RNAsubopt - manual page for RNAsubopt 2.5.1
RNAsubopt [
OPTION]...
RNAsubopt 2.5.1
calculate suboptimal secondary structures of RNAs
Reads RNA sequences from stdin and (in the default
-e mode) calculates
all suboptimal secondary structures within a user defined energy range above
the minimum free energy (mfe). It prints the suboptimal structures in
dot-bracket notation followed by the energy in kcal/mol to stdout. Be careful,
the number of structures returned grows exponentially with both sequence
length and energy range.
Alternatively, when used with the
-p option, RNAsubopt produces Boltzmann
weighted samples of secondary structures.
-
-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
- Command line options which alter the general behavior of
this program
-
-v, --verbose
- Be verbose. (default=off)
- --noconv
- Do not automatically substitude nucleotide "T"
with "U". (default=off)
-
-i, --infile=<filename>
- Read a file instead of reading from stdin.
- The default behavior of RNAsubopt is to read input from
stdin. Using this parameter the user can specify an input file name where
data is read from.
-
-o, --outfile[=<filename>]
- Print output to file instead of stdout.
- This option may be used to write all output to output files
rather than printing to stdout. The default filename is
"RNAsubopt_output.sub" if no FASTA header precedes the input
sequences and the --auto-id feature is inactive. Otherwise, output
files with the scheme "prefix.sub" are generated, where the
"prefix" is taken from the sequence id. The user may specify a
single output file name for all data generated from the input by supplying
an optional string as argument to this parameter. In case a file with the
same filename already exists, any output of the program 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 "--filename-delim"
parameter)
- --auto-id
- Automatically generate an ID for each sequence.
(default=off)
- The default mode of RNAsubopt is to automatically determine
an ID from the input sequence data if the input file format allows to do
that. Sequence IDs are usually given in the FASTA header of input
sequences. If this flag is active, RNAsubopt ignores any IDs retrieved
from the input and automatically generates an ID for each sequence. This
ID consists of a prefix and an increasing number. This flag can also be
used to add a FASTA header to the output even if the input has none.
-
--id-prefix=prefix
- Prefix for automatically generated IDs (as used in output
file names). (default=`sequence')
- If this parameter is set, each sequences' FASTA id will be
prefixed with the provided string. FASTA ids then take the form
">prefix_xxxx" where xxxx is the sequence number. Note:
Setting this parameter implies --auto-id.
-
--id-delim=STRING
- 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
automatically 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]. This option implies
--auto-id.
-
--id-start=LONG
- Specify the first number in automatically generated
alignment IDs. (default=`1')
- When sequence IDs are automatically generated, they receive
an increasing number, usually starting with 1. Using this parameter, the
first number can be specified to the users requirements. Note: negative
numbers are not allowed. Note: Setting this parameter implies to ignore
any IDs retrieved from the input data, i.e. it activates the
--auto-id flag.
-
--filename-delim=STRING
- Change the delimiting character that is used for sanitized
filenames. (default=`ID-delimiter')
- This parameter can be used to change the delimiting
character used while sanitizing filenames, i.e. replacing invalid
characters. Note, that the default delimiter ALWAYS is the first character
of the "ID delimiter" as supplied through the --id-delim
option. If the delimiter is a whitespace character or empty, invalid
characters will be simply removed rather than substituted. Currently, we
regard the following characters as illegal for use in filenames: backslash
'\', slash '/', question mark '?', percent sign '%', asterisk '*', colon
':', pipe symbol '|', double quote '"', triangular brackets '<'
and '>'.
- --filename-full
- Use full FASTA header to create filenames.
(default=off)
- This parameter can be used to deactivate the default
behavior of limiting output filenames to the first word of the sequence
ID. Consider the following example: An input with FASTA header
">NM_0001 Homo Sapiens some gene" usually produces output
files with the prefix "NM_0001" without the additional data
available in the FASTA header, e.g. "NM_0001.sub". With this
flag set, no truncation of the output filenames is performed, i.e. output
filenames receive the full FASTA header data as prefixes. Note, however,
that invalid characters (such as whitespace) will be substituted by a
delimiting character or simply removed, (see also the parameter option
--filename-delim).
