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

25/08/2016
1 sample
DAC: EGAC00001000076

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Metadata

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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
EGAS00001000769	Whole genome sequencing of 50 trios, where the child is affected with ID, and the parents are unaffected	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
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)