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ednainvar | 
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Phylip dnainvar documentation.
% ednainvar Nucleic acid sequence invariants method Input (aligned) nucleotide sequence set: dnainvar.dat Phylip dnainvar program output file [ednainvar.outfile]:  | 
Go to the input files for this example
Go to the output files for this example
Nucleic acid sequence invariants method
Version: EMBOSS:6.6.0.0
   Standard (Mandatory) qualifiers:
  [-sequence]          seqset     File containing sequences
  [-outfile]           outfile    [ednainvar.outfile] Phylip dnainvar program
                                  output file
   Additional (Optional) qualifiers:
   -printdata          boolean    [N] Print out the data at start of run
   -progress           boolean    [N] Print indications of progress of run
   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
   -scircular1         boolean    Sequence is circular
   -squick1            boolean    Read id and sequence only
   -sformat1           string     Input sequence format
   -iquery1            string     Input query fields or ID list
   -ioffset1           integer    Input start position offset
   -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 first file to standard output
   -filter             boolean    Read first file from standard input, write
                                  first file to 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 and exit. 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 messages
   -version            boolean    Report version number and exit
 | 
| Qualifier | Type | Description | Allowed values | Default | 
|---|---|---|---|---|
| Standard (Mandatory) qualifiers | ||||
| [-sequence] (Parameter 1)  | 
seqset | File containing sequences | Readable set of sequences | Required | 
| [-outfile] (Parameter 2)  | 
outfile | Phylip dnainvar program output file | Output file | ednainvar.outfile | 
| Additional (Optional) qualifiers | ||||
| -printdata | boolean | Print out the data at start of run | Boolean value Yes/No | No | 
| -progress | boolean | Print indications of progress of run | Boolean value Yes/No | No | 
| Advanced (Unprompted) qualifiers | ||||
| (none) | ||||
| Associated qualifiers | ||||
| "-sequence" associated seqset qualifiers | ||||
|  -sbegin1 -sbegin_sequence  | 
integer | Start of each sequence to be used | Any integer value | 0 | 
|  -send1 -send_sequence  | 
integer | End of each sequence to be used | Any integer value | 0 | 
|  -sreverse1 -sreverse_sequence  | 
boolean | Reverse (if DNA) | Boolean value Yes/No | N | 
|  -sask1 -sask_sequence  | 
boolean | Ask for begin/end/reverse | Boolean value Yes/No | N | 
|  -snucleotide1 -snucleotide_sequence  | 
boolean | Sequence is nucleotide | Boolean value Yes/No | N | 
|  -sprotein1 -sprotein_sequence  | 
boolean | Sequence is protein | Boolean value Yes/No | N | 
|  -slower1 -slower_sequence  | 
boolean | Make lower case | Boolean value Yes/No | N | 
|  -supper1 -supper_sequence  | 
boolean | Make upper case | Boolean value Yes/No | N | 
|  -scircular1 -scircular_sequence  | 
boolean | Sequence is circular | Boolean value Yes/No | N | 
|  -squick1 -squick_sequence  | 
boolean | Read id and sequence only | Boolean value Yes/No | N | 
|  -sformat1 -sformat_sequence  | 
string | Input sequence format | Any string | |
|  -iquery1 -iquery_sequence  | 
string | Input query fields or ID list | Any string | |
|  -ioffset1 -ioffset_sequence  | 
integer | Input start position offset | Any integer value | 0 | 
|  -sdbname1 -sdbname_sequence  | 
string | Database name | Any string | |
|  -sid1 -sid_sequence  | 
string | Entryname | Any string | |
|  -ufo1 -ufo_sequence  | 
string | UFO features | Any string | |
|  -fformat1 -fformat_sequence  | 
string | Features format | Any string | |
|  -fopenfile1 -fopenfile_sequence  | 
string | Features file name | Any string | |
| "-outfile" associated outfile qualifiers | ||||
|  -odirectory2 -odirectory_outfile  | 
string | Output directory | Any string | |
| General qualifiers | ||||
| -auto | boolean | Turn off prompts | Boolean value Yes/No | N | 
| -stdout | boolean | Write first file to standard output | Boolean value Yes/No | N | 
| -filter | boolean | Read first file from standard input, write first file to standard output | Boolean value Yes/No | N | 
| -options | boolean | Prompt for standard and additional values | Boolean value Yes/No | N | 
| -debug | boolean | Write debug output to program.dbg | Boolean value Yes/No | N | 
| -verbose | boolean | Report some/full command line options | Boolean value Yes/No | Y | 
