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Many NGS projects will not have access to data from inbred lines. This will cause problems in the assembly. How can this be solved?
Current technology generate short reads, or low coverage. Extent and nature of DNA duplications is unknown. Which NGS approach is best?
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LF: this is a research topic, especially for multiploid genomes. At the moment no solution exist. We could invite people how worked on similar projects or specialised in phasing.