NAME

SYNOPSIS

DESCRIPTION

The alignment file must be in Stockholm or SELEX format, and must contain consensus secondary structure annotation. cmbuild uses the consensus structure to determine the architecture of the CM.

<msafile> may be '-' (dash), which means reading this input from stdin rather than a file. To use '-', you must also specify the alignment file format with --informat <s>, as in --informat stockholm (because of a current limitation in our implementation, MSA file formats cannot be autodetected in a nonrewindable input stream.)

<cmfile_out> may not be '-' (stdout), because sending the CM file to stdout would conflict with the other text output of the program.

In addition to writing CM(s) to <cmfile_out>, cmbuild also outputs a single line for each model created to stdout. Each line has the following fields: "aln": the index of the alignment used to build the CM; "idx": the index of the CM in the <cmfile_out>; "name": the name of the CM; "nseq": the number of sequences in the alignment used to build the CM; "eff_nseq": the effective number of sequences used to build the model; "alen": the length of the alignment used to build the CM; "clen": the number of columns from the alignment defined as consensus (match) columns; "bps": the number of basepairs in the CM; "bifs": the number of bifurcations in the CM; "rel entropy: CM": the total relative entropy of the model divided by the number of consensus columns; "rel entropy: HMM": the total relative entropy of the model ignoring secondary structure divided by the number of consensus columns. "description": description of the model/alignment.

OPTIONS

-h

Help; print a brief reminder of command line usage and available options.

-n <s>

Name the new CM <s>. The default is to use the name of the alignment (if one is present in the <msafile>), or, failing that, the name of the <msafile>. If <msafile> contains more than one alignment, -n doesn't work, and every alignment must have a name annotated in the <msafile> (as in Stockholm #=GF ID annotation).

-F

Allow <cmfile_out> to be overwritten. Without this option, if <cmfile_out> already exists, cmbuild exits with an error.

-o <f>

Direct the summary output to file <f>, rather than to stdout.

-O <f>

After each model is constructed, resave annotated source alignments to a file <f> in Stockholm format. Sequences are annoted with what relative sequence weights were assigned. The alignments are also annotated with a reference annotation line indicating which columns were assigned as consensus. If the source alignment had reference annotation ("#=GC RF") it will be replaced with the consensus residue of the model for consensus columns and '.' for insert columns, unless the --hand option was used for specifying consensus positions, in which case it will be unchanged.

--devhelp Print help, as with -h , but also include expert options that are not displayed with -h . These expert options are not expected to be relevant for the vast majority of users and so are not described in the manual page. The only resources for understanding what they actually do are the brief one-line descriptions output when --devhelp is enabled, and the source code.

OPTIONS CONTROLLING MODEL CONSTRUCTION

--fast

Define consensus columns automatically as those that have a fraction >= symfrac of residues as opposed to gaps. (See below for the --symfrac option.) This is the default.

--hand

Use reference coordinate annotation (#=GC RF line, in Stockholm) to determine which columns are consensus, and which are inserts. Any non-gap character indicates a consensus column. (For example, mark consensus columns with "x", and insert columns with ".".) This option was called --rf in previous versions of Infernal (0.1 through 1.0.2).

--symfrac <x>

Define the residue fraction threshold necessary to define a consensus column when not using --hand. The default is 0.5. The symbol fraction in each column is calculated after taking relative sequence weighting into account. Setting this to 0.0 means that every alignment column will be assigned as consensus, which may be useful in some cases. Setting it to 1.0 means that only columns that include 0 gaps will be assigned as consensus. This option replaces the --gapthresh <y> option from previous versions of Infernal (0.1 through 1.0.2), with <x> equal to (1.0 - <y>). For example to reproduce behavior for a command of cmbuild --gapthresh 0.8 in a previous version, use cmbuild --symfrac 0.2 with this version.

