FIN cohort
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| 1000 Genomes Project | associated_with | FIN | — | 1 |
Mentioned in (10)
Papers in which this entity is mentioned.
- Genome-wide association testing beyond SNPs. (2025)
- Variant interpretation using population databases: Lessons from gnomAD. (2022)
- Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
- Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
- Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
- Rare variant phasing using paired tumor:normal sequence data. (2019)
- A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
- Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
- A global reference for human genetic variation. (2015)
- Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. (2015)
Merged raw entities (3)
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 |
|---|---|---|---|
| fin | cohort | 8 | 20 |
| finnish | cohort | 8 | 12 |
| finnish from finland | cohort | — | — |