- Guide
- Working with Sequences
- Manage sequences
Manage Genetic Sequences
The Genetics workspace imports, views, annotates, and analyzes DNA, RNA, and protein sequences. Whether you're planning a cloning experiment, comparing constructs, or cataloging a sequence library, Genetics gives you the molecular-biology tools to work with the data directly.
Genetics workspace with the sequence viewer open, annotation track, and the sidebar tool list
Importing Sequences
Supported Formats
- FASTA for simple sequence data (nucleotide or protein)
- GenBank for annotated sequences with features, references, and metadata
How to Import
- Click New Sequence or Import on the workspace landing page
- Pick your file or paste sequence text into the dialog box
- Conspecta auto-detects the sequence type (DNA, RNA, or protein)
- GenBank annotations are imported automatically
Tip: GenBank preserves annotations like CDS, promoters, and restriction sites. Use GenBank whenever possible to keep your metadata intact.
Sequence Viewer
Each sequence opens in a viewer that shows:
- A linear view with position numbering you can scroll through
- An annotation track with color-coded features above the sequence
- A minimap for fast navigation in long sequences
- Click-and-drag selection for highlighting regions
Annotations
Add, edit, and view feature annotations on any sequence. Annotations imported from GenBank carry over with their feature types, colors, and qualifiers. New annotations can be drawn directly on the viewer.
Analysis Tools
Open the sidebar to find the analysis tools:
General
- Multiple alignment for comparing sequences
- Dot plot for visual pairwise comparison
- Sequence logo for conservation analysis across a set
- Phylogenetic tree for evolutionary relationships
- Export figure to save a publication-quality viewer image
DNA and RNA
- Translate frames to render the six reading frames
- RNA structure predictions
- Restriction digest simulation, with downstream ligation for assembly planning
Protein
- Hydropathy plot
- Protein properties (length, MW, pI, extinction coefficient)
- Secondary structure prediction
Cloning and Assembly
- Construct assembly for designing multi-fragment assemblies
- Part library for managing reusable fragments
- Contig assembly for stitching reads or fragments together
- Register item to capture an assembly as a new sequence with full lineage
Sample Linking
- Lineage tree to visualize the relationships between sequences and the samples they came from
Visualization
- Linear map for a feature map along a linear sequence
- Circular map for a plasmid-style view, when the sequence is circular
- Export figure saves either map at publication scale
Organization
Grid and Table Views
Browse the library in Grid view (cards with sequence type, length, and annotation count) or switch to Table for metadata-heavy browsing.
Sharing
Each sequence has a sharing toggle that controls visibility to your project members.
Next Steps
- Write notes to embed sequences in your notebook
- Track your samples to link sequences back to the samples they came from
- Share and export to export sequences and maps for collaborators