📄 cusp.txt
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cusp Function Create a codon usage tableDescription Reads one or more coding sequences (CDS sequence only) and calculates a codon frequency table. The output file can be used as a codon usage table in other applications.Usage Here is a sample session with cusp This example uses only one input sequence. The normal use would be to use a set of coding sequences as the input.% cusp -sbeg 135 -send 1292 Create a codon usage tableInput nucleotide sequence(s): tembl:paamirOutput file [paamir.cusp]: Go to the input files for this example Go to the output files for this exampleCommand line arguments Standard (Mandatory) qualifiers: [-sequence] seqall Nucleotide sequence(s) filename and optional format, or reference (input USA) [-outfile] outfile [*.cusp] Output file name Additional (Optional) qualifiers: (none) Advanced (Unprompted) qualifiers: (none) Associated qualifiers: "-sequence" associated qualifiers -sbegin1 integer Start of each sequence to be used -send1 integer End of each sequence to be used -sreverse1 boolean Reverse (if DNA) -sask1 boolean Ask for begin/end/reverse -snucleotide1 boolean Sequence is nucleotide -sprotein1 boolean Sequence is protein -slower1 boolean Make lower case -supper1 boolean Make upper case -sformat1 string Input sequence format -sdbname1 string Database name -sid1 string Entryname -ufo1 string UFO features -fformat1 string Features format -fopenfile1 string Features file name "-outfile" associated qualifiers -odirectory2 string Output directory General qualifiers: -auto boolean Turn off prompts -stdout boolean Write standard output -filter boolean Read standard input, write standard output -options boolean Prompt for standard and additional values -debug boolean Write debug output to program.dbg -verbose boolean Report some/full command line options -help boolean Report command line options. More information on associated and general qualifiers can be found with -help -verbose -warning boolean Report warnings -error boolean Report errors -fatal boolean Report fatal errors -die boolean Report dying program messagesInput file format Input files for usage example 'tembl:paamir' is a sequence entry in the example nucleic acid database 'tembl' Database entry: tembl:paamirID PAAMIR standard; DNA; PRO; 2167 BP.XXAC X13776; M43175;XXSV X13776.1XXDT 19-APR-1989 (Rel. 19, Created)DT 17-FEB-1997 (Rel. 50, Last updated, Version 22)XXDE Pseudomonas aeruginosa amiC and amiR gene for aliphatic amidase regulationXXKW aliphatic amidase regulator; amiC gene; amiR gene.XXOS Pseudomonas aeruginosaOC Bacteria; Proteobacteria; gamma subdivision; Pseudomonadaceae; Pseudomonas.XXRN [1]RP 1167-2167RA Rice P.M.;RT ;RL Submitted (16-DEC-1988) to the EMBL/GenBank/DDBJ databases.RL Rice P.M., EMBL, Postfach 10-2209, Meyerhofstrasse 1, 6900 Heidelberg, FRG.XXRN [2]RP 1167-2167RX MEDLINE; 89211409.RA Lowe N., Rice P.M., Drew R.E.;RT "Nucleotide sequence of the aliphatic amidase regulator gene of PseudomonasRT aeruginosa";RL FEBS Lett. 246:39-43(1989).XXRN [3]RP 1-1292RX MEDLINE; 91317707.RA Wilson S., Drew R.;RT "Cloning and DNA seqence of amiC, a new gene regulating expression of theRT Pseudomonas aeruginosa aliphatic amidase, and purification of the amiCRT product.";RL J. Bacteriol. 