trainphd1
Interpretation of dna sanger sequencing data
Overview
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-h -
(Help) This message
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-C <consensusfile> -
Specify the name of the FASTA file which contains the consensus sequence
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-V <vector> -
Specify the name of the FASTA file which contains the vector sequence
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-P <primer> -
Specify the name of the FASTA file which contains the primer sequence
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-S <site> -
Specify the name of the FASTA file which contains the restriction site sequence
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-M <match> -
Specify the match premium (default is 10)
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-X <mismatch> -
Specify the mismatch penalty (default is 20)
-G<gap_penalty >-
Specify the gap initiation or extension penalty (default is 40)
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-r <repeat_fraction> -
Specify the repeat_fraction (default is 0.85)
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-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)
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-l <min_read_length> -
Instructs trainphd to ignore a read of length less than specified number of basepairs (0 by default)
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-o <output_file> -
Specify the name of the output file. By default, the output will be made to stdout
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-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
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-d <dir> -
Read the input PHD files from specified directory
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-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
Releases
Unchanged in 4 releases since Debian 10 (Buster).