- 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>] Apply
structural constraint(s) during
- prediction. (default=`')
- The program first reads the sequence(s), then a dot-bracket
like string containing constraints on the structure. The following symbols
are recognized:
- '.' ... no constraint for this base
- 'x' ... the base is unpaired
- '<' ... the base pairs downstream, i.e. i is paired with
j > i
- '>' ... the base pairs upstream, i.e. i is paired with j
< i
- '|' ... the corresponding base has to be paired
- '()' ... base i pairs with base j
- Due to historic behavior of this program, all pairing
constraints will only
- disallow pairs that conflict with the constraint. This is
usually sufficient to enforce the constraint, but occasionally a base may
stay unpaired in spite of constraints. Use the --enforceConstraint
to really exclude unpaired states.
- --batch
- Use constraints for multiple sequences. (default=off)
- Usually, constraints provided from input file only apply to
a single input sequence. Therefore, RNAsubopt will stop its computation
and quit after the first input sequence was processed. Using this switch,
RNAsubopt processes multiple input sequences and applies the same provided
constraints to each of them.
- --canonicalBPonly
- Remove non-canonical base pairs from the structure
constraint. (default=off)
- --enforceConstraint
- Enforce base pairs given by round brackets ( ) in structure
constraint. (default=off)
-
--shape=<filename>
- Use SHAPE reactivity data in the folding recursions (does
not work for Zuker suboptimals).
-
--shapeMethod=STRING
- Specify the method how to convert SHAPE reactivity data to
pseudo energy contributions. (default=`D')
- The following methods can be used to convert SHAPE
reactivities into pseudo energy contributions.
- 'D': Convert by using a linear equation according to Deigan
et al 2009. The calculated pseudo energies will be applied for every
nucleotide involved in a stacked pair. This method is recognized 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. 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".
- 'Z': Convert SHAPE reactivities to pseudo energies
according to Zarringhalam et al 2012. SHAPE reactivities will be converted
to pairing probabilities by using linear mapping. Aberration from the
observed pairing probabilities will be penalized during the folding
recursion. The magnitude of the penalties can affected by adjusting the
factor beta (e.g. --shapeMethod="Zb0.8").
- 'W': Apply a given vector of perturbation energies to
unpaired nucleotides according to Washietl et al 2012. Perturbation
vectors can be calculated by using RNApvmin.
-
--shapeConversion=STRING
- Specify the method used to convert SHAPE reactivities to
pairing probabilities when using the SHAPE approach of Zarringhalam et al.
(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.
- 'C': Use a cutoff-approach to divide into paired and
unpaired nucleotides (e.g. "C0.25")
- 'S': Skip the normalizing step since the input data already
represents 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)
-
--commands=<filename>
- Read additional commands from file
- Commands include hard and soft constraints, but also
structure motifs in hairpin and interior loops that need to be treeted
differently. Furthermore, commands can be set for unstructured and
structured domains.
- Select the algorithms which should be applied to the given
RNA sequence.
-
-e, --deltaEnergy=range
- Compute suboptimal structures with energy in a certain
range of the optimum (kcal/mol).
- Default is calculation of mfe structure only.
-
--deltaEnergyPost=range
- Only print structures with energy within range of the mfe
after post reevaluation of energies.
- Useful in conjunction with -logML, -d1 or
-d3: while the -e option specifies the range before energies
are re-evaluated, this option specifies the maximum energy after
re-evaluation.
-
-s, --sorted
- Sort the suboptimal structures by energy and
lexicographical order. (default=off)
- Structures are first sorted by energy in ascending order.
