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RNAALIFOLD(1) User Commands RNAALIFOLD(1) NAME RNAalifold - manual page for RNAalifold 2.7.0 SYNOPSIS RNAalifold [options] [<input0.aln>] [<input1.aln>]... DESCRIPTION RNAalifold 2.7.0 calculate secondary structures for a set of aligned RNAs Read aligned RNA sequences from stdin or file.aln and calculate their minimum free energy (mfe) structure, partition function (pf) and base pairing probability matrix. Currently, input alignments have to be in CLUSTAL, Stockholm, FASTA, or MAF format. The input format must be set manually in interactive mode (default is Clustal), but will be deter- mined automagically from the input file, if not expplicitly set. It re- turns the mfe structure in bracket notation, its energy, the free en- ergy of the thermodynamic ensemble and the frequency of the mfe struc- ture in the ensemble to stdout. It also produces Postscript files with plots of the resulting secondary structure graph ("alirna.ps") and a "dot plot" of the base pairing matrix ("alidot.ps"). The file "ali- fold.out" will contain a list of likely pairs sorted by credibility, suitable for viewing with "AliDot.pl". Be warned that output file will overwrite any existing files of the same name. -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. -q, --quiet Be quiet. (default=off) This option can be used to minimize the output of additional in- formation and non-severe warnings which otherwise might spam stdout/stderr. I/O Options: Command line options for input and output (pre-)processing -f, --input-format=C|S|F|M File format of the input multiple sequence alignment (MSA). If this parameter is set, the input is considered to be in a particular file format. Otherwise, the program tries to deter- mine the file format automatically, if an input file was pro- vided in the set of parameters. In case the input MSA is pro- vided in interactive mode, or from a terminal (TTY), the pro- grams default is to assume CLUSTALW format. Currently, the fol- lowing formats are available: ClustalW ('C'), Stockholm 1.0 ('S'), FASTA/Pearson ('F'), and MAF ('M'). --mis Output "most informative sequence" instead of simple consensus: For each column of the alignment output the set of nucleotides with frequency greater than average in IUPAC notation. (default=off) -j, --jobs[=number] Split batch input into jobs and start processing in parallel us- ing multiple threads. A value of 0 indicates to use as many par- allel threads as computation cores are available. (default=`0') Default processing of input data is performed in a serial fash- ion, i.e. one alignment at a time. Using this switch, a user can instead start the computation for many alignments in the input in parallel. RNAalifold will create as many parallel computation slots as specified and assigns input alignments of the input file(s) to the available slots. Note, that this increases memory consumption since input alignments have to be kept in memory un- til an empty compute slot is available and each running job re- quires its own dynamic programming matrices. --unordered Do not try to keep output in order with input while parallel processing is in place. (default=off) When parallel input processing (--jobs flag) is enabled, the or- der in which input is processed depends on the host machines job scheduler. Therefore, any output to stdout or files generated by this program will most likely not follow the order of the corre- sponding input data set. The default of RNAalifold is to use a specialized data structure to still keep the results output in order with the input data. However, this comes with a trade-off in terms of memory consumption, since all output must be kept in memory for as long as no chunks of consecutive, ordered output are available. By setting this flag, RNAalifold will not buffer individual results but print them as soon as they have been com- putated. --noconv Do not automatically substitute nucleotide "T" with "U". (default=off) -n, --continuous-ids Use continuous alignment ID numbering when no alignment ID can be retrieved from input data. (default=off) Due to its past, RNAalifold produces a specific set of output file names for the first input alignment, "alirna.ps", "ali- dot.ps", etc. But