Australian Genomics

oliver.hofmann@unimelb.edu.au

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Dataset ID	Description	Technology	Samples
EGAD00001011260	A prospective study of individuals with suspicion of a hereditary cancer syndrome for whom previous clinical targeted genetic testing was either not informative or was not available. To identify pathogenic disease-causing variants explaining participant presentation, germline whole-genome sequencing and a comprehensive cancer virtual gene panel analysis were undertaken.	Illumina NovaSeq 6000	182