translocation variant

Aliases

translocations

External links

ClinVar

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Mentioned in (39)

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)
• 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)
• 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)

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