for all further alignments in the input, it usually adopts a naming scheme based on IDs, which may be re- trieved from the input alignment's meta-data, or generated by a prefix followed by an increasing counter. Setting this flag in- structs RNAalifold to use the ID naming scheme also for the first alignment. --auto-id Automatically generate an ID for each alignment. (default=off) The default mode of RNAalifold is to automatically determine an ID from the input alignment if the input file format allows to do that. Alignment IDs are, for instance, usually given in Stockholm 1.0 formatted input. If this flag is active, RNAali- fold ignores any IDs retrieved from the input and automatically generates an ID for each alignment. --id-prefix=STRING Prefix for automatically generated IDs (as used in output file names). (default=`alignment') If this parameter is set, each alignment will be prefixed with the provided string. Hence, the output files will obey the fol- lowing naming scheme: "prefix_xxxx_ss.ps" (secondary structure plot), "prefix_xxxx_dp.ps" (dot-plot), "prefix_xxxx_aln.ps" (an- notated alignment), etc. where xxxx is the alignment number be- ginning with the second alignment in the input. Use this setting in conjunction with the --continuous-ids flag to assign IDs be- ginning with the first input alignment. --id-delim=CHAR Change the delimiter between prefix and increasing number for automatically generated IDs (as used in output file names). (default=`_') This parameter can be used to change the default delimiter '_' between the prefix string and the increasing number for automat- ically generated ID. --id-digits=INT Specify the number of digits of the counter in automatically generated alignment IDs. (default=`4') When alignments IDs are automatically generated, they receive an increasing number, starting with 1. This number will always be left-padded by leading zeros, such that the number takes up a certain width. Using this parameter, the width can be specified to the users need. We allow numbers in the range [1:18]. --id-start=LONG Specify the first number in automatically generated alignment IDs. (default=`1') When alignment IDs are automatically generated, they receive an increasing number, usually starting with 1. Using this parame- ter, the first number can be specified to the users require- ments. Note: negative numbers are not allowed. Note: Setting this parameter implies continuous alignment IDs, i.e. it acti- vates the --continuous-ids flag. --filename-delim=CHAR Change the delimiting character used in sanitized filenames. (default=`ID-delimiter') This parameter can be used to change the delimiting character used while sanitizing filenames, i.e. replacing invalid charac- ters. Note, that the default delimiter ALWAYS is the first char- acter of the "ID delimiter" as supplied through the --id-delim option. If the delimiter is a whitespace character or empty, in- valid characters will be simply removed rather than substituted. Currently, we regard the following characters as illegal for use in filenames: backslash '\', slash '/', question mark '?', per- cent sign '%', asterisk '*', colon ':', pipe symbol '|', double quote '"', triangular brackets '<' and '>'. --log-level=level Set log level threshold. (default=`2') By default, any log messages are filtered such that only warn- ings (level 2) or errors (level 3) are printed. This setting al- lows 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=`RNAalifold.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 calculations. -p, --partfunc[=INT] Calculate the partition function and base pairing probability matrix in addition to the mfe structure. Default is calculation of mfe structure only. (default=`1') In addition to the MFE structure we print a coarse representa- tion of the pair probabilities in form of a pseudo bracket nota- tion, followed by the ensemble free energy, as well as the cen- troid structure derived from the pair probabilities together with its free energy and distance to the ensemble. Finally it prints the frequency of the mfe structure. An additionally passed value to this option changes the behavior of partition function calculation: -p0 deactivates the calcula- tion of the pair probabilities, saving about 