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DuplexFold is used to predict lowest free energy structures
containing two strands. The structures
will not contain intramolecular
pairs.
Note that output is written to a CT file where the sequences are
concatenated, with an intermolecular linker between them ("III").
USAGE: DuplexFold <seq file 1> <seq file 2>
<ct file> [options]
| <seq file 1> |
The name of a file containing a first input sequence.Note that lowercase nucleotides are forced single-stranded in structure prediction. |
| <seq file 2> |
The name of a file containing a second input sequence. Note that lowercase nucleotides are forced single-stranded in structure prediction. |
| <ct file> |
The name of a CT file to which output will be written. |
| -d, -D, --DNA |
Specify that the sequence is DNA, and DNA parameters are to
be used. Note that the backbone type must be the same for
both sequences.
Default is to use RNA parameters.
|
| -h, -H, --help |
Display the usage details message. |
| -l, -L, --loop |
Specify the maximum number of unpaired nucleotides in an internal or bulge loop.
Default is 6 unpaired nucleotides.
|
| -m, -M, --maximum |
Specify a maximum number of structures. Note that suboptimal
structures are generated until either the maximum number of
structures are reached or the maximum percent difference is
reached (below).
Default is 10 structures.
|
| -p, -P, --percent |
Specify a maximum percent difference in folding free energy
change in suboptimal structures. Note that suboptimal
structures are generated until either the maximum percent
free energy difference is reached or until the maximum number
of structures is reached (above).
Default is 40 percent (specified as 40, not 0.4).
|
| -t, -T, --temperature |
Specify the temperature at which calculation takes place in
Kelvin.
Default is 310.15 K, which is 37 degrees C.
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| -w, -W, --window |
Specify a window size for generating suboptimal structures. Smaller windows (down to zero) will result in a larger set of structures that are similar. Larger windows result in fewer structures that are more different in predicted pairs.
Default is 0 nucleotides.
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-
Reuter, J.S. and Mathews, D.H.
"RNAstructure: software for RNA secondary structure prediction
and analysis."
BMC Bioinformatics, 11:129. (2010).
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Piekna-Przybylska, D., DiChiacchio, L., Mathews, D.H. and Bambara, R.A.
"A sequence similar to tRNA3Lys gene is embedded in HIV-1 U3/R and promotes minus strand transfer."
Nature Structural & Molecular Biology, 17:83-89. (2010).
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