Fig. 1From: Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defectsWorkflow for identification of homozygous blocks and candidate genes. Whole-exome data (variant calling file) is used for homozygosity mapping. Homozygosity mapper is integrated with gene distillers to search for candidate genes and sort the genes in the candidate regionBack to article page