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DNASTAR - Identifying Causal Genes of Rare Mendelian Disease using Lasergene

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Published on Jan 29, 2014

In this webinar, we will use DNASTAR's Lasergene Genomics Suite software to analyze exome sequencing data from the breakthrough work of Ng et. al. (Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome. Nat. Genet. 42, 30-35 (2010)).
This case study confirms the discovery of mutations in the MLL2 gene as a cause of the rare autosomal dominant Kabuki syndrome. Through this case study, we will give a live demonstration of the capabilities of Lasergene Genomics Suite as applicable to similar association studies.

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