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

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

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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
EGAS00001000026 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
EGAF00000058126 srf 17.1 GB
EGAF00000058127 srf 17.4 GB
EGAF00000058128 srf 17.3 GB
EGAF00000058129 srf 23.1 GB
EGAF00000058130 srf 23.1 GB
EGAF00000058131 srf 22.3 GB
EGAF00000058132 srf 16.1 GB
EGAF00000058133 srf 15.8 GB
EGAF00000058134 srf 16.3 GB
EGAF00000058135 srf 24.0 GB
EGAF00000058136 srf 24.2 GB
EGAF00000058137 srf 24.2 GB
12 Files (240.8 GB)