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(Looks for tandem repeats in a nucleotide sequence)

Fields with a coloured background are optional and can safely be ignored...
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1. Set the parameters for the run (or accept the defaults...)
input section
Select an input sequence.

Use one of the following three fields:   (file must contain a DNA sequence)

  1. To access a sequence from a database, enter the USA path here: (dbname:entry)

  2. Or, upload a sequence file from your local computer here:

  3. Or enter the sequence data manually here:

required section
Minimum repeat size   (Integer, 2 or higher)    
Maximum repeat size   (Integer, same as -minrepeat or higher)     (default is same as -minrepeat)
advanced section
Threshold score   (integer)    
Allow N as a mismatch?  
Allow uniform consensus?  
output section
Report format:
Sanger Centre program tandem output file (optional)  
2. Submit to etandem...
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