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Share national and regional initiatives to establish standardized microbiome data platforms.
Share national and regional initiatives to establish standardized microbiome data platforms.
Showcase recent scientific advances and clinical applications in human microbiome research.
Discuss regulatory considerations and opportunities for innovation in microbiome-based therapeutics and diagnostics.

The Microbiome Leadership Forum is an international forum dedicated to advancing human microbiome science and fostering collaboration across the Asia-Pacific region. Our goal is to advance Human Microbiome Science & Collaboration in APAC.
Also join us in Seoul as we shape the future of microbiome science in Asia and beyond. The event will bring together leaders from government, academia, and industry to accelerate the adoption of human microbiome research for public health and precision medicine.
Andaz Seoul Gangnam, Seoul, South Korea
Thursday, 20 November 2025, 8:30 AM – 5:30 PM

Opening Remarks/The Current Landscape of Korea’s Microbiome Industry

Welcome Remarks

Introduction to PacBio and innovations in Microbiome HiFi Sequencing

Clinical-Based Human Microbiome Project in Korea

Bridging Clinical and Translational Microbiome Research through PacBio HiFi Full-Length 16S Sequencing

HiFi Long-Read Metagenomic Sequencing Advances FMT Research for Ulcerative Colitis

Functional study of gut microbiome association with colorectal adenoma

Oral Microbiome Dynamics with Periodontal Disease Progression

Novel insights into the ecological and evolutionary microbial dynamics of CPE colonized subjects using high-quality long reads
Complete genomes from complex soils: Long-Read PacBio metagenomics for high-resolution microbial ecology

Advancing Human Microbiome Research with Comprehensive Bioinformatics and Analysis Tools

Long-Read Metagenomic Analysis (MAG)

Influence of the gut microbiota on immunotherapy response

A Molecule-First Approach to Next-Generation Microbiome Therapeutics

Closing Remarks
Authors: Jacob Brandenburg, Aaron Wenger, Christine Lambert, Heather Ferrao

Long-read whole genome sequencing (WGS) for plants and animals has allowed scientists to tackle the assembly of genomes ranging in size, ploidy, and repeat content. HiFi WGS enables complete, accurate, and contiguous assemblies of even the most complex genomes. As a result, HiFi WGS has been adopted by many biodiversity genomics consortia and agriculture researchers to assemble thousands of genomes.
While HiFi WGS simplifies the bioinformatics of genome assembly, library preparation remains a common challenge, especially for scientists sequencing organisms which yield low quantities of DNA or have very large genomes that require multiple libraries for a single de novo assembly.
We describe a new workgow using the PacBio SMRTbell prep kit 3.0 that is amenable to automation while significantly reducing the time (by 50%), cost, and DNA quantity (by 40%) necessary to prepare a sequencing library. We applied the workflow to rice and fly samples and demonstrate that the assembly quality matches that of the previous, more time-consuming library prep workgows. This new workflow offers a more efficient solution for all WGS applications, regardless of organism size or complexity.
Authors: Greg Concepcion, Michelle Vierra

With the increasing prevalence of high-quality assembled genomes, access to the pangenomes of species is now an achievable possibility for researchers with all research budgets. However, the tools to visualize, analyze, and extract actionable information from these pangenome datasets are still in their infancy. Using a large plant pangenome dataset, we evaluated the pangenome graph builder pipeline for building a pangenome graph of the species and use these evaluations to provide basic recommendations for how to best manipulate and visualize these pangenomic datasets with other downstream tools including the vg toolkit.
Authors: Greg Concepcion, Michelle Vierra

With the increasing prevalence of high-quality assembled genomes, access to the pangenomes of species is now an achievable possibility for researchers with all research budgets. However, the tools to visualize, analyze, and extract actionable information from these pangenome datasets are still in their infancy. Using a large plant pangenome dataset, we evaluated the pangenome graph builder pipeline for building a pangenome graph of the species and use these evaluations to provide basic recommendations for how to best manipulate and visualize these pangenomic datasets with other downstream tools including the vg toolkit.
Authors: Greg Concepcion, Michelle Vierra

With the increasing prevalence of high-quality assembled genomes, access to the pangenomes of species is now an achievable possibility for researchers with all research budgets. However, the tools to visualize, analyze, and extract actionable information from these pangenome datasets are still in their infancy. Using a large plant pangenome dataset, we evaluated the pangenome graph builder pipeline for building a pangenome graph of the species and use these evaluations to provide basic recommendations for how to best manipulate and visualize these pangenomic datasets with other downstream tools including the vg toolkit.
Monday, June 12, 2022 14:15–15:45 PST
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Title, credentials, PacBio

