Inputsection-sequenceseqall-datafiledatafile-mfiledatafile
Default value: Emethylsites.dat
Requiredsection-siteleninteger
This sets the minimum length of the restriction enzyme recognition site. Any enzymes with sites
shorter than this will be ignored. Default value: 4
-enzymesstring
The name 'all' reads in all enzyme names from the REBASE database. You can specify enzymes by giving
their names with commas between then, such as: 'HincII,hinfI,ppiI,hindiii'. The case of the names is
not important. You can specify a file of enzyme names to read in by giving the name of the file
holding the enzyme names with a '@' character in front of it, for example, '@enz.list'. Blank lines
and lines starting with a hash character or '!' are ignored and all other lines are concatenated
together with a comma character ',' and then treated as the list of enzymes to search for. An example
of a file of enzyme names is: ! my enzymes HincII, ppiII ! other enzymes hindiii HinfI PpiI Default
value: all
Advancedsection-mininteger
This sets the minimum number of cuts for any restriction enzyme that will be considered. Any enzymes
that cut fewer times than this will be ignored. Default value: 1
-maxinteger
This sets the maximum number of cuts for any restriction enzyme that will be considered. Any enzymes
that cut more times than this will be ignored. Default value: 2000000000
-solofragmentboolean
This gives the fragment lengths of the forward sense strand produced by complete restriction by each
restriction enzyme on its own. Results are added to the tail section of the report. Default value: N
-singleboolean
If this is set then this forces the values of the mincuts and maxcuts qualifiers to both be 1. Any
other value you may have set them to will be ignored. Default value: N
-bluntboolean
This allows those enzymes which cut at the same position on the forward and reverse strands to be
considered. Default value: Y
-stickyboolean
This allows those enzymes which cut at different positions on the forward and reverse strands,
leaving an overhang, to be considered. Default value: Y
-ambiguityboolean
This allows those enzymes which have one or more 'N' ambiguity codes in their pattern to be
considered Default value: Y
-plasmidboolean
If this is set then this allows searches for restriction enzyme recognition site and cut positions
that span the end of the sequence to be considered. Default value: N
-methylationboolean
If this is set then RE recognition sites will not match methylated bases. Default value: N
-commercialboolean
If this is set, then only those enzymes with a commercial supplier will be searched for. This
qualifier is ignored if you have specified an explicit list of enzymes to search for, rather than
searching through 'all' the enzymes in the REBASE database. It is assumed that, if you are asking for
an explicit enzyme, then you probably know where to get it from and so all enzymes names that you
have asked to be searched for, and which cut, will be reported whether or not they have a commercial
supplier. Default value: Y
Outputsection-limitboolean
This limits the reporting of enzymes to just one enzyme from each group of isoschizomers. The enzyme
chosen to represent an isoschizomer group is the prototype indicated in the data file 'embossre.equ',
which is created by the program 'rebaseextract'. If you prefer different prototypes to be used, make
a copy of embossre.equ in your home directory and edit it. If this value is set to be false then all
of the input enzymes will be reported. You might like to set this to false if you are supplying an
explicit set of enzymes rather than searching 'all' of them. Default value: Y
-alphabeticboolean
Default value: N
-fragmentsboolean
This gives the fragment lengths of the forward sense strand produced by complete restriction using
all of the input enzymes together. Results are added to the tail section of the report. Default
value: N
-nameboolean
Default value: N
-outfilereport