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RNAPVMIN(1) User Commands RNAPVMIN(1) NAME RNApvmin - manual page for RNApvmin 2.7.2 SYNOPSIS RNApvmin [options] <file.shape> DESCRIPTION RNApvmin 2.7.2 Calculate a perturbation vector that minimizes discripancies between pre- dicted and observed pairing probabilities The program reads a RNA sequence from stdin and uses an iterative minimiza- tion process to calculate a perturbation vector that minimizes the dis- cripancies between predicted pairing probabilites and observed pairing probabilities (deduced from given shape reactivities). Experimental data is read from a given SHAPE file and normalized to pairing probabilities. The experimental data has to be provided in a multiline plain text file where each line has the format '[position] [nucleotide] [absolute shape reactiv- ity]' (e.g. '3 A 0.7'). The objective function used for the minimization may be weighted by choosing appropriate values for sigma and tau. The minimization progress will be written to stderr. Once the minimization has terminated, the obtained perturbation vector is written to stdout. -h, --help Print help and exit --detailed-help Print help, including all details and hidden options, and exit --full-help Print help, including hidden options, and exit -V, --version Print version and exit -v, --verbose Be verbose. (default=off) Lower the log level setting such that even INFO messages are passed through. I/O Options: Command line options for input and output (pre-)processing -j, --numThreads=INT Set the number of threads used for calculations. --log-level=level Set log level threshold. (default=`2') By default, any log messages are filtered such that only warnings (level 2) or errors (level 3) are printed. This setting allows for specifying the log level threshold, where higher values result in fewer information. Log-level 5 turns off all messages, even errors and other critical information. --log-file[=filename] Print log messages to a file instead of stderr. (de- fault=`RNApvmin.log') --log-time Include time stamp in log messages. (default=off) --log-call Include file and line of log calling function. (default=off) Algorithms: Select additional algorithms which should be included in the calcu- lations. The Minimum free energy (MFE) and a structure representa- tive are calculated in any case. --shapeConversion=STRING Specify the method used to convert SHAPE reactivities to pairing probabilities. (default=`O') The following methods can be used to convert SHAPE reactivities into the probability for a certain nucleotide to be unpaired. 'M': Use linear mapping according to Zarringhalam et al. 2012 'C': Use a cutoff-approach to divide into paired and unpaired nu- cleotides (e.g. "C0.25") 'S': Skip the normalizing step since the input data already repre- sents probabilities for being unpaired rather than raw reactivity values 'L': Use a linear model to convert the reactivity into a probability for being unpaired (e.g. "Ls0.68i0.2" to use a slope of 0.68 and an intercept of 0.2) 'O': Use a linear model to convert the log of the reactivity into a probability for being unpaired (e.g. "Os1.6i-2.29" to use a slope of 1.6 and an intercept of -2.29) --tauSigmaRatio=DOUBLE Ratio of the weighting factors tau and sigma. (default=`1.0') A high ratio will lead to a solution as close as possible to the ex- perimental data, while a low ratio will lead to results close to the thermodynamic prediction without guiding pseudo energies. --objectiveFunction=INT The energies of the perturbation vector and the discripancies be- tween predicted and observed pairing probabilities contribute to the objective function. This parameter defines, which function is used to process the contributions before summing them up. 0 square 1 ab- solute. (default=`0') --sampleSize=INT The iterative minimization process requires to evaluate the gradient of the objective function. (default=`1000') A sample size of 0 leads to an analytical evaluation which scales as O(N^4). Choosing a sample size >0 estimates the gradient by sam- pling the given number of sequences from the ensemble, which is much faster. -N, --nonRedundant Enable non-redundant sampling strategy. (default=off) --intermediatePath=STRING Write an output file for each iteration of the minimization process. Each file contains the used perturbation vector and the score of the objective function. The number of the iteration will be appended to the given path. --initialVector=DOUBLE Specify the vector of initial pertubations. (default=`0') Defines the initial perturbation vector which will be used as start- ing vector for the minimization process. The value 0 results in a null vector. Every other value x will be used to populate the ini- tial vector with random numbers from the interval [-x,x]. --minimizer=ENUM Set the minimizing algorithm used for finding an appropriate pertur- bation vector. (possible values="conjugate_fr", "conjugate_pr", "vector_bfgs", "vector_bfgs2", "steepest_descent", "default" default=`default') The default option uses a custom implementation of the gradient de- scent algorithms while all other options represent various algo- rithms implemented in the GNU Scientific Library. When the GNU Sci- entific Library can not be found, only the default minimizer is available. --initialStepSize=DOUBLE The initial stepsize for the minimizer methods. (default=`0.01') --minStepSize=DOUBLE The minimal stepsize for the minizimer methods. (default=`1e-15') --minImprovement=DOUBLE The minimal improvement in the default minizimer method that has to be surpassed to considered a new result a better one. (default=`1e-3') --minimizerTolerance=DOUBLE The tolerance to be used in the GSL minimizer methods. (default=`1e-3') -S, --pfScale=DOUBLE In the calculation of the pf use scale*mfe as an estimate for the ensemble free energy (used to avoid overflows). (default=`1.07') The default is 1.07, useful values are 1.0 to 1.2. Occasionally needed for