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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.

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:

DAC_for_study_Transcriptome_PLX4032
Contact person: David Adams
Email: da1 [at] sanger [dot] ac [dot] uk
More details: EGAC00001000108

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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

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Dataset Description

Who controls access to this dataset

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This dataset is featured in 1 study

The European Genome-phenome Archive (EGA) is part of the ELIXIR infrastructure.