TOPMed data

URI: https://gptkb.org/entity/TOPMed_data
GPTKB entity
Statements (100)
Predicate Object
gptkbp:instanceOf genomic dataset
gptkbp:accessibleBy gptkb:dbGaP
gptkb:BRAVO_variant_browser
gptkb:TOPMed_Imputation_Server
gptkbp:contains omics data
phenotypic data
whole genome sequencing data
gptkbp:fundedBy National Heart, Lung, and Blood Institute
https://www.w3.org/2000/01/rdf-schema#label TOPMed data
gptkbp:includes family studies
clinical trial data
data from diverse populations
longitudinal cohort studies
multi-omics data (e.g., RNA-seq, methylation)
over 150,000 participants
gptkbp:launched 2014
gptkbp:notableCollection gptkb:NHLBI_Trans-Omics_for_Precision_Medicine_(TOPMed)_Program
gptkbp:subjectArea biomedical research
genomics
public health
gptkbp:type gptkb:RNA-seq
family history
metabolomics
proteomics
electronic health records
laboratory measurements
clinical data
epigenomic data
proteomic data
transcriptomic data
variant annotation
lifestyle data
demographic data
DNA methylation
phenotype data
longitudinal data
survey data
clinical outcomes
whole genome sequencing
imaging data
gene expression data
environmental exposures
biospecimen data
funding information
omics data
genotype data
structural variant data
vital signs
ancestry information
ancestry-informative markers
biomarker data
cellular phenotype data
collaborator information
common variant data
consent information
copy number variation data
data access requests
data release notes
data sharing policies
data use limitations
disease status
family structure data
follow-up data
functional genomics data
genome-wide association study (GWAS) data
haplotype data
hospitalization records
imputed genotypes
imputed sequence data
indel data
medication data
metabolomic data
microbiome data
mortality data
multi-ethnic data
pedigree data
phased genotype data
phenome-wide association study (PheWAS) data
physical examination data
population structure data
principal component analysis data
project metadata
publication references
quality control metrics
questionnaire data
rare variant data
relatedness data
sample metadata
sample tracking data
sequencing platform information
single nucleotide variant data
splicing data
study design information
variant calls
gptkbp:usedFor precision medicine
genetic research
population health studies
studying heart, lung, blood, and sleep disorders
gptkbp:bfsParent gptkb:NHLBI_BioData_Catalyst
gptkbp:bfsLayer 5