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Implement a system to use GNN and/or LLM to use knowledge graphs to integrate literature with knowledge graphs made from large public datasets (CIVIC, TCGA, CPTAC)
Identifying novel TR loci and motifs in individuals that are not in the reference genome
Benchmarking of how the quality of the reference genome assembly affects the discovery of structural variants, using aligners: Minimap2 & Winnowmap
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