1000 Genomes
Provided by: National Institutes of Health, part of the AWS Open Data Sponsorship Program
Provided by: National Institutes of Health, part of the AWS Open Data Sponsorship Program
1000 Genomes
Provided by: National Institutes of Health, part of the AWS Open Data Sponsorship Program
Provided by: National Institutes of Health, part of the AWS Open Data Sponsorship Program
This product is part of the AWS Open Data Sponsorship Program and contains data sets that are publicly available for anyone to access and use. No subscription is required. Unless specifically stated in the applicable data set documentation, data sets available through the AWS Open Data Sponsorship Program are not provided and maintained by AWS.
Description
The 1000 Genomes Project is an international collaboration which has established the most detailed catalogue of human genetic variation, including SNPs, structural variants, and their haplotype context. The final phase of the project sequenced more than 2500 individuals from 26 different populations around the world and produced an integrated set of phased haplotypes with more than 80 million variants for these individuals.
License
Data from the 1000 Genomes Project is now available without embargo, following the final publication from the project. Use of the data should be cited in the usual way, with current details available at http://www.internationalgenome.org/faq/how-do-i-cite-1000-genomes-project .
How to cite
1000 Genomes was accessed on DATE from https://registry.opendata.aws/1000-genomes .
Update frequency
Not updated
Support information
Managed by: National Institutes of Health
General AWS Data Exchange support
Resources on AWS
Description
Resource type
S3 Bucket
Amazon Resource Name (ARN)
arn:aws:s3:::1000genomesAWS Region
us-east-1AWS CLI Access (No AWS account required)
aws s3 ls --no-sign-request s3://1000genomes/Usage examples
Tools & Applications
- Examine genomic variation across populations with AWS by Konstantinos Tzouvanas