Provided by: emboss_6.6.0-1_amd64
NAME
megamerger - Merge two large overlapping DNA sequences
SYNOPSIS
megamerger -asequence sequence -bsequence sequence -wordsize integer [-prefer boolean] -outseq seqout -outfile outfile megamerger -help
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).
OPTIONS
Input section -asequence sequence -bsequence sequence Required section -wordsize integer Default value: 20 Additional section -prefer boolean 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 Output section -outseq seqout -outfile outfile
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).
SEE ALSO
megamerger is fully documented via the tfm(1) system.
AUTHOR
Debian Med Packaging Team <debian-med-packaging@lists.alioth.debian.org> Wrote the script used to autogenerate this manual page.
COPYRIGHT
This manual page was autogenerated from an Ajax Control Definition of the EMBOSS package. It can be redistributed under the same terms as EMBOSS itself.