全基因组关联分析维基百科,自由的 encyclopedia 全基因组关联分析(Genome-wide association study)是指在人类全基因组范围内找出存在的序列变异,即单核苷酸多态性(SNP),从中筛选出与疾病相关的SNPs。 An illustration of a Manhattan plot depicting several strongly associated risk loci. Each dot represents a SNP, with the X-axis showing genomic location and Y-axis showing association level. This example is taken from a GWA study investigating microcirculation, so the tops indicates genetic variants that more often are found in individuals with constrictions in small blood vessels.[1]
全基因组关联分析(Genome-wide association study)是指在人类全基因组范围内找出存在的序列变异,即单核苷酸多态性(SNP),从中筛选出与疾病相关的SNPs。 An illustration of a Manhattan plot depicting several strongly associated risk loci. Each dot represents a SNP, with the X-axis showing genomic location and Y-axis showing association level. This example is taken from a GWA study investigating microcirculation, so the tops indicates genetic variants that more often are found in individuals with constrictions in small blood vessels.[1]