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
- Gene Fusion Visualiser☆51Updated 2 years ago
- An interactive web-tool for RNA-seq analysis☆69Updated 7 months ago
- Prepare Sailfish and Salmon output for downstream analysis☆42Updated 6 years ago
- A standalone interactive application for detecting biological significance on a set of genes☆40Updated 4 years ago
- A pipeline for differential expression and differential alternative splicing analysis☆66Updated last year
- Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)☆42Updated last month
- Repository of Nextflow+BioContainers workflows☆14Updated 4 years ago
- Mapped QC analysis program☆44Updated 7 years ago
- rnasplice is a bioinformatics pipeline for RNA-seq alternative splicing analysis☆59Updated 4 months ago
- Making Snakemake workflows into full-fledged command line tools since 1999.☆51Updated 7 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 4 months ago
- Python package to annotate and visualize gene fusions.☆64Updated last year
- ☆26Updated 10 months ago
- Assembly of RNA reads to determine the effect of a cancer mutation on protein sequence☆25Updated last year
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- Bioinformatic pipeline for identifying dsDNA breaks by marker based incorporation, such as breaks induced by designer nucleases like Cas9…☆23Updated 2 months ago
- ☆29Updated 6 years ago
- EditR: an algorithm for simple and cost effective measurement of base editing by quantifying Sanger trace fluorescence☆32Updated 2 years ago
- Galaxy RNA workbench☆40Updated 5 years ago
- B-cell and T-cell Adaptive Immune Receptor Repertoire (AIRR) sequencing analysis pipeline using the Immcantation framework☆66Updated last week
- Nextflow RNA-Seq Best Practice analysis pipeline, used at the SciLifeLab National Genomics Infrastructure.☆51Updated 7 years ago
- A guide to running MaxQuant in Linux☆34Updated 5 years ago
- 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
- Interactive multiscale visualization for structural variation in human genomes☆70Updated last week
- A workflow for enhanced protein isoform detection through integration of long-read RNA-seq and mass spectrometry-based proteomics.☆49Updated 2 years ago
- Genomic data interpretation and visualization Workshop☆21Updated last month
- Website to analyze conflicting assertions in ClinVar☆19Updated last year
- Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer☆53Updated this week
- Unsorted scripts for bioinformatics☆61Updated 4 years ago