50% in runtime. This prints the ensemble free energy 'dG=-kT ln(Z)'. --betaScale=DOUBLE Set the scaling of the Boltzmann factors. (default=`1.') The argument provided with this option is used to scale the thermodynamic temperature in the Boltzmann factors independently from the temperature of the individual loop energy contribu- tions. The Boltzmann factors then become 'exp(- dG/(kTn*betaS- cale))' where 'k' is the Boltzmann constant, 'dG' the free en- ergy contribution of the state, 'T' the absolute temperature and 'n' the number of sequences. -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. --MEA[=gamma] Compute MEA (maximum expected accuracy) structure. (default=`1.') The expected accuracy is computed from the pair probabilities: each base pair '(i,j)' receives a score '2*gamma*p_ij' and the score of an unpaired base is given by the probability of not forming a pair. The parameter gamma tunes the importance of cor- rectly predicted pairs versus unpaired bases. Thus, for small values of gamma the MEA structure will contain only pairs with very high probability. Using --MEA implies -p for computing the pair probabilities. --sci Compute the structure conservation index (SCI) for the MFE con- sensus structure of the alignment. (default=off) -c, --circ Assume a circular (instead of linear) RNA molecule. (default=off) --bppmThreshold=cutoff Set the threshold/cutoff for base pair probabilities included in the postscript output. (default=`1e-6') By setting the threshold the base pair probabilities that are included in the output can be varied. By default only those ex- ceeding '1e-6' in probability will be shown as squares in the dot plot. Changing the threshold to any other value allows for increase or decrease of data. -g, --gquad Incoorporate G-Quadruplex formation into the structure predic- tion algorithm. (default=off) -s, --stochBT=INT Stochastic backtrack. Compute a certain number of random struc- tures with a probability dependend on the partition function. See -p option in RNAsubopt. --stochBT_en=INT same as -s option but also print out the energies and probabili- ties of the backtraced structures. -N, --nonRedundant Enable non-redundant sampling strategy. (default=off) --random-seed=INT Set the seed for the random number generator Structure Constraints: Command line options to interact with the structure constraints feature of this program --maxBPspan=INT Set the maximum base pair span. (default=`-1') -C, --constraint[=filename] Calculate structures subject to constraints. The constraining structure will be read from 'stdin', the alignment has to be given as a file name on the command line. (default=`') The program reads first the sequence, then a string containing constraints on the structure encoded with the symbols: '.' (no constraint for this base) '|' (the corresponding base has to be paired 'x' (the base is unpaired) '<' (base i is paired with a base j>i) '>' (base i is paired with a base j<i) and matching brackets '(' ')' (base i pairs base j) With the exception of '|', constraints will disallow all pairs conflicting with the constraint. This is usually sufficient to enforce the constraint, but occasionally a base may stay un- paired in spite of constraints. PF folding ignores constraints of type '|'. --batch Use constraints for all alignment records. (default=off) Usually, constraints provided from input file are only applied to a single sequence alignment. Therefore, RNAalifold will stop its computation and quit after the first input alignment was processed. Using this switch, RNAalifold processes all sequence alignments in the input and applies the same provided con- straints to each of them. --enforceConstraint Enforce base pairs given by round brackets '(' ')' in structure constraint. (default=off) --SS_cons Use consensus structures from Stockholm file ('#=GF SS_cons') as constraint. (default=off) Stockholm formatted alignment files have the possibility to store a secondary structure string in one of if ('#=GC') column annotation meta tags. The corresponding tag name is usually 'SS_cons', a consensus secondary structure. Activating this flag allows one to use this consensus secondary structure from the input file as structure constraint. Currently, only the fol- lowing