--noss

Ignore the secondary structure annotation, if any, in <msafile> and build a CM with zero basepairs. This model will be similar to a profile HMM and the cmsearch and cmscan programs will use HMM algorithms which are faster than CM ones for this model. Additionally, a zero basepair model need not be calibrated with cmcalibrate prior to running cmsearch with it. The --noss option must be used if there is no secondary structure annotation in <msafile>.

--rsearch <f>

Parameterize emission scores a la RSEARCH, using the RIBOSUM matrix in file <f>. With --rsearch enabled, all alignments in <msafile> must contain exactly one sequence or the --call option must also be enabled. All positions in each sequence will be considered consensus "columns". Actually, the emission scores for these models will not be identical to RIBOSUM scores due of differences in the modelling strategy between Infernal and RSEARCH, but they will be as similar as possible. RIBOSUM matrix files are included with Infernal in the "matrices/" subdirectory of the top-level "infernal-xxx" directory. RIBOSUM matrices are substitution score matrices trained specifically for structural RNAs with separate single stranded residue and base pair substitution scores. For more information see the RSEARCH publication (Klein and Eddy, BMC Bioinformatics 4:44, 2003).

OTHER MODEL CONSTRUCTION OPTIONS

--null <f>

Read a null model from <f>. The null model defines the probability of each RNA nucleotide in background sequence, the default is to use 0.25 for each nucleotide. The format of null files is specified in the user guide.

--prior <f>

Read a Dirichlet prior from <f>, replacing the default mixture Dirichlet. The format of prior files is specified in the user guide.

Use --devhelp to see additional, otherwise undocumented, model construction options.

OPTIONS CONTROLLING RELATIVE WEIGHTS

--wpb

Use the Henikoff position-based sequence weighting scheme [Henikoff and Henikoff, J. Mol. Biol. 243:574, 1994]. This is the default.

--wgsc

Use the Gerstein/Sonnhammer/Chothia weighting algorithm [Gerstein et al, J. Mol. Biol. 235:1067, 1994].

--wnone

Turn sequence weighting off; e.g. explicitly set all sequence weights to 1.0.

--wgiven

Use sequence weights as given in annotation in the input alignment file. If no weights were given, assume they are all 1.0. The default is to determine new sequence weights by the Gerstein/Sonnhammer/Chothia algorithm, ignoring any annotated weights.

--wblosum

Use the BLOSUM filtering algorithm to weight the sequences, instead of the default GSC weighting. Cluster the sequences at a given percentage identity (see --wid); assign each cluster a total weight of 1.0, distributed equally amongst the members of that cluster.

--wid <x>

Controls the behavior of the --wblosum weighting option by setting the percent identity for clustering the alignment to <x>.

OPTIONS CONTROLLING EFFECTIVE SEQUENCE NUMBER

--eent

Use the entropy weighting strategy to determine the effective sequence number that gives a target mean match state relative entropy. This option is the default, and can be turned off with --enone. The default target mean match state relative entropy is 0.59 bits for models with at least 1 basepair and 0.38 bits for models with zero basepairs, but can be changed with --ere. The default of 0.59 or 0.38 bits is automatically changed if the total relative entropy of the model (summed match state relative entropy) is less than a cutoff, which is controlled by the --esigma option. If you really want to play with that option, consult the source code. Additionally, the effective sequence number cannot be larger than the number of sequences in the alignment, although this can be overridden to set the maximum possible effective sequence number with the --emaxseq option.

--enone

Turn off the entropy weighting strategy. The effective sequence number is just the number of sequences in the alignment.

--ere <x>

Set the target mean match state relative entropy as <x>. By default the target relative entropy per match position is 0.59 bits for models with at least 1 basepair and 0.38 for models with zero basepairs.

--eminseq <x>

Define the minimum allowed effective sequence number as <x>.

--emaxseq <x>

Define the maximum allowed effective sequence number as <x>. This number can be larger than the number of sequences in the alignment.

--ehmmre <x>

Set the target HMM mean match state relative entropy as <x>. Entropy for basepairing match states is calculated using marginalized basepair emission probabilities.

--eset <x>

Set the effective sequence number for entropy weighting as <x>.

