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

Dataset Accession Technology Samples
EGAD00001000024 Illumina Genome Analyzer II 4

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This dataset is featured in 1 studies

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 Accessions below to find out more.

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

Who controls access to this dataset

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

DAC for study PK Exome Seq 439-sc-2011-05-27T14:46:29Z-439

Contact Person: Christopher Tyler-Smith