SYNTHETIC DATA: WGS sample with variants related hearing loss
SYNTHETIC DATA: 1 sample with a set of paired fastq files, cram reference alignment file (with index) and GATK called variant vcf file (with index)
- 26/05/2023
- 1 sample
- DAC: EGAC50000000005
- Technology: Illumina HiSeq 4000
- HMB DUO:0000006 (version: 2021-02-23)health or medical or biomedical researchThis data use permission indicates that use is allowed for health/medical/biomedical purposes; does not include the study of population origins or ancestry.
- NPUNCU DUO:0000018 (version: 2021-02-23)not for profit, non commercial use onlyThis data use modifier indicates that use of the data is limited to not-for-profit organizations and not-for-profit use, non-commercial use.
- US DUO:0000026 (version: 2021-02-23)user specific restrictionThis data use modifier indicates that use is limited to use by approved users.
Access policy for SYNTHETIC DATA in FEGA Norway test instance
The synthetic data is approved for research and explorations of data sharing infrastructures and bioinformatics workflows.
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 |
---|---|---|
Synthetic Genomics |
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 | |
---|---|---|---|---|
EGAF50000104027 | fastq.gz | 20.7 GB | ||
EGAF50000104028 | fastq.gz | 20.7 GB | ||
EGAF50000104029 | cram | 7.3 GB | ||
EGAF50000104030 | crai | 909.0 kB | ||
EGAF50000104031 | vcf.gz | 349.8 MB | ||
EGAF50000104032 | tbi | 1.7 MB | ||
6 Files (49.0 GB) |