SNAPGENE VIEWER SEQUENCE ALIGNMENT SOFTWARE

Any feature type or qualifier can be defined (added / deleted) The silent mutation enzyme site tool allows you to easily add or remove restriction enzyme sites from your coding sequence (you can add / remove restriction sites to your coding sequence without changing the translation).Ģ. Addition and removal of restriction enzymes by silent mutation – Convert various file formats in molecular biology to SnapGene

– Automatically create change history with excellent identification such as color coding

Data management with Data Retention & Folder Self-Service explained.

– Plasmid sequence and annotation, alignment, agarose gel electrophoresis – Automatically record all operations in the cloning procedure – Visualization of DNA and chromosomes (chromosome size sequences) – Simulation of PCR and common cloning methods

SNAPGENE VIEWER SEQUENCE ALIGNMENT SOFTWARE

Planning, visualization, and documentation software for gene analysis in molecular biology methods that support the range of cloning and PCR operations.Make the DNA constructs created in your research an easy-to-read electronic document.These document files can be shared among researchers using the free viewer (SnapGene Viewer). Functional annotation in pairwise and multiple alignment Agarose gel simulation can be saved as a.

Snapgene viewer sequence alignment