E-GEUV-5 - Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

Released on 6 November 2013, last updated on 2 May 2014
Homo sapiens
Samples (300)
Protocols (2)
Intellectual disability is a common condition that carries lifelong severe medical and developmental consequences. The causes of intellectual disability (ID) remain unknown for the majority of patients due to the extensive clinical and genetic heterogeneity of this disorder. De novo mutations may play an important role in ID as most individuals with ID present as isolated cases without family history and/or clear syndromic indication. In addition, the involvement of such mutations have recently been demonstrated in a small number of individuals with ID. Here we evaluate the diagnostic potential and role of de novo mutations in a cohort of 100 patients with ID of unknown cause using family-based exome sequencing. Single end short-read (50 bp) SOLiD 4 sequencing data for 300 individuals, constituting 100 patient-parent trios. For more details please read; http://www.nejm.org/doi/full/10.1056/NEJMoa1206524. Dataset is created by RUNMC (Radboud University, Nijmegen Medical Center), partner of Geuvadis consortium (http://www.geuvadis.org).
Experiment types
DNA-seq, family based design
Diagnostic exome sequencing in persons with severe intellectual disability. de Ligt J, Willemsen MH, van Bon BW, Kleefstra T, Yntema HG, Kroes T, Vulto-van Silfhout AT, Koolen DA, de Vries P, Gilissen C, del Rosario M, Hoischen A, Scheffer H, de Vries BB, Brunner HG, Veltman JA, Vissers LE. , Europe PMC 23033978
Exp. designProtocolsFactorsProcessedSeq. reads
Investigation descriptionE-GEUV-5.idf.txt
Sample and data relationshipE-GEUV-5.sdrf.txt