The document describes analyzing data sets of patients diagnosed with Familial Dilated Cardiomyopathy. The analysis involved aligning the data sets to a reference genome, marking duplicates, calling variants using GATK, quality filtering results, annotating variants using Annovar and 1000g project. Familial Dilated Cardiomyopathy is characterized by thinning of the heart muscle and chamber enlargement which can lead to heart failure. More than 30 genes are associated with the condition, with the TTN gene associated with 20% of cases. The next steps outlined are to investigate annotation results, research alternative views on variant relevance, create a script to extract specific filtered results, and prepare a list of around 10 variants stating their details