This post was contribued by guest bloggers Aline and Benjamin Glick from SnapGene.
SnapGene was created to meet a need. While there were software tools available to biomedical researchers manipulating DNA sequences on a daily basis, many found these tools inadequate for planning, visualizing, and documenting their procedures. Preventable errors in the design of cloning strategies set experiments back days or even weeks. Primer design was done painstakingly by hand. Records of plasmid construction were often incomplete or nonexistent. In the 21st century, many molecular biologists didn’t know the complete sequences or properties of the DNA molecules they were using.