translocation variant
Evidence from:
primary |
all sources
Related entities (3)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| translocation | associated_with | diabetes | — | 1 |
| translocation | associated_with | obesity | — | 1 |
| translocation | associated_with | smoking | — | 1 |
Mentioned in (43)
Papers in which this entity is mentioned.
- Three-dimensional genome landscape of primary human cancers. (2025)
- ConsensuSV-ONT - A modern method for accurate structural variant calling. (2025)
- Genome-wide association testing beyond SNPs. (2025)
- Comprehensive analysis of mutational signatures reveals distinct patterns and molecular processes across 27 pediatric cancers. (2023)
- Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers. (2022)
- Application of third-generation sequencing in cancer research. (2021)
- Detection of somatic structural variants from short-read next-generation sequencing data. (2021)
- A Comprehensive Circulating Tumor DNA Assay for Detection of Translocation and Copy-Number Changes in Pediatric Sarcomas. (2021)
- Integrative reconstruction of cancer genome karyotypes using InfoGenomeR. (2021)
- Structural variation in the sequencing era. (2020)
- SVXplorer: Three-tier approach to identification of structural variants via sequential recombination of discordant cluster signatures. (2020)
- Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs. (2020)
- Inferring structural variant cancer cell fraction. (2020)
- Pan-cancer landscape of homologous recombination deficiency. (2020)
- Diverse noncoding mutations contribute to deregulation of cis-regulatory landscape in pediatric cancers. (2020)
- Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing. (2020)
- Highly Efficient CRISPR-Cas9-Based Methods for Generating Deletion Mutations and F0 Embryos that Lack Gene Function in Zebrafish. (2019)
- Structural variant calling: the long and the short of it. (2019)
- Best practices for bioinformatic characterization of neoantigens for clinical utility. (2019)
- Comprehensive analysis of structural variants in breast cancer genomes using single molecule sequencing (2019)
- Pan-cancer whole-genome analyses of metastatic solid tumours. (2019)
- Identifying simultaneous rearrangements in cancer genomes. (2018)
- Driver Fusions and Their Implications in the Development and Treatment of Human Cancers. (2018)
- Detection of Somatic Structural Variants Enables Quantification and Characterization of Circulating Tumor DNA in Children With Solid Tumors. (2018)
- Widespread Selection for Oncogenic Mutant Allele Imbalance in Cancer. (2018)
- Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line. (2018)
- Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes. (2018)
- Predicting T cell recognition of MHC class I restricted neoepitopes. (2018)
- The 3D Genome Browser: a web-based browser for visualizing 3D genome organization and long-range chromatin interactions. (2018)
- Patterns and mechanisms of structural variations in human cancer. (2018)
- Picky comprehensively detects high-resolution structural variants in nanopore long reads. (2018)
- Nanopore Sequencing Reveals High-Resolution Structural Variation in the Cancer Genome (2017)
- PGBD5 promotes site-specific oncogenic mutations in human tumors. (2017)
- Copy-number signatures and mutational processes in ovarian carcinoma (2017)
- Landscape of somatic mutations in 560 breast cancer whole-genome sequences. (2016)
- Cancer genome landscapes. (2013)
- ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. (2013)
- DELLY: structural variant discovery by integrated paired-end and split-read analysis. (2012)
- Uncovering hidden variance: pair-wise SNP analysis accounts for additional variance in nicotine dependence. (2011)
- Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion. (2011)
- BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. (2009)
- Finding the missing heritability of complex diseases. (2009)
- Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009)
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 |
|---|---|---|---|
| translocation | variant | 36 | 65 |
| translocations | variant | 19 | 28 |