Statements (50)
| Predicate | Object |
|---|---|
| gptkbp:instance_of |
gptkb:DNA
|
| gptkbp:affiliated_with |
gptkb:University_of_California,_Santa_Cruz
gptkb:Wellcome_Trust_Sanger_Institute gptkb:National_Institutes_of_Health gptkb:Broad_Institute |
| gptkbp:analysis |
population genetics
variant calling haplotype phasing imputation |
| gptkbp:collaboration |
international consortium
multidisciplinary approach contribution from various scientists involvement of multiple research institutions |
| gptkbp:data_type |
whole genome sequencing
genotype data phenotype data exome sequencing |
| gptkbp:ended |
gptkb:2015
|
| gptkbp:focus |
human populations
|
| gptkbp:goal |
to provide a comprehensive resource on human genetic variation
|
| https://www.w3.org/2000/01/rdf-schema#label |
1000 Genomes Project
|
| gptkbp:impact |
identification of genetic variants associated with diseases
advancement of genomic technologies contribution to personalized medicine understanding of human genetic diversity |
| gptkbp:involved_countries |
gptkb:Brazil
gptkb:China gptkb:Iceland gptkb:India gptkb:Japan gptkb:Mexico gptkb:Nigeria gptkb:United_Kingdom gptkb:United_States |
| gptkbp:is_funded_by |
gptkb:National_Institutes_of_Health
|
| gptkbp:legacy |
resource for researchers
foundation for future genomic studies data for clinical applications influence on population genomics |
| gptkbp:number_of_genomes_sequenced |
over 2500
|
| gptkbp:public_access |
data available for clinical research
data available for educational purposes data available for policy making data available to researchers |
| gptkbp:released |
gptkb:2010
gptkb:2012 gptkb:2015 |
| gptkbp:started_in |
gptkb:2008
|
| gptkbp:bfsParent |
gptkb:Human_Genome_Project
|
| gptkbp:bfsLayer |
4
|