subclonal mutations variant
Evidence from:
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all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| subclonal mutations | associated_with | cancer | — | 1 |
| subclonal mutations | biomarker_for | chronic lymphocytic leukemia | — | 1 |
Mentioned in (12)
Papers in which this entity is mentioned.
- Immune selection determines tumor antigenicity and influences response to checkpoint inhibitors. (2023)
- Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes. (2021)
- Multi-cancer analysis of clonality and the timing of systemic spread in paired primary tumors and metastases. (2020)
- Quantification of subclonal selection in cancer from bulk sequencing data. (2018)
- Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes (2018)
- Quantifying Clonal and Subclonal Passenger Mutations in Cancer Evolution. (2016)
- Clock-like mutational processes in human somatic cells. (2015)
- Detecting ultralow-frequency mutations by Duplex Sequencing. (2014)
- Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. (2013)
- Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. (2013)
- Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. (2013)
- Absolute quantification of somatic DNA alterations in human cancer. (2012)
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 |
|---|---|---|---|
| subclonal mutations | variant | 12 | 21 |
| subclonal driver mutations | variant | 1 | 1 |