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HUMAN GENOME
MEETING 2026

Zappeion Hall
Athens, Greece

 

Events

Human Genome Meeting

HGM2026

Human Genome Meeting (HGM) is a series of annual conferences organized by the Human Genome Organisation (HUGO). It started as a meeting dedicated for Human Genome Mapping. Over the years, with the completion of the Human Genome Project, HGM has evolved from a small targeted meeting into a scientific conference for all genetic and genomic researchers; an excellent platform for industry partners and bio-technology companies as well as pharmaceutical giants; and a fantastic reunion for fellow scientists and networking opportunity for established and young investigators.

HGM2026

https://www.hugo-hgm2026.org/

Events

 

9th Variant Effect Prediction Training Course

 

Variant interpretation is one of the most complex and time-intensive aspects of genomic testing. VEPTC 2025 is designed to provide participants with the tools, skills, and confidence to navigate this challenging landscape. Next-Generation Sequencing (NGS) has revolutionised the speed of generating variation data, yet data analysis and variant interpretation remain the most time-consuming and complex steps. As genomic testing becomes increasingly integral in diagnostics, it’s crucial to gather and curate evidence to determine whether an identified variant has been previously reported and its potential effects. This in-person event is designed to empower professionals with the knowledge and tools to excel in DNA variant analysis and interpretation.

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HUGO 16th International Symposium on Variants in the Genome

 

This biennial conference, formerly known as the Mutation Detection meeting series, will delve into the latest advancements in scanning, sequencing, databasing, and bioinformatics analysis of genetic variants in DNA, RNA, and protein. As technology rapidly evolves, understanding the impact of these variants on individual health is becoming increasingly vital, transforming how we interpret genomic data. This year’s symposium will place special emphasis on the methodologies and capabilities for functional testing and classification of genomic variants associated with disease.

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