Whole genome sequencing of AVM endothelial and non-endothelial cell fractions
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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.
Study Datasets 1 dataset.
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Whole genome sequencing data of brain AVM endothelial and non-endothelial cell fractions, as well as paired blood samples