Terminal-based circular plasmid map viewer, sequence editor, and Primer3/Golden Braid primer design workbench
Project description
SpliceCraft
A plasmid workbench you live in. SpliceCraft is a terminal-native viewer, sequence editor, primer + mutagenesis designer, Golden Braid / MoClo cloning workbench, and in-process BLAST / HMMscan engine — all rendered as crisp Unicode braille graphics in any modern terminal.
Built by a practicing bioengineer for daily lab work. Bug reports come from the bench; releases ship from the bench.
Quick start
pipx install splicecraft
splicecraft # empty canvas
splicecraft L09137 # fetch pUC19 from NCBI on launch
splicecraft myplasmid.gb # local GenBank or .dna
Press ? once running for the full keyboard-shortcut reference.
See docs/install.md for pip / uv / conda / source
installs and the user-data directory location.
What it does
- View circular and linear braille-dot maps, per-base sequence panel with two-strand display, AA translation, restriction overlays (200+ NEB enzymes incl. Type IIS).
- Edit in-place with deepcopy undo / redo, feature CRUD, 3-second-debounced crash-recovery autosave.
- Clone through a multi-tab Constructor (Traditional / Gibson / Golden Braid / MoClo / custom grammar) with a 4-source part picker. Every save path — L0 Domesticator, Constructor TU / MOD / L3+, Traditional cloning, Gibson, MoClo — lands as a single complete library entry (payload + overhangs + backbone) carrying every parent L0 / TU feature as its own annotation, so the L0 → TU → MOD provenance chain is browsable from the Library panel.
- Design primers via Primer3 (detection / cloning / GB / generic) with a persistent Designed → Ordered → Validated lifecycle.
- Mutagenize any CDS via SOE-PCR site-directed mutagenesis with edge-case fallback to 2-primer modified-outer PCR.
- Simulate PCR + agarose gels (0.5–4% with the Helling-Goodman- Boyer mobility curve and form corrections).
- Align sequencing runs from the Sequencing toolbar — drop in a
Plasmidsaurus
.zip, browse a nested 4-tab view of the run (General overview · per-Samples table · Quality metrics including k-mer + contamination + coverage · Align), pick a sample + target plasmid; the pairwise alignment lands as a sequencing-read lane on the linear map right next to the rail, and the target's library entry auto-tags to linear view for future opens. - Log experiments from the Experiments toolbar — full-screen
lab-notebook workbench with a split-pane layout: entries list on
the left (Updated · Title with horizontal scroll for long titles)
- full-width markdown
TextAreaeditor on the right. Group entries into named projects (Ctrl+P → Projects… picker: Open / New / Rename / Duplicate / Delete) — projects are to experiments what plasmid collections are to plasmids. In-editor colored cross-references —@<plasmid>(lime),!<action>(purple),&<gel>(orange) — backspace deletes the whole tag, and Ctrl+G or double-click on a tag opens its source modal focused on that entry. Persistentexperiments.json+experiment_projects.json+gels.json, per-entry image attachments (file picker on Linux/WSL · Pillow clipboard grab on Win/Mac), and F7 spellcheck viapyspellcheckerwith a user-maintained custom dictionary.
- full-width markdown
- Save Simulator gels from the
Simulator → Gel → Librarybutton — name + save the current lane layout + agarose %, load it back later, or reference it as&<id>in an Experiments entry. - Search your library with in-process BLASTN / BLASTP / HMMscan
(via
pyhmmer— no externalblast+install). - Drive from outside via a 60+ endpoint localhost JSON API
(
splicecraft --agent) and a stdlib-only CLI sidecar (splicecraft-cli).
Full feature reference: docs/features.md.
Robustness is a feature
- Load-time collision detection across parts bin, plasmid library, and primer library. An exact duplicate (same name + same content) prompts skip (default) or keep as " COPY" so duplicates can coexist with their twin. A name-match with different content prompts three-way keep original (default) / overwrite / cancel the load — never silently clobbers existing data.
- Four-layer JSON safety net per save: atomic write +
.bak+ rotating timestamped backups + daily snapshots + suspicious-shrink guard. - Pre-update snapshots before any pip / pipx / uv subprocess; stored in a sibling directory so a hypothetical recursive-wipe bug in a new version cannot kill recovery.
- 2,600+ tests anchored on 41 sacred invariants (see
CLAUDE.md), hypothesis property-based fuzzing on biology primitives. - Defence-in-depth size caps on every external input (NCBI / PyPI
/ Kazusa fetch,
.dnahistory packets, JSON saves, agent-API bodies, CLI responses). - Lock-file PID-fsync + stale-PID detection so a SpliceCraft killed on a shared filesystem releases its lock on next launch.
- Master Delete under File → "⚠ Master Delete (wipe all user
data)…" lets you wipe every plasmid, collection, experiment, gel,
primer, part, grammar, codon table, feature, setting, backup,
snapshot, and pre-update recovery copy in one go — true clean
slate. Triple-gated: typed
YES(case-sensitive) to enable the Delete button, then a default-No confirm with a 3-second cool-down on the destructive button. No keyboard shortcut. No agent endpoint. - Entry-vector auto-detection. When you import a folder via Collections → New Collection, SpliceCraft scans every plasmid, identifies acceptors (UPD / α1 / α2 / Ω1 / Ω2 for Golden Braid), and auto-binds them to their roles. Manual review + override via Settings → Entry Vectors…. Configured acceptors flip TU classification from the lenient fallback to strict per-acceptor matching with explicit role labels.
Full data-safety writeup: docs/data-safety.md.
Security policy: SECURITY.md.
Documentation
| Topic | Where |
|---|---|
| Install methods | docs/install.md |
| First five seconds with pUC19 | docs/getting-started.md |
| Full feature list | docs/features.md |
| Keybindings + menus | docs/keybindings.md |
| Data safety + backups | docs/data-safety.md |
| Agent API (HTTP) | docs/agent-api.md |
| CLI sidecar | docs/cli.md |
| Architecture | docs/architecture.md |
| Sacred invariants | CLAUDE.md |
| Contributing | CONTRIBUTING.md |
| Security policy | SECURITY.md |
| v1.0.0 acceptance gate | V1_GATE.md |
| Changelog | CHANGELOG.md |
| Release checklist | RELEASE_CHECKLIST.md |
Tests
python3 -m pytest -n auto -q # full suite (~5–6 min on 8 cores)
python3 -m pytest tests/test_dna_sanity.py # biology correctness only (< 2 s)
python3 -m pytest tests/test_perf_regression.py # perf gates (~3 s)
All tests run offline against synthetic SeqRecords and monkeypatched
data paths; the autouse _protect_user_data fixture in
tests/conftest.py guarantees no test can write to real user files.
Maintenance
SpliceCraft is actively maintained. The maintainer is a practicing bioengineer running real cloning workflows in it daily; releases typically go out the same week a problem surfaces at the bench. Issues and PRs welcome at github.com/Binomica-Labs/SpliceCraft/issues.
See CONTRIBUTING.md before opening a non-trivial
PR — it walks through the sacred invariants, the test cadence, and
the security-sensitive code surfaces.
License
MIT
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