A Data Fusion Method for Multi Source (VCF4.0+) Structural Variation Analysis
☆23Feb 4, 2025Updated last year
Alternatives and similar repositories for FusorSV
Users that are interested in FusorSV are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ☆51Aug 27, 2019Updated 6 years ago
- This repository is comprised of notebooks, datasets, and other related materials for the Python Bootcamp☆11Feb 1, 2025Updated last year
- Integrative analysis of structural variations.☆40Dec 20, 2023Updated 2 years ago
- ☆11May 12, 2021Updated 4 years ago
- Combine structural variation outputs from long sequencing reads into a superior call set☆18Aug 6, 2025Updated 7 months ago
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- MetaSV: An accurate and integrative structural-variant caller for next generation sequencing☆59Jun 30, 2017Updated 8 years ago
- Runs a combination of tools to generate structural variant calls on whole-genome sequencing data☆103Nov 5, 2020Updated 5 years ago
- Toolset for SV simulation, comparison and filtering☆414Dec 1, 2023Updated 2 years ago
- TIDDIT - structural variant calling☆10Dec 8, 2025Updated 3 months ago
- ☆12Dec 12, 2014Updated 11 years ago
- ☆37Apr 13, 2024Updated last year
- Complex structural variant detection from WGS data☆31Jan 10, 2025Updated last year
- Snakemake-based workflow for detecting structural variants in genomic data☆82Feb 14, 2025Updated last year
- FunctionaL Omics Processing platform☆13Jul 25, 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.
- Gene model transfer from closely related reference genomes using cDNA alignments☆10Aug 27, 2020Updated 5 years ago
- Adaptive haplotype assembly for efficiently leveraging high coverage in long reads☆13Sep 4, 2018Updated 7 years ago
- Phase reads, assemble haplotypes and detect SVs☆19Nov 11, 2020Updated 5 years ago
- An R package to detect, classify, and visualize genome rearrangements☆15Aug 4, 2020Updated 5 years ago
- a python extension of CNVnator -- a tool for CNV analysis from depth-of-coverage by mapped reads☆212Mar 16, 2026Updated last week
- ☆17Nov 26, 2023Updated 2 years ago
- Approach to identify simple and complex structural genomic rearrangements using a randomized approach☆21Nov 14, 2018Updated 7 years ago
- Code for the Brassica oleracea/rapa/napus genomic comparison☆16Apr 29, 2021Updated 4 years ago
- This repository contains material for the python workshop on deep learning in computer vision☆14Jul 20, 2022Updated 3 years ago
- DigitalOcean Gradient AI Platform • AdBuild production-ready AI agents using customizable tools or access multiple LLMs through a single endpoint. Create custom knowledge bases or connect external data.
- CN-Learn☆30Jan 24, 2020Updated 6 years ago
- dbVar☆41Sep 13, 2022Updated 3 years ago
- Tools for processing and analyzing structural variants.☆157May 2, 2022Updated 3 years ago
- This tool performs an automatic identification, annotation, and analysis of the MYB gene family in plants. It can be applied to new trans…☆20Oct 12, 2025Updated 5 months ago
- Structural Variant Identification Method using Long Reads☆181Jun 29, 2021Updated 4 years ago
- SV caller for nanopore data☆92Jun 7, 2020Updated 5 years ago
- Structural Variation and fusion detection using targeted sequencing data from circulating cell free DNA☆29Jun 6, 2024Updated last year
- Easy batch submission of adhoc jobs onto GCP☆13Mar 19, 2026Updated last week
- Pangenome-based genome inference☆163Dec 1, 2025Updated 3 months ago
- Proton VPN Special Offer - Get 70% off • AdSpecial partner offer. Trusted by over 100 million users worldwide. Tested, Approved and Recommended by Experts.
- Runs a combination of tools to generate structural variant calls on whole-genome sequencing data☆49Jun 2, 2020Updated 5 years ago
- A python package from Pacific Biosciences to analyze centromeric sequences☆21Oct 7, 2015Updated 10 years ago
- Updated figures for "A benchmarking of WGS-based structural variant callers" paper☆27Apr 3, 2022Updated 3 years ago
- ☆45Dec 11, 2016Updated 9 years ago
- Study of TE evolution in a population of genomes☆10Dec 11, 2023Updated 2 years ago
- Scripts to do haplotype analysis on pan genomes.☆20Sep 24, 2020Updated 5 years ago
- Powerful statistics for VCF files☆73Nov 16, 2025Updated 4 months ago