Need Help?

WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW32_M

50 trios were whole genome sequenced with Complete Genomics to a depth of 80x. For each trio the child was affected with severe ID, and the parents were unaffected. All trios were negative for array, targeted gene and whole exome screening. Dataset consists of sample: MW32_M

Request Access

This document refers to the data set, EGAS00001000287 which has been submitted to the European Genome Archive (EGA) for the restricted access by legitimate academic institutions that have agreed to comply with the terms of a Data Access Agreement drafted by the Data Access Committee.For more information see the complete policy document and our webpage on data sharing;https://www.umcn.nl/Research/Departments/HumanGenetics/Pages/SharingData.aspx

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.

Study ID Study Title Study Type
Other

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID File Type Size Located in
EGAF00001029242 tsv 1.8 kB
EGAF00001029243 tsv 709 Bytes
EGAF00001029244 tsv 3.1 MB
EGAF00001029245 tsv 378.7 kB
EGAF00001029246 tsv 585.9 kB
EGAF00001029247 tsv.bz2 12.2 MB
EGAF00001029248 tsv 763.7 kB
EGAF00001029249 tsv 138.8 kB
EGAF00001029250 tsv 551 Bytes
EGAF00001029251 tsv 769.6 kB
EGAF00001029252 tsv 394.3 kB
EGAF00001029253 tsv 20.5 kB
EGAF00001029254 tsv 769.6 kB
EGAF00001029995 tsv 394.3 kB
14 Files (19.5 MB)