Salmon
v1.10.3 - defaultQuasi-mapping against a reference transcriptome. Fast, accurate, and the right call for most experiments.
library type - ISR (auto)
GC bias correction - on
bootstraps - 30
Run complete RNA-seq workflows with trusted tools, customizable analyses, and publication-ready results - without setup, scripts, or infrastructure.
Bulk RNA-seq analysis workspace for sample setup, execution, and results.
Samples
Upload and annotate data
Run
Launch or monitor analysis
Results
Review outputs and findings
Tune thresholds, inspect genes, and explore the plots interactively.
16,119
Total Genes
8
Significant (padj c <= 0.050)
~ 3
Upregulated
~ 5
Downregulated
Gene: IFITM1
Gene: IFITM1
Bulk RNA-seq analysis workspace for sample setup, execution, and results.
Assign every sample to a group, and confirm at least two groups are represented.
| Sample Name | Size | Type | Group | Cell line |
|---|---|---|---|---|
| SRR36938853 | 2.81 GB | FASTQ | Control | A549 |
| SRR36938854 | 1.97 GB | FASTQ | Control | A549 |
| SRR36938855 | 2.43 GB | FASTQ | Control | A549 |
| SRR36938856 | 1.98 GB | FASTQ | Treatment | A549 |
| SRR36938857 | 2.14 GB | FASTQ | Treatment | A549 |
| SRR36938858 | 2.32 GB | FASTQ | Treatment | A549 |
Bulk RNA-seq analysis workspace for sample setup, execution, and results.
Recommended
Balanced trimming for most bulk RNA-seq datasets.
Sensitive
More aggressive cleanup for noisy libraries.
Minimal trimming
Keep reads close to raw input with only basic filtering.
Trim preview - across 6 samples
Bulk RNA-seq analysis workspace for sample setup, execution, and results.
Quasi-mapping against a reference transcriptome. Fast, accurate, and the right call for most experiments.
library type - ISR (auto)
GC bias correction - on
bootstraps - 30
Splice-aware genome alignment when you need BAM files or novel-junction discovery.
2-pass mode - off
min splice overhang - 8
output - BAM + counts
Reference
Species
Library
Bulk RNA-seq analysis workspace for sample setup, execution, and results.
Group / Condition
Primary treatment, condition, or experimental group.
6/6 assigned - 2 levels
Cell line
Control for cell line or genetic background differences.
6/6 assigned - 1 level
Blocking variables
Cell line
Control for cell line or genetic background differences.
Design formula
Bulk RNA-seq analysis workspace for sample setup, execution, and results.
Gene sets
Permutation type
Scoring metric
Bulk RNA-seq analysis workspace for sample setup, execution, and results.
16,119
Total genes
412
Significant (p-adj < 0.05)
248
Upregulated
164
Downregulated
Research path
Three things matter for an RNA-seq tool: the methods, the figures, and the path from raw data to interpretation.
Trust
Workflows use standard methods reviewers already trust. Every run records exact tool versions and parameters.
Customize
Adjust labels, thresholds, gene callouts, palettes, and legend placement before downloading the figure and source table.
No setup
Skip package conflicts, tutorials, and compute provisioning. Open the workspace, attach data, configure the run.
$ pip install ...
$ conda env create ...
$ docker run ...
// not your job anymore
Workflow
Configure the experiment, pick the processes you need, and run with tools and outputs your team already understands.
Sources & options
Drag in FASTQ files or paste an accession
GSE183852 - SRP345670 - PRJNA1108812
Pick a reference genome and species
GRCh38 - GRCm39 - custom transcriptome
Annotate samples with metadata
group - condition - cell line - replicate - batch
Sample sheet
6 samples - 2 groups| sample | group | condition | cell line | rep |
|---|---|---|---|---|
| SRR15278 | Control | Untreated | A549 | R1 |
| SRR15279 | Control | Untreated | A549 | R2 |
| SRR15280 | Control | Untreated | A549 | R3 |
| SRR15281 | Treatment | Drug A | A549 | R1 |
| SRR15282 | Treatment | Drug A | A549 | R2 |
| SRR15283 | Treatment | Drug A | A549 | R3 |
Tools we wire together
QC + adapter trimming
Transcript quantification
Splice-aware alignment
Differential expression
Pathway analysis
Build the contrast
REFERENCE GROUP
3 replicates
COMPARE AGAINST
BLOCKING / COVARIATES
What this gives you
Replicate-aware comparisons
DESeq2 models batch effects and replicate structure automatically.
