Need Help?

WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB28_C

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: BvB28_C

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
EGAF00000983028 tsv.bz2 9.4 kB
EGAF00000983029 tsv 7.4 kB
EGAF00000983030 tsv.bz2 234.8 MB
EGAF00000983031 vcf.bz2 187.5 MB
EGAF00000983032 tsv.bz2 11.4 MB
EGAF00000983033 tsv.bz2 227.4 kB
EGAF00000983034 tsv 465.8 kB
EGAF00000983035 tsv 23.3 kB
EGAF00000983036 tsv 1.4 MB
EGAF00000983037 tsv.bz2 768.1 MB
EGAF00000983038 tsv.bz2 1.8 GB
EGAF00000983039 tsv.bz2 473.8 MB
EGAF00000983040 tsv.bz2 997.1 MB
EGAF00000983041 tsv.bz2 340.5 MB
14 Files (4.8 GB)