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megamerger - Merge two large overlapping DNA sequences

Author

DebianMedPackagingTeam <debian-med-packaging@lists.alioth.debian.org>
           Wrote the script used to autogenerate this manual page.

Bugs

       Bugs can be reported to the Debian Bug Tracking system (http://bugs.debian.org/emboss), or directly to
       the EMBOSS developers (http://sourceforge.net/tracker/?group_id=93650&atid=605031).

Description

megamerger is a command line program from EMBOSS (“the European Molecular Biology Open Software Suite”).
       It is part of the "Alignment:Consensus" command group(s).

Name

       megamerger - Merge two large overlapping DNA sequences

Options

Inputsection-asequencesequence-bsequencesequenceRequiredsection-wordsizeinteger
           Default value: 20

   Additionalsection-preferboolean
           When a mismatch between the two sequence is discovered, one or other of the two sequences must be
           used to create the merged sequence over this mismatch region. The default action is to create the
           merged sequence using the sequence where the mismatch is closest to that sequence's centre. If this
           option is used, then the first sequence (seqa) will always be used in preference to the other
           sequence when there is a mismatch. Default value: N

   Outputsection-outseqseqout-outfileoutfile

See Also

       megamerger is fully documented via the tfm(1) system.

Synopsis

megamerger-asequencesequence-bsequencesequence-wordsizeinteger [-preferboolean] -outseqseqout-outfileoutfilemegamerger-help

See Also