Availability of next gen sequence (NGS) data for you to use/analyze (e.g. “I have illumina RAD data [200 M reads] from xxx individuals for my PhD project. I will have 200M more reads before the ConGen2.0 meeting”). Note: It’s ok if you only have microsatellite or SNP-chip data for ConGen, for example, but you should have a basic understanding of NGS data production and analysis (e.g., filtering/genotype calling) before ConGen to maximally benefit from ConGen. *