trf(1)
locate and display tandem repeats in DNA sequences
Description
TRF
NAME
trf - locate and display tandem repeats in DNA sequences
SYNOPSIS
trf (File|Match|Mismatch|Delta|PM|PI|Minscore|MaxPeriod) [options]
OPTIONS
Where: (all weights, penalties, and scores are positive)
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File |
sequences input file |
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Match |
matching weight |
Mismatch
mismatching penalty
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Delta |
indel penalty |
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PM |
match probability (whole number) |
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PI |
indel probability (whole number) |
Minscore
minimum alignment score to report
MaxPeriod
maximum period size to report
[options] = one or more of the following:
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-m |
masked sequence file |
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-f |
flanking sequence |
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-d |
data file |
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-h |
suppress html output |
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-r |
no redundancy elimination |
-l <n>
maximum TR length expected (in millions) (eg, -l 3 or -l=3 for 3 million) Human genome HG38 would need -l 6
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-ngs |
more compact .dat output on multisequence files, returns 0 on success. Output is printed to the screen, not a file. You may pipe input in with this option using - for file name. Short 50 flanks are appended to .dat output. |
SEE ALSO
See more information on the TRF Unix Help web page: https://tandem.bu.edu/trf/trf.unix.help.html
NOTE
Note the sequence file should be in FASTA format:
>Name of sequence aggaaacctgccatggcctcctggtgagctgtcctcatccactgctcgctgcctctccag atactctgacccatggatcccctgggtgcagccaagccacaatggccatggcgccgctgt actcccacccgccccaccctcctgatcctgctatggacatggcctttccacatccctgtg
AUTHOR
Copyright © 1999-2020 Gary Benson
This manpage was written by Andreas Tille for the Debian distribution and can be used for any other usage of the program.