Generating amplicon reads for microbial community assessment with next-generation sequencing

被引:59
作者
Golebiewski, M. [1 ,2 ]
Tretyn, A. [1 ,2 ]
机构
[1] Nicolaus Copernicus Univ, Plant Physiol & Biotechnol, Lwowska 1, PL-87100 Torun, Poland
[2] Nicolaus Copernicus Univ, Ctr Modern Interdisciplinary Technol, Torun, Poland
关键词
16S rRNA gene; error and bias sources; experimental workflow; marker gene amplicons; microbial community assessment; next-generation sequencing; 16S RIBOSOMAL-RNA; BACTERIAL DIVERSITY; PCR AMPLIFICATION; CHIMERA FORMATION; BARCODED PRIMERS; DNA; EXTRACTION; GENOME; BIAS; ACCURATE;
D O I
10.1111/jam.14380
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Marker gene amplicon sequencing is often preferred over whole genome sequencing for microbial community characterization, due to its lower cost while still enabling assessment of uncultivable organisms. This technique involves many experimental steps, each of which can be a source of errors and bias. We present an up-to-date overview of the whole experimental pipeline, from sampling to sequencing reads, and give information allowing for informed choices at each step of both planning and execution of a microbial community assessment study. When applicable, we also suggest ways of avoiding inherent pitfalls in amplicon sequencing.
引用
收藏
页码:330 / 354
页数:25
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