Run analyses together, get results in hours, and copy and send large genomic datasets to collaborators in seconds, no file transfers or ticket queues.
The Research Scientist Reality
Then: everything stops while you wait for someone else to look at your data
You hand off your samples and wait days, sometimes weeks, before the bioinformatics team can get to your run.
When results finally arrive, they're a folder of files and a PDF. You can't tweak parameters or explore alternate cuts on your own.
Asking a follow-up question means another email, another upload, another round of waiting. With Horizon, you share large genomic datasets with collaborators in seconds and everyone sees the same data.
You can't see when a run finishes, what version produced your results, or who else is looking at your data.
Before vs After
PIs and bench researchers lose days moving data around. With Bridge Horizon, you copy and send large genomic datasets to collaborators in seconds and work from one shared, traceable analysis.
Data lives in zip files and shared drives. Every analysis starts with a transfer, a request, and a wait.
One shared dataset, fast data distribution to collaborators with shareable links, and analyses your bioinformatician can review and reproduce.
The Platform
1. Pick a pipeline. 2. Choose your data. 3. Get results. No bioinformatics queue needed.



Drag and drop your FASTQ files, and Horizon organizes them into your project. No shared drives, no waiting on IT.

Video walkthrough: Navigate to the Data page → select a project folder → drag and drop FASTQ files → monitor upload progress → files are ready for analysis.
Drag-and-drop your sequencing files from anywhere
Files are automatically organized into your project
See upload progress and know exactly when files are ready
Get a tailored walkthrough of how Bridge Horizon replaces handoffs with controlled, traceable collaboration.
How we compare
Other platforms assume there's always a bioinformatician available. Horizon is built so research scientists can move from raw data to results without waiting in the queue.
| Where teams get stuck | Horizon | Terra | Seqera | DNAnexus | LLMs |
|---|---|---|---|---|---|
| Research scientists can run pipelines without bioinformatics support | |||||
| Getting from raw data to results quickly | |||||
| Sharing results without exporting or re-explaining | |||||
| Understanding what actually happened in an analysis | |||||
| Setup without dedicated platform engineering | |||||
| Bringing in specialists without file transfers or context loss | |||||
| Reproducible and defensible at peer review |
Last reviewed April 2026 · Hover any for context
Key Features
No more file transfers. Your data lives in one place, accessible to everyone who needs it, instantly.
Share datasets with collaborators when needed. No copies, no drift, no version confusion.
Per-dataset permissions let you decide exactly who can view, run, or share. Revoke access at any time.
Every pipeline run, every parameter, every input and output, logged and versioned automatically.
Move from sample prep to analysis to results without context switching, waiting, or manual coordination.
Core facilities send large genomic datasets to customers with one shareable link. Researchers share results with collaborators in seconds, with no re-uploading or file-transfer overhead.
Send terabyte-scale genomic datasets to collaborators with a single shareable link. Recipients get access in seconds from any location, no downloads, no re-uploads, no FTP delays.
Research Scientist Impact
Weeks to Days
From sequencer to first results
As confirmed by our clients when moving genomics data
5×
More hypotheses tested per week
Zero
Tickets filed to see your own data
"This is phenomenal. I'm impressed. the user interface is very easy, and uploading data feels seamless. This is very exciting; I really like it."
"For the first time, I've seen an environment that's both collaborative and genuinely easy to use. I wish I had this years ago. It just makes sense."
Why we built this
The starting point
Bridge Informatics founded. Embedded bioinformatics support for genomics teams from day one.
The pattern emerges
After 100+ client engagements, the same friction kept surfacing: handoffs, lost context, and siloed tools.
Horizon launches
Horizon goes generally available. Production-tested expertise lands in the hands of every team member, working from the same data.
Horizon grew out of Bridge Informatics, a services firm embedded in production genomics teams since 2020. The same friction kept appearing. Handoffs broke, context got lost, and anyone outside bioinformatics was left waiting.
We built the tool we wished existed. Every step visible and understandable as it runs.
Pricing
Plans scale with the analyses you run, the data you keep, and the people who need access, from a free single-user tier to team and enterprise workspaces.
Individual researchers and small labs can run validated pipelines with full run provenance without a budget conversation. Larger teams are quoted on real usage: compute, storage, and seats.
FAQ
Everything you need to know about analyzing your own sequencing data in Bridge Horizon.
Built on production genomics experience since 2020, Horizon makes every dataset, pipeline run, and parameter shared and traceable across your entire team.