173:4914-4921(1991).XXRN [4]RP 1-2167RA Rice P.M.;RT ;RL Submitted (04-SEP-1991) to the EMBL/GenBank/DDBJ databases.RL Rice P.M., EMBL, Postfach 10-2209, Meyerhofstrasse 1, 6900 Heidelberg, FRG.XXDR SWISS-PROT; P10932; AMIR_PSEAE.DR SWISS-PROT; P27017; AMIC_PSEAE.DR SWISS-PROT; Q51417; AMIS_PSEAE. [Part of this file has been deleted for brevity]FT phenotype"FT /replace=""FT /gene="amiC"FT misc_feature 1FT /note="last base of an XhoI site"FT misc_feature 648..653FT /note="end of 658bp XhoI fragment, deletion in pSW3 causesFT constitutive expression of amiE"FT conflict 1281FT /replace="g"FT /citation=[3]XXSQ Sequence 2167 BP; 363 A; 712 C; 730 G; 362 T; 0 other; ggtaccgctg gccgagcatc tgctcgatca ccaccagccg ggcgacggga actgcacgat 60 ctacctggcg agcctggagc acgagcgggt tcgcttcgta cggcgctgag cgacagtcac 120 aggagaggaa acggatggga tcgcaccagg agcggccgct gatcggcctg ctgttctccg 180 aaaccggcgt caccgccgat atcgagcgct cgcacgcgta tggcgcattg ctcgcggtcg 240 agcaactgaa ccgcgagggc ggcgtcggcg gtcgcccgat cgaaacgctg tcccaggacc 300 ccggcggcga cccggaccgc tatcggctgt gcgccgagga cttcattcgc aaccgggggg 360 tacggttcct cgtgggctgc tacatgtcgc acacgcgcaa ggcggtgatg ccggtggtcg 420 agcgcgccga cgcgctgctc tgctacccga ccccctacga gggcttcgag tattcgccga 480 acatcgtcta cggcggtccg gcgccgaacc agaacagtgc gccgctggcg gcgtacctga 540 ttcgccacta cggcgagcgg gtggtgttca tcggctcgga ctacatctat ccgcgggaaa 600 gcaaccatgt gatgcgccac ctgtatcgcc agcacggcgg cacggtgctc gaggaaatct 660 acattccgct gtatccctcc gacgacgact tgcagcgcgc cgtcgagcgc atctaccagg 720 cgcgcgccga cgtggtcttc tccaccgtgg tgggcaccgg caccgccgag ctgtatcgcg 780 ccatcgcccg tcgctacggc gacggcaggc ggccgccgat cgccagcctg accaccagcg 840 aggcggaggt ggcgaagatg gagagtgacg tggcagaggg gcaggtggtg gtcgcgcctt 900 acttctccag catcgatacg cccgccagcc gggccttcgt ccaggcctgc catggtttct 960 tcccggagaa cgcgaccatc accgcctggg ccgaggcggc ctactggcag accttgttgc 1020 tcggccgcgc cgcgcaggcc gcaggcaact ggcgggtgga agacgtgcag cggcacctgt 1080 acgacatcga catcgacgcg ccacaggggc cggtccgggt ggagcgccag aacaaccaca 1140 gccgcctgtc ttcgcgcatc gcggaaatcg atgcgcgcgg cgtgttccag gtccgctggc 1200 agtcgcccga accgattcgc cccgaccctt atgtcgtcgt gcataacctc gacgactggt 1260 ccgccagcat gggcggggga ccgctcccat gagcgccaac tcgctgctcg gcagcctgcg 1320 cgagttgcag gtgctggtcc tcaacccgcc gggggaggtc agcgacgccc tggtcttgca 1380 gctgatccgc atcggttgtt cggtgcgcca gtgctggccg ccgccggaag ccttcgacgt 1440 gccggtggac gtggtcttca ccagcatttt ccagaatggc caccacgacg agatcgctgc 1500 gctgctcgcc gccgggactc cgcgcactac cctggtggcg ctggtggagt acgaaagccc 1560 cgcggtgctc tcgcagatca tcgagctgga gtgccacggc gtgatcaccc agccgctcga 1620 tgcccaccgg gtgctgcctg tgctggtatc ggcgcggcgc atcagcgagg aaatggcgaa 1680 gctgaagcag aagaccgagc agctccagga ccgcatcgcc ggccaggccc ggatcaacca 1740 ggccaaggtg ttgctgatgc agcgccatgg ctgggacgag cgcgaggcgc accagcacct 1800 gtcgcgggaa gcgatgaagc ggcgcgagcc gatcctgaag atcgctcagg agttgctggg 1860 aaacgagccg tccgcctgag cgatccgggc cgaccagaac aataacaaga ggggtatcgt 1920 catcatgctg ggactggttc tgctgtacgt tggcgcggtg ctgtttctca atgccgtctg 1980 gttgctgggc aagatcagcg gtcgggaggt ggcggtgatc aacttcctgg tcggcgtgct 2040 gagcgcctgc gtcgcgttct acctgatctt ttccgcagca gccgggcagg gctcgctgaa 2100 ggccggagcg ctgaccctgc tattcgcttt tacctatctg tgggtggccg ccaaccagtt 2160 cctcgag 2167//Output file format Output files for usage example File: paamir.cusp#CdsCount: 1#Coding GC 67.79%#1st letter GC 67.88%#2nd letter GC 46.89%#3rd letter GC 88.60%#Codon AA Fraction Frequency NumberGCA A 0.077 7.772 3GCC A 0.462 46.632 18GCG A 0.462 