Sequences are
not designs.

Nucleora is the CAD system molecular biology never had - assemble constructs from parametric parts, run continuous design-rule checks, fold and simulate locally, and ship an auditable release record.

Continuous design rules · ViennaRNA fold · 33 species codon tables · Local-first
33
Species codon
tables
350+
Tools in the
workbench
0
Sequences
uploaded

Electronics has CAD.
Mechanical has CAD.
Architecture has CAD.

Molecular biology has a text box with ATGC in it, a folder of Benchling tabs, and a spreadsheet.

Nucleora treats a DNA or mRNA construct the way an engineer treats any other design. Parts. Constraints. Checks. Simulation. A release you can hand to someone.

FROM

A sequence you type and then analyze

TO

A design you assemble, constrain, simulate, verify, and release

One environment. The full workflow.

From antigen to auditable release record - without switching tabs.

Nucleora dashboard - Recent Constructs, Quick Actions, and Recent Analyses

HOME - Dashboard and project overview

Nucleora Design Studio - cloning, codon optimization, and sequence editing

DESIGN STUDIO - 41 tools including cloning, codon optimization, and mutagenesis

Nucleora sequence editor - mRNA linear view with feature map

SEQUENCE EDITOR - mRNA linear, IVT plasmid circular, with auto-annotation

Nucleora sequencing QC - align result to reference

ANALYSIS & QC - Align sequencing results to your design, classify every variant

Home & Projects
1 / 4

Five pillars. Every mature CAD system has them.
No nucleic-acid tool has had all five.

01

Canvas

Schematic capture

Construct your design from parametric parts - not by typing characters. Change poly(A) from 80 to 120 and the sequence regenerates underneath you. The sequence is a rendering of the design, never its source of truth.

  • Drag-and-drop part assembly
  • Bidirectional sequence sync
  • mRNA, DNA, IVT plasmid views
02

Library

Versioned, provenanced parts

Every part carries its provenance - the database, the accession number, the date it was fetched. Codon tables tallied from real RefSeq coding sequences. When a species doesn't have one, Nucleora names the proxy it used.

  • Real codon data, or it tells you
  • Provenance on every part
  • Sample library included
03

Constraint Engine

Design rules that fail loudly

Design rules run continuously - like a spell-checker. It finds the homopolymer run your synthesis vendor would have rejected, explains why in plain language, and offers the fix before you ever place an order.

  • Rules across multiple categories
  • Plain-language failure explanations
  • Synonymous-substitution fixes
04

Simulator

Physics in the loop

Fold locally with ViennaRNA. Watch the structure change as you edit. Walk the template through the IVT run before it costs anything: predicted yield, manufacturability grade, and an itemised order form - all computed on your machine.

  • ViennaRNA local fold
  • Manufacturability grade + yield
  • IVT run simulation
05

Release Path

From intent to auditable artifact

One signed, immutable release record: the design revision, every check, every waiver, every simulation result, and the bill of materials. SBOL export. 21 CFR 11 signatures. The full audit trail - in a format another person can verify.

  • Signed, immutable release records
  • SBOL export
  • 21 CFR 11 audit trail

It fails here.
Not at the bench.

A homopolymer run of A×9 will cause your synthesis vendor to reject the order. Nucleora's DRC-014 catches it before you send it. Three synonymous substitutions later - the protein is unchanged, the construct ships.

The error costs you ten seconds on screen. At the bench it costs $4,000 and three weeks.

DRC Design rules
6 Rule packs
0 Surprises at the vendor
<10s Time to detect & fix
MOLECULAR ANALYSIS  ·  CONTINUOUS CHECKING LIVE SCAN
DRC-001 GC content in range PASS
DRC-008 No internal Kozak conflicts PASS
DRC-014 Homopolymer run A×9 at pos 847 ERROR

Synthesis vendors reject homopolymer runs ≥ 8 nt.
Your vendor would have rejected this order.

SUGGESTED FIX 3 synonymous substitutions · protein unchanged · Δlum = 0.002
DRC-015 No restriction site conflicts PASS
DRC-031 5′ UTR secondary structure ΔG PASS
DRC-047 No GC-rich window > 80% in 20nt window PASS
DRC-089 Poly(A) tail length in acceptable range PASS

Paste a sequence. See the checks fire.

No install. No account. A preview of what Nucleora does - right here, right now.

0 nt
Paste a sequence above — checks fire instantly.

Runs entirely in your browser — no data leaves this page. Full analysis (design rules + ViennaRNA folding) available in the Nucleora app.

Your sequences never leave the building.

Not a data-harvesting cloud. Works on a plane, in a BSL-3, air-gapped.

Runs on your machine

ViennaRNA, codon tables, DRC, fold simulation - all local. No API keys. No account required.

BSL-3 and air-gap ready

No outbound connections required after install. Works in regulated environments where cloud tools cannot go.

Method-transparent

Every computed number traces to a named, published method. No confident guesses. We publish the benchmarks we lose.

