CNVs variant
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| CNVs | associated_with | alcohol dependence | — | 1 |
Mentioned in (17)
Papers in which this entity is mentioned.
- Three-dimensional genome landscape of primary human cancers. (2025)
- Genome-wide association testing beyond SNPs. (2025)
- Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X. (2020)
- Best practices for variant calling in clinical sequencing. (2020)
- SVXplorer: Three-tier approach to identification of structural variants via sequential recombination of discordant cluster signatures. (2020)
- Accucopy: Accurate and Fast Inference of Allele-specific Copy Number Alterations from Low-coverage Low-purity Tumor Sequencing Data (2020)
- Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing. (2020)
- Longitudinal therapy monitoring of ALK-positive lung cancer by combined copy number and targeted mutation profiling of cell-free DNA. (2020)
- Structural variant calling: the long and the short of it. (2019)
- The evolution of tumour phylogenetics: principles and practice. (2017)
- Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia. (2015)
- Hidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping Microarrays. (2014)
- Recurrent somatic structural variations contribute to tumorigenesis in pediatric osteosarcoma. (2014)
- ACMG clinical laboratory standards for next-generation sequencing. (2013)
- Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence. (2012)
- cn.MOPS: mixture of Poissons for discovering copy number variations in next-generation sequencing data with a low false discovery rate. (2012)
- A hidden Markov model for copy number variant prediction from whole genome resequencing data. (2011)
Merged raw entities (1)
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 |
|---|---|---|---|
| cnvs | variant | 34 | 47 |