DAC: Dr. Majewski's lab

Somayyeh Fahiminiya
somayyeh.fahiminiya@mcgill.ca

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Dataset ID	Description	Technology	Samples
EGAD00001001033	Whole exome sequencing (WES) was performed on genomic DNA derived from two patients with Sotos Syndrome Features. Sequencing (100 base pair paired-end) was performed on an Illumina Hiseq 2000 sequencer after enrichment of 62Mb of exonic and adjacent intronic sequences with TruSeq Exome Enrichment Kit (Illumina, San Diego, CA, USA).	Illumina HiSeq 2000	2
EGAD00001001042	In this work, using exome sequencing, we identified biallelic PNLPA6 mutations in patients with childhood blindness due to severe photoreceptor death and clinical features of Leber congenital amaurosis (LCA) and, interestingly, also of the rare Oliver McFarlane Syndrome	AB SOLiD 4 System Illumina HiSeq 2000	7