# HG changeset patch # User mrvollger # Date 1418424666 18000 # Node ID 6ddffb742bf1875486ab94cf6d59c89fe58153f9 # Parent 5c3ec718c26f4deb6c20ad5b79ff94f0c450128f Deleted selected files diff -r 5c3ec718c26f -r 6ddffb742bf1 myTools/trtr.xml --- a/myTools/trtr.xml Fri Dec 12 17:51:00 2014 -0500 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,43 +0,0 @@ - - - trtr - - - Trim Reads of Tandem Repeat in a fastq file. - - - trtr $input $max_repeat $aggressive > $output - - - - - - - - - - - - - - - - - - - - - - - - -This tool removes tandem repeats from ends of unaligned sequencing reads (leaving one copy). This prevents reads that don't span the repeated region from overlapping and leading to innaccurate SNPs calls. - -The maximimum repeat length is adjustable (use 1 to trim only homopolymers). - -The "aggressive" option should not be touched in general. Setting to 0 will prevent the program from trimming to exactly 1 copy of the repeat, instead leaving between 1 and 2 copies. - -This could also be a useful first step before assembly. More testing needs to be done. - - -