///////////////////////////////////////////////////////////////////////////////////// // // // INDELible V1.03 control file - settings.txt // // // // How to include paup blocks, set seeds for the random number generator, // // change the output format for generated data, or how to print "reports" // // // ///////////////////////////////////////////////////////////////////////////////////// [TYPE] NUCLEOTIDE 2 // nucleotide simulation using algorithm from method 2 // // * If a command is not specified in the [SETTINGS] block then it will have the // default value shown below. The only exception to this is [randomseed] whose // value will be randomly chosen if not specified. // * If no [SETTINGS] block is specified all commands will have these default values. // * More information on each of the commands can be found at the end of the file. // [SETTINGS] [ancestralprint] FALSE // NEW, SAME or FALSE [output] PHYLIP // FASTA, NEXUS, PHYLIP or PHYLIPT [phylipextension] phy // any alpha-numeric string [nexusextension] nex // any alpha-numeric string [fastaextension] fas // any alpha-numeric string [randomseed] 1568746 // any integer [printrates] FALSE // FALSE or TRUE [insertaslowercase] TRUE // FALSE or TRUE [markdeletedinsertions] FALSE // FALSE or TRUE [printcodonsasaminoacids] FALSE // FALSE or TRUE [fileperrep] FALSE // FALSE or TRUE [MODEL] mymodel [submodel] JC [TREE] t1 ((A:0.1,B:0.1):0.1,(C:0.1,D:0.1):0.1); [PARTITIONS] Pname [t1 mymodel 1000] // tree t1, model mymodel, root length 1000 [EVOLVE] Pname 10 filename // 10 replicates generated from partition Pname /* [ancestralprint] * NEW will print ancestral sequences in a separate file to leaf sequences. * SAME prints ancestral sequences in the same file as the leaf sequences. * FALSE will not print any ancestral sequences. * It should be noted that if you used different guide trees for different partitions in a partitioned (multi-gene) analysis then only the root sequence will be printed in the SAME/NEW file specified in this command. [output] * Unaligned sequences are always output in FASTA format as e.g. filename.fas * This command sets the output type for the true alignment and prints it to a file named e.g. filename_TRUE.phy * FASTA, NEXUS, PHYLIP will print out sequences to file in either fasta, nexus, or phylip format respectively. * FASTA is used by NCBI and accepted by most sequence alignment programs. NEXUS is used by e.g. MacClade, Mesquite, ModelTest, MrBayes and PAUP*. PHYLIP is used by PHYLIP and PAML. * PHYLIPT gives PHYLIP format with filenames truncated to 10 characters. [phylipextension] * This command sets the file extension for true alignments in phylip format so they are e.g. filename.phy or whatever you choose them to be. [nexusextension] * This command sets the file extension for true alignments in nexus format so they are e.g. filename.nex or whatever you choose them to be. [fastaextension] * This command sets the file extension for fasta formatted output files so they are e.g. filename.fas or whatever you choose them to be. [randomseed] * This must be an integer value and is used to seed the random number generator. * Running simulations with the same random seed value (and the same control file) will produce identical datasets. [printrates] * TRUE will print out a detailed output file for each replicate of each block that lists what the site-classes or relative rates of substitution are. * FALSE will not print any rates information. * Follow these links for examples of the output for NUCLEOTIDE / AMINOACID simulations, or for CODON simulations. [markdeletedinsertions] * TRUE will output inserted bases/residues that have been subsequently been deleted as * rather than - for easy identification. * FALSE will leave them as -. [insertaslowercase] * TRUE will output inserted bases/residues as lower case letters for easy identification. * FALSE will output all bases/residues as upper case letters. [printcodonsasaminoacids] * TRUE will output codon datasets as amino-acids - how they are translated will depend on the genetic code specified in the model. * FALSE will print codons as nucleotide triplets. [fileperrep] * TRUE will output each replicate dataset in a separate file. Unaligned sequences will go in e.g. filename_1.fas, filename_2.fas, etc The true alignment will go in e.g. filename_TRUE_1.phy, filename_TRUE_2.phy, etc * FALSE will print all replicates in a single file. Unaligned sequences for each dataset will all go in e.g. filename.fas All the true alignments will go in e.g. filename_TRUE.phy * If a file called paupstart.txt (or paupend.txt) exists in the same directory as INDELible then it will be copied to the beginning (or end) of each file. * If a file called paupmiddle.txt exists in the same directory as INDELible then it will be copied to e.g. filename_TRUE.phy after each replicate datset. * These features are useful if you want to include PAUP or MrBayes blocks in your files. */
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