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ProbKnot is used to predict a maximum expected accuracy structure that can contain pseudoknots.
USAGE: ProbKnot <input file> <ct file> [options]
| <input file> |
The name of a file containing input data. This input data can be in one of three formats:
- Partition function save file (holds base pairing probability data for all pairs and can be generated using the partition interface).
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Sequence file (holds raw sequence: .seq or .fasta).
Note that lowercase nucleotides are forced single-stranded in structure prediction.
Note that in order to use a squence file, the "sequence" flag must be specified (see "--sequence" below).
- ct file (holds a set of structures). This should be a stochastic sample. (see "--ensemble") below.
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| <ct file> |
The name of a CT file to which output will be written. |
| -d, -D, --DNA |
This flag only matters if the input file is a squence file and has been identified as such (see "--sequence" below).
Specify that the sequence is DNA, and DNA parameters are to be used.
Default is to use RNA parameters. |
| --ensemble |
Read a ct file of a stochastic sample as the input of the program. The base pairing probabilities for each pair are the calculated from the fraction of structures with that pair. |
| -h, -H, --help |
Display the usage details message. |
| --sequence |
Identify the input file format as a sequence file. |
| -i, -I, --iterations |
Specify the number of iterations the calculation will undergo. More iterations can result in more predicted pairs, although a single iteration is generally sufficient.
Default is 1 iteration.
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| -m, -M, --minimum |
Specify the minimum length accepted for a helix. A post-processing filter removes short helices.
Default is 3 base pairs.
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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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Bellaousov, S., and Mathews, D.H.
"ProbKnot: fast prediction of RNA secondary structure including pseudoknots."
RNA, 16:1870-1880. (2010).
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