基因组
离子半导体测序
生物
微生物群
DNA测序
计算生物学
放大器
扩增子测序
DNA提取
梭状芽孢杆菌
生物信息学
遗传学
DNA
聚合酶链反应
细菌
16S核糖体RNA
基因
作者
Georg Conrads,Mohamed M. H. Abdelbary
出处
期刊:Anaerobe
[Elsevier BV]
日期:2019-08-01
卷期号:58: 47-52
被引量:22
标识
DOI:10.1016/j.anaerobe.2019.02.006
摘要
Next-generation sequencing allows for investigating the composition of microbiomes that are associated with infection (clinical microbiology) or dysbiosis (microbial ecology). The most commonly applied short-read sequencing technologies are Illumina MiSeq/HiSeq and Ion Torrent PGM, however, other platforms that generate long-reads are under way and optimized. A pre-condition for representative results is an appropriate method for contamination-free collection, homogenization, storage of specimens and a subsequent efficient DNA extraction protocol. As some of the anaerobes such as Clostridia or anaerobe Archaea are robust while others of the same environment, such as spirochetes, possess a very thin cell wall, a chemico-mechanical lysing strategy is recommended but with some precautions to avoid DNA-sheering and overheating. For amplicon sequencing, the Silva-TestPrime online tool helps to find the optimal 16S directed primers for individual studies. For metagenome profiling, the classifier tool has to be selected with helpful decision trees available but a combination based on different strategies seems to be indispensable. Further development of both hard- and software is needed before microbiome results become free of a substantial technology-dependent bias.
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