Trusted by leading research teams at
Built for the speed and scale of modern genomics.
From raw FASTQ ingestion to publication-ready variant analysis—every step runs in your browser with the performance of native tooling.
Zero-latency rendering.
Custom WebAssembly parsers stream and index heavy BAM, VCF, and h5ad files directly in the browser. Query millions of reads without round-trips to the server.
Dynamic filtering.
Explore volcano plots, t-SNE clustering, and UMAP embeddings with real-time p-value sliders. Slice transcriptomics data by cell type, condition, or metadata instantly.
Enterprise-grade compliance.
End-to-end encrypted storage with SOC 2 Type II controls. Enable local-first processing for sensitive clinical genomics—your data never leaves the secure enclave.
FAQ
Common questions.
We natively support BAM, CRAM, VCF, BCF, FASTQ, h5ad, and Loom formats. Files are parsed using custom WebAssembly modules built on htslib and anndata. No server-side preprocessing required—everything runs directly in your browser tab.
Our WebAssembly parsers compile standard genomics libraries to run inside your browser's sandboxed environment. Files are streamed in chunks, indexed in-memory, and rendered with GPU-accelerated canvas—without sending a single byte to a server.
Yes. We use chunked streaming and virtual file system APIs to handle arbitrarily large files. Users regularly process BAM files exceeding 40 GB in a standard browser session, with indexed regions loading in under two seconds.
In local-first mode, your data never leaves your machine. The browser's sandboxed memory handles all processing. For cloud workflows, all transfers are encrypted end-to-end with AES-256 in transit and at rest.
Our cloud infrastructure is SOC 2 Type II certified and supports HIPAA Business Associate Agreements. EU-based teams can choose data residency in Frankfurt or Dublin, with GDPR Data Processing Agreements available on request.
Academic institutions get unlimited local-file processing and 50 GB of cloud storage at no cost. Projects funded by NIH, ERC, or equivalent grants qualify for extended cloud quotas—just provide your grant ID during signup.
Yes. Enterprise plans include dedicated cloud infrastructure, SSO/SAML auth, custom data residency, audit logging, priority support, and SLA-backed uptime. Contact our sales team for a custom quote.
Sign up with your institutional email to receive early access. Onboarding takes under five minutes—upload a BAM, VCF, or h5ad file and the explorer launches your first analysis automatically. No configuration or pipeline setup required.
Contact
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Start exploring your genomic data today.
Xplore runs entirely in your browser — no servers to provision, no data leaving your network.
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