16s bioinformatics pipeline Search Results


90
BugSeq Bioinformatics 16s pipeline bugseq (v5.0)
Average relative abundance (%) of bacterial organisms present in MCM2α and MCM2β obtained by ONT sequencing using the R10.4.1 MinION flow cell and ONT <t>16S</t> Barcoding all-in-one kit (v14). Three concentrations of the MCM2α and MCM2β materials were tested in triplicate (neat, 1:10 and 1:100) and analysis by EPI2ME Desktop agent. The species abundance (%) of each dilution is reported, including the dPCR reported composition for the two materials ( <xref ref-type= Supplementary Data 3 ). " width="250" height="auto" />
16s Pipeline Bugseq (V5.0), supplied by BugSeq Bioinformatics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/16s+bioinformatics+pipeline/bugseq+16s/pmc11922894-278-10-8
Average 90 stars, based on 1 article reviews
16s pipeline bugseq (v5.0) - by Bioz Stars, 2026-10
90/100 stars
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86
1928 Diagnostics 16s bioinformatic pipeline
Workflow overview used by the participating laboratories. Seven different extraction methods were followed by library preparation using a modified ONT <t>16S</t> Barcoding kit 24 V14 protocol (52 °C annealing, 40 cycles), or in-house PCR systems with the Ligation Sequencing V14 kit. Sequencing was conducted on various ONT devices. Species identification was performed using the commercial 1928 Diagnostics-16S pipeline and the GMS-16S pipeline (EMU classification tool). Created in BioRender. Wang, H. (2024) https://BioRender.com/i45i214
16s Bioinformatic Pipeline, supplied by 1928 Diagnostics, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/16s+bioinformatics+pipeline/16s+pipeline/pmc12321653-4-2-6
Average 86 stars, based on 1 article reviews
16s bioinformatic pipeline - by Bioz Stars, 2026-10
86/100 stars
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90
Oxford Nanopore 16s oxford nanopore long read protocol
Workflow overview used by the participating laboratories. Seven different extraction methods were followed by library preparation using a modified ONT <t>16S</t> Barcoding kit 24 V14 protocol (52 °C annealing, 40 cycles), or in-house PCR systems with the Ligation Sequencing V14 kit. Sequencing was conducted on various ONT devices. Species identification was performed using the commercial 1928 Diagnostics-16S pipeline and the GMS-16S pipeline (EMU classification tool). Created in BioRender. Wang, H. (2024) https://BioRender.com/i45i214
16s Oxford Nanopore Long Read Protocol, supplied by Oxford Nanopore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/16s+bioinformatics+pipeline/16s+oxford+nanopore+long+read+protocol/pmc11112893-40-17-4
Average 90 stars, based on 1 article reviews
16s oxford nanopore long read protocol - by Bioz Stars, 2026-10
90/100 stars
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90
Oxford Nanopore minion™ sequencer
Workflow overview used by the participating laboratories. Seven different extraction methods were followed by library preparation using a modified ONT <t>16S</t> Barcoding kit 24 V14 protocol (52 °C annealing, 40 cycles), or in-house PCR systems with the Ligation Sequencing V14 kit. Sequencing was conducted on various ONT devices. Species identification was performed using the commercial 1928 Diagnostics-16S pipeline and the GMS-16S pipeline (EMU classification tool). Created in BioRender. Wang, H. (2024) https://BioRender.com/i45i214
Minion™ Sequencer, supplied by Oxford Nanopore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/16s+bioinformatics+pipeline/minion+sequencer/pmc06396348-23-20-17
Average 90 stars, based on 1 article reviews
minion™ sequencer - by Bioz Stars, 2026-10
90/100 stars
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90
Oxford Nanopore nanopore minion sequencer
Workflow overview used by the participating laboratories. Seven different extraction methods were followed by library preparation using a modified ONT <t>16S</t> Barcoding kit 24 V14 protocol (52 °C annealing, 40 cycles), or in-house PCR systems with the Ligation Sequencing V14 kit. Sequencing was conducted on various ONT devices. Species identification was performed using the commercial 1928 Diagnostics-16S pipeline and the GMS-16S pipeline (EMU classification tool). Created in BioRender. Wang, H. (2024) https://BioRender.com/i45i214
Nanopore Minion Sequencer, supplied by Oxford Nanopore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/16s+bioinformatics+pipeline/oxford+nanopore+sequencing/pm39869650-94-23-0
Average 90 stars, based on 1 article reviews
nanopore minion sequencer - by Bioz Stars, 2026-10
90/100 stars
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86
Pyrosequencing Inc 16s rrna v4 region
Workflow overview used by the participating laboratories. Seven different extraction methods were followed by library preparation using a modified ONT <t>16S</t> Barcoding kit 24 V14 protocol (52 °C annealing, 40 cycles), or in-house PCR systems with the Ligation Sequencing V14 kit. Sequencing was conducted on various ONT devices. Species identification was performed using the commercial 1928 Diagnostics-16S pipeline and the GMS-16S pipeline (EMU classification tool). Created in BioRender. Wang, H. (2024) https://BioRender.com/i45i214
