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Targeted oligonucleotide-mediated microsatellite identification (TOMMI) from large-insert library clones

机译:大插入文库克隆的靶向寡核苷酸介导的微卫星鉴定(TOMMI)

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摘要

BackgroundIn the last few years, microsatellites have become the most popular molecular marker system and have intensively been applied in genome mapping, biodiversity and phylogeny studies of livestock. Compared to single nucleotide polymorphism (SNP) as another popular marker system, microsatellites reveal obvious advantages. They are multi-allelic, possibly more polymorphic and cheaper to genotype. Calculations showed that a multi-allelic marker system always has more power to detect Linkage Disequilibrium (LD) than does a di-allelic marker system []. Traditional isolation methods using partial genomic libraries are time-consuming and cost-intensive. In order to directly generate microsatellites from large-insert libraries a sequencing approach with repeat-containing oligonucleotides is introduced.
机译:背景技术在过去的几年中,微卫星已成为最受欢迎的分子标记系统,并已广泛应用于牲畜的基因组图谱,生物多样性和系统发育研究。与单核苷酸多态性(SNP)作为另一种流行的标记系统相比,微卫星具有明显的优势。它们是多等位基因,可能更具多态性,且基因型便宜。计算表明,与双等位基因标记系统相比,多等位基因标记系统始终具有更大的检测连锁不平衡(LD)的能力。使用部分基因组文库的传统分离方法既费时又费钱。为了直接从大插入文库中生成微卫星,引入了一种包含重复序列的寡核苷酸的测序方法。

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