HG001_dataset
The following dataset contains chromosome 22 alignment file and whole genome variant calls for sample HG001 from 1KGP. Analyses were performed using GRCh38 reference genome. BWA was used for the genomic alignment. GATK4 for variant calling.
- 04/09/2026
- 1 sample
- DAC: EGAC50000000008
- Technology: Illumina NovaSeq 6000
- Archive: Federated EGA France Federated EGA Node
DUO:0000006 version: 2021-02-23
health or medical or biomedical research
This data use permission indicates that use is allowed for health/medical/biomedical purposes; does not include the study of population origins or ancestry.
DUO:0000028 version: 2021-02-23
institution specific restriction
This data use modifier indicates that use is limited to use within an approved institution.
Research-only at French DEMO institute
Text for Access Policy for research use @Demo only.
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 |
|---|---|---|
| EGAS50000000542 | Whole Genome Sequencing |
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 | Quality Report | |
|---|---|---|---|---|
| EGAF50000106636 | vcf.gz | 269.5 MB | ||
| EGAF50000106640 | bam | 589.8 MB | ||
| 2 Files (859.2 MB) | ||||
