank data. We identified 380 genes at 129 genomic loci to be significantly associated with breast cancer at the Bonferroni threshold (p < 2.36 × 10 −6 ). Of them, 29 genes were located in 11 novel regions that were at least 1Mb away from published GWAS hits. The rest of TWAS-significant genes were located in 118 known genomic loci from previous GWAS of breast cancer. After conditioning on previous GWAS index variants, we found that 22 genes located in known GWAS loci remained statistically significant. Our study maps potential target genes in more than half of known GWAS loci and discovers multiple new loci, providing new insights into breast cancer genetics.
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