characters are interpreted: '(' ')' [mathing parenthesis: column i pairs with column j] '<' '>' [matching angular brackets: column i pairs with column j] All other characters are not interpreted (yet). Note: Activat- ing this flag implies --constraint. --shape=file1,file2 Use SHAPE reactivity data to guide structure predictions. Multiple shapefiles for the individual sequences in the align- ment may be specified as a comma separated list. An optional association of particular shape files to a specific sequence in the alignment can be expressed by prepending the sequence number to the filename, e.g. "5=seq5.shape,3=seq3.shape" will assign the reactivity values from file seq5.shape to the fifth se- quence in the alignment, and the values from file seq3.shape to sequence 3. If no assignment is specified, the reactivity val- ues are assigned to corresponding sequences in the order they are given. --shapeMethod=D[mX][bY] Specify the method how to convert SHAPE reactivity data to pseudo energy contributions. (default=`D') Currently, the only data conversion method available is that of to Deigan et al 2009. This method is the default and is recog- nized by a capital 'D' in the provided parameter, i.e.: --shapeMethod="D" is the default setting. The slope 'm' and the intercept 'b' can be set to a non-default value if necessary. Otherwise m=1.8 and b=-0.6 as stated in the paper mentionen be- fore. To alter these parameters, e.g. m=1.9 and b=-0.7, use a parameter string like this: --shapeMethod="Dm1.9b-0.7". You may also provide only one of the two parameters like: --shapeMethod="Dm1.9" or --shapeMethod="Db-0.7". Energy Parameters: Energy parameter sets can be adapted or loaded from user-pro- vided 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 de- fault parameter set. Different sets of energy parameters for RNA and DNA should ac- company your distribution. See the RNAlib documentation for de- tails 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 following parameters -d, --dangles=INT How to treat "dangling end" energies for bases adjacent to he- lices in free ends and multi-loops. (default=`2') With -d2 dangling energies will be added for the bases adjacent to a helix on both sides in any case. The option -d0 ignores dangling ends altogether (mostly for de- bugging). --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 oc- cur as helices of length 1. --noGU Do not allow GU pairs. (default=off) --noClosingGU Do not allow GU pairs at the end of helices. (default=off) --cfactor=DOUBLE Set the weight of the covariance term in the energy function (default=`1.0') --nfactor=DOUBLE Set the penalty for non-compatible sequences in the covariance term of the energy function (default=`1.0') -E, --endgaps Score pairs with endgaps same as gap-gap pairs. (default=off) -R, --ribosum_file=ribosumfile use specified Ribosum Matrix instead of normal energy model. Matrixes to use should be 6x6 matrices, the order of the terms is 'AU', 'CG', 'GC', 'GU', 'UA', 'UG'. -r, --ribosum_scoring use ribosum scoring matrix. (default=off) The matrix is chosen according to the minimal and maximal pair- wise identities of the sequences in the file. --old use old energy evaluation, treating gaps as characters. (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... alphabet, 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. Plotting: Command line options for changing the default behavior of struc- ture layout and pairing probability plots --color Produce a colored version of the consensus structure plot "alirna.ps" (default b&w only) (default=off) --color-threshold=FLOAT Set the threshold of maximum counter examples for coloring con- sensus structure plot. (default=`2') Floating point numbers between 0 and 1 are treated as frequen- cies among all sequencesin the alignment. All other will be truncated to integer and used as absolute number of counter ex- amples. --color-min-sat=FLOAT Set the minimum saturation for coloring consensus structure plot. (default=`0.2') Floating point number >= 0 and smaller than 1. --aln Produce a colored and structure annotated alignment in Post- Script format in the file "aln.ps" in the current directory. (default=off) --aln-EPS-cols=INT Number of columns in colored EPS alignment