Bulk RNA-seq
From read quality and STAR alignment to count matrices, DESeq2 contrasts, and publication-ready plots.
Upload raw FASTQ files and run Bulk RNA-seq, scRNA-seq, ChIP-seq, Ribo-seq, and more. Go fully autonomous or stay in the loop. No data yet? Drop in a GEO accession and try it FREE!
Autonomous run
The pipeline continues even when this tab is closed.
Quality control
12 FASTQ files
Read preparation
Adapters resolved
STAR alignment
GRCh38 · 94.2% mapped
Quantification
18,742 genes
DE + plots
Running DESeq2
Mapped reads
94.2%
Notifications ready
Email and Telegram reports will include each stage and any failure reason.
Workflow library
Clear availability labels tell you what can run today and what is still being developed.
From read quality and STAR alignment to count matrices, DESeq2 contrasts, and publication-ready plots.
Ribosome-footprint analysis with adapter and UMI handling, RPF diagnostics, alignment, and differential analysis.
A focused workspace for cell-level exploration and future end-to-end single-cell processing.
ChIP-seq and variant-analysis workspaces are part of the roadmap—not presented as finished features.
Autonomous, not opaque
Xplore removes pipeline babysitting without hiding what happened along the way.
Autonomous execution
Long-running workflows continue on the server, with recorded stage progress and clear failure diagnostics when intervention is needed.
Transparent results
Move from QC through differential analysis with the inputs, outputs, summaries, and reused results visible inside one project.
Reporting
Receive detailed email or Telegram notifications, then open the workspace or skim a generated PDF summary.
Contact
Have a question or want to learn more? Drop us a message and we'll get back to you shortly.
Create a workspace, bring FASTQ files or a GEO accession, and follow every stage from quality control to interpretable results.
No credit card · FASTQ or GEO input · Transparent stages