labsquare / cutevariantLinks
A standalone and free application to explore genetics variations from VCF file
☆108Updated last year
Alternatives and similar repositories for cutevariant
Users that are interested in cutevariant are comparing it to the libraries listed below
Sorting:
- An extensible python-based genomics visualization engine☆145Updated 2 years ago
- simple viewer for variant call format using htslib☆32Updated 9 years ago
- PGxPOP☆17Updated 3 years ago
- Functionality for working with pipeline and sample sheet schema files in Nextflow pipelines☆50Updated this week
- Efficiently read and write sequencing data from Python☆69Updated 3 months ago
- NEAT (NExt-generation Analysis Toolkit) simulates next-gen sequencing reads and can learn simulation parameters from real data.☆66Updated last week
- Julia package powering VIVA, our tool for visualization of genomic variation data. Manual:☆87Updated 2 years ago
- Analysis pipelines from Oxford Nanopore Technologies' Research Division☆48Updated 5 years ago
- Generic human DNA variant annotation pipeline☆59Updated last year
- A Python package for pharmacogenomics (PGx) research☆82Updated 3 weeks ago
- VarFish: comprehensive DNA variant analysis for diagnostics and research☆51Updated this week
- Monitor computational workflows in real time☆73Updated last year
- Data and information about the Polaris study☆55Updated 6 years ago
- cDNA read preprocessing☆83Updated last year
- Scallop is a reference-based transcriptome assembler for RNA-seq☆92Updated 4 years ago
- An open-source, cloud-ready web application for simplified deployment of big data workflows.☆36Updated 8 months ago
- R package designed to simplify structural variant analysis☆74Updated 4 years ago
- A comprehensive cancer DNA/RNA analysis and reporting pipeline☆100Updated this week
- A tool to design highly specific PCR primers for the validation of genomic alterations including structural variants☆47Updated 8 years ago
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆70Updated 2 years ago
- Transcript versions for HGVS libraries☆33Updated 3 months ago
- (WIP) best-practices workflow for rare disease☆62Updated last year
- vembrane filters VCF records using python expressions☆68Updated 3 weeks ago
- TIDDIT - structural variant calling☆78Updated last month
- ☆18Updated 3 years ago
- Structural Variant Prediction Viewer☆35Updated 8 years ago
- Platypus Variant Caller☆108Updated last year
- A tool for genotyping Variable Number Tandem Repeats (VNTR) from sequence data☆47Updated last year
- Comprehensive benchmark of structural variant callers☆48Updated 4 years ago
- VCF-kit: Assorted utilities for the variant call format☆132Updated 6 months ago