SAS cohort
Evidence from:
primary |
all sources
Related entities (7)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| 1000 Genomes Project | associated_with | SAS | — | 1 |
| AFR | interacts_with | SAS | — | 1 |
| EAs | interacts_with | SAS | — | 1 |
| EUR | interacts_with | SAS | — | 1 |
| His | interacts_with | SAS | — | 1 |
| SAS | associated_with | UKB | — | 1 |
| SNP | associated_with | SAS | — | 1 |
Mentioned in (13)
Papers in which this entity is mentioned.
- Meta-analysis reveals differences in somatic alterations by genetic ancestry across common cancers. (2025)
- MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups. (2024)
- Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
- Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
- Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. (2023)
- A saturated map of common genetic variants associated with human height. (2022)
- The complete sequence of a human genome. (2022)
- Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. (2022)
- Rapid genotype imputation from sequence with reference panels. (2021)
- Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
- A global reference for human genetic variation. (2015)
- Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. (2009)
- Using whole-genome sequencing to evaluate copy number variants of the LPA Kringle-IV type 2 domain with DRAGEN
Merged raw entities (1)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| sas | cohort | 13 | 45 |