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Using GWAS SNPs to Determine Association between COVID-19 and Comorbid Diseases

机译:使用GWAS SNP来确定Covid-19和可同经疾病之间的关联

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This paper analyzed the associations between COVID severity conditions and 7 comorbid diseases - Breast Cancer, Chronic Kidney Disease, Chronic Obstructive Pulmonary Disease, Coronary Artery Disease, Lung Cancer, Obesity, and Type 2 Diabetes. Genome-wide Association Study (GWAS) results were used to obtain Single-nucleotide Polymorphisms (SNP) for each disease. QQ plots were then used to compare the distribution of p-values for the GWAS SNPs with a uniform distribution to allow for the filtering out of insignificant SNPs. A co-association algorithm, based off of a fixed position window, was then applied to the filtered GWAS data to identify the degree of influence each of the 7 diseases have on the 3 COVID severities. A haplotype- block-based algorithm was then applied to identify specific genes that drives observed comorbidity patterns. Results showed that Chronic Kidney Diseases or Obesity are better predictors for COVID Infection, but not good predictors for Severe or Hospitalized COVID. It was also found that TRPC7, EXOC6, RNGTT, XPO7, PEX19, EDC4 and 7 more genes display recurring patterns of coassociation with multiple comorbid disease and clear inclination towards specific severity conditions.
机译:本文分析了Covid严重程度条件和7种同种式疾病 - 乳腺癌,慢性肾病,慢性阻塞性肺病,冠状动脉疾病,肺癌,肥胖症和2型糖尿病之间的关联。基因组 - 范围的协会研究(GWAS)结果用于获得每种疾病的单核苷酸多态性(SNP)。然后使用QQ图来比较GWAS SNP的P值的分布,具有均匀的分布,以允许滤除不显着的SNP。然后将基于固定位置窗口的共关联算法应用于过滤的GWAS数据,以识别每种7个疾病对3个Covid严重主义的影响程度。然后应用单倍型块的算法以识别驱动观察到的合并图案的特定基因。结果表明,慢性肾疾病或肥胖是Covid感染的更好的预测因子,但对于严重或住院的Covid来说不是良好的预测因子。还发现TRPC7,EXOC6,RNGTT,XPO7,PEX19,EDC4和7种更大的基因显示多种同血管疾病的经常性模式,并透明朝向特定的严重性条件。

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