46.632 18GCT A 0.000 0.000 0TGC C 1.000 10.363 4TGT C 0.000 0.000 0GAC D 0.864 49.223 19GAT D 0.136 7.772 3GAA E 0.269 18.135 7GAG E 0.731 49.223 19TTC F 1.000 28.497 11TTT F 0.000 0.000 0GGA G 0.062 5.181 2GGC G 0.719 59.585 23GGG G 0.125 10.363 4GGT G 0.094 7.772 3CAC H 0.727 20.725 8CAT H 0.273 7.772 3ATA I 0.000 0.000 0ATC I 0.800 41.451 16ATT I 0.200 10.363 4AAA K 0.000 0.000 0AAG K 1.000 5.181 2CTA L 0.000 0.000 0CTC L 0.269 18.135 7CTG L 0.577 38.860 15CTT L 0.000 0.000 0TTA L 0.000 0.000 0TTG L 0.154 10.363 4ATG M 1.000 15.544 6AAC N 1.000 28.497 11AAT N 0.000 0.000 0CCA P 0.074 5.181 2CCC P 0.222 15.544 6CCG P 0.630 44.041 17CCT P 0.074 5.181 2CAA Q 0.062 2.591 1CAG Q 0.938 38.860 15AGA R 0.000 0.000 0AGG R 0.029 2.591 1CGA R 0.000 0.000 0CGC R 0.629 56.995 22CGG R 0.314 28.497 11CGT R 0.029 2.591 1AGC S 0.304 18.135 7AGT S 0.087 5.181 2TCA S 0.000 0.000 0TCC S 0.261 15.544 6TCG S 0.304 18.135 7TCT S 0.043 2.591 1ACA T 0.000 0.000 0ACC T 0.733 28.497 11ACG T 0.267 10.363 4ACT T 0.000 0.000 0GTA V 0.030 2.591 1GTC V 0.394 33.679 13GTG V 0.576 49.223 19GTT V 0.000 0.000 0TGG W 1.000 12.953 5TAC Y 0.619 33.679 13TAT Y 0.381 20.725 8TAA * 0.000 0.000 0TAG * 0.000 0.000 0TGA * 1.000 2.591 1 The example usage read in a single CDS from Pseudomonas aeruginosa which has a very high GC content ands a strong coding bias, as shown by the codons for Alanine where those ending with G or C are used almost exclusively. The 'Fract' column gives that proportion of usage of a given codon among its redundant set (i.e. the set of codons which code for this codon's amino acid). For example, the sum of the 6 codons representing serine will add up to 1.00. The /1000 column represents the number of codons, given the input sequence(s), there are per 1000 bases. This will be an extrapolation if the sequence is shorter than 1000 bases. If multiple sequences are input then the statistics are given for all of the sequences together, not individually.Data files cusp reads a codon usage file, but only as a template and does not use any of the data so any codon usage file from any species will give the same results. EMBOSS data files are distributed with the application and stored in the standard EMBOSS data directory, which is defined by the EMBOSS environment variable EMBOSS_DATA. To see the available EMBOSS data files, run:% embossdata -showall To fetch one of the data files (for example 'Exxx.dat') into your current directory for you to inspect or modify, run:% embossdata -fetch -file Exxx.dat Users can provide their own data files in their own directories. Project specific files can be put in the current directory, or for tidier directory listings in a subdirectory called ".embossdata". Files for all EMBOSS runs can be put in the user's home directory, or again in a subdirectory called ".embossdata". The directories are searched in the following order: * . (your current directory) * .embossdata (under your current directory) * ~/ (your home directory) * ~/.embossdataNotes None.References None.Warnings None.Diagnostic Error Messages None.Exit status Always exits with status 0.Known bugs None.See also Program name Description cai CAI codon adaptation index chips Codon usage statistics codcmp Codon usage table comparison syco Synonymous codon usage Gribskov statistic plotAuthor(s) Alan Bleasby (ajb
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