Congenital anosmia 1
Congenital anosmias can be complete (the lack of a sense of smell) or specific (the inability to detect specific smells). To date, only a single recessive gene underlying complete anosmia has been identified. Here we sequenced the exomes of 10 individuals from a single family, including three with complete anosmia, across three generations to identify the genetic basis of congenital anosmia in this family. This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/
- 28/06/2016
- 10 samples
- DAC: EGAC00001000205
- Technology: Illumina HiSeq 2000
Wellcome Trust Sanger Institute Data Sharing Policy
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 |
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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 | |
---|---|---|---|---|
EGAF00000827813 | cram | 3.0 GB | ||
EGAF00000827814 | cram | 2.8 GB | ||
EGAF00000827815 | cram | 2.7 GB | ||
EGAF00000827816 | cram | 2.8 GB | ||
EGAF00000827817 | cram | 3.0 GB | ||
EGAF00000827818 | cram | 2.8 GB | ||
EGAF00000827819 | cram | 2.6 GB | ||
EGAF00000827820 | cram | 3.0 GB | ||
EGAF00000827821 | cram | 2.9 GB | ||
EGAF00000827822 | cram | 2.8 GB | ||
10 Files (28.5 GB) |