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SnapGene使克隆技术更智能,更快速。改进核心分子生物学过程,提升研究结果的正确率。
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
限制站点指示器
确认限制站点适合克隆。
历史记录颜色
使用可选的历史记录标上颜色来标识序列的更改。
拥有您的数据
SnapGene可以帮助您选择读取和共享文件,同时保持对数据的完全控制。
安全文件管理
把您的SnapGene文件放在您想要的地方。
从另一种格式导入时,目标不仅是捕获DNA序列,还要捕获注释和注解。如果在导入文件时遇到故障,或者想要支持新的文件格式,请与我们联系。
SnapGene可适用于Windows和Mac系统。