-c (--collapse)
Collapse sequences to haplotypes.
-cg (--collapseGaps)
Treat gaps as missing data when collapsing.
-cl (--collapseLimit) N
Connection limit (sequences differing at <= l sites will be collapsed) (default is l=0).
-cm (--collapseMissing)
Count missing data as differences when collapsing.
-i (--input) FILE
Input file.
-ia (--inputAutodetect)
Autodetect format (other input options are omitted).
-if (--inputFormat) VAL
Input format (ALN, FASTA, GDE, MEGA, MSF, NEXUS, PHYLIP or PIR).
-io (--inputOS) VAL
Input operating system (Linux, MacOS or Windows)
-ip (--inputProgram) VAL
Input program (Clustal, MAFFT, MUSCLE, PROBCONS or TCoffee).
-o (--output) FILE
Output file.
-of (--outputFormat) VAL
Output format (ALN, FASTA, GDE, MEGA, MSF, NEXUS, PHYLIP or PIR).
-ol (--outputLowerCase)
Lowe case output.
-om (--outputMatch)
Output match characters.
-on (--outputResidueNumbers)
Output residue numbers (only ALN format).
-oo (--outputOS) VAL
Output operating system (Linux, MacOS or Windows).
-op (--outputProgram) VAL
Output program (jModelTest, MrBayes, PAML, PAUP, PhyML, ProtTest, RAxML, TCS, CodABC, BioEdit,
MEGA, dnaSP, Se-Al, Mesquite, SplitsTree, Clustal , MAFFT, MUSCLE, PROBCONS, TCoffee, Gblocks,
SeaView, trimAl or GENERAL)
-os (--outputSequential)
Sequential output (only NEXUS and PHYLIP formats).
alter-sequence-alignment 1.3.3 September 2015 ALTER-SEQUENCE-ALIGNMENT(1)