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Full Discussion: C command not found
Top Forums Shell Programming and Scripting C command not found Post 302916937 by Corona688 on Friday 12th of September 2014 02:59:52 PM
Old 09-12-2014
It builds here without those errors, running mfold gives me

Code:
./mfold: line 7: mfold_datdir: command not found
Usage is
mfold SEQ='file_name' with optional parameters:
    [ AUX='auxfile_name' ] [ RUN_TYPE=text (default) or html ]
    [ NA=RNA (default) or DNA ] [ LC=sequence type (default = linear) ]
    [ T=temperature (default = 37 deg C) ] [ P=percent (default = 5) ]
    [ NA_CONC=Na+ molar concentration (default = 1.0) ]
    [ MG_CONC=Mg++ molar concentration (default = 0.0) ]
    [ W=window parameter (default - set by sequence length) ]
    [ MAXBP=max base pair distance (default - no limit) ]
    [ MAX=maximum number of foldings to be computed (default 100) ]
    [ MAX_LP=maximum bulge/interior loop size (default 30) ]
    [ MAX_AS=maximum asymmetry of a bulge/interior loop (default 30) ]
    [ ANN=structure annotation type: none (default), p-num or ss-count ]
    [ MODE=structure display mode: auto (default), bases or lines ]
    [ LAB_FR=base numbering frequency ] [ ROT_ANG=structure rotation angle ]
    [ START=5' base # (default = 1)] [ STOP=3' base # (default = end) ]
    [ REUSE=NO/YES (default=NO) reuse existing .sav file ]

That first error is just because I didn't bother putting the folder I installed it into, into my PATH.

I don't know what's provoking those 'command not found' errors. Maybe check in config.log.
 

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RNAEFFECTIVE(1) 					      General Commands Manual						   RNAEFFECTIVE(1)

NAME
RNAeffective - calculation of effective numbers of orthologous miRNA targets SYNOPSIS
RNAeffective [-h] [-d frequency_file] [-f from,to] [-k sample_size] [-l mean,std] [-m max_target_length] [-n max_query_length] [-u iloop_upper_limit] [-v bloop_upper_limit] [-s] [-t target_file] [-q query_file] [query] DESCRIPTION
RNAeffective is a tool for determining the effective number of orthologous miRNA targets. This number can be used for the calculation of more accurate joint p-values in multi-species analyses. RNAeffective searches a set of target sequences with random miRNAs that can be given on the command line or otherwise generates random sequences according to given sample size, length distribution parameters and dinu- cleotide frequencies. The empirical distribution of joint p-values is compared to the p-values themselves, and the effective number of independent targets is the one that reduces the deviation between the two distributions. OPTIONS
-h Give a short summary of command line options. -d frequency_file Generate random sequences according to dinucleotide frequencies given in frequency_file. See example directory for example files. -f from,to Forces all structures to have a helix from position from to position to with respect to the query. The first base has position 1. -k sample_size Generate sample_size random sequences. Default value is 5000. -l mean,std Generate random sequences with a normal length distribution of mean mean and standard deviation std. Default values are 22 and 0, respectively. -m max_target_length The maximum allowed length of a target sequence. The default value is 2000. This option only has an effect if a target file is given with the -t option (see below). -n max_query_length The maximum allowed length of a query sequence. The default value is 30. This option only has an effect if a query file is given with the -q option (see below). -u iloop_upper_limit The maximally allowed number of unpaired nucleotides in either side of an internal loop. -v bloop_upper_limit The maximally allowed number of unpaired nucleotides in a bulge loop. -s Generate random sequences according to the dinucleotide distribution of given queries (either with the -q option or on command line. If no -q is given, the last argument to RNAeffective is taken as a query). See -q option. -q query_file Without the -s option, each of the query sequences in query_file is subject to hybridisation with each of the targets (which are from the target_file; see -t below). The sequences in the query_file have to be in FASTA format, ie. one line starting with a > and directly followed by a name, then one or more following lines with the sequence itself. Each individual sequence line must not have more than 1000 characters. With the -s option, the query (or query file) dinucleotide distribution is counted, and random sequences are generated according to this distribution. If no -q is given, random sequences are generated as described above (see -d option). -t target_file See -q option above. REFERENCES
The energy parameters are taken from: Mathews DH, Sabina J, Zuker M, Turner DH. "Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure" J Mol Biol., 288 (5), pp 911-940, 1999 VERSION
This man page documents version 2.0 of RNAeffective. AUTHORS
Marc Rehmsmeier, Peter Steffen, Matthias Hoechsmann. LIMITATIONS
Character dependent energy values are only defined for [acgtuACGTU]. All other characters lead to values of zero in these cases. SEE ALSO
RNAhybrid, RNAcalibrate RNAEFFECTIVE(1)
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