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Don't put all your eggs in one basket: a cost-effective and powerful method to optimize primer choice for rRNA environmental community analyses using the Fluidigm Access Array

机译:不要把所有的鸡蛋都放在一个篮子里:这是一种经济高效的方法,可使用Fluidigm Access Array优化引物选择,用于rRNA环境群落分析

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摘要

With the increasing democratization of high-throughput sequencing (HTS) technologies, along with the concomitant increase in sequence yield per dollar, many researchers are exploring HTS for microbial community ecology. Many elements of experimental design can drastically affect the final observed community structure, notably the choice of primers for amplification prior to sequencing. Some targeted microbes can fail to amplify due to primer-targeted sequence divergence and be omitted from obtained sequences, leading to differences among primer pairs in the sequenced organisms even when targeting the same community. This potential source of taxonomic bias in HTS makes it prudent to investigate how primer choice will affect the sequenced community prior to investing in a costly community-wide sequencing effort. Here, we use Fluidigm's microfluidic Access Arrays (IFC) followed by Illumina (R) MiSeq Nano sequencing on a culture-derived local mock community to demonstrate how this approach allows for a low-cost combinatorial investigation of primer pairs and experimental samples (up to 48 primer pairs and 48 samples) to determine the most effective primers that maximize obtained communities whilst minimizing taxonomic biases.
机译:随着高通量测序(HTS)技术的日益民主化,以及随之而来的每美元测序产量的增加,许多研究人员正在探索HTS用于微生物群落生态学。实验设计的许多要素会极大地影响最终观察到的群落结构,特别是在测序之前选择用于扩增的引物。由于靶向引物的序列差异,某些靶向微生物可能无法扩增,因此无法从获得的序列中删除,即使在靶向同一群落的情况下,也会导致测序生物中引物对之间的差异。在HTS中这种潜在的分类学偏见来源使得在投资昂贵的社区范围内的测序工作之前,应仔细研究引物选择将如何影响测序社区。在这里,我们使用Fluidigm的微流控访问阵列(IFC),然后在源自培养物的本地模拟社区上进行Illumina(R)MiSeq Nano测序,以证明该方法如何实现低成本的引物对和实验样品组合研究(最多48个引物对和48个样本)来确定最有效的引物,这些引物可最大程度地提高获得的群落,同时最大程度地减少分类学偏差。

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