We are currently trying to other researchers actively engaged in whole genome sequencing to both confirm currently known SNPs and variants/alleles as well as potentially identify novel genetic variants in scoliosis patients compared to a non-scoliotic control population.
Laura Marie-Hardy
Good morning, we are in Paris doing exome sequencing in a cohort of familial scoliosis (idiopathic scoliosis, more than 3 cases in the family).
You do whole-genome sequencing??
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