User Guides

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SnapGene

Installation
- Download and Register SnapGene
- Adjust the Configuration
- Generate an Email with a Download Link
- Unregister the Computer You Are Using
- Unregister a Computer Remotely
- Retrieve a License from a Computer
- Reactivate a Blacklisted Computer
- Set Up a License Server on a Mac
- Set Up a License Server on Windows
- Set Up a License Server on Linux
- Command Line: Installation and Activation
- Shared License Administration: Replace a Vendor Daemon License File
Preferences
- Open Full Screen Windows By Default
- Hide or Show the Description Panel By Default
- Show the Launch Window on macOS
- Set the Background Color
- Set the Default Font Size for New Files
- Set the Default Transformation Strain
- Set When SnapGene Checks for Updates
- Choose if SnapGene Sends Anonymous Statistics and Crash Reports
- Reset All Warning Messages
- Set the Default Location for Opening and Saving Files
- Set the Default Author For Files and Collections
- Set the Ancestor Limit for History Trees
- Set the Default Export Formats
- Prohibit /label Qualifiers in Exported GenBank Files
- Transfer Source Features During Cloning Simulations
- Set the Default Display Preferences for New Collections
- Set the Display Preferences for New and Imported DNA Sequences
- Display Feature Labels Below or Inside a Map
- Italicize Restriction Enzyme Names
- Don't Show Unique Cutters in Bold
- Highlight Blunt Cutters in Green
- Show Full Structures for Primer-Template Duplexes
- Set the Default Display Preferences for New Protein Sequences
- Prohibit Region Labels Above a Protein Map
- Show Protein Molecular Weights in Daltons
- Set the Default Stringency for Hiding Chromatogram Ends
Display Options
- View a Sequence with a Split Window
- View Sequence Traces with Color Vision Disabilities
- Show a Plot of GC Content
Description Panel
- Show or Hide the Description Panel
- Add Descriptive Information to a Sequence File
- Add Reference Information to a Sequence File
- Embed Files from Other Programs in a Sequence File
Enzymes
- Show or Hide Individual Enzymes
- Choose an Enzyme Set
- Choose Enzymes Manually
- Highlight an Enzyme Site
- Display a Restriction Site Overview
- Sort Enzymes
- View Enzyme Information
- View Noncutters
- Save or Export Enzyme Set
- Manage Enzyme Sets
- Set the Preferences for Enzymes
Features
- Create a Simple Feature
- Create a Translated Feature
- Adjust Translated Feature Numbering
- Create a Feature Segment
- Annotate Introns
- Add a Cleavage Arrow
- Create a Point Feature
- Edit Multiple Features
- Delete Features
- Confirm an In-Frame Gene Fusion
- Set the Genetic Code for a Feature
- Designate a Non-ATG Start Codon
- Show or Hide Features
- Sort the Feature List
- Import Feature Data
- Export Feature Data
- Splice to Remove Introns
- Detect Common Features
- Detect Custom Features
- Edit Common Features
- Share Custom Feature List
- Add Reference Information to a Feature
- Create a Feature with Introns Using an Aligned cDNA
Primers
- Create a Primer
- Edit Multiple Primers
- Adjust Primer Hybridization Parameters
- Show or Hide Primers
- Sort the Primers List
- Import Primers
- Export Primers
Translations
- Show or Hide Translations and ORFs
- Choose the Translation Frames
- Choose the Translation Format
- Choose the Translation Genetic Code
- Display Open Reading Frames
- Convert an ORF to a Feature
Colors
- Customize DNA Sequence Colors
- Show or Hide DNA Colors
- Choose a Color Mode
- Show Colors in History View
Searching
- Search for an Exact DNA Sequence
- Search for Similar DNA Sequences
- Search for a Protein Sequence
- Search for an Enzyme, Feature, or Primer
Zooming
- Show or Hide the Zoom Controls
- Zoom In
- Pan Across a Sequence
Single Stranded Sequences
- Create or Import a Single-Stranded DNA Sequence
- Convert Between Single-Stranded and Double-Stranded Formats
Restriction Cloning and Linear Ligation
- Insert a Fragment into a Plasmid
- Insert Multiple Fragments into a plasmid
- Delete Restriction Fragment
- Destroy a Restriction Site
- Linear Ligation
TOPO Cloning
- Simulate Directional TOPO® Cloning
- Simulate TA TOPO® cloning
- Simulate Blunt TOPO® Cloning
PCR and Mutagenesis
- PCR
- Inverse PCR
- Mutagenesis
Agarose Gel Simulation
- Initiate an Agarose Gel Simulation
- Choose a MW Marker
- Set the Default MW marker
- Configure the Gel Properties
- Choose a Sequence for Digestion or PCR
- Simulate a Restriction Digest
- Simulate a PCR Amplification
- Rearrange the Gel Lanes
- Export the Gel Data
- Set Preferences for Agarose Gel Simulations
Collections
- Make a New Collection
- Designate a Main Collection
- Open a Collection
- Add Files to a Collection
- Organize Sequences in a Collection
- Import from a Database to a Collection
- Export Files from a Collection
- Save Changes in a Collection
- Adjust the Collection Display Options
- Rename a File or Folder in a Collection
- Search a Collection
- Do Bulk Replacement in a Collection
- Define a Working Set
- Specify a Description and Authors for a Collection
- Configure Code Numbers for a Collection
- Create Links Between Collection Areas
Batch Operations
- Add Description Data to Multiple Sequences
- Add Common Features to Multiple DNA Sequences
- Import Features into Multiple SnapGene Files
- Import Primers into Multiple SnapGene Files
- Flip Multiple DNA Sequences
- Blast Multiple Sequences
Electronic Laboratory Notebooks
- Exchange Files with the LabArchives ELN
Command Line Interface
- Command Line: Converting File Formats
- Command Line: Creating Maps
Importing and Exporting
- Import Features from a GTF, GFF3, or BED File
Assembly and Alignment
- Align Reads to a Reference Sequence