Other phenotype
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| 1000 Genomes Project | associated_with | Other | — | 1 |
Mentioned in (9)
Papers in which this entity is mentioned.
- Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasets. (2023)
- Anatomy-Aware Contrastive Representation Learning for Fetal Ultrasound. (2022)
- Variant interpretation using population databases: Lessons from gnomAD. (2022)
- Single-cell genomic variation induced by mutational processes in cancer. (2022)
- Detection and characterization of lung cancer using cell-free DNA fragmentomes. (2021)
- Rare variant phasing using paired tumor:normal sequence data. (2019)
- Genome-wide association studies of alcohol dependence, DSM-IV criterion count and individual criteria. (2019)
- Molecular profiling and sequential somatic mutation shift in hypermutator tumours harbouring POLE mutations. (2018)
- Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden. (2017)
Merged raw entities (4)
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 |
|---|---|---|---|
| other | phenotype | 11 | 11 |
| other | cohort | 10 | 11 |
| other race/ethnicity adolescents | phenotype | — | — |
| undetermined | phenotype | — | — |