ESP cohort
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| African American | associated_with | ESP | — | 1 |
| European population | associated_with | ESP | — | 1 |
Mentioned in (13)
Papers in which this entity is mentioned.
- Variant interpretation using population databases: Lessons from gnomAD. (2022)
- The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
- The GenomeAsia 100K Project enables genetic discoveries across Asia. (2019)
- A SNP panel for identification of DNA and RNA specimens. (2018)
- Identification of novel candidate disease genes from de novo exonic copy number variants. (2017)
- CRAVAT 4: Cancer-Related Analysis of Variants Toolkit. (2017)
- A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease. (2016)
- The discovery of integrated gene networks for autism and related disorders. (2015)
- 708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. (2014)
- VariantDB: a flexible annotation and filtering portal for next generation sequencing data. (2014)
- Signatures of mutational processes in human cancer. (2013)
- Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
- Evolution and functional impact of rare coding variation from deep sequencing of human exomes. (2012)
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 |
|---|---|---|---|
| esp | cohort | 6 | 6 |
| exome sequencing project | cohort | 5 | 6 |
| nhlbi go exome sequencing project | cohort | 3 | 3 |