ednamlk |
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% ednamlk -categories -catnum 2 -catvals "1.0 3.2" -catprob "0.4 0.6" -lambda 1.5 Phylogenies from nucleic acid maximum likelihood with clock Input (aligned) nucleotide sequence set: dnaml.dat Search for best tree [Y]: Global rearrangements [N]: Randomize input order of species [N]: Use empirical base frequencies [Y]: Use Default Mean block length of sites [N]: Phylip dnamlk program output file [ednamlk.outfile]: Create a tree file [Y]: Phylip tree output file [ednamlk.treefile]: |
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Phylogenies from nucleic acid maximum likelihood with clock Version: EMBOSS:6.6.0.0 Standard (Mandatory) qualifiers (* if not always prompted): [-sequence] seqset File containing a sequence alignment -[no]besttree toggle [Y] Search for best tree * -lengths boolean [N] Use lengths from user trees * -global boolean [N] Global rearrangements * -random toggle [N] Randomize input order of species * -randseed integer [3] Random number seed (must be odd) (Any integer value) * -randtimes integer [3] How many times to randomise (Any integer value) -[no]basefrequency toggle [Y] Use empirical base frequencies * -freqa float [0.25] Frequency for A (Number from 0.000 to 1.000) * -freqc float [0.25] Frequency for C (Number from 0.000 to 1.000) * -freqg float [0.25] Frequency for G (Number from 0.000 to 1.000) * -freqt float [0.25] Frequency for T/U (Number from 0.000 to 1.000) -categories toggle [N] More than one category of substitution rates * -catnum integer [2] Number of categories of substitution rates (Integer from 2 to 9) * -catvals string Space separated category values (Any string) * -catprob string Space separated probability values (Any string) * -uselambda toggle [N] Use Default Mean block length of sites * -lambda float [1.0] Mean block length of sites having the same rate (greater than 1) (Number 1.000 or more) [-outfile] outfile [ednamlk.outfile] Phylip dnamlk program output file [-[no]trout] toggle [Y] Create a tree file * -treefile outfile [ednamlk.treefile] Phylip tree output file Additional (Optional) qualifiers: -ttratio float [2.0] Transition/transversion ratio (Any numeric value) -printdata boolean [N] Print out the data at start of run -progress boolean [N] Print indications of progress of run -[no]drawtree boolean [Y] Draw tree 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 "-treefile" associated qualifiers -odirectory 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 a sequence alignment | Readable set of sequences | Required |
-[no]besttree | toggle | Search for best tree | Toggle value Yes/No | Yes |
-lengths | boolean | Use lengths from user trees | Boolean value Yes/No | No |
-global | boolean | Global rearrangements | Boolean value Yes/No | No |
-random | toggle | Randomize input order of species | Toggle value Yes/No | No |
-randseed | integer | Random number seed (must be odd) | Any integer value | 3 |
-randtimes | integer | How many times to randomise | Any integer value | 3 |
-[no]basefrequency | toggle | Use empirical base frequencies | Toggle value Yes/No | Yes |
-freqa | float | Frequency for A | Number from 0.000 to 1.000 | 0.25 |
-freqc | float | Frequency for C | Number from 0.000 to 1.000 | 0.25 |
-freqg | float | Frequency for G | Number from 0.000 to 1.000 | 0.25 |
-freqt | float | Frequency for T/U | Number from 0.000 to 1.000 | 0.25 |
-categories | toggle | More than one category of substitution rates | Toggle value Yes/No | No |
-catnum | integer | Number of categories of substitution rates | Integer from 2 to 9 | 2 |
-catvals | string | Space separated category values | Any string | |
-catprob | string | Space separated probability values | Any string | |
-uselambda | toggle | Use Default Mean block length of sites | Toggle value Yes/No | No |
-lambda | float | Mean block length of sites having the same rate (greater than 1) | Number 1.000 or more | 1.0 |
[-outfile] (Parameter 2) |
outfile | Phylip dnamlk program output file | Output file | ednamlk.outfile |
[-[no]trout] (Parameter 3) |
toggle | Create a tree file | Toggle value Yes/No | Yes |
-treefile | outfile | Phylip tree output file | Output file | ednamlk.treefile |
Additional (Optional) qualifiers | ||||
-ttratio | float | Transition/transversion ratio | Any numeric value | 2.0 |
-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 |
-[no]drawtree | boolean | Draw tree | Boolean value Yes/No | Yes |
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 | |
"-treefile" associated outfile qualifiers | ||||
-odirectory | 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 |
5 13 Alpha AACGTGGCCAAAT Beta AAGGTCGCCAAAC Gamma CATTTCGTCACAA Delta GGTATTTCGGCCT Epsilon GGGATCTCGGCCC |
Nucleic acid sequence Maximum Likelihood method with molecular clock, version 3.57c.650 Site category Rate of change Probability 1 1.000 0.400 2 3.200 0.600 Expected length of a patch of sites having the same rate = 1.500 Empirical Base Frequencies: A 0.24615 C 0.29231 G 0.24615 T(U) 0.21538 Transition/transversion ratio = 2.000000 (Transition/transversion parameter = 1.523077) +--Delta +--------------------------------------------------------4 ! +--Epsilon --3 ! +-------------Gamma +---------------------------------------------2 ! +--Alpha +----------1 +--Beta Ln Likelihood = -72.40499 Ancestor Node Node Time Length -------- ---- ---- ---- ------ root 3 3 4 3.40036 3.40036 4 Delta 3.55871 0.15834 4 Epsilon 3.55871 0.15834 3 2 2.75249 2.75249 2 Gamma 3.55871 0.80621 2 1 3.38652 0.63403 1 Alpha 3.55871 0.17218 1 Beta 3.55871 0.17218 Combination of categories that contributes the most to the likelihood: 2222221111 112 |
((Delta:0.15834,Epsilon:0.15834):3.40036,(Gamma:0.80621, (Alpha:0.17218,Beta:0.17218):0.63403):2.75249); |
Program name | Description |
---|---|
distmat | Create a distance matrix from a multiple sequence alignment |
ednacomp | DNA compatibility algorithm |
ednadist | Nucleic acid sequence distance matrix program |
ednainvar | Nucleic acid sequence invariants method |
ednaml | Phylogenies from nucleic acid maximum likelihood |
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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