Technical note: High fidelity of whole-genome amplified sheep (Ovis aries) deoxyribonucleic acid using a high-density single nucleotide polymorphism array-based genotyping platform

被引:10
|
作者
Magee, D. A. [1 ]
Park, S. D. E. [1 ]
Scraggs, E. [1 ]
Murphy, A. M. [2 ]
Doherty, M. L.
Kijas, J. W. [3 ]
MacHugh, D. E. [1 ,4 ]
机构
[1] Natl Univ Ireland Univ Coll Dublin, UCD Coll Life Sci, UCD Sch Agr Food Sci & Vet Med, Anim Genom Lab, Dublin 4, Ireland
[2] Univ London Royal Vet Coll, London NW1 0TU, England
[3] CSIRO, Div Livestock Ind, Brisbane, Qld 4067, Australia
[4] Natl Univ Ireland Univ Coll Dublin, UCD Conway Inst Biomol & Biomed Res, Dublin 4, Ireland
基金
爱尔兰科学基金会;
关键词
BeadChip array; genotyping; Ovis aries; sheep; single nucleotide polymorphism; whole-genome amplified DNA; DNA; AMPLIFICATION;
D O I
10.2527/jas.2009-2723
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Advances in high-throughput genotyping technologies have afforded researchers the opportunity to study ever-increasing numbers of SNP in animal genomes. However, many studies encounter difficulties in obtaining sufficient quantities of high-quality DNA for such analyses, particularly when the source biological material is limited or degraded. The recent development of in vitro whole-genome amplification approaches has permitted researchers to circumvent these challenges by increasing the amount of usable DNA in normally small-quantity samples. Here, we assess the performance of whole-genome amplification products generated from ovine genomic DNA using a high-throughput SNP genotyping platform, the newly developed Illumina ovineSNP50 BeadChip. Our results demonstrate a high genotype call rate for conventional genomic DNA and whole-genome amplified genomic DNA. The data also reveal an exceptionally high concordance rate (>= 99%) between the genotypes generated from whole-genome amplified products and their conventional genomic DNA counterparts. This study supports the use of whole-genome amplification as a viable solution for the analysis of high-density SNP genotypic data using compromised or limited starting material.
引用
收藏
页码:3183 / 3186
页数:4
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