霰弹枪测序
微生物群
放大器
康蒂格
生物
计算生物学
猎枪
扩增子测序
基因组
基因组
核糖体RNA
16S核糖体RNA
人类微生物组计划
人体微生物群
遗传学
DNA测序
顺序装配
深度测序
基因
聚合酶链反应
转录组
基因表达
作者
Ravi Ranjan,Asha Rani,Ammal M. Metwally,Halvor S. McGee,David L. Perkins
标识
DOI:10.1016/j.bbrc.2015.12.083
摘要
The human microbiome has emerged as a major player in regulating human health and disease. Translational studies of the microbiome have the potential to indicate clinical applications such as fecal transplants and probiotics. However, one major issue is accurate identification of microbes constituting the microbiota. Studies of the microbiome have frequently utilized sequencing of the conserved 16S ribosomal RNA (rRNA) gene. We present a comparative study of an alternative approach using whole genome shotgun sequencing (WGS). In the present study, we analyzed the human fecal microbiome compiling a total of 194.1 × 10(6) reads from a single sample using multiple sequencing methods and platforms. Specifically, after establishing the reproducibility of our methods with extensive multiplexing, we compared: 1) The 16S rRNA amplicon versus the WGS method, 2) the Illumina HiSeq versus MiSeq platforms, 3) the analysis of reads versus de novo assembled contigs, and 4) the effect of shorter versus longer reads. Our study demonstrates that whole genome shotgun sequencing has multiple advantages compared with the 16S amplicon method including enhanced detection of bacterial species, increased detection of diversity and increased prediction of genes. In addition, increased length, either due to longer reads or the assembly of contigs, improved the accuracy of species detection.
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