long sequences. Structure Constraints: Command line options to interact with the structure constraints fea- ture of this program --maxBPspan=INT Set the maximum base pair span. (default=`-1') Energy Parameters: Energy parameter sets can be adapted or loaded from user-provided input files -T, --temp=DOUBLE Rescale energy parameters to a temperature of temp C. Default is 37C. (default=`37.0') -P, --paramFile=paramfile Read energy parameters from paramfile, instead of using the default parameter set. Different sets of energy parameters for RNA and DNA should accompany your distribution. See the RNAlib documentation for details on the file format. The placeholder file name 'DNA' can be used to load DNA parameters without the need to actually specify any input file. -4, --noTetra Do not include special tabulated stabilizing energies for tri-, tetra- and hexaloop hairpins. (default=off) Mostly for testing. --salt=DOUBLE Set salt concentration in molar (M). Default is 1.021M. Model Details: Tweak the energy model and pairing rules additionally using the fol- lowing parameters -d, --dangles=INT How to treat "dangling end" energies for bases adjacent to helices in free ends and multi-loops. (default=`2') With -d1 only unpaired bases can participate in at most one dangling end. With -d2 this check is ignored, dangling energies will be added for the bases adjacent to a helix on both sides in any case; this is the default for mfe and partition function folding (-p). The option -d0 ignores dangling ends altogether (mostly for debug- ging). With -d3 mfe folding will allow coaxial stacking of adjacent helices in multi-loops. At the moment the implementation will not allow coaxial stacking of the two enclosed pairs in a loop of degree 3 and works only for mfe folding. Note that with -d1 and -d3 only the MFE computations will be using this setting while partition function uses -d2 setting, i.e. dan- gling ends will be treated differently. --noLP Produce structures without lonely pairs (helices of length 1). (default=off) For partition function folding this only disallows pairs that can only occur isolated. Other pairs may still occasionally occur as he- lices of length 1. --noGU Do not allow GU pairs. (default=off) --noClosingGU Do not allow GU pairs at the end of helices. (default=off) --nsp=STRING Allow other pairs in addition to the usual AU,GC,and GU pairs. Its argument is a comma separated list of additionally allowed pairs. If the first character is a "-" then AB will imply that AB and BA are allowed pairs, e.g. --nsp="-GA" will allow GA and AG pairs. Nonstandard pairs are given 0 stacking energy. --energyModel=INT Set energy model. Rarely used option to fold sequences from the artificial ABCD... al- phabet, where A pairs B, C-D etc. Use the energy parameters for GC (--energyModel 1) or AU (--energyModel 2) pairs. --helical-rise=FLOAT Set the helical rise of the helix in units of Angstrom. (default=`2.8') Use with caution! This value will be re-set automatically to 3.4 in case DNA parameters are loaded via -P DNA and no further value is provided. --backbone-length=FLOAT Set the average backbone length for looped regions in units of Angstrom. (default=`6.0') Use with caution! This value will be re-set automatically to 6.76 in case DNA parameters are loaded via -P DNA and no further value is provided. REFERENCES If you use this program in your work you might want to cite: R. Lorenz, S.H. Bernhart, C. Hoener zu Siederdissen, H. Tafer, C. Flamm, P.F. Stadler and I.L. Hofacker (2011), "ViennaRNA Package 2.0", Algorithms for Molecular Biology: 6:26 I.L. Hofacker, W. Fontana, P.F. Stadler, S. Bonhoeffer, M. Tacker, P. Schuster (1994), "Fast Folding and Comparison of RNA Secondary Structures", Monatshefte f. Chemie: 125, pp 167-188 R. Lorenz, I.L. Hofacker, P.F. Stadler (2016), "RNA folding with hard and soft constraints", Algorithms for Molecular Biology 11:1 pp 1-13 S. Washietl, I.L. Hofacker, P.F. Stadler, M. Kellis (2012) "RNA folding with soft constraints: reconciliation of probing data and thermodynamics secondary structure prediction" Nucl Acids Res: 40(10), pp 4261-4272 The energy parameters are taken from: D.H. Mathews, M.D. Disney, D. Matthew, J.L. Childs, S.J. Schroeder, J. Su- san, M. Zuker, D.H. Turner (2004), "Incorporating chemical modification constraints into a dynamic programming algorithm for prediction of RNA sec- ondary structure", Proc. Natl. Acad. Sci. USA: 101, pp 7287-7292 D.H Turner, D.H. Mathews (2009), "NNDB: The nearest neighbor parameter database for predicting stability of nucleic acid secondary structure", Nu- cleic Acids Research: 38, pp 280-282 EXAMPLES RNApvmin acceptes a SHAPE file and a corresponding nucleotide sequence, which is read form stdin. RNApvmin sequence.shape < sequence.fasta > sequence.pv The normalized SHAPE reactivity data has to be stored in a text file, where each line contains the position and the reactivity for a certain nucleotide ([position] [nucleotide] [SHAPE reactivity]). 1 A 1.286 2 U 0.383 3 C 0.033 4 C 0.017 ... ... 98 U 0.234 99 G 0.885 The nucleotide information in the SHAPE file is optional and will be used to cross check the given input sequence if present. If SHAPE reactivities could not be determined for every nucleotide, missing values can simply be omited. The progress of the minimization will be printed to stderr. Once a solution was found, the calculated perturbation vector will be print to stdout and can then further be used to constrain RNAfold's MFE/partition function cal- culation by applying the perturbation energies as soft constraints. RNAfold --shape=sequence.pv --shapeMethod=W < sequence.fasta AUTHOR Dominik Luntzer, Ronny Lorenz REPORTING BUGS If in doubt our program is right, nature is at fault. Comments should be sent to rna@tbi.univie.ac.at. RNApvmin 2.7.2 December 2025 RNAPVMIN(1)
NAME | SYNOPSIS | DESCRIPTION | REFERENCES | EXAMPLES | AUTHOR | REPORTING BUGS
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