SPATC1L variants associated with age-related and hereditary hearing loss.
The dataset contains three BAM files that include SPATC1L variants identified in Italian patients affected by hearing loss (both hereditary and age-related hearing loss). Data have been produced by whole exome sequencing and targeted re-sequencing, using Ion Proton and Ion Torrent PGM platforms respectively.
- 3 samples
- DAC: EGAC00001000933
- Technologies: Ion Torrent PGM, Ion Torrent Proton
SPATC1L variants in hearing loss patients
Data availability is subject to restrictions. A username and password are needed to access the dataset and will be granted after signing a proper data access agreement.
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.
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| Other |