DOKK / manpages / debian 12 / tracetuner / train.1.en
TRAIN(1) User Commands TRAIN(1)

train - interpretation of DNA Sanger sequencing data

(Help) This message
Disable base recalling and just use the original called bases read from the input sample file
Disable adding bases to or deleting from the original called sequence. Only recall Ns
Disable adding bases to or deleting from the original called sequence. Only recall Ns and dye blobs
Similar to -recalln, but all bases, not only Ns will be recalled from original locations
Start base recalling from the ABI's edited bases
Call heterozygous bases
Call mixed bases
Override the default threshold ratio of heights of the lowest peak to the highest peak at a given position
(default is 0.85)
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)
Specify the name of the output file. By default, the output will be made to stdout
Specify the name of the FASTA file which contains the consensus sequence
Specify the name of the FASTA file which contains the vector sequence
Specify the name of the FASTA file which contains the primer sequence
Specify the name of the FASTA file which contains the restriction site sequence
Specify the match premium (default is 10)
Specify the mismatch penalty (default is 20)
Specify the gap initiation or extension penalty (default is 40)
Read the input sample files from specified directory
Specify the name of the projectfile which consists of two columns. Each line in this file contains the full path to the sample file to be processed and the full path to the FASTA file which contains the consensus sequence that should be used with this sample file

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

October 2018 train 3.0.6~beta