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).

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Studies are experimental investigations of a particular phenomenon. e.g. case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients. Click on one of the Study IDs below to find out more.

Study ID Study Title Study Type
EGAS00001000993 Other
ID File Type Size Located in Quality Control
EGAF00000650107 fastq.gz 2.0 GB
EGAF00000650108 fastq.gz 2.0 GB
EGAF00000650109 fastq.gz 2.0 GB
EGAF00000650110 fastq.gz 2.1 GB
EGAF00000650111 fastq.gz 2.4 GB
EGAF00000650112 fastq.gz 2.5 GB
EGAF00000650113 fastq.gz 2.5 GB
EGAF00000650114 fastq.gz 2.5 GB
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