output. (default=`60') A value less than 1 indicates that the output should not be wrapped at all. --aln-stk[=prefix] Create a multi-Stockholm formatted output file. (de- fault=`RNAalifold_results') The default file name used for the output is "RNAalifold_re- sults.stk". Users may change the filename to "prefix.stk" by specifying the prefix as optional argument. The file will be create in the current directory if it does not already exist. In case the file already exists, output will be appended to it. Note: Any special characters in the filename will be replaced by the filename delimiter, hence there is no way to pass an entire directory path through this option yet. (See also the "--file- name-delim" parameter) --noPS Do not produce postscript drawing of the mfe structure. (default=off) --noDP Do not produce dot-plot postscript file containing base pair or stack probabilitities. (default=off) In combination with the -p option, this flag turns-off creation of individual dot-plot files. Consequently, computed base pair probability output is omitted but centroid and MEA structure prediction is still performed. -t, --layout-type=INT Choose the layout algorithm. (default=`1') Select the layout algorithm that computes the nucleotide coordi- nates. Currently, the following algorithms are available: '0': simple radial layout '1': Naview layout (Bruccoleri et al. 1988) '2': circular layout '3': RNAturtle (Wiegreffe et al. 2018) '4': RNApuzzler (Wiegreffe et al. 2018) Caveats: Sequences are not weighted. If possible, do not mix very similar and dissimilar sequences. Duplicate sequences, for example, can distort the prediction. 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 Struc- tures", 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 The algorithm is a variant of the dynamic programming algorithms of M. Zuker and P. Stiegler (mfe) and J.S. McCaskill (pf) adapted for sets of aligned sequences with covariance information. Ivo L. Hofacker, Martin Fekete, and Peter F. Stadler (2002), "Secondary Structure Prediction for Aligned RNA Sequences", J.Mol.Biol.: 319, pp 1059-1066. Stephan H. Bernhart, Ivo L. Hofacker, Sebastian Will, Andreas R. Gru- ber, and Peter F. Stadler (2008), "RNAalifold: Improved consensus structure prediction for RNA alignments", BMC Bioinformatics: 9, pp 474 The energy parameters are taken from: D.H. Mathews, M.D. Disney, D. Matthew, J.L. Childs, S.J. Schroeder, J. Susan, M. Zuker, D.H. Turner (2004), "Incorporating chemical modifica- tion constraints into a dynamic programming algorithm for prediction of RNA secondary 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", Nucleic Acids Research: 38, pp 280-282 EXAMPLES A simple call to compute consensus MFE structure, ensemble free energy, base pair probabilities, centroid structure, and MEA structure for a multiple sequence alignment (MSA) provided as Stockholm formatted file alignment.stk might look like: $ RNAalifold -p --MEA alignment.stk Consider the following MSA file for three sequences # STOCKHOLM 1.0 #=GF AC RF01293 #=GF ID ACA59 #=GF DE Small nucleolar RNA ACA59 #=GF AU Wilkinson A #=GF SE Predicted; WAR; Wilkinson A #=GF SS Predicted; WAR; Wilkinson A #=GF GA 43.00 #=GF TC 44.90 #=GF NC 40.30 #=GF TP Gene; snRNA; snoRNA; HACA-box; #=GF BM cmbuild -F CM SEED #=GF CB cmcalibrate --mpi CM #=GF SM cmsearch --cpu 4 --verbose --nohmmonly -E 1000 -Z 549862.597050 CM SEQDB #=GF DR snoRNABase; ACA59; #=GF DR SO; 0001263; ncRNA_gene; #=GF DR GO; 0006396; RNA processing; #=GF DR GO; 0005730; nucleolus; #=GF RN [1] #=GF RM 15199136 #=GF RT Human box H/ACA pseudouridylation guide RNA machinery. #=GF RA Kiss AM, Jady BE, Bertrand E, Kiss T #=GF RL Mol Cell Biol. 2004;24:5797-5807. #=GF WK Small_nucleolar_RNA #=GF SQ 3 AL031296.1/85969-86120 CUGCCUCACAACGUUUGUGCCUCAGUUACCCGUAGAUGUAGUGAGGGUAACAAUACUUACUCUCGUUGGUGAUAAGGAACAGCU AANU01225121.1/438-603 CUGCCUCACAACAUUUGUGCCUCAGUUACUCAUAGAUGUAGUGAGGGUGACAAUACUUACUCUCGUUGGUGAUAAGGAACAGCU AAWR02037329.1/29294-29150 ---CUCGACACCACU---GCCUCGGUUACCCAUCGGUGCAGUGCGGGUAGUAGUACCAAUGCUAAUUAGUUGUGAGGACCAACU #=GC SS_cons -----((((,<<<<<<<<<___________>>>>>>>>>,,,,<<<<<<<______>>>>>>>,,,,,)))):::::::::::: #=GC RF CUGCcccaCAaCacuuguGCCUCaGUUACcCauagguGuAGUGaGgGuggcAaUACccaCcCucgUUgGuggUaAGGAaCAgCU // Then, the above program call will produce this output: 3 sequences; length of alignment 84. >ACA59 CUGCCUCACAACAUUUGUGCCUCAGUUACCCAUAGAUGUAGUGAGGGUAACAAUACUUACUCUCGUUGGUGAUAAGGAACAGCU ...