Finder of Somatic Fusion Genes in RNA-seq data
☆150Sep 9, 2025Updated 7 months ago
Alternatives and similar repositories for fusioncatcher
Users that are interested in fusioncatcher are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- STAR-Fusion codebase☆250Oct 4, 2025Updated 6 months ago
- Tool for parsing outputs from fusion detection tools. Part of a nf-core/rnafusion pipeline. Checkout a live demo at https://matq007.githu…☆28Jun 13, 2025Updated 9 months ago
- Fast fusion detection using kallisto☆79Jun 11, 2025Updated 10 months ago
- Gene fusion detection and visualization☆133Feb 21, 2022Updated 4 years ago
- Concordance and contamination estimator for tumor–normal pairs☆59Oct 22, 2024Updated last year
- NordVPN Special Discount Offer • AdSave on top-rated NordVPN 1 or 2-year plans with secure browsing, privacy protection, and support for for all major platforms.
- FusionInspector code☆59Apr 1, 2026Updated last week
- Python package to annotate and visualize gene fusions.☆67Sep 30, 2024Updated last year
- Fast and accurate gene fusion detection from RNA-Seq data☆267Sep 21, 2025Updated 6 months ago
- RADIA: RNA and DNA Integrated Analysis for Somatic Mutation Detection☆29Oct 1, 2020Updated 5 years ago
- chimeraviz is an R package that automates the creation of chimeric RNA visualizations.☆39Nov 25, 2023Updated 2 years ago
- 肿瘤突变负荷学习笔记(tumor mutation burden)☆16Dec 10, 2019Updated 6 years ago
- Toolkit for benchmarking fusion transcript predictions☆19Dec 24, 2025Updated 3 months ago
- A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region exp…☆27Mar 16, 2026Updated 3 weeks ago
- RNA-seq analysis pipeline for detection of gene-fusions☆173Mar 18, 2026Updated 3 weeks ago
- Wordpress hosting with auto-scaling on Cloudways • AdFully Managed hosting built for WordPress-powered businesses that need reliable, auto-scalable hosting. Cloudways SafeUpdates now available.
- A set of tools to annotate VCF files with expression and readcount data☆30Jan 30, 2026Updated 2 months ago
- Pindel can detect breakpoints of large deletions, medium sized insertions, inversions, tandem duplications and other structural variants …☆176Jan 7, 2020Updated 6 years ago
- ☆33May 2, 2022Updated 3 years ago
- DELLY2: Structural variant discovery by integrated paired-end and split-read analysis☆509Feb 26, 2026Updated last month
- microsatellite instability detection using tumor only or paired tumor-normal data☆132Jan 6, 2021Updated 5 years ago
- Control-FREEC: Copy number and genotype annotation in whole genome and whole exome sequencing data☆176Aug 22, 2024Updated last year
- TransVar - multiway annotator for precision medicine☆127Apr 19, 2023Updated 2 years ago
- Canvas - Copy number variant (CNV) calling from DNA sequencing data☆129Sep 3, 2019Updated 6 years ago
- Work supporting the comparison of SnpEff and VEP effect prediction and HGVS identifiers☆11Mar 15, 2017Updated 9 years ago
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting with the flexibility to host WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Cloudways by DigitalOcean.
- GRIDSS: the Genomic Rearrangement IDentification Software Suite☆282May 21, 2025Updated 10 months ago
- Combined mutation recurrence and functional impact to identify coding and non-coding cancer drivers☆15Oct 26, 2018Updated 7 years ago
- RNA Fusion Detection and Quantification☆18Oct 31, 2018Updated 7 years ago
- Summarize, Analyze and Visualize MAF files from TCGA or in-house studies.☆486Feb 25, 2026Updated last month
- ☆120Sep 5, 2023Updated 2 years ago
- Convert a VCF into a MAF, where each variant is annotated to only one of all possible gene isoforms☆416Mar 13, 2026Updated 3 weeks ago
- Plot structural variant signals from many BAMs and CRAMs☆563Jul 13, 2024Updated last year
- Microsatellite instability (MSI) detection for tumor only data.☆114Apr 23, 2024Updated last year
- RTG Tools: Utilities for accurate VCF comparison and manipulation☆334May 27, 2025Updated 10 months ago
- Wordpress hosting with auto-scaling on Cloudways • AdFully Managed hosting built for WordPress-powered businesses that need reliable, auto-scalable hosting. Cloudways SafeUpdates now available.
- Software program for checking sample matching for NGS data☆139Jun 20, 2024Updated last year
- Personal Cancer Genome Reporter (PCGR)☆274Apr 1, 2026Updated last week
- goleft is a collection of bioinformatics tools distributed under MIT license in a single static binary☆225Sep 18, 2025Updated 6 months ago
- ☆123Sep 5, 2023Updated 2 years ago
- Copy Number Variation Detection In Next-generation sequencing Gene panels was designed for small (single-exon) copy number variation (CNV…☆21Jun 30, 2020Updated 5 years ago
- structural variant database software☆48Feb 16, 2026Updated last month
- ☆55Jan 11, 2023Updated 3 years ago