Within groups of the same energy, structures are then sorted in ascending
in lexicographical order of their dot-bracket notation. See the
--en-only flag to deactivate this second step. Note that sorting is
done in memory, thus it can easily lead to exhaution of RAM! This is
especially true if the number of structures produced becomes large or the
RNA sequence is rather long. In such cases better use an external sort
method, such as UNIX "sort".
- --en-only
- Only sort structures by free energy. (default=off)
- In combination with --sorted, this flag deactivates
the second sorting criteria and sorts structures solely by their free
energy instead of additionally sorting by lexicographic order in each
energy band. This might save some time during the sorting process in
situations where lexicographic order is not required.
-
-p, --stochBT=number
- Randomly draw structures according to their probability in
the Boltzmann ensemble.
- Instead of producing all suboptimals in an energy range,
produce a random sample of suboptimal structures, drawn with probabilities
equal to their Boltzmann weights via stochastic backtracking in the
partition function. The -e and -p options are mutually
exclusive.
-
--stochBT_en=number
- Same as "--stochBT" but also print free energies
and probabilities of the backtraced structures.
-
-N, --nonRedundant
- Enable non-redundant sampling strategy. (default=off)
-
-S, --pfScale=DOUBLE
- Set scaling factor for Boltzmann factors to prevent
under/overflows.
- In the calculation of the pf use scale*mfe as an estimate
for the ensemble free energy (used to avoid overflows). The default is
1.07, useful values are 1.0 to 1.2. Occasionally needed for long
sequences. You can also recompile the program to use double precision (see
the README file).
-
-c, --circ
- Assume a circular (instead of linear) RNA molecule.
(default=off)
-
-D, --dos
- Compute density of states instead of secondary structures.
(default=off)
- This option enables the evaluation of the number of
secondary structures in certain energy bands around the MFE.
-
-z, --zuker
- Compute Zuker suboptimals instead of all suboptimal
structures within an energy band around the MFE. (default=off)
-
-g, --gquad
- Incoorporate G-Quadruplex formation. (default=off)
- No support of G-quadruplex prediction for stochastic
backtracking and Zuker-style suboptimals yet).
-
-T, --temp=DOUBLE
- Rescale energy parameters to a temperature in degrees
centigrade. (default=`37.0')
-
-4, --noTetra
- Do not include special tabulated stabilizing energies for
tri-, tetra- and hexaloop hairpins. (default=off)
- Mostly for testing.
-
-d, --dangles=INT
- Specify "dangling end" model 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 debugging). 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 interior 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. dangling 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
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)
- --logML
- Recompute energies of structures using a logarithmic energy
function for multi-loops before output. (default=off)
- This option does not effect structure generation, only the
energies that are printed out. Since logML lowers energies somewhat, some
structures may be missing.
-
-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. When passing the placeholder file name "DNA",
DNA parameters are loaded without the need to actually specify any input
file.
-
--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. RNAsubopt -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 ( -e 1) or AU (-e 2) pairs.
-
--betaScale=DOUBLE
- Set the scaling of the Boltzmann factors.
(default=`1.')
- The argument provided with this option enables to scale the
thermodynamic temperature used in the Boltzmann factors independently from
the temperature used to scale the individual energy contributions of the
loop types. The Boltzmann factors then become exp(
-dG/(kT*betaScale)) where k is the Boltzmann constant, dG the free
energy contribution of the state and T the absolute temperature.
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. Wuchty, W. Fontana, I. L. Hofacker and P. Schuster (1999), "Complete
Suboptimal Folding of RNA and the Stability of Secondary Structures",
Biopolymers: 49, pp 145-165
M. Zuker (1989), "On Finding All Suboptimal Foldings of an RNA
Molecule", Science 244.4900, pp 48-52
Y. Ding, and C.E. Lawrence (2003), "A statistical sampling algorithm for
RNA secondary structure prediction", Nucleic Acids Research 31.24, pp
7280-7301
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 modification
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
Ivo L Hofacker, Stefan Wuchty, Walter Fontana, Ronny Lorenz
If in doubt our program is right, nature is at fault. Comments should be sent to
[email protected].