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Dataset

Whole Exome Sequencing for Characterization of Disease Causing Mutations in two Pakistani Families Suffering from Autosomal Recessive Ocular Disorders.

Dataset ID	Technology	Samples
EGAD00001000024	Illumina Genome Analyzer II	4

Dataset Description

Whole Exome Sequencing for Characterization of Disease Causing Mutations in two Pakistani Families Suffering from Autosomal Recessive Ocular Disorders.

Data Use Conditions

IS PUB US PS

See further information on Data Use Conditions

Label	Code	Version
general research use	DUO:0000042	2021-02-23
institution specific restriction	DUO:0000028	2021-02-23
publication required	DUO:0000019	2021-02-23
user specific restriction	DUO:0000026	2021-02-23
project specific restriction	DUO:0000027	2021-02-23

Who controls access to this dataset

For each dataset that requires controlled access, there is a corresponding Data Access Committee (DAC) who determine access permissions. Access to actual data files is not managed by the EGA. If you need to request access to this data set, please contact:

Wellcome Trust Sanger Institute
Contact person: Data Sharing
Email: datasharing [at] sanger [dot] ac [dot] uk
Access information: https://www.sanger.ac.uk/legal/DAA/MasterController
More details: EGAC00001000205

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This dataset is featured in 1 study

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
EGAS00001000026	Whole Exome Sequencing for Characterization of Disease Causing Mutations in two Pakistani Families Suffering from Autosomal Recessive Ocular Disorders	Other

EGA Beacon