An Illumina metabarcoding pipeline for fungi

被引:93
作者
Balint, Miklos [1 ]
Schmidt, Philipp-Andre [1 ,2 ]
Sharma, Rahul [2 ]
Thines, Marco [1 ,2 ]
Schmitt, Imke [1 ,2 ]
机构
[1] Senckenberg Gesell Nat Forsch, Biodivers & Climate Res Ctr, D-60325 Frankfurt, Germany
[2] Goethe Univ Frankfurt, Inst Okol Evolut & Diversitat, D-60438 Frankfurt, Germany
关键词
community ecology; data pruning; high throughput; internal transcribed spacer rDNA; next-generation sequencing; AMPLICON READS; SEQUENCES; COMMUNITY; GENERATION; DATABASE; IDENTIFICATION; MAGNITUDE; ALIGNMENT; WORKFLOW; SEARCH;
D O I
10.1002/ece3.1107
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
High-throughput metabarcoding studies on fungi and other eukaryotic microorganisms are rapidly becoming more frequent and more complex, requiring researchers to handle ever increasing amounts of raw sequence data. Here, we provide a flexible pipeline for pruning and analyzing fungal barcode (ITS rDNA) data generated as paired-end reads on Illumina MiSeq sequencers. The pipeline presented includes specific steps fine-tuned for ITS, that are mostly missing from pipelines developed for prokaryotes. It (1) employs state of the art programs and follows best practices in fungal high-throughput metabarcoding; (2) consists of modules and scripts easily modifiable by the user to ensure maximum flexibility with regard to specific needs of a project or future methodological developments; and (3) is straightforward to use, also in classroom settings. We provide detailed descriptions and revision techniques for each step, thus giving the user maximum control over data treatment and avoiding a black-box approach. Employing this pipeline will improve and speed up the tedious and error-prone process of cleaning fungal Illumina metabarcoding data.
引用
收藏
页码:2642 / 2653
页数:12
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