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在配对的血液和口腔样本中成功进行全基因组扫描。

Successful genome-wide scan in paired blood and buccal samples.

作者信息

Feigelson Heather Spencer, Rodriguez Carmen, Welch Robert, Hutchinson Amy, Shao Wen, Jacobs Kevin, Diver W Ryan, Calle Eugenia E, Thun Michael J, Hunter David J, Thomas Gilles, Chanock Stephen J

机构信息

Department of Epidemiology and Surveillance Research, American Cancer Society, 1599 Clifton Road, NE, Atlanta, GA, USA.

出版信息

Cancer Epidemiol Biomarkers Prev. 2007 May;16(5):1023-5. doi: 10.1158/1055-9965.EPI-06-0859.

DOI:10.1158/1055-9965.EPI-06-0859
PMID:17507632
Abstract

Interest in genome-wide association studies to identify susceptibility alleles for cancer is growing, and several are currently planned or under way. Although the feasibility of collecting buccal cell samples as an alternative to venous blood samples as a source of genomic DNA has been shown, the validity of using DNA from buccal cells for genome-wide scans has not been assessed. We used 46 paired buffy coat and buccal cell samples to test the feasibility of using DNA from buccal cells for genotyping with the HumanHap300 Bead Chip (v.1.0.0) on the Illumina Infinium II platform. Genotyping was successful in every sample, regardless of DNA yield or sample type. Of the 317,502 genotypes attempted, 315,314 (99.3%) were successfully called. Completion rates were similar for buffy coat and buccal cell samples (99.63% and 99.44%, respectively; P = 0.15). Completion rates <99% were observed in only four samples and did not differ by specimen type. The paired samples showed exceptionally high concordance (99.96%). These results show that buccal cell samples collected and processed under optimal conditions can be used for genome-wide association studies with results comparable to those obtained from DNA extracted from buffy coat.

摘要

识别癌症易感性等位基因的全基因组关联研究正日益受到关注,目前有几项研究正在计划中或正在进行。虽然已证明收集颊细胞样本作为基因组DNA来源以替代静脉血样本的可行性,但尚未评估使用颊细胞DNA进行全基因组扫描的有效性。我们使用46对血沉棕黄层和颊细胞样本,在Illumina Infinium II平台上,测试使用颊细胞DNA通过HumanHap300 Bead Chip(v.1.0.0)进行基因分型的可行性。无论DNA产量或样本类型如何,每个样本的基因分型均成功。在尝试的317,502个基因型中,315,314个(99.3%)被成功检出。血沉棕黄层和颊细胞样本的完成率相似(分别为99.63%和99.44%;P = 0.15)。仅在4个样本中观察到完成率<99%,且未因样本类型而异。配对样本显示出极高的一致性(99.96%)。这些结果表明,在最佳条件下收集和处理的颊细胞样本可用于全基因组关联研究,其结果与从血沉棕黄层提取的DNA所获得的结果相当。

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