Suppr超能文献

基因组 DNA 制备的质量要求和高密度寡核苷酸微阵列的储存条件。

Quality requirements for genomic DNA preparations and storage conditions for a high-density oligonucleotide microarray.

机构信息

Division of Medicinal Safety Science, National Institute of Health Sciences, 1–18–1 Kamiyoga, Setagaya-ku, Tokyo 158–8501, Japan.

出版信息

Biol Pharm Bull. 2012;35(10):1846-8. doi: 10.1248/bpb.b12-00523.

Abstract

High-density oligonucleotide microarrays are widely used in genome-wide association studies. The purpose of this study was to assess the influence of various factors during the preparation of DNA on genotype calling for the Affymetrix high-density oligonucleotide microarray 250K GeneChip. DNA was extracted from peripheral whole blood by solution-based and silica-membrane-based methods. Blood was stored at 4°C or 25°C for 4 or 24 h, followed by DNA extraction. To examine the effects of freeze-thaw cycles, blood and DNA were also subjected to 5 and 10 or 20 of freeze-thaw cycles, respectively. The suitability of variously DNA preparations for the array was assessed by the call rate resulting from genotyping. All DNA samples showed mean call rates of more than 0.99, which passed the quality criteria for genotyping (greater than 0.95). The results indicated that the solution-based method and the silica-membrane-based DNA extraction method could provide DNA of sufficient quality for genotyping. In addition, DNA quality suitable for high-density oligonucleotide microarrays is not strongly dependent on the preparation conditions under standard procedures.

摘要

高密度寡核苷酸微阵列被广泛应用于全基因组关联研究。本研究旨在评估在 DNA 制备过程中的各种因素对 Affymetrix 高密度寡核苷酸微阵列 250K GeneChip 基因分型的影响。DNA 采用基于溶液的和基于硅膜的方法从外周全血中提取。血液在 4°C 或 25°C 下储存 4 或 24 小时后,再进行 DNA 提取。为了研究冻融循环的影响,血液和 DNA 分别经历了 5 次、10 次或 20 次冻融循环。通过基因分型的调用率来评估各种 DNA 制备方法对微阵列的适用性。所有 DNA 样本的平均调用率均超过 0.99,符合基因分型的质量标准(大于 0.95)。结果表明,基于溶液的方法和基于硅膜的 DNA 提取方法能够提供足够质量用于基因分型的 DNA。此外,在标准程序下,适用于高密度寡核苷酸微阵列的 DNA 质量并不强烈依赖于制备条件。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验