A simple procedure to generate 2-way alignments and associated data
in a few steps.
- select or upload a Target genome
- select or upload a Query genome
- press the OK bottom to generate the alignment.
To customize the size of the genome files for low-quality genomes,
the size distribution can be visualized (Distribution) and short
reads can be excluded from analysis via the Min length
parameter. Queued, running, finished, or erroneous runs are
color-coded and listed as Previous IDs in the left panel. After
request, the new 2-way combination can be transferred to the n-way
module and organized in client-specific projects.