oncojs / lolliplot
Chart to aid in understanding mutations and their location on a gene.
☆22Updated last year
Related projects: ⓘ
- Javascript library for visualizing OncoGrids and related tracks☆26Updated 4 years ago
- Analysis Framework for Biological Data from High Throughput Experiments☆34Updated 8 years ago
- RNA-seq Viewer Team at the NCBI-assisted Boston Genomics Hackathon☆36Updated 7 years ago
- TOPMed analysis pipeline☆52Updated 11 months ago
- gnomAD browser pre-ASHG 2018☆33Updated 3 years ago
- paplot creates various dynamic and interactive reports for cancer genome analysis.☆25Updated last year
- Deprecated : Use https://github.com/drpowell/degust☆44Updated 7 years ago
- An interactive learning resource for next-generation sequencing (NGS) techniques☆26Updated 5 years ago
- MuSiCa - Mutational Signatures in Cancer☆23Updated 8 months ago
- Parallel merging, squaring off and ensemble calling for genomic variants☆20Updated 5 years ago
- Annotation and Prediction of Oncogenic Gene Fusions in RNAseq☆11Updated 8 years ago
- ☆20Updated 7 years ago
- deepStats: a stastitical toolbox for deeptools and genomic signals☆32Updated 3 years ago
- A nextflow implementation of Kallisto & Sleuth RNA-Seq Tools☆21Updated 6 years ago
- Subclonal Hierarchy Inference from Somatic Mutations☆21Updated 5 years ago
- ☆15Updated this week
- EpiGenome Gateway - WashU EpiGenome Browser☆21Updated 2 years ago
- Genomes on the Cloud, Mapping & Variant Calling Pipelines☆32Updated 7 years ago
- Rna-seq pipeline, From FASTQ to differential expression analysis...☆20Updated 7 years ago
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆28Updated 3 years ago
- BigWig manpulation tools using libBigWig and htslib☆28Updated last month
- Prepare Sailfish and Salmon output for downstream analysis☆43Updated 5 years ago
- Nextflow basic tutorial for newbie users☆32Updated 6 years ago
- Curated collection of open-source bioinformatics tools☆28Updated 5 years ago
- Integrative visualization of multiple omic datasets onto KEGG pathways.☆11Updated 2 years ago
- WebApp for DNA variants interpretation☆13Updated 2 weeks ago
- Modular blocks to build Snakemake workflows for reproducible NGS analyses☆21Updated 5 years ago
- R tools to interact with hap.py output☆15Updated 5 years ago
- EpiViz is a scientific information visualization tool for genetic and epigenetic data, used to aid in the exploration and understanding o…☆68Updated last year
- Differential Count Data Analysis Toolbox☆60Updated 7 months ago