
The 16S rRNA amplicon sequencing technique is a microbiome analysis where different samples are analyzed at the same time using multiplexing. The results can be used to evaluate microbial diversity at genus, family, order, class, and phylum levels. The resolution is normally insufficient to evaluate the species level. The different steps in the bioinformatical analysis allow both the analysis of all samples combined and comparisons between samples. The bioinformatical analysis focuses on quality control of reads, merging of identical reads, and grouping of reads into operational taxonomic units (OTUs) with a threshold of 97%. The threshold is inherited from the species threshold for classification of species based on 16S rRNA sequence comparison. The distribution of reads and OTUs within and between samples can be used to estimate α- and β-diversity, respectively. The relative occurrence of the taxonomic units at the levels of genus, family, order, class, and phylum can be compared between samples. These distributions can be related to metadata by principal component analysis.
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 8 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
