dlal-group / Simple-ClinVarLinks
Shiny ClinVar web server source code
☆12Updated 6 years ago
Alternatives and similar repositories for Simple-ClinVar
Users that are interested in Simple-ClinVar are comparing it to the libraries listed below
Sorting:
- Tool for RNA-Seq analysis.☆39Updated 3 years ago
- ☆27Updated last year
- Python package to annotate and visualize gene fusions.☆65Updated last year
- B-cell and T-cell Adaptive Immune Receptor Repertoire (AIRR) sequencing analysis pipeline using the Immcantation framework☆74Updated this week
- Workflow management with Nextflow and nf-core☆29Updated last year
- Prepare Sailfish and Salmon output for downstream analysis☆42Updated 6 years ago
- A nextflow pipeline to perform state-of-the-art genome-wide association studies.☆78Updated 4 months ago
- Mapped QC analysis program☆43Updated 7 years ago
- Gene Fusion Visualiser☆51Updated 3 years ago
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆57Updated this week
- utilities for working with IGV: opening files remotely in either desktop IGV or a web viewer (igv.js), creating screenshots, etc.☆49Updated 6 years ago
- rnasplice is a bioinformatics pipeline for RNA-seq alternative splicing analysis☆63Updated 8 months ago
- Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)☆42Updated 5 months ago
- Python program designed to reconstruct immunoglobulin gene rearrangements and oncogenic translocations from WGS, WES and capture NGS in l…☆21Updated 2 years ago
- The Zavolab Automated RNA-seq Pipeline☆36Updated 2 weeks ago
- Genomic data interpretation and visualization Workshop☆21Updated 2 months ago
- An interactive web-tool for RNA-seq analysis☆70Updated last month
- visual analysis of your VCF files☆39Updated 3 years ago
- Known and Novel IsoForm Explorer. Statistically based splicing detection for circular and linear isoforms☆33Updated 8 years ago
- Unsorted scripts for bioinformatics☆61Updated 4 years ago
- SeqMonk NGS visualisation and analysis tool☆51Updated 3 months ago
- Full-spectrum copy number variation detection by high-throughput DNA sequencing☆40Updated 4 years ago
- A standalone interactive application for detecting biological significance on a set of genes☆40Updated 4 years ago
- Tool for parsing outputs from fusion detection tools. Part of a nf-core/rnafusion pipeline. Checkout a live demo at https://matq007.githu…☆28Updated 7 months ago
- gnomAD browser pre-ASHG 2018☆33Updated 5 years ago
- Variant catalogue pipeline☆26Updated last week
- R package for inferring copy number from read depth☆32Updated 3 years ago
- A pipeline for differential expression and differential alternative splicing analysis☆67Updated last year
- VEP Plugin to annotate high-impact five prime UTR variants☆28Updated last year
- ☆29Updated 6 years ago