Built for Research Scientists

    From sequencing to insight
    in no time

    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

    Your experiments move faster than your data analysis

    1. 1Design experiment
    2. 2Prep samples
    3. 3Run sequencer

    Then: everything stops while you wait for someone else to look at your data

    Stuck in the Queue

    You hand off your samples and wait days, sometimes weeks, before the bioinformatics team can get to your run.

    Black-Box Results

    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.

    File-Transfer Ping-Pong

    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.

    No Visibility

    You can't see when a run finishes, what version produced your results, or who else is looking at your data.

    Before vs After

    From file-transfer ping-pong to shared, instant collaboration

    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.

    Before HorizonWith Horizon

    Before Horizon

    Data lives in zip files and shared drives. Every analysis starts with a transfer, a request, and a wait.

    1. Zip and upload FASTQs to a file-sharing service
    2. Ping the bioinformatician and wait in the queue
    3. Lose days to transfers and back-and-forth
    4. Results arrive with the wrong parameters
    5. Forward files again to collaborators

    With Horizon

    One shared dataset, fast data distribution to collaborators with shareable links, and analyses your bioinformatician can review and reproduce.

    1. One shared dataset for the lab and collaborators
    2. Fast data distribution via shareable links, in seconds
    3. Run validated pipelines yourself, fully tracked
    4. Results with parameters and version history attached
    5. Your bioinformatician reviews in the same workspace
    Drag to reveal the after state

    The Platform

    Run your own analyses, start to finish

    1. Pick a pipeline. 2. Choose your data. 3. Get results. No bioinformatics queue needed.

    Pipeline Config screenshot of the Bridge Horizon genomics workspace
    Video demo
    Run History screenshot of the Bridge Horizon genomics workspace
    Run Results screenshot of the Bridge Horizon genomics workspace

    Get your data in without filing a ticket.

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

    Horizon Data Upload interface for uploading FASTQ files and organizing them into projects
    🔇 No audio

    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

    Ready to see it in action?

    Get a tailored walkthrough of how Bridge Horizon replaces handoffs with controlled, traceable collaboration.

    How we compare

    Why research scientists pick Horizon

    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 stuckHorizonTerraSeqeraDNAnexusLLMs
    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
    Native / built-in Requires setup or expertise Not the focus

    Last reviewed April 2026 · Hover any for context

    Key Features

    Everything you need to collaborate on genomics

    Instant Data Sharing

    No more file transfers. Your data lives in one place, accessible to everyone who needs it, instantly.

    Shared Datasets

    Share datasets with collaborators when needed. No copies, no drift, no version confusion.

    Granular Access Control

    Per-dataset permissions let you decide exactly who can view, run, or share. Revoke access at any time.

    Full Traceability

    Every pipeline run, every parameter, every input and output, logged and versioned automatically.

    Seamless Handoff

    Move from sample prep to analysis to results without context switching, waiting, or manual coordination.

    Fast Data Distribution

    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.

    Shareable Links for Terabyte-Scale Data

    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

    Move from samples to insight without waiting

    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."
    Adrienne GreeneDirector, Tessera Therapeutics
    "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."
    Jonathan JacksonDirector of R&D, Life Net Health

    Why we built this

    Built from real bioinformatics workflows

    6 yrsEmbedded in genomics
    100+Client engagements
    2026Horizon launch
    • 2020

      The starting point

      Bridge Informatics founded. Embedded bioinformatics support for genomics teams from day one.

    • 2023

      The pattern emerges

      After 100+ client engagements, the same friction kept surfacing: handoffs, lost context, and siloed tools.

    • 2026

      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.
    The Bridge Informatics team · since 2020

    Pricing

    Built to be accessible

    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.

    There will always be a free tier

    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.

    See plans and estimate your usage

    FAQ

    Questions from research scientists

    Everything you need to know about analyzing your own sequencing data in Bridge Horizon.

    See how Horizon fits your team.

    Built on production genomics experience since 2020, Horizon makes every dataset, pipeline run, and parameter shared and traceable across your entire team.