Testing available upon request

Full workbench. No crippled tier. Academic and commercial use welcome. Request access - join the list.

"Assemble a construct from parametric parts, fold it as you edit, and catch the homopolymer run before your vendor does. 350+ tools underneath when you need them."

Real codon tables.
Real species. Real data.

Codon usage tables calculated from RefSeq CDS sequences - not interpolated, not approximated. Every table names its source.

Browse codon usage data →
HumanMouseTigerChimpanzee ElephantDolphinGorillaLion Polar BearGiant PandaCheetahWhite Rhino Axolotl+ more →

Every part of the construct.
Designed, not typed.

Nucleora lets you assemble mRNA constructs from parametric parts. Change one element - the sequence regenerates underneath you.

Common questions.

Cloud tools vs. Nucleora.

What happens to your sequences depends entirely on where computation runs.

Cloud-based tools
☁️
Sequences uploaded to vendor serversEvery FASTA, every construct, every edit is transmitted over the internet.
🔑
Account requiredTied to a vendor login, a credit card, a subscription - and their terms of service.
📶
Requires internetCannot be used in BSL-3, on a plane, or on an air-gapped network.
🔒
Sequences stored on third-party infrastructureSubject to vendor data policies, breaches, and government disclosure requests.
VS
Nucleora - local-first
💻
All computation runs on your machineViennaRNA, DRC, codon optimization - no data leaves your machine.
🚫
No account requiredJoin the waitlist, get access, design. No sign-up, no credit card, no vendor lock-in.
✈️
Works offline, on planes, in BSL-3After initial install, no network connection is ever required.
🛡️
Your sequences stay yoursNo vendor terms govern what they can do with your IP, because they never have it.

How Nucleora compares.

An honest look at the tools people actually use for DNA and mRNA design.

Nucleora feature comparison versus Benchling, SnapGene, and UGENE
Feature Nucleora Benchling SnapGene UGENE
Local-first (no upload) -
Continuous design-rule check Continuous Partial - -
Codon optimization 33 species - Basic
Local RNA folding (ViennaRNA) - - mfold
mRNA full construct workflow End-to-end Limited - -
IVT run simulation - - -
21 CFR 11 audit trail - -
SBOL export SBOL 3 SBOL 1 -
Access model By request Limited Paid

Features reflect publicly stated capabilities as of mid-2026. Partial = feature exists with limitations. Nucleora is in active development.

What's new.

Nucleora is in active development. We ship regularly.

v1.0.0 August 2026 New
Public release - full workbench available
Canvas, Library, Constraint Engine, Simulator, and Release Path - all five pillars available in the first public release. macOS (Apple Silicon + Intel) and Windows 10/11.
v1.0.0 New
Continuous design rules across multiple categories
Continuous DRC runs on every edit - homopolymer detection, GC content windows, Kozak conflicts, restriction site screening, mRNA 5′ UTR structure, and IVT manufacturability rules.
v1.0.0 New
33-species codon optimization with RefSeq data
Codon tables tallied directly from RefSeq CDS sequences. Every table names its source database, accession count, and proxy species if applicable.
v0.9 beta June 2026 Fix
ViennaRNA local fold: performance improvements
Reduced fold latency by 40% on Apple Silicon. Structures now update in real-time as you edit the sequence canvas.
v0.8 beta April 2026 Improvement
Signed release records with 21 CFR 11 audit trail
Every release record now includes cryptographic signatures, a full audit trail of checks and waivers, and a verifiable bill of materials in SBOL 3 format.

What's coming.

Nucleora is in active development. These features are in progress or planned for the next release cycle.

✓ Shipped
Continuous DRC
Real-time design rule checking across all 6 rule packs as you edit.
✓ Shipped
Local RNA folding (ViennaRNA)
Full ViennaRNA integration - fold locally, no API, no upload.
✓ Shipped
33-species codon optimization
RefSeq-based codon tables for 33 species, with transparent proxy naming.
▶ In progress
Linux native build
Ubuntu 22.04 LTS and later - same full feature set as macOS and Windows.
▶ In progress
Expanded codon species database
60+ species including additional conservation and marine organisms.
◎ Planned
Team collaboration (local-network)
Share projects and release records with colleagues on the same LAN - no cloud required.
◎ Planned
Custom DRC rule authoring
Write your own design rules in a structured rule language - check your organisation's specific constraints.
◎ Planned
Python scripting API
Automate construct generation, batch codon optimization, and DRC runs from Python scripts.
◎ Planned
GenBank / EMBL import
Import annotated sequences directly from NCBI GenBank and EMBL format - auto-mapped to the part library.

In active development.

We're building the CAD tool molecular biology never had. See how it works →

Request early access

Nucleora is a research and education tool for designing DNA and mRNA sequences using public reference genomes. Not a medical device. Constructs intended for cells, animals, or humans require institutional biosafety review and applicable regulatory approval.

In development Join early access