16s Rrna V4 Region, supplied by Pyrosequencing Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/16s+bioinformatics+pipeline/16s+pyrosequencing+rrna/pmc12429330-108-6-10
Average 86 stars, based on 1 article reviews
16s rrna v4 region - by Bioz Stars, 2026-10
86/100 stars
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99
Illumina Inc miseq illumina sequencing platform
Workflow overview used by the participating laboratories. Seven different extraction methods were followed by library preparation using a modified ONT <t>16S</t> Barcoding kit 24 V14 protocol (52 °C annealing, 40 cycles), or in-house PCR systems with the Ligation Sequencing V14 kit. Sequencing was conducted on various ONT devices. Species identification was performed using the commercial 1928 Diagnostics-16S pipeline and the GMS-16S pipeline (EMU classification tool). Created in BioRender. Wang, H. (2024) https://BioRender.com/i45i214
Miseq Illumina Sequencing Platform, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/16s+bioinformatics+pipeline/MiSeq+System/10__4172_slash_2161___0525__1000493-5-8-9
Average 99 stars, based on 1 article reviews
miseq illumina sequencing platform - by Bioz Stars, 2026-10
99/100 stars
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99
Akoya Biosciences one codex pipeline
Workflow overview used by the participating laboratories. Seven different extraction methods were followed by library preparation using a modified ONT <t>16S</t> Barcoding kit 24 V14 protocol (52 °C annealing, 40 cycles), or in-house PCR systems with the Ligation Sequencing V14 kit. Sequencing was conducted on various ONT devices. Species identification was performed using the commercial 1928 Diagnostics-16S pipeline and the GMS-16S pipeline (EMU classification tool). Created in BioRender. Wang, H. (2024) https://BioRender.com/i45i214
One Codex Pipeline, supplied by Akoya Biosciences, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/16s+bioinformatics+pipeline/PhenoCycler-Fusion+2%2E0/pm30166151-541-50-51
Average 99 stars, based on 1 article reviews
one codex pipeline - by Bioz Stars, 2026-10
99/100 stars
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99
Valiant Co Ltd fastdna spin kit 193 for soil
Workflow overview used by the participating laboratories. Seven different extraction methods were followed by library preparation using a modified ONT <t>16S</t> Barcoding kit 24 V14 protocol (52 °C annealing, 40 cycles), or in-house PCR systems with the Ligation Sequencing V14 kit. Sequencing was conducted on various ONT devices. Species identification was performed using the commercial 1928 Diagnostics-16S pipeline and the GMS-16S pipeline (EMU classification tool). Created in BioRender. Wang, H. (2024) https://BioRender.com/i45i214
Fastdna Spin Kit 193 For Soil, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/16s+bioinformatics+pipeline/FastDNA+Spin+Kit/10__2139_slash_ssrn__4013649-90-24-30
Average 99 stars, based on 1 article reviews
fastdna spin kit 193 for soil - by Bioz Stars, 2026-10
99/100 stars
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99
Qiagen saliva qiaamp dna blood mini kit
Workflow overview used by the participating laboratories. Seven different extraction methods were followed by library preparation using a modified ONT <t>16S</t> Barcoding kit 24 V14 protocol (52 °C annealing, 40 cycles), or in-house PCR systems with the Ligation Sequencing V14 kit. Sequencing was conducted on various ONT devices. Species identification was performed using the commercial 1928 Diagnostics-16S pipeline and the GMS-16S pipeline (EMU classification tool). Created in BioRender. Wang, H. (2024) https://BioRender.com/i45i214
Saliva Qiaamp Dna Blood Mini Kit, supplied by Qiagen, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/16s+bioinformatics+pipeline/QIAamp+DNA+Blood+Mini+Kit/pmc12068744-39-37-50
Average 99 stars, based on 1 article reviews
saliva qiaamp dna blood mini kit - by Bioz Stars, 2026-10
99/100 stars
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90
SourceForge net clinqc
Popular Bioinformatics Tools Used for 16S rRNA Metagenome Analysis.
Clinqc, supplied by SourceForge net, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/16s+bioinformatics+pipeline/clinqc/pmc06363981-191-52-53
Average 90 stars, based on 1 article reviews
clinqc - by Bioz Stars, 2026-10
90/100 stars
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99
Illumina Inc miseq reagent kit v3
Popular Bioinformatics Tools Used for 16S rRNA Metagenome Analysis.
Miseq Reagent Kit V3, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/16s+bioinformatics+pipeline/MiSeq+Reagent+Kit+v3/10__1002_slash_jper__18___0167-75-23-27
Average 99 stars, based on 1 article reviews
miseq reagent kit v3 - by Bioz Stars, 2026-10
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Image Search Results


