
The REPuter Program Family

- REPfind
- detects degenerate repeats with insertions, deletions, mismatches
- detects direct repeats as well as reverse complemented
- output size: control via parameters for min. length and max. error
- these parameters can also be calculated heuristically by the program, according to the number of repeats required by the user
- output is sorted by significance scores (E-values, as in BLAST)
- REPselect
- selects interesting repeats from the output of REPfind as specified by user-defined criteria
- delivers a list of repeats of chosen length, degeneracy or significance
- simple interfacing to other
- analysis program via executable object code that is linked dynamically
- REPvis
- state of the art interactive visualization tool to display large amount of repeats data
- designed to be used by the biologist, thus putting the data in the hands of those who can best interpret it
- written in ANSI C using GTK
- overview of the repeats over whole genome / chromosome
- repeats displayed as lines connecting their starting positions
- further display modes: circular graph and dot plot
- color coded repeat lengths and significance scores
- scroll bar controls amount of data displayed
- zoom function to display details of a particular repetitive region
- single repeat can be selected to view the alignment
- submit corresponding nucleotide sequence to FASTA / BLAST
- subsequences can be exported to a file
- display additional user provided annotation
- batch mode to produce publishable graphic of repeat structure
The REPuter programs are freely available for universities.
Get the appropriate license here: