CGGOxford / BrowseVCFView external linksLinks
BrowseVCF is a web-based application and workflow to quickly prioritise disease-causative variants in VCF files.
☆47Jun 26, 2020Updated 5 years ago
Alternatives and similar repositories for BrowseVCF
Users that are interested in BrowseVCF are comparing it to the libraries listed below
Sorting:
- VCF-Miner: A graphical user interface for sorting, filtering and querying annotated VCF Files☆37Nov 19, 2019Updated 6 years ago
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Apr 18, 2019Updated 6 years ago
- Gene Exploration System for Variance☆22Dec 8, 2022Updated 3 years ago
- Automated ACMG/AMP classification for human variants associated with congenital hearing loss☆11May 14, 2025Updated 8 months ago
- PathOS is a clinical application for filtering, analysing and reporting on NGS variants☆29Mar 30, 2021Updated 4 years ago
- A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region exp…☆27Jan 15, 2026Updated 3 weeks ago
- Generic human DNA variant annotation pipeline☆60Feb 13, 2024Updated 2 years ago
- myVCF: a web-based platform for target and exome mutations data management☆20Apr 13, 2021Updated 4 years ago
- dv-trio provides a pipeline to call variants for a trio (father-mother-child) using DeepVariants [1]. Genomic Variant Calling Files (gVCF…☆11Feb 3, 2021Updated 5 years ago
- Compare assembly graph file formats☆16Jul 23, 2015Updated 10 years ago
- a pileup library that embraces the huge☆43Oct 2, 2020Updated 5 years ago
- Allele frequency filtering for Mendelian variant discovery☆18Sep 27, 2016Updated 9 years ago
- Whole Genome Sequenceing Structural Variation Pipelines☆18Apr 4, 2019Updated 6 years ago
- web-based analysis tool for rare disease genomics☆200Updated this week
- Ancestry and Kinship Tools☆70Nov 16, 2022Updated 3 years ago
- Pan gGnome Viewer☆10Jul 10, 2025Updated 7 months ago
- Sequence Bloom Trees with All/Some split☆11Oct 30, 2018Updated 7 years ago
- VVP (VAAST Variant Prioritizer) rapidly prioritizes genetic variants☆19Mar 10, 2018Updated 7 years ago
- Characterization of Germline variants☆100Mar 15, 2022Updated 3 years ago
- Online material and code base for the article Coordinates and Intervals in Graph Based Reference Genomes☆11May 2, 2017Updated 8 years ago
- Bacterial typing pipeline for clinical NGS data. Written in NextFlow, Python & Bash.☆12Feb 6, 2026Updated last week
- Hemang Parikh☆11Jan 12, 2016Updated 10 years ago
- A tool to detect postzygotic single-nucleotide mosaicism from unpaired, trio, or paired samples.☆13Feb 23, 2021Updated 4 years ago
- Curated list of resources for variant prioritization☆12Nov 18, 2025Updated 2 months ago
- A read alignment visualization library for long reads☆10Aug 6, 2022Updated 3 years ago
- Clin.iobio - Workflow and reporting for iobio variant analysis pipeline☆12Oct 7, 2025Updated 4 months ago
- Non-parametric structural variant genotyper☆15Nov 18, 2021Updated 4 years ago
- Visualizing genetic sequence variation☆13Apr 27, 2020Updated 5 years ago
- Genomic Visualization Catalog☆13Oct 6, 2022Updated 3 years ago
- VAPr: A Python package for NoSQL variant data storage, annotation and prioritization☆37Jun 30, 2021Updated 4 years ago
- Population-wide Deletion Calling☆35Apr 16, 2025Updated 9 months ago
- VEP-like tool for sequence ontology and HGVS annotation of VCF files☆24Updated this week
- Ultra-efficient mapping-free structural variation genotyper☆20Jul 28, 2021Updated 4 years ago
- Julia package powering VIVA, our tool for visualization of genomic variation data. Manual:☆87Aug 7, 2023Updated 2 years ago
- A small repo for storing the code for making the files and html for CCRs.☆22Oct 22, 2019Updated 6 years ago
- ☆11Dec 8, 2022Updated 3 years ago
- Visualisation and prioritisation of genomic variants from human exome sequencing projects☆13Apr 23, 2019Updated 6 years ago
- Multiple sequence alignment browser☆11Dec 12, 2022Updated 3 years ago
- Call regions of homozygosity and make tentative UPD calls☆12Jun 27, 2025Updated 7 months ago