Average relative abundance (%) of bacterial organisms present in MCM2α and MCM2β obtained by ONT sequencing using the R10.4.1 MinION flow cell and ONT 16S Barcoding all-in-one kit (v14). Three concentrations of the MCM2α and MCM2β materials were tested in triplicate (neat, 1:10 and 1:100) and analysis by EPI2ME Desktop agent. The species abundance (%) of each dilution is reported, including the dPCR reported composition for the two materials ( <xref ref-type= Supplementary Data 3 ). " width="100%" height="100%">

Journal: Frontiers in Cellular and Infection Microbiology

Article Title: Standardization of 16S rRNA gene sequencing using nanopore long read sequencing technology for clinical diagnosis of culture negative infections

doi: 10.3389/fcimb.2025.1517208

Figure Lengend Snippet: Average relative abundance (%) of bacterial organisms present in MCM2α and MCM2β obtained by ONT sequencing using the R10.4.1 MinION flow cell and ONT 16S Barcoding all-in-one kit (v14). Three concentrations of the MCM2α and MCM2β materials were tested in triplicate (neat, 1:10 and 1:100) and analysis by EPI2ME Desktop agent. The species abundance (%) of each dilution is reported, including the dPCR reported composition for the two materials ( Supplementary Data 3 ).

Article Snippet: To ensure the quality of the output, the BugSeq (v5.0) 16S pipeline requires both 80% query coverage and 80% sequence identity for the classification of consensus sequences ( ).

Techniques: Sequencing

Average relative abundance (%) of bacterial organisms present in MCM2α and MCM2β obtained by ONT sequencing using the R10.4.1 MinION flow cell and the in-house developed 16S ONT RBK method. Three concentrations of the MCM2α and MCM2β materials were tested in triplicate (neat, 1:10 and 1:100) and amplified in two PCRs targeting the V1-V2 and V1-V9 genomic regions of the 16S rRNA gene; analysis by EPI2ME Desktop agent. The species abundance (%) of each dilution is reported, including the dPCR reported composition for the two materials ( <xref ref-type= Supplementary data 3 ). " width="100%" height="100%">

Journal: Frontiers in Cellular and Infection Microbiology

Article Title: Standardization of 16S rRNA gene sequencing using nanopore long read sequencing technology for clinical diagnosis of culture negative infections

doi: 10.3389/fcimb.2025.1517208

Figure Lengend Snippet: Average relative abundance (%) of bacterial organisms present in MCM2α and MCM2β obtained by ONT sequencing using the R10.4.1 MinION flow cell and the in-house developed 16S ONT RBK method. Three concentrations of the MCM2α and MCM2β materials were tested in triplicate (neat, 1:10 and 1:100) and amplified in two PCRs targeting the V1-V2 and V1-V9 genomic regions of the 16S rRNA gene; analysis by EPI2ME Desktop agent. The species abundance (%) of each dilution is reported, including the dPCR reported composition for the two materials ( Supplementary data 3 ).

Article Snippet: To ensure the quality of the output, the BugSeq (v5.0) 16S pipeline requires both 80% query coverage and 80% sequence identity for the classification of consensus sequences ( ).

Techniques: Sequencing, Amplification

Workflow overview used by the participating laboratories. Seven different extraction methods were followed by library preparation using a modified ONT 16S Barcoding kit 24 V14 protocol (52 °C annealing, 40 cycles), or in-house PCR systems with the Ligation Sequencing V14 kit. Sequencing was conducted on various ONT devices. Species identification was performed using the commercial 1928 Diagnostics-16S pipeline and the GMS-16S pipeline (EMU classification tool). Created in BioRender. Wang, H. (2024) https://BioRender.com/i45i214

Journal: European Journal of Clinical Microbiology & Infectious Diseases

Article Title: Nationwide multicentre study of Nanopore long-read sequencing for 16S rRNA-species identification

doi: 10.1007/s10096-025-05158-w

Figure Lengend Snippet: Workflow overview used by the participating laboratories. Seven different extraction methods were followed by library preparation using a modified ONT 16S Barcoding kit 24 V14 protocol (52 °C annealing, 40 cycles), or in-house PCR systems with the Ligation Sequencing V14 kit. Sequencing was conducted on various ONT devices. Species identification was performed using the commercial 1928 Diagnostics-16S pipeline and the GMS-16S pipeline (EMU classification tool). Created in BioRender. Wang, H. (2024) https://BioRender.com/i45i214

Article Snippet: The commercial 16S bioinformatic pipeline from 1928 Diagnostics (1928-16S) was evaluated and compared with the open-sourced gms_16S pipeline that is based on the EMU classification tool (GMS-16S).