((((((.(((((((((...........))))))))).))))))..........(((((......)))))............ (-12.54 = -12.77 + 0.23) ...((((((.(((((((((...........))))))))).)))))){{,.......{{{{,......}))))............ [-14.38] ...((((((.(((((((((...........))))))))).))))))..........((((........))))............ {-12.44 = -12.33 + -0.10 d=10.94} ...((((((.(((((((((...........))))))))).))))))..........((((........))))............ {-12.44 = -12.33 + -0.10 MEA=66.65} frequency of mfe structure in ensemble 0.368739; ensemble diversity 17.77 Here, the first line is written to stderr and simply states the number of sequences and the length of the alignment. This line can be sup- pressed using the --quiet option. The main output then consists of 7 lines, where the first two resemble the FASTA header with the ID as read from the input data set, followed by the consensus sequence in the second line. The third line consists of the consensus secondary struc- ture in dot-bracket notation followed by the averaged minimum free en- ergy in parenthesis. This energy is composed of two major contribu- tions, the actual free energies derived from the Nearest Neighbor model, and the covariance pseudo-energy term, which are both displayed after the equal sign. The fourth line shows the base pair propensity in pseudo dot-bracket notation followed by the ensemble free energy dG = -kT ln(Z) in square brackets. Similarly, the next two lines state the controid- and the MEA structure in dot-bracket notation, followed by their corresponding free energy contributions, the mean distance (d) to the ensemble as well as the maximum expected accuracy (MEA). Again, the free energies are split into Nearest Neighbor contribution and the co- variance pseudo-energy term. Furthermore, RNAalifold will produce three output files: ACA59_ss.ps, ACA59_dp.ps, and ACA59_ali.out that contain the secondary structure drawing, the base pair probability dot-plot, and a detailed table of base pair probabilities, respectively. THE ALIOUT FILE When computing base pair probabilities (--partfunc option), RNAalifold will produce a file with the suffix `ali.out`. This file contains the base pairing probabilities between different alignment columns together with some detailed statistics for the individual sequences within the alignment. The file is a simple text file with a two line header that states the number of sequences and length of the alignment. The first couple of lines of this file may look like: 3 sequence; length of alignment 84 alifold output 14 36 0 92.7% 0.212 CG:1 UA:2 13 37 0 92.7% 0.218 GU:1 AU:2 12 38 0 92.7% 0.231 CG:3 15 35 0 91.9% 0.239 UG:3 16 34 0 85.2% 0.434 UA:2 --:1 8 42 0 80.7% 0.526 AU:3 + 9 41 0 80.4% 0.542 CG:3 + 7 43 1 80.1% 0.541 CG:2 + Starting with the third row, there are at least six and at most 13 columns separated by whitespaces stating: (1) the i-position and (2) the j-position of a potential base pair (i, j), followed by (3) the number of counter examples, i.e. the number of sequences in the align- ment that can't form a canonical base pair with their respective se- quence positions. Next is (4) the base pair probabilitiy in percent, (5) a pseudo entropy measure S_ij = S_i + S_j - p_ij ln(p_ij), where S_i and S_j are the positional entropies for the two alignment columns i and j, and p_ij is the base pair probability. Finally, the last columns (6-12) state the number of particular base pairs for the indi- vidual sequences in the alignment. Here, we distinguish the base pairs "GC","CG","AU","UA","GU","UG", and the special case "--" that repre- sents gaps at both positions i and j. Finally, base pairs that are not part of the MFE structure are marked by an additional "+" sign in the last column. AUTHOR Ivo L Hofacker, Stephan Bernhart, 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. SEE ALSO The ALIDOT package http://www.tbi.univie.ac.at/RNA/Alidot/ RNAalifold 2.7.0 October 2024 RNAALIFOLD(1)
NAME | SYNOPSIS | DESCRIPTION | REFERENCES | EXAMPLES | THE ALIOUT FILE | AUTHOR | REPORTING BUGS | SEE ALSO
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