Division of Epidemiology and Clinical Research, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA.
Methods Mol Biol. 2021;2195:189-223. doi: 10.1007/978-1-0716-0860-9_14.
Genomewide association studies (GWAS) have been widely used in recent years to identify common variants that are associated with multiple types of cancer, including testicular germ cell tumors. These studies require no a priori hypotheses and have advantages, including the ability to highlight new pathways relevant to the biology of common diseases. GWAS require collection of germline DNA from individuals with and without the disease of interest. Following DNA extraction and quantification, a variety of array based platforms are available to evaluate common and moderately rare germline variation throughout the genome in an agnostic fashion. Here, we describe DNA extraction methods from samples typically used in the evaluation of germline genetic variation (blood and saliva). We also describe assays used to assess DNA quality and quantity. Finally, we include methods describing array based genotyping using the Illumina platform and validation of relevant variants using the iPLEX Agena Multiplexed Genotyping (formerly Sequenom).
全基因组关联研究(GWAS)近年来已被广泛应用于鉴定与多种癌症相关的常见变异,包括睾丸生殖细胞肿瘤。这些研究不需要先验假设,具有优势,包括能够突出与常见疾病生物学相关的新途径。GWAS 需要从有和没有所关注疾病的个体中收集种系 DNA。在提取和定量 DNA 后,有多种基于阵列的平台可用于以一种不可知的方式评估整个基因组中常见和中度罕见的种系变异。在这里,我们描述了通常用于评估种系遗传变异(血液和唾液)的样本的 DNA 提取方法。我们还描述了用于评估 DNA 质量和数量的检测方法。最后,我们包括了使用 Illumina 平台进行基于阵列的基因分型的方法和使用 iPLEX Agena 多重基因分型(前身为 Sequenom)验证相关变体的方法。