首页> 美国卫生研究院文献>BMC Genomics >Interspecies hybridization on DNA resequencing microarrays: efficiency of sequence recovery and accuracy of SNP detection in human ape and codfish mitochondrial DNA genomes sequenced on a human-specific MitoChip
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Interspecies hybridization on DNA resequencing microarrays: efficiency of sequence recovery and accuracy of SNP detection in human ape and codfish mitochondrial DNA genomes sequenced on a human-specific MitoChip

机译:在DNA重测序微阵列上进行种间杂交:在人类特异性MitoChip上测序的人类猿和鳕鱼线粒体DNA基因组中的序列恢复效率和SNP检测的准确性

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摘要

BackgroundIterative DNA "resequencing" on oligonucleotide microarrays offers a high-throughput method to measure intraspecific biodiversity, one that is especially suited to SNP-dense gene regions such as vertebrate mitochondrial (mtDNA) genomes. However, costs of single-species design and microarray fabrication are prohibitive. A cost-effective, multi-species strategy is to hybridize experimental DNAs from diverse species to a common microarray that is tiled with oligonucleotide sets from multiple, homologous reference genomes. Such a strategy requires that cross-hybridization between the experimental DNAs and reference oligos from the different species not interfere with the accurate recovery of species-specific data. To determine the pattern and limits of such interspecific hybridization, we compared the efficiency of sequence recovery and accuracy of SNP identification by a 15,452-base human-specific microarray challenged with human, chimpanzee, gorilla, and codfish mtDNA genomes.
机译:背景技术寡核苷酸微阵列上的迭代DNA“重测序”提供了一种高通量方法来测量种内生物多样性,该方法特别适用于SNP密集基因区域,例如脊椎动物线粒体(mtDNA)基因组。但是,单一物种设计和微阵列制造的成本高昂。一种经济有效的多物种​​策略是将来自不同物种的实验DNA杂交到一个普通的微阵列,该微阵列上铺有来自多个同源参考基因组的寡核苷酸集。这种策略要求实验DNA和来自不同物种的参考寡核苷酸之间的交叉杂交不干扰物种特异性数据的准确恢复。为了确定这种种间杂交的模式和限制,我们比较了15,452个碱基的人特异性微阵列对人类,黑猩猩,大猩猩和银鳕鱼mtDNA基因组的攻击,从而比较了序列恢复的效率和SNP鉴定的准确性。

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