Whole exome sequencing of two patients with Sotos Syndrome Features
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).
- Technology: Illumina HiSeq 2000
- 2 samples
- DAC: EGAC00001000249
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