Statements (22)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genomic reference panel
|
| gptkbp:availableOn |
Michigan Imputation Server
|
| gptkbp:developedBy |
Trans-Omics for Precision Medicine (TOPMed) Program
|
| gptkbp:firstReleased |
2019
|
| https://www.w3.org/2000/01/rdf-schema#label |
TOPMed reference panel
|
| gptkbp:includes |
common variants
rare variants |
| gptkbp:numberOfSamples |
over 97,000
|
| gptkbp:provides |
diverse populations
whole genome sequencing |
| gptkbp:relatedTo |
gptkb:1000_Genomes_Project
Haplotype Reference Consortium (HRC) |
| gptkbp:releaseYear |
gptkb:National_Heart,_Lung,_and_Blood_Institute_(NHLBI)
|
| gptkbp:type |
genotype data
haplotype data |
| gptkbp:updated |
TOPMed Imputation Panel v2
|
| gptkbp:usedFor |
genotype imputation
|
| gptkbp:usedIn |
genome-wide association studies (GWAS)
|
| gptkbp:website |
https://imputation.biodatacatalyst.nhlbi.nih.gov/
|
| gptkbp:bfsParent |
gptkb:NHLBI_TOPMed_Imputation_Server
gptkb:TOPMed_Imputation_Server |
| gptkbp:bfsLayer |
7
|