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]: |
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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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