This dataset contains the whole genome sequencing variants detected in prostate cancer samples used in the first tranche of papers from the Pan Prostate Cancer Group. Further details on this data rele
50 trios were whole genome sequenced with Complete Genomics to a depth of 80x. For each trio the child was affected with severe ID, and the parents were unaffected. All trios were negative for array,
We identified a family segregating ASD in three siblings with an unidentified cause. We performed WGS in the three probands in order to use a state-of-the-art comprehensive bioinformatic analysis pipe
