Your sequences, in the same place as everything else.
A built-in DNA/RNA viewer means no more switching to a desktop tool just to look at a plasmid map. Linear and circular views, feature annotations, and inline comments — embedded directly in your workspace.
Capabilities
What you can do without leaving the page.
Native imports
- › FASTA, GenBank, EMBL, SnapGene-compatible exports
- › Auto-detect features (CDS, promoter, terminator, primer-binding)
- › Round-trip preserves annotations
Linear and circular views
- › Linear scrolling with feature tracks
- › Circular plasmid map view
- › Zoom from whole-construct to base-level
- › Jump-to-coordinate
Annotations & restriction sites
- › Click-to-annotate any region
- › Show / hide restriction enzymes by recognition site
- › Inline comments on any base or feature
Embed anywhere
- › Drop a sequence block into any editor page
- › Sample records show their associated sequence
- › Comments and annotations sync across embeds
Why it matters
The desktop-viewer detour costs more than time.
Every time a scientist opens IGV, SnapGene, or Geneious to look at a sequence, the evidence trail breaks. The viewer's session is on a laptop. The annotation lives in a personal file. The discussion happens in Slack. None of it is connected to the sample, the experiment, or the auditor's record.
Labitron's viewer is a first-class block inside the workspace. The annotation lives on the sequence record, the comment lives on the page, and both stay tied to the sample. When the auditor asks "show me the construct used in this study," the answer is one click — not a forensic excavation of someone's downloads folder.
Get started
See the sequence viewer in context.
Bring a plasmid; we'll import it and show you the whole flow — from sample to sequence to annotated page.