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A 454 multiplex sequencing method for rapid and reliable genotyping of highly polymorphic genes in large-scale studies

机译:大规模研究中快速,可靠地对高度多态基因进行基因分型的454多重测序方法

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摘要

Background: High-throughput sequencing technologies offer new perspectives for biomedical, agronomical and evolutionary research. Promising progresses now concern the application of these technologies to large-scale studies of genetic variation. Such studies require the genotyping of high numbers of samples. This is theoretically possible using 454 pyrosequencing, which generates billions of base pairs of sequence data. However several challenges arise: first in the attribution of each read produced to its original sample, and second, in bioinformatic analyses to distinguish true from artifactual sequence variation. This pilot study proposes a new application for the 454 GS FLX platform, allowing the individual genotyping of thousands of samples in one run. A probabilistic model has been developed to demonstrate the reliability of this method. Results: DNA amplicons from 1,710 rodent samples were individually barcoded using a combination of tags located in forward and reverse primers. Amplicons consisted in 222 bp fragments corresponding to DRB exon 2, a highly polymorphic gene in mammals. A total of 221,789 reads were obtained, of which 153,349 were finally assigned to original samples. Rules based on a probabilistic model and a four-step procedure, were developed to validate sequences and provide a confidence level for each genotype. The method gave promising results, with the genotyping of DRB exon 2 sequences for 1,407 samples from 24 different rodent species and the sequencing of 392 variants in one half of a 454 run. Using replicates, we estimated that the reproducibility of genotyping reached 95%. Conclusions: This new approach is a promising alternative to classical methods involving electrophoresis-based techniques for variant separation and cloning-sequencing for sequence determination. The 454 system is less costly and time consuming and may enhance the reliability of genotypes obtained when high numbers of samples are studied. It opens up new perspectives for the study of evolutionary and functional genetics of highly polymorphic genes like major histocompatibility complex genes in vertebrates or loci regulating self-compatibility in plants. Important applications in biomedical research will include the detection of individual variation in disease susceptibility. Similarly, agronomy will benefit from this approach, through the study of genes implicated in productivity or disease susceptibility traits
机译:背景:高通量测序技术为生物医学,农艺学和进化研究提供了新的视角。现在有希望的进展涉及这些技术在大规模遗传变异研究中的应用。此类研究需要对大量样品进行基因分型。从理论上讲,使用454焦磷酸测序是可行的,它可以生成数十亿个碱基对的序列数据。但是,出现了一些挑战:首先是将每个读数的归因于其原始样本,其次是在生物信息学分析中,以区分真实序列与人为序列变异。这项初步研究提出了454 GS FLX平台的新应用,允许一次运行对数千个样品进行单独的基因分型。已经开发了概率模型来证明该方法的可靠性。结果:使用位于正向和反向引物中的标签组合,分别对来自1,710个啮齿动物样品的DNA扩增子进行条形码编码。扩增子包含222 bp的片段,对应于DRB外显子2,DRB外显子2是哺乳动物中的高度多态性基因。总共获得221,789次读取,其中最终将153,349次分配给原始样本。开发了基于概率模型和四步过程的规则,以验证序列并为每种基因型提供置信度。该方法给出了令人鼓舞的结果,对来自24种不同啮齿动物的1,407个样品的DRB外显子2序列进行了基因分型,并在454次运行的一半中对392个变异体进行了测序。使用复制品,我们估计基因分型的可重复性达到了95%。结论:这种新方法是经典方法的有希望的替代方法,经典方法涉及基于电泳的技术用于变体分离和克隆测序以进行序列测定。 454系统成本更低,耗时更少,并且可以提高研究大量样本时获得的基因型的可靠性。它为研究高度多态性基因(如脊椎动物的主要组织相容性复杂基因或调节植物自我适应性的基因座)的进化和功能遗传学开辟了新的视野。生物医学研究中的重要应用将包括检测疾病易感性的个体差异。同样,通过研究与生产力或疾病易感性状有关的基因,农艺学将从这种方法中受益

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