Title, credentials, PacBio

Title, credentials, PacBio

Title, credentials, PacBio
| # | Title | First Author | Date/Time |
| 2314 | Increased Diagnostic Yield With Long Read Sequencing In Patients With Undiagnosed Neurodevelopmental Disorder | S. Jamuar | October 26, 3:00 - 4:45 pm PDT |
| 2322 | Long-read HiFi genome sequencing reveals a 2.7 kilobase intronic insertion in NR5A1as a cause of 46,XY disorder of sexual development | G. Del Gobbo | October 26, 3:00 - 4:45 pm PDT |
| 2354 | Ultra-low DNA input with long-read sequencing identified complex chromosomal rearrangements involving NIPBL in a Cornelia de Lange syndrome patient | N. Jiang | October 26, 3:00 - 4:45 pm PDT |
| 2723 | Accurate CYP2D6 star (*) allele diplotyping for long-read PacBio HiFi sequencing | J. Harting | October 26, 3:00 - 4:45 pm PDT |
| 3096 | PacBio HiFi sequencing provides highly accurate CpG methylation calls without bisulfite treatment | C. Saunders | October 26, 3:00 - 4:45 pm PDT |
| 3133 | Sequencing By Binding (SBB) enables a lower limit of detection for Tuberculosis resistance genes gyrA and katG | C. Wike | October 26, 3:00 - 4:45 pm PDT |
| 2269 | Clinical long-read genome sequencing: Analytical performance of germline small variant detection using HiFi genome sequencing | N. Hammond | October 27, 3:00 - 4:45 pm PDT |
| 2954 | De novo variant detection with HiFi reads | J. Lake | October 27, 3:00 - 4:45 pm PDT |
| 3012 | High throughput workflow for human whole genome sequencing using PacBio HiFi | J. Rocha | October 27, 3:00 - 4:45 pm PDT |
| 3132 | Sequencing By Binding (SBB) demonstrates superior performance in low-pass whole-human-sequencing applications | KY. Chen | October 27, 3:00 - 4:45 pm PDT |
| 2938 | Closing the gap: Solving complex medically relevant regions of the human genome | F. Sedlazeck | October 27, 3:00 - 4:45 pm PDT |
| # | Title | First Author | Date/Time |
| 2314 | Increased Diagnostic Yield With Long Read Sequencing In Patients With Undiagnosed Neurodevelopmental Disorder | S. Jamuar | October 26, 3:00 - 4:45 pm PDT |
| 2322 | Long-read HiFi genome sequencing reveals a 2.7 kilobase intronic insertion in NR5A1as a cause of 46,XY disorder of sexual development | G. Del Gobbo | October 26, 3:00 - 4:45 pm PDT |
| 2354 | Ultra-low DNA input with long-read sequencing identified complex chromosomal rearrangements involving NIPBL in a Cornelia de Lange syndrome patient | N. Jiang | October 26, 3:00 - 4:45 pm PDT |
| 2723 | Accurate CYP2D6 star (*) allele diplotyping for long-read PacBio HiFi sequencing | J. Harting | October 26, 3:00 - 4:45 pm PDT |
| 3096 | PacBio HiFi sequencing provides highly accurate CpG methylation calls without bisulfite treatment | C. Saunders | October 26, 3:00 - 4:45 pm PDT |
| 3133 | Sequencing By Binding (SBB) enables a lower limit of detection for Tuberculosis resistance genes gyrA and katG | C. Wike | October 26, 3:00 - 4:45 pm PDT |
| 2269 | Clinical long-read genome sequencing: Analytical performance of germline small variant detection using HiFi genome sequencing | N. Hammond | October 27, 3:00 - 4:45 pm PDT |
| 2954 | De novo variant detection with HiFi reads | J. Lake | October 27, 3:00 - 4:45 pm PDT |
| 3012 | High throughput workflow for human whole genome sequencing using PacBio HiFi | J. Rocha | October 27, 3:00 - 4:45 pm PDT |
| 3132 | Sequencing By Binding (SBB) demonstrates superior performance in low-pass whole-human-sequencing applications | KY. Chen | October 27, 3:00 - 4:45 pm PDT |
| 2938 | Closing the gap: Solving complex medically relevant regions of the human genome | F. Sedlazeck | October 27, 3:00 - 4:45 pm PDT |

Stop by our booth to chat with PacBio staff and have your questions answered. We are excited to learn about your sequencing goals and learn more about your research.
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