OPTIONS CONTROLLING FILTER P7 HMM CONSTRUCTION

--p7ere <x>

Set the target mean match state relative entropy for the filter p7 HMM as <x>. By default the target relative entropy per match position is 0.38 bits.

--p7ml

Use a maximum likelihood p7 HMM built from the CM as the filter HMM. This HMM will be as similar as possible to the CM (while necessarily ignorant of secondary structure).

Use --devhelp to see additional, otherwise undocumented, filter HMM construction options.

OPTIONS CONTROLLING FILTER P7 HMM CALIBRATION

--EmN <n> Set the number of sampled sequences for local MSV filter HMM calibration to <n>. 200 by default.

--EvN <n> Set the number of sampled sequences for local Viterbi filter HMM calibration to <n>. 200 by default.

--ElfN <n> Set the number of sampled sequences for local Forward filter HMM calibration to <n>. 200 by default.

--EgfN <n> Set the number of sampled sequences for glocal Forward filter HMM calibration to <n>. 200 by default.

Use --devhelp to see additional, otherwise undocumented, filter HMM calibration options.

OPTIONS FOR REFINING THE INPUT ALIGNMENT

--refine <f>

Attempt to refine the alignment before building the CM using expectation-maximization (EM). A CM is first built from the initial alignment as usual. Then, the sequences in the alignment are realigned optimally (with the HMM banded CYK algorithm, optimal means optimal given the bands) to the CM, and a new CM is built from the resulting alignment. The sequences are then realigned to the new CM, and a new CM is built from that alignment. This is continued until convergence, specifically when the alignments for two successive iterations are not significantly different (the summed bit scores of all the sequences in the alignment changes less than 1% between two successive iterations). The final alignment (the alignment used to build the CM that gets written to <cmfile_out>) is written to <f>.

-l

With --refine, turn on the local alignment algorithm, which allows the alignment to span two or more subsequences if necessary (e.g. if the structures of the query model and target sequence are only partially shared), allowing certain large insertions and deletions in the structure to be penalized differently than normal indels. The default is to globally align the query model to the target sequences.

--gibbs

Modifies the behavior of --refine so Gibbs sampling is used instead of EM. The difference is that during the alignment stage the alignment is not necessarily optimal, instead an alignment (parsetree) for each sequences is sampled from the posterior distribution of alignments as determined by the Inside algorithm. Due to this sampling step --gibbs is non-deterministic, so different runs with the same alignment may yield different results. This is not true when --refine is used without the --gibbs option, in which case the final alignment and CM will always be the same. When --gibbs is enabled, the --seed <n> option can be used to seed the random number generator predictably, making the results reproducible. The goal of the --gibbs option is to help expert RNA alignment curators refine structural alignments by allowing them to observe alternative high scoring alignments.

--seed <n>

Seed the random number generator with <n>, an integer >= 0. This option can only be used in combination with --gibbs. If <n> is nonzero, stochastic sampling of alignments will be reproducible; the same command will give the same results. If <n> is 0, the random number generator is seeded arbitrarily, and stochastic samplings may vary from run to run of the same command. The default seed is 0.

--cyk

With --refine, align with the CYK algorithm. By default the optimal accuracy algorithm is used. There is more information on this in the cmalign manual page.

--notrunc

With --refine, turn off the the truncated alignment algorithm. There is more information on this in the cmalign manual page.

Use --devhelp to see additional, otherwise undocumented, alignment refinement options as well as other output file options and options for building multiple models for a single alignment.

SEE ALSO

For complete documentation, see the user guide that came with your Infernal distribution (Userguide.pdf); or see the Infernal web page ().

COPYRIGHT

Copyright (C) 2019 Howard Hughes Medical Institute.
Freely distributed under the BSD open source license.

For additional information on copyright and licensing, see the file called COPYRIGHT in your Infernal source distribution, or see the Infernal web page ().

AUTHOR

The Eddy/Rivas Laboratory
Janelia Farm Research Campus
19700 Helix Drive
Ashburn VA 20147 USA
http://eddylab.org