描述
SnapGene 分子生物學軟體
產品特色
Molecular Cloning
- Restriction Cloning
- Gateway Cloning
- Gibson Assembly
- NEBuilder HiFi Assembly
- In-Fusion Cloning
- TA & GC Cloning
- TOPO Cloning
Primers
- Design primers
- Anneal two oligos to form a double-stranded product
PCR and Mutagenesis
- Simulate PCR
- Overlap extension PCR
- Primer-directed mutagenesis
Enzyme Sets
- Predefined enzyme sets – by company or cutter
- Create custom enzyme sets
- View detailed enzyme information
- Rich support for methylation sensitivity and associated error prevention
Convert File Formats
- Alignment Formats
- ApE
- CLC Bio
- Clone Manager
- DNA Strider
- DNADynamo
- DNASIS
- DNAssist
- DNASTAR Lasergene®
- DS Gene
- EMBL (ENA)
- EnzymeX
- GenBank / DDBJ
- Gene Construction Kit®
- Geneious
- GeneTool
- Genome Compiler
- Jellyfish
- MacVector
- pDRAW32
- Serial Cloner
- Swiss-Prot
- Vector NTI®
- Visual Cloning
Agarose Gel Simulation
- Simulate an agarose gel
- Simulate a Restriction Digest
- Simulate a PCR Amplification
- Large collection of MW markers
Features / Annotations
- Create and edit features
- Automatic annotation of common features
- Annotate novel features manually
- Choose Alternative Codons
- Sophisticated numbering of feature translations
- Support for ribosomal slippage
Translations
- View and edit translated features
- Open reading frames (ORFs)
- Whole-sequence translations
- Check reading frames for gene fusions
- Make Protein (from DNA)
- Reverse Translate (from Protein)
Alignment
- Align DNA sequences with a reference sequence
- Verify cloning or mutagenesis
- Align cDNA to a chromosome
- Pairwise and multi sequence DNA and Protein alignment
- Choice of alignment algorithms – Clustal Omega, MAFFT, MUSCLE, T-Coffee
- Contig Assembly
Visualizing
- See multiple views of a DNA sequence
- Large sequence support – browse chromosome size sequences
- Edit DNA and protein sequences
- Color code sequences
History Tracking
- Comprehensive “undo” capability
- See a graphical history of a product
- Use optional history colors to identify the most recent change to a sequence
Data Management
- Import from common file formats including annotations and notes
- Export to standard formats
- Create and share Collections
- Share data with SnapGene Viewer
- Run batch operations
Search
- Search for DNA or protein sequences
- Search for enzymes, features or primers
General
- Cross platform compatibility – Windows, macOS, Linux