Find out about the future of NGS and benefit from critical discussions in the accuracy, cost and coverage of short and long read sequencing. Gain .. Read more insights from thought-provoking presentations on Long read sequencing for human genomes and De Novo Studies, data analysis in de-novo assembly and structural variants, bioinformatics and mapping tools. Over 600 end users representing internationally renowned research & academic institutions, clinical research institutions, healthcare organisations as well as leading pharmaceutical and biotech companies. We produce cutting edge congresses and summits for the Life Sciences Industry, bringing together industry leaders and solution providers at a senior level, creating the opportunity to partner, network and knowledge share.
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