The 'mfold' software is a tool for nucleic acid folding and hybridization prediction. It was developed by M. Zuker in the late 1980s for RNA folding and improved for DNA folding in 1996. mfold uses nearest neighbor energy rules.
Tool home page: mfold.org. Similar results to those produced by UGENE can be obtained using the mfold web server (DNA prediction, RNA prediction) or using the OligoAnalyzer tool. For complete documentation on the tool, see a) on the website, b) in the article, c) in the source code in the corresponding folder.
UGENE uses Ghostscript to convert PS files to PNG and PDF.
ToC
Prerequisites
For mfold to work correctly, the path to the temporary directory must not contain spaces, non-printable characters and non-ASCII characters (Unicode characters such as emoji, Cyrillic, Chinese family of scripts, etc.). In this case, you need to change the path to the temporary directory in the appropriate setting.
UGENE itself must be installed to a path that does not contain non-printable characters or non-ASCII characters (Unicode characters). If installed incorrectly, a corresponding error will be displayed.
Open the dialog
mfold only works with DNA or RNA sequences. You can trigger the dialog from
by selecting the appropriate Sequence View Global action 
or through the Main Menu→Actions→Analyze 
or through the Sequence Context Menu→Analyze 
This is what the mfold dialog looks like
Input parameters
The tool is passed explicit and implicit parameters. Explicit parameters are set in the dialog, implicit parameters are taken from the sequence context.
Algorithm settings
For complete settings details, see the documentation on the mfold website or documentation in source.
This is the Settings section of the mfold settings tab.
| Parameter | Unit | Default | Limits | Tool argument name | Description |
|---|---|---|---|---|---|
| Temperature | °C | 37 | [0,100] | T | The folding temperature. For RNA this is always the default value. For DNA it is taken from the dialog. |
| Ionic conditions | M | Na=1 | [0,1.5] | NA_CONC | Ionic conditions are used to enter total monovalent (Na) and divalent (Mg) ions concentrations. For RNA this is always the default values. For DNA it is taken from the dialog. |
| Mg=0 | MG_CONC | ||||
| Percent suboptimality | % | 5 | [1,100] | P | The suboptimality percentage controls the free energy increment δδG for computing suboptimal foldings. Only foldings with a free energy ≤ΔG+δδG will be computed, where ΔG is the predicted minimum free energy. Normally, δδG=(P/100)|ΔG|, but it is rounded up to 1 kcal/mol or down to 12 kcal/mol if it is outside this range. |
| Max num of foldings | 50 | [1,100] | MAX | This is the maximum number of foldings that mfold will compute. It is better to limit the number of foldings by careful selection of the P and W parameters. | |
| Window | 0 (len≤29) 1 (30≤len≤49) 2 (50≤len≤119) 3 (120≤len≤199) 5 (200≤len≤299) 7 (300≤len≤399) 8 (400≤len≤499) 10 (500≤len≤599) 11 (600≤len≤699) 12 (700≤len≤799) 15 (800≤len≤1199) 20 (1200≤len≤1999) 25 (2000≤len) | [0,50] | W | The window parameter, W, controls the number of foldings that are computed. It may be thought of as a distance parameter. The distance between 2 base pairs, ri rj and ri' rj' may be defined as max{|i-i′|, |j-j′|}. If k-1 foldings have already been predicted by mfold, the kth folding must have at least W base pairs that are at least a distance W from any of the base pairs in the first k-1 foldings. A new folding is not added to the output list unless this criterion is fulfilled. As W increases, the number of predicted foldings decreases. A smaller value of this parameter will usually result in more computed foldings that may be quite similar to one another. A larger value will result in fewer foldings that are very different from one another. If the parameter is set to the default value, then in the calculations the real value of W will be set according to the described algorithm, based on the length of the selected region of the input sequence (see the Default column). | |
| Max base pair distance | ∞ | [1,∞] | MAXBP | If the maximum distance between paired bases parameter, MAXBP, is specified, then any base pair, ri rj, in a folding must satisfy Thus small values of MAXBP ensure that only short range base pairs will be predicted. For example, in a sequence of 1000 nucleotides, setting MAXBP to 50 will force mfold to compute foldings involving only short range base pairs. The default is MAXBP=∞, which means no constraint. |
Display settings
Corresponds to the Extended settings section on the main tab.
| Parameter | Unit | Default | Limits | Tool argument name | Description |
|---|---|---|---|---|---|
| Base numbering frequency | 10 (len≤50) 20 (51≤len≤300) 50 (301≤len) | [0,1000] | LAB_FR | Each image marks the number of the base (nucleotide) starting from the beginning 5'. The frequency with which this number will be displayed on an image depends on this parameter: Compare images above with the same algorithm settings to see the difference. | |
| Rotation angle | ° | 0 | [-180,180] | ROT_ANG | Specifying the orientation of the folded molecule by selecting the rotation angle. Positive values correspond to counter-clockwise. |
Region settings
Specifies the part of the sequence that will be analyzed. The tool will only work with this piece of the sequence in isolation from the whole sequence.
You can select the entire sequence, a custom region, or a selected region if there was one. The region must be less than 3000 bases. It is acceptable to select a small region (<10bp), but there will almost certainly be no folding there.
Rules for substituting the selected region:
- If several regions have been selected in a sequence (using the GenBank format), then the dialog will only accept the first of them. The remaining selected regions are ignored.
- The first rule has an exception: if the sequence is marked circular and the region passing through the end/beginning is selected, then such a region is considered as a whole region and mfold will be launched on it as on an ordinary piece of the sequence (2 parts of the region – one that goes to end and another that starts from the beginning of the sequence – will be combined into one sequence and analyzed).
Output settings
UGENE&Ghostscript settings in the "Output" tab.
| Parameter | Default | Description |
|---|---|---|
| Save output to | /path/to/sequence/ | The folder where the "mfold" subdirectory will be created with the output data in it. By default, this folder is the same as the folder where the input sequence is stored. For example, let's say our OS is Windows and the analyzed sequence has the path "C:\path\to\sequence\my_sequence.fa". After running the task, the folder structure will look something like this C:.
└───path
└───to
└───sequence
│ my_sequence.fa
│
└───mfold
└───2024.03.19_16-31-34
inp.fa_1.pdf
inp.fa_1.png
inp.fa_2.pdf
inp.fa_2.png
inp.fa_3.pdf
inp.fa_3.png
out.html
Settings are not saved between dialog calls. If you need to change the output folder to something other than the default, you will have to do this manually each time. This behavior may be corrected in future releases of UGENE. |
| DPI | 96 | Setting up the Ghostscript converter from ps files to PNG. Quality of saved images (PNG files). The higher this parameter, the higher the quality, size and resolution of the resulting images. This setting only affects images in the output folder. This setting does not affect images in UGENE. This setting does not affect PDF. |
Internal parameters
Settings that the user cannot explicitly influence.
- Molecule Type (DNA/RNA). mfold gets sequence information from command line arguments. Information about what type will be passed to the tool can be seen next to the sequence name
- Molecule Topology (linear/circular). mfold gets sequence information from command line arguments.
- If the sequence is marked as circular
, then mfold will work with it as a circular one.
- Otherwise
- Part of a circular sequence will also be considered a circular sequence. If you want to change this behavior, uncheck "Mark sequence as circular" and then call the mfold dialog
- If the sequence is marked as circular
- DPI of images in UGENE. Ghostscript has a default DPI of 72. Therefore, this value is used for images for the internal UGENE report and this value cannot be changed.
Tool comparison
хранение результатов
подключение к интернету
какие настройки есть
исправлены баги
размер входных последовательностей
Links