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151 lines
6.1 KiB
Plaintext
151 lines
6.1 KiB
Plaintext
trimAl/readAl v1.3. April 2011.
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[General]
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* Rewritten all file format parsers.
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* Added a new file format for compatibility with some programs.
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* phylip_paml
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* Extended some file format parsers.
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* fasta_m10
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* phylip_m10
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* phylip3.2_m10
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* phylip_paml_m10
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* A new control versions system is used: git.
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* Improved general system for tracking builds/revisions.
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* Refactored some portion of codes for improving its legibility and
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comprehension.
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[trimAl]
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* Improved HTML functionality. Now trimAl's summary shows which scores have been used
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for trimming the alignment along with scores scales bars.
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* Now it is possible to get an HTML trimAl's summary of previously no-allowed combinations
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of trimming methods. No-allowed combinations were related to the use of methods based on
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several alignments (consistency based scores) and methods based on a single alignment.
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* Some previously no allowed combinations between different trimming methods now are permitted.
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This is oriented to trim a given alignment using scores from several alignments along with
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scores computed from a single alignment.
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* When several alignment are given now it is possible to force the selection of one
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of them using a new option "-forceselect". This is useful to trim a specific alignment
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based on its consistency scores computed from a given set of alignments independently
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if that alignment is the most consistent among the set of those alignments.
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The selected alignment should not be present among alignments in the "-compareset"
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input file.
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* Former "-select" option has been converted into "-selectcols" for removing specific
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columns/range of columns.
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* Added the possibility, using "-selectseqs" option, to remove specific sequences/range
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of sequences from input alignment.
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* Using "-backtrans" option it is possible to trim an input protein alignment and then
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get a back-translated CDS alignment. Coding DNA sequences are mapped before trimming
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to protein sequences through sequences identifiers controlling stop codons, sequences
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lengths, etc, etc.
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* Using "-splitbystopcodon" option is possible, when a back-translation is done, to split
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input coding sequences for its stop codons (at positions multiple of 3).
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* Added a new option "-terminalonly" for removing only columns out of internal boundaries.
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Internal boundaries are defined as the first and last column in the alignment without
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gaps. The columns removal depends on the applied trimming method, that means, if there
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is not columns to be deleted out of internal boundaries, no-columns will be deleted.
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All columns in-between internal boundaries are kept independently of any trimming methods
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decision.
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* Added a new option "-clusters" for getting the most Nth representative sequences from
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input alignment. Representativeness is computed in terms of identity between each pair
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of sequences in the alignment. Then an algorithm is applied for constructing a set of
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clusters based on those identities values. The longest sequences is selected as the
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cluster representative for the final alignment.
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* Added a new option "-maxidentity" for getting sequences representatives at given identity
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threshold. This option allows to get the set of sequences/cluster representatives with an
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identity below to that threshold regarding to rest of the sequences. Sequences with identities
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scores higher than established threshold are clusters to the most similar sequence. The
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longest sequences are selected as cluster representatives for the final alignment.
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* Added a new option "-block" for keeping only columns blocks equal or higher to that size
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in the final alignment. This option is available for manual trimming methods and only for
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"gappyout" method among automated ones.
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* Changed identity scores matrix. Now it is shown "100.000" in the diagonal instead of
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"0". It makes more sense to have a score of 100 for each sequence against itself.
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* Changed options name for making clear their meaning.
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* scc => ssc - Similarity scores for columns in the alignment.
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* sct => sst - Cumulative distribution of similarities scores in the alignment.
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[readAl]
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* Added new option "-reverse" for getting the reverse of the input alignment.
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* Added new option "-onlyseqs" for getting only sequences from the alignment. This option
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destroys input alignment and returns a fasta file with unaligned sequences.
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* Added new option "-html" for getting an HTML file with alignments residues colored
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according to CLUSTAL scheme. This functionality is similar to SeaView/JalView visualization.
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* Changed option "-format". Now it informs about input file format and if sequences are
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aligned or not.
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* Updated option "-type". Now it informs more about nucleotides datatype: dna or rna.
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trimAl/readAl v1.2. April 2009.
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* Added the htmlout to track the trimAl's trimming.
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* Added the possibility to delete spurious sequences from the alignment.
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* Added the complementary and colnumbering options.
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* Added the manual selection of columns.
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* Added one new heuristic method to select the best automated trimming method.
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* Automated1
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* Added two new automated methods to work with gaps and similarity distribution.
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* Strict
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* Strictplus
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* Select only one automated method to work with gaps distribution.
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* Strict => Gappyout
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* Relaxed was deleted
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* Added the version/revisions system.
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* Improved the file format.
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* Added support for phylip 3.2
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* Added support for clustal
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* Added support for fasta
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* Added support for nexus
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* Added support for mega
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* Added support for nbrf/pir
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* Improved of statistics methods.
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* Improved the information of the available methods.
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* Added the identity statistics.
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* Improved of windows size methods.
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* Consistency windows size.
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* Improved the similarity-matrices handling.
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* Improved the support for DNA/RNA alignments.
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* Added readAl.
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* Fixed some bugs from the previous version.
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trimAl v1.1. February 2008.
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* Initial public version of trimAl.
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