ASHG 2026 · Tier 2–3 Academic

Korea Research Institute of Bioscience and Biotechnology at ASHG 2026

Name: ASHG 2026 Annual Meeting
Start: 2026-10-20
End: 2026-10-24
Location: Montréal

Daejeon, South Korea

Korea Research Institute of Bioscience and Biotechnology at ASHG 2026 in Montréal: 6 presentations (4 posters, 2 platform talks); 4 research groups.

presentations on the program

research groups identified

Reviewers’ Choice abstracts

Explore everyone at ASHG 2026 →

Organization	ASHG 2026 Attendance
Korea Research Institute of Bioscience and Biotechnology Daejeon, South Korea	1 Staff Scientist
Korea Bioinformation Center (KOBIC)vnd.kobic.re.kr Wet + dry lab Produces and analyzes 30x blood WGS, 60x tissue WGS, and proteomic, metabolomic and transcriptomic data. Supports Korea’s National Integrated Bio Big Data project. Funded by Not stated › Not stated, 국가 통합 바이오 빅데이터 구축 · active “「국가 통합 바이오 빅데이터 구축」의 연구개발과제로써 ... 과제를 수행 중입니다.” Source: lab pages 6 platforms and techniques › Runs 30x blood WGS, 60x tissue WGS Techniques Genomic data quality control, Advanced genomic analysis, Batch-effect detection and correction, Allele-balance bias analysis Source: lab pages No openings posted	Talk Wed Oct 21 11:30 am Large-scale whole-genome landscape of rare diseases in 15K Koreans Rare Variants, Big Insights: Illuminating Human Disease Genetics Rare variantsIdentification of disease genesGenetic variationLarge-scale biobanks Poster Wed Oct 21 2:30 pm Development of a fully automated open-source whole genome analysis pipeline for efficient high-throughput processing Genetic, Genomic, and Epigenomic Resources and Databases BioinformaticsComputational toolsGenomicsLarge-scale biobanks
Biomedical Genomics Research Center Works in population genetics and computational genetics.	Poster Thu Oct 22 4:15 pm ★ Reviewers’ Choice Constructing a Korean pangenome enhances structural variant detection in short-read sequencing Genetic, Genomic, and Epigenomic Resources and Databases Long-read sequencingCopy number/structural variationVariant callingPopulation genetics
Genomic Medicine Research Center Works in computational genetics and clinical genetics.	Poster Wed Oct 21 2:30 pm HImprint: an HMM-based tool for detecting imprinted differentially methylated regions from long-read sequencing data Genetic, Genomic, and Epigenomic Resources and Databases Computational toolsEpigeneticsLong-read sequencingMethodology
KRIBB Bioinformatics Group Works in computational genetics.	Talk Thu Oct 22 8:45 am HiVerse: A multi-resolution genomic language model atlas integrating 5-methylcytosine for tissue- and cell-type-specific epigenome and transcriptome prediction Sequence Models Transforming Genetics and Genomics Artificial intelligenceBioinformaticsComplex diseasesEpigenetics
1 more presenter — research group not yet identified

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