Techniques: Extraction, Modification, Ligation, Sequencing

Relative abundance (%) of reads per sample for each laboratory ( r-y ) and species using the GMS-16S pipeline. (a) monomicrobial QCMD samples (top), (b) monomicrobial GMS samples (middle) (c) polymicrobial samples for both sample sets (bottom). Bacterial load (CFU/mL) is provided for the GMS panel, while QCMD concentrations are unknown (N/A). See Supplementary file for detailed classification

Journal: European Journal of Clinical Microbiology & Infectious Diseases

Article Title: Nationwide multicentre study of Nanopore long-read sequencing for 16S rRNA-species identification

doi: 10.1007/s10096-025-05158-w

Figure Lengend Snippet: Relative abundance (%) of reads per sample for each laboratory ( r-y ) and species using the GMS-16S pipeline. (a) monomicrobial QCMD samples (top), (b) monomicrobial GMS samples (middle) (c) polymicrobial samples for both sample sets (bottom). Bacterial load (CFU/mL) is provided for the GMS panel, while QCMD concentrations are unknown (N/A). See Supplementary file for detailed classification

Article Snippet: The commercial 16S bioinformatic pipeline from 1928 Diagnostics (1928-16S) was evaluated and compared with the open-sourced gms_16S pipeline that is based on the EMU classification tool (GMS-16S).

Techniques:

a Comparison of species identification between GMS-16S and 1928-16S for samples with the largest discrepancies (G12-G4). The relative abundance (%) for each laboratory is represented by a box, with similar identification on the left and differences on the right . See Supplementary File and for details. b Comparison of species distribution in the polymicrobial samples G11 and Q6 across the laboratories ( a - y ). Relative abundance (%) of reads are shown for both pipelines (GMS-16S vs 1928-16S)

Journal: European Journal of Clinical Microbiology & Infectious Diseases

Article Title: Nationwide multicentre study of Nanopore long-read sequencing for 16S rRNA-species identification

doi: 10.1007/s10096-025-05158-w

Figure Lengend Snippet: a Comparison of species identification between GMS-16S and 1928-16S for samples with the largest discrepancies (G12-G4). The relative abundance (%) for each laboratory is represented by a box, with similar identification on the left and differences on the right . See Supplementary File and for details. b Comparison of species distribution in the polymicrobial samples G11 and Q6 across the laboratories ( a - y ). Relative abundance (%) of reads are shown for both pipelines (GMS-16S vs 1928-16S)

Article Snippet: The commercial 16S bioinformatic pipeline from 1928 Diagnostics (1928-16S) was evaluated and compared with the open-sourced gms_16S pipeline that is based on the EMU classification tool (GMS-16S).

Techniques: Comparison

Popular Bioinformatics Tools Used for 16S rRNA Metagenome Analysis.

Journal: Journal of Clinical and Experimental Hepatology

Article Title: Methods for Studying Gut Microbiota: A Primer for Physicians

doi: 10.1016/j.jceh.2018.04.016

Figure Lengend Snippet: Popular Bioinformatics Tools Used for 16S rRNA Metagenome Analysis.

Article Snippet: Details on the usage, selectable features, strengths and limitations of these tools are usually available on the servers where these are hosted. table ft1 table-wrap mode="anchored" t5 caption a7 Purpose Tools URL Trimming of primers and adapters Cutadapt https://github.com/marcelm/cutadapt Sickle https://github.com/najoshi/sickle cutPrimers https://github.com/aakechin/cutPrimers AdaperRemoval https://github.com/MikkelSchubert/adapterremoval Quality control NGS-QC ToolKit http://www.nipgr.res.in/ngsqctoolkit.html Trimmomatic http://www.usadellab.org/cms/?page=trimmomatic clinQC https://sourceforge.net/projects/clinqc/ AfterQC https://github.com/OpenGene/AfterQC Merger of paired-end reads Pandaseq https://github.com/neufeld/pandaseq PEAR https://sco.h-its.org/exelixis/web/software/pear/ FLASH https://ccb.jhu.edu/software/FLASH/ MeFiT https://github.com/nisheth/MeFiT 16S-rRNA metagenome analysis pipelines QIIME http://qiime.org/ MOTHUR https://www.mothur.org/ MG-RAST http://metagenomics.anl.gov/ MICCA http://micca.org/ Open in a separate window Popular Bioinformatics Tools Used for 16S rRNA Metagenome Analysis.

Techniques: Control