See your genome in a new light.
Prism is a purpose-built IDE for epigenomics — designed to visualize, explore, and understand raw and processed genomic data without leaving your development environment.
Built on VSCode. Focused on science.
Existing genome browsers (IGV, UCSC, Seqmonk) are viewers — not workspaces. Prism brings visualization directly into your analysis environment, so you never context-switch between your pipeline and your data.
| Format | Type |
|---|---|
| FASTQ | Raw sequencing reads |
| BAM / SAM | Aligned reads |
| bigWig / bedGraph | Signal tracks |
| BED / narrowPeak | Peak calls |
- VSCode fork + upstream sync
- Epigenomics file associations
- Signal track renderer (bigWig/bedGraph)
- Peak call viewer (BED/narrowPeak)
- BAM read-level visualization
- Multi-track comparison view
git clone https://github.com/AtlasMindAI/Prism.git
cd Prism
yarn
yarn run watchAtlasMindAI — building scientific infrastructure for the next generation of genomics research.
Prism is in active development. Epigenomics-first. More formats coming.