Multi-group contrasts
Treatment-vs-control, drug-A-vs-drug-B, and interaction terms in one run.
Cell-line and condition grouping
Metadata follows every downstream plot and table.
Reproducible re-runs
Change one parameter and a new versioned run is forked. Nothing is overwritten.
Cutoffs & comparisons
Top significant genes
n = 412 sigEverything generated by a run
PCA plot
PNG / SVG / PDF / CSV
Volcano plot
PNG / SVG / PDF / CSV
Heatmap
PNG / SVG / PDF / CSV
MA plot
PNG / SVG / PDF / CSV
QC report
PNG / SVG / PDF / CSV
Gene table
PNG / SVG / PDF / CSV
DE results
PNG / SVG / PDF / CSV
GSEA bundle
PNG / SVG / PDF / CSV
Run parameters
PNG / SVG / PDF / CSV
The plots in the workspace are the same ones you'll ship in a paper. Tune thresholds, labels, and colors, then export at the resolution you need. The underlying table downloads with every figure.
Volcano
PCA
Heatmap
MA plot
Gene expression
Outputs
Every run produces a versioned bundle of tables, plots, reports, and parameters you can inspect in the workspace or download as a package.
run_2026-05-15_idh1-vs-ctrl
6 samples - 412 sig genes - 28 enriched pathways
Clean gene-level results with fold change, p-values, FDR, and significance flags.
Per-sample quality summaries and processing metrics so you can validate the run before interpretation.
PCA, volcano, MA, heatmap, GSEA, and gene-expression plots with vector exports.
Parameters, comparisons, tool versions, and execution traces captured for every run.
Inputs, runs, comparisons, and outputs organized in one place.
Workspace
Past the pipeline, NotchBio is a real workspace: parameters, runs, plots, files, and people, all in one place.
Elastic CPU and memory pools. The platform spins up the right size for your run.
Step through inputs, QC, quant, design, and DE with sensible defaults at every fork.
Override anything you need: trimming thresholds, library type, contrasts, shrinkage.
Each run captures inputs, parameters, tool versions, and outputs as a frozen record.
Pan, zoom, filter, and label inside the browser before you decide what to export.
Tables, reports, plots, and JSON parameters in one zip. Drop straight into a paper.
Invite collaborators with role-based access. Comments and run history stay with the project.
Projects are isolated, encrypted at rest, and access-controlled at the project level.
Use cases
The shape of an RNA-seq workspace varies by team. NotchBio carries the same pipeline across the contexts that matter most.
Lab members run the same workflow, get the same plot styles, and ship comparable results. Onboarding a new grad student takes an afternoon, not a semester.
Sequencing data lands in NotchBio and comes out as DE tables and pathway maps the same day. No internal pipeline team required.
Run dozens of projects from the same workspace, branded reports, and predictable deliverables. Charge per project, not per support ticket.
Drop in FASTQ, configure the contrast, export a deliverable. The pipeline isn't your product, the analysis is.
Compare across treatments, time points, and cell lines. Customize figures and drop them straight into a paper draft.
Security
Built for the way labs and biotech teams actually want to handle data: isolated workspaces, encrypted storage, and records that hold up to internal review.
Each analysis workspace keeps files, runs, and outputs separated. Nothing leaks across projects.
Uploaded data and generated results remain yours. We provide the software layer, not your IP.
Invite only the people who should be on a project, with role-based permissions.
Encrypted at rest, encrypted in transit. Computation is isolated per project.
Every run captures parameters, workflow versions, and tool versions for full traceability.
Upload your data, run a complete workflow, customize your visuals, and export everything your research needs.