NAME

       trainphd - interpretation of DNA Sanger sequencing data

DESCRIPTION

       -h     (Help) This message

       -C <consensusfile>
              Specify the name of the FASTA file which contains the consensus sequence

       -V <vector>
              Specify the name of the FASTA file which contains the vector sequence

       -P <primer>
              Specify the name of the FASTA file which contains the primer sequence

       -S <site>
              Specify the name of the FASTA file which contains the restriction site sequence

       -M <match>
              Specify the match premium     (default is 10)

       -X <mismatch>
              Specify the mismatch penalty  (default is 20)

       -G <gap_penalty >
              Specify the gap initiation or extension penalty (default is 40)

       -r <repeat_fraction>
              Specify the repeat_fraction   (default is 0.85)

       -f <max_frac_of_err>
              Specify  the  allowable  fraction  of  errors within the best alignment region. Default is 0.1. If
              actual fraction of errors exceeds this vale, the fragment will be rejected (=not used in  training
              process)

       -a <min_portion_aligned> Instructs trainphd to ignore a read if less than
              the specified portion of its bases is aligned with reference sequence (default is 0)

       -l <min_read_length>
              Instructs  trainphd  to  ignore  a  read  of  length less than specified number of basepairs (0 by
              default)

       -o <output_file>
              Specify the name of the output file. By default, the output will be made to stdout

       -t <tab_dir>
              Instructs trainphd extract alternative base calls from TAB files stored in directory  tab_dir  and
              to output these calls, together with quality value for each alternative call

       -d <dir>
              Read the input PHD files from specified directory

       -j <projectfile>
              Specify  the  name of the projectfile which comprises two columns: the full path to the FASTA file
              which contains the consensus sequence, followed by the full path to the sample file

AUTHOR

       This manpage was written by Andreas Tille for the Debian distribution and can be used for any other usage
       of the program.