SeeCiTe: a method to assess CNV calls from SNP arrays using trio data
Single nucleotide polymorphism (SNP) genotyping arrays stay a sexy platform for assaying copy quantity variants (CNVs) in massive population-wide cohorts. Nevertheless present instruments for calling CNVs are nonetheless liable to intensive false optimistic calls when utilized to biobank scale arrays. Furthermore, there’s a lack of strategies exploiting cohorts with trios out there (e.g. nuclear household) … Read more