The Variance Table
A powerful tool for SNP analysis and more
Now there is a very simple way to compare DNA sequences or contig consensus sequences and find all the differences between those sequences in just a few keystrokes. The Variance Table lets you sift through large quantities of sequence data so you can quickly visualize the bases of greatest interest to you. Each cell in the Variance table is linked to its original data, so you can easily validate or edit each putative difference directly in the Table, and have the sequence and chromatogram data updated automatically. Once you’ve found all the differences, Sequencher provides you with a variety of export and reporting options. These are described in greater detail in the Reports Page.
Multiple Contig Variance Table
Single Contig Variance Table