Assessment of bacterial diversity through sequencing of 16S ribosomal RNA (16S rRNA) genes has been an approach widely used in environmental microbiology, particularly since the advent of high-throughput sequencing technology. Oxford Nanopore Technology (ONT) provides the long reads sequencing that cover the full-length sequence of 16S rRNA gene (V1-V9 regions) through a fast, cheap, and high throughput process. Since all the informative sites of 16S rRNA genes are considered, the full-length 16S rRNA sequences offer a higher level of taxonomic and phylogenetic resolution for bacterial identification [1].
DNA concentration was determined using both NanoDrop spectrophotometers and Qubit fluorometer. Library preparations were conducted using Kits from Oxford Nanopore Technology.
Nanopore sequencing was operated by MinKNOW software version 24.02.16. Basecalling was performed using Dorado version 7.3.11 with high-accuracy model [2]. The quality of FASTQ files were visualized using NanoPlot, and quality filtering was performed using NanoFilt [3][4].
Filtered reads were classified using Centrifuge classifier [5]. Bacteria and Archaea index was built using NCBI 16S RefSeq database (https://ftp.ncbi.nlm.nih.gov/refseq/TargetedLoci/). Downstream analysis and visualizations were performed using Pavian (https://github.com/fbreitwieser/pavian), Krona Tools (https://github.com/marbl/Krona), and RStudio using R version 4.3.3 (https://www.R-project.org/).


The quality of FASTQ files were assessed by NanoPlot.
| Sample ID | Raw | Filtered | ||
|---|---|---|---|---|
| QC Stats | Full Report | QC Stats | Full Report | |
| G_Gk1 | view | download | view | download |
| G_Gk2 | view | download | view | download |
| G_Bt1 | view | download | view | download |
| G_Bt2 | view | download | view | download |
| G_KP1 | view | download | view | download |
| G_KP2 | view | download | view | download |
Reads classification table contains the output of reads classification by Centrifuge software. Click "CSV" button to download the raw data and open it in another viewer, such as Microsoft Excel.
Please select sample:Top 10 of relative abundance from each taxonomic level (Phylum to Species).
Total count & relative abundance of each taxonomic level are presented in the CSV table. Download each file and open with Excel application.
| Rank | Count | Relative |
|---|---|---|
| Phylum | view | view |
| Class | view | view |
| Order | view | view |
| Family | view | view |
| Genus | view | view |
| Species | view | view |
Krona visualization allows us to intuitively explore the relative abundances within the complex hierarchies of metagenomic classifications. The count in Krona was based on the numReads from Centrifuge Report. Click "snapshot" to convert the chart into a static image.
Sankey diagrams are used to visualize microbial species of samples. In this diagram, the arrow width is proportional to the quantity to depict changes over time hierarchy between nodes.
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Alpha diversity describes the mean species diversity in sites or habitats at local scale.
Heatmap depicts taxon relative abundance of each sample using shades of colour to easily identify patterns among samples. Red indicates a taxon with high distribution while black shows low relative abundance. Top 50 most abundant OTUs were shown on the graph.
Venn diagram illustrates the logical relationship between samples.
Beta diversity provides measurement of the differences among samples or groups.
Figures below are beta diversity metrics that grouped using Principle Coordinate Analysis (PCoA) plot, based on Bray-Curtis dissimilarity.
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