Whole genome sequencing of AVM endothelial and non-endothelial cell fractions

We previously identified somatic activating KRAS mutations in a majority of human arteriovenous malformations (AVMs), using whole exome sequencing, which were enhanced in AVM endothelial cell fractions. We have now performed whole genome sequencing on AVM endothelial and non-endothelial cell fractions, as well as paired blood samples, in order to identify further somatic mutations.

Type: Other
Archiver: European Genome-Phenome Archive (EGA)

1 Dataset

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Dataset ID	Description	Technology	Samples
EGAD00001009696	Whole genome sequencing data of brain AVM endothelial and non-endothelial cell fractions, as well as paired blood samples	unspecified	31