| -help | boolean | Report command line options and exit. More information on associated and general qualifiers can be found with -help -verbose | Boolean value Yes/No | N | 
| -warning | boolean | Report warnings | Boolean value Yes/No | Y | 
| -error | boolean | Report errors | Boolean value Yes/No | Y | 
| -fatal | boolean | Report fatal errors | Boolean value Yes/No | Y | 
| -die | boolean | Report dying program messages | Boolean value Yes/No | Y | 
| -version | boolean | Report version number and exit | Boolean value Yes/No | N | 
4 13 Alpha AACGTGGCCAAAT Beta AAGGTCGCCAAAC Gamma CATTTCGTCACAA Delta GGTATTTCGGCCT  | 
Nucleic acid sequence Invariants method, version 3.57c.650
   Pattern   Number of times
     AAAC         1
     AAAG         2
     AACC         1
     AACG         1
     CCCG         1
     CCTC         1
     CGTT         1
     GCCT         1
     GGGT         1
     GGTA         1
     TCAT         1
     TTTT         1
Symmetrized patterns (1, 2 = the two purines  and  3, 4 = the two pyrimidines
                  or  1, 2 = the two pyrimidines  and  3, 4 = the two purines)
     1111         1
     1112         2
     1113         3
     1121         1
     1132         2
     1133         1
     1231         1
     1322         1
     1334         1
Tree topologies (unrooted): 
    I:  ((Alpha,Beta),(Gamma,Delta))
   II:  ((Alpha,Gamma),(Beta,Delta))
  III:  ((Alpha,Delta),(Beta,Gamma))
Lake's linear invariants
 (these are expected to be zero for the two incorrect tree topologies.
  This is tested by testing the equality of the two parts
  of each expression using a one-sided exact binomial test.
  The null hypothesis is that the first part is no larger than the second.)
 Tree                             Exact test P value    Significant?
   I      1    -     0   =     1       0.5000               no
   II     0    -     0   =     0       1.0000               no
  [Part of this file has been deleted for brevity]
different purine:pyrimidine ratios from 1:1.
  Tree I:
   Contingency Table
      2     8
      1     2
   Quadratic invariant =             4.0
   Chi-square =    0.23111 (not significant)
  Tree II:
   Contingency Table
      1     5
      1     6
   Quadratic invariant =            -1.0
   Chi-square =    0.01407 (not significant)
  Tree III:
   Contingency Table
      1     2
      6     4
   Quadratic invariant =             8.0
   Chi-square =    0.66032 (not significant)
Cavender's quadratic invariants (type K) using purines vs. pyrimidines
 (these are expected to be zero for the correct tree topology)
They will be misled if there are substantially
different evolutionary rate between sites, or
different purine:pyrimidine ratios from 1:1.
No statistical test is done on them here.
  Tree I:              -9.0
  Tree II:              4.0
  Tree III:             5.0
 | 
| Program name | Description | 
|---|---|
| distmat | Create a distance matrix from a multiple sequence alignment | 
| ednacomp | DNA compatibility algorithm | 
| ednadist | Nucleic acid sequence distance matrix program | 
| ednaml | Phylogenies from nucleic acid maximum likelihood | 
| ednamlk | Phylogenies from nucleic acid maximum likelihood with clock | 
| ednapars | DNA parsimony algorithm | 
| ednapenny | Penny algorithm for DNA | 
| eprotdist | Protein distance algorithm | 
| eprotpars | Protein parsimony algorithm | 
| erestml | Restriction site maximum likelihood method | 
| eseqboot | Bootstrapped sequences algorithm | 
| fdiscboot | Bootstrapped discrete sites algorithm | 
| fdnacomp | DNA compatibility algorithm | 
| fdnadist | Nucleic acid sequence distance matrix program | 
| fdnainvar | Nucleic acid sequence invariants method | 
| fdnaml | Estimate nucleotide phylogeny by maximum likelihood | 
| fdnamlk | Estimates nucleotide phylogeny by maximum likelihood | 
| fdnamove | Interactive DNA parsimony | 
| fdnapars | DNA parsimony algorithm | 
| fdnapenny | Penny algorithm for DNA | 
| fdolmove | Interactive Dollo or polymorphism parsimony | 
| ffreqboot | Bootstrapped genetic frequencies algorithm | 
| fproml | Protein phylogeny by maximum likelihood | 
| fpromlk | Protein phylogeny by maximum likelihood | 
| fprotdist | Protein distance algorithm | 
| fprotpars | Protein parsimony algorithm | 
| frestboot | Bootstrapped restriction sites algorithm | 
| frestdist | Calculate distance matrix from restriction sites or fragments | 
| frestml | Restriction site maximum likelihood method | 
| fseqboot | Bootstrapped sequences algorithm | 
| fseqbootall | Bootstrapped sequences algorithm | 
This application was modified for inclusion in EMBOSS by Ian Longden (il@sanger.ac.uk) Informatics Division, The Sanger Centre, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.
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