oncojs / lolliplot
Chart to aid in understanding mutations and their location on a gene.
☆22Updated 2 years ago
Alternatives and similar repositories for lolliplot:
Users that are interested in lolliplot are comparing it to the libraries listed below
- Javascript library for visualizing OncoGrids and related tracks☆26Updated 4 years ago
- RNA-seq Viewer Team at the NCBI-assisted Boston Genomics Hackathon☆37Updated 7 years ago
- deepStats: a stastitical toolbox for deeptools and genomic signals☆34Updated 3 years ago
- EpiGenome Gateway - WashU EpiGenome Browser☆21Updated 3 years ago
- Tutorial for working with cloud infrastructure and AWS from R☆20Updated 7 years ago
- Prepare Sailfish and Salmon output for downstream analysis☆43Updated 5 years ago
- Linking GWAS studies to genes through cis-regulatory datasets☆39Updated last year
- SNV expectation maximisation based mutation calling algorithm aimed at detecting somatic mutations in paired (tumour/normal) cancer sampl…☆60Updated 2 months ago
- TOPMed analysis pipeline☆52Updated last year
- Rna-seq pipeline, From FASTQ to differential expression analysis...☆20Updated 7 years ago
- Mapped QC analysis program☆42Updated 6 years ago
- MuSiCa - Mutational Signatures in Cancer☆23Updated last year
- gnomAD browser pre-ASHG 2018☆33Updated 4 years ago
- Platform for Interactive analysis and Visualization Of Transcriptomics data☆27Updated 4 years ago
- Subclonal Hierarchy Inference from Somatic Mutations☆21Updated 5 years ago
- Repository for resources we'd like to share with the community.☆24Updated 2 years ago
- See the main fork of this repository here >>>☆38Updated last month
- Class materials for the NIH HPC snakemake class☆16Updated 3 months ago
- Deprecated : Use https://github.com/drpowell/degust☆44Updated 7 years ago
- Prioritization of functional rare genetic variants by integrating genomic annotations and RNA-seq☆18Updated 2 years ago
- Toil workflows for common genomic pipelines☆33Updated 5 years ago
- Predict mutated T-cell epitopes from sequencing data☆27Updated 6 years ago
- Integrative visualization of multiple omic datasets onto KEGG pathways.☆11Updated 3 years ago
- A standalone interactive application for detecting biological significance on a set of genes☆40Updated 3 years ago
- Detect somatic variants from tumor and normal WGS/WXS data☆15Updated last week
- Computational correction of copy-number effect in CRISPR-Cas9 essentiality screens☆27Updated 5 years ago
- A nextflow implementation of Kallisto & Sleuth RNA-Seq Tools☆22Updated 6 years ago
- Seven Bridges API Client, CWL Schema, Meta Schema, and SDK Helper in R☆35Updated 2 years ago
- A Shiny web server for interactive visualization and analysis of RNA-seq data☆22Updated 3 years ago
- WebApp for DNA variants interpretation☆13Updated last week