speakers

using single-cell rna-sequencing to study transcriptional and post-transcriptional gene regulation

Rickard Sandberg, Professor, Karolinska Institutet / Department of Cell and Molecular Biology

ADVANCING OUR UNDERSTANDING OF HUMAN TRAITS AND DISEASE THROUGH NGS AND THE T2T-CHM13 REFERENCE GENOME

Åsa Johansson,  Associate Professor, Uppsala Universitet / Department of Immunology, Genetics and Pathology

NEW INSIGHTS INTO THE STRUCTURE AND FUNCTION OF THE NORWAY SPRUCE AND SCOTS PINE GENOMES

Nathaniel Street, Professor, Umeå Universitet / Umeå Plant Science Center

An intronic copy number variation in the gene STX17 determines speed of greying and melanoma incidence in horses

Carl-Johan Rubin, Researcher, Uppsala Universitet / Department of Medical Biochemistry and Microbiology

The known, the unknown and the “can you quickly” – lessons learnt automating NGS workflows

Inken Dillmann, Senior Research Scientist - NGS Automation specialist AstraZeneca

Adaptive Sampling using ONT sequencing

Anja Mezger, Head of Genomics Application Development, National Genomics Infrastructure (NGI)

Go Long project: A short-long story

Carolina Rocha, Research Scientist, Novonesis/ Next Generation Sequencing Department

bacterial wgs in clinical microbiology laboratory

Marianne Gunell,  adjunct professor, Turku University Hospital/ Department of Clinical Microbiology

scRNA Sequencing Reveals Hallmarks of Mitochondrial Diseases in Stem Cell Models

Tsering Yangzom,  PhD student, University of Bergen

NEBNext Product Development: Streamlining workflows & addressing new applications

Keerthana Krishnan, Associate Director NGS, New England Biolabs, USA