insertion/deletion variant
Evidence from:
primary |
all sources
Related entities (3)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| insertion/deletion | associated_with | diabetes | — | 1 |
| insertion/deletion | associated_with | obesity | — | 1 |
| insertion/deletion | associated_with | smoking | — | 1 |
Mentioned in (10)
Papers in which this entity is mentioned.
- ConsensuSV-ONT - A modern method for accurate structural variant calling. (2025)
- The Application of Long-Read Sequencing to Cancer. (2024)
- Detection of somatic structural variants from short-read next-generation sequencing data. (2021)
- Multi-cancer analysis of clonality and the timing of systemic spread in paired primary tumors and metastases. (2020)
- Best practices for bioinformatic characterization of neoantigens for clinical utility. (2019)
- HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures. (2017)
- The impact of structural variation on human gene expression. (2017)
- Track data hubs enable visualization of user-defined genome-wide annotations on the UCSC Genome Browser. (2014)
- VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. (2012)
- Uncovering hidden variance: pair-wise SNP analysis accounts for additional variance in nicotine dependence. (2011)
Merged raw entities (2)
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 |
|---|---|---|---|
| insertion/deletion | variant | 8 | 9 |
| insertions/deletions | variant | 2 | 2 |