Statements (61)
| Predicate | Object |
|---|---|
| gptkbp:instance_of |
gptkb:DNA
|
| gptkbp:aims_to |
reduce healthcare costs
improve patient outcomes improve public health foster international collaboration develop new treatments create a genomic database advance genomic technologies improve diagnosis foster innovation in healthcare promote ethical research practices enhance disease prevention strategies support clinical trials improve research reproducibility enhance genetic literacy facilitate genetic counseling identify genetic predispositions increase genetic testing availability sequence 100,000 genomes support genomic education |
| gptkbp:analyzes |
ethnic diversity
genetic variants |
| gptkbp:collaborated_with |
gptkb:NHS_England
|
| gptkbp:collaborates_with |
academic institutions
biotechnology companies |
| gptkbp:contributes_to |
gptkb:Health_Insurance
personalized medicine global health initiatives |
| gptkbp:ended |
gptkb:2020
|
| gptkbp:enhances |
understanding of genomics
|
| gptkbp:focuses_on |
rare diseases
common diseases |
| https://www.w3.org/2000/01/rdf-schema#label |
100,000 Genomes Project
|
| gptkbp:includes |
participants from the UK
|
| gptkbp:involves |
community engagement
data sharing whole genome sequencing patient consent longitudinal studies data privacy measures multi-disciplinary teams |
| gptkbp:is_funded_by |
gptkb:British_government
|
| gptkbp:is_led_by |
gptkb:Genomics_England
|
| gptkbp:provides |
data for research
training for researchers data for public health research insights into population genetics resources for genetic research insights into genetic disorders |
| gptkbp:result |
gptkb:academic_journals
|
| gptkbp:started_in |
gptkb:2012
|
| gptkbp:supports |
evidence-based medicine
healthcare innovation clinical genomics |
| gptkbp:uses |
clinical data
next-generation sequencing |
| gptkbp:utilizes |
bioinformatics
|
| gptkbp:bfsParent |
gptkb:Genomics_England
gptkb:Sanger_Institute gptkb:Broad_Institute_of_MIT_and_Harvard |
| gptkbp:bfsLayer |
6
|