mutalyzer / mutalyzer2Links
HGVS variant nomenclature checker
☆98Updated 2 years ago
Alternatives and similar repositories for mutalyzer2
Users that are interested in mutalyzer2 are comparing it to the libraries listed below
Sorting:
- HGVS variant name parsing and generation☆175Updated 2 years ago
- TransVar - multiway annotator for precision medicine☆126Updated 2 years ago
- This repo has been archived, these workflows are still available in the GATK repository under the scripts directory. The workflows are al…☆77Updated 5 years ago
- Somatic and germline variant caller for amplicon data. Recommended caller for tumor-only workflows.☆98Updated 3 years ago
- This repo provides tools to convert ClinVar data into a tab-delimited flat file, and also provides that resulting tab-delimited flat file…☆126Updated 5 years ago
- Annotation of VCF variants with functional impact and from databases (executable+library)☆62Updated 2 weeks ago
- Universal Transcript Archive: comprehensive genome-transcript alignments; multiple transcript sources, versions, and alignment methods; a…☆65Updated 5 months ago
- ☆57Updated 5 years ago
- phenotype-based prioritization of candidate genes for human diseases☆65Updated 2 years ago
- ☆69Updated 3 years ago
- Public repository for VariantValidator project☆77Updated this week
- Platypus Variant Caller☆108Updated last year
- Pure-python implementation of UCSC liftOver genome coordinate conversion☆97Updated last year
- DEPRECATED. This tool has been superseded by https://github.com/griffithlab/pVACtools☆61Updated 6 years ago
- C++ Library to parse Illumina InterOp files☆79Updated 2 months ago
- Extensible specification for representing and uniquely identifying biological sequence variation☆93Updated last month
- Simple FASTQ quality assessment using Python☆109Updated 4 years ago
- ABRA2☆92Updated 2 years ago
- A collection of reusable WDL tasks. Category:Other☆88Updated 2 weeks ago
- Annotate models of genetic inheritance patterns in variant files (vcf files)☆82Updated 2 weeks ago
- Phenotype driven gene prioritization for HPO☆47Updated 4 years ago
- Galaxy RNA workbench☆40Updated 4 years ago
- Documentation and description of AWS iGenomes S3 resource.☆116Updated 8 months ago
- ☆82Updated 6 years ago
- Read visualizer for structural variants☆84Updated 7 years ago
- A modular annotation tool for genomic variants☆127Updated last week
- This repository contains information about latest release from Genome in a Bottle project☆74Updated 6 years ago
- Tools for processing and analyzing structural variants.☆154Updated 3 years ago
- Gene fusion detection and visualization☆128Updated 3 years ago
- Finder of Somatic Fusion Genes in RNA-seq data☆146Updated 2 years ago