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首页> 外文期刊>Biology and fertility of soils: Cooperating Journal of the International Society of Soil Science >Analysis of soil fungal communities by amplicon pyrosequencing: current approaches to data analysis and the introduction of the pipeline SEED.
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Analysis of soil fungal communities by amplicon pyrosequencing: current approaches to data analysis and the introduction of the pipeline SEED.

机译:通过扩增子焦磷酸测序分析土壤真菌群落:当前的数据分析方法和管道SEED的引入。

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摘要

Fungi are important in soils as both decomposers and plant symbionts, and an understanding of the composition of their complex communities is thus indispensable to answer a variety of ecological questions. 454 Pyrosequencing is currently the method of choice for the in-depth analysis of fungal communities. However, the interpretation of its results is complicated by differences in data analysis approaches that make inter-study comparisons difficult. The pyrosequencing studies published so far have also used variable molecular targets in fungal rDNA. Although the ITS region and, in particular, ITS1 appear to be the most frequent sequencing targets, the use of various primers with different coverages of fungal groups remains a serious problem. Sequence length limits also vary widely across studies, and in many studies, length differences may negatively affect sequence similarity clustering or identification. Unfortunately, many studies neglect the need to correct for method-dependent errors, such as pyrosequencing noise or chimeric sequences. Even when performed, error rates in sequences may be high, and consensus sequences created by sequence clustering therefore better represent operational taxonomic units. We recommend a data analysis workflow that includes sequence denoising, chimera removal, sequence trimming before clustering and random resampling before calculating diversity parameters. The newly developed free pipeline (SEED) introduced here can be used to perform all the required analytical steps. The improvement and unification of data analysis procedures should make future studies both more reliable and comparable and allow meta-studies to be performed to provide more general views on fungal diversity, biogeography or ecology.
机译:真菌在土壤中既是分解者又是植物共生体的重要来源,因此,了解其复杂群落的组成对于回答各种生态问题必不可少。 454焦磷酸测序是目前深入分析真菌群落的一种选择方法。但是,其结果的解释由于数据分析方法的差异而变得复杂,这使得研究之间的比较变得困难。迄今为止发表的焦磷酸测序研究还在真菌rDNA中使用了可变的分子靶标。尽管ITS区,尤其是ITS1似乎是最常见的测序靶标,但是使用具有不同覆盖率的真菌基团的各种引物仍然是一个严重的问题。序列长度限制在各个研究中也相差很大,在许多研究中,长度差异可能会对序列相似性聚类或鉴定产生负面影响。不幸的是,许多研究忽略了校正依赖于方法的错误的需要,例如焦磷酸测序噪音或嵌合序列。即使执行时,序列中的错误率也可能很高,因此通过序列聚类创建的共有序列会更好地表示可操作的分类单位。我们建议使用一种数据分析工作流程,包括序列去噪,嵌合体去除,聚类之前的序列修剪和计算多样性参数之前的随机重采样。此处介绍的新开发的免费管道(SEED)可用于执行所有必需的分析步骤。数据分析程序的改进和统一将使未来的研究更加可靠和可比,并允许进行元研究以提供有关真菌多样性,生物地理学或生态学的更一般的观点。

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