# HG changeset patch # User mrvollger # Date 1418448263 18000 # Node ID fb4591a06949b342b1ded29ac35849e82ad0e016 # Parent 25dcbaaeedab527ea8c9d9871734e7746376d395 Deleted selected files diff -r 25dcbaaeedab -r fb4591a06949 tool_dependencies.xml --- a/tool_dependencies.xml Fri Dec 12 22:51:00 2014 -0500 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,6 +0,0 @@ - - - - - - diff -r 25dcbaaeedab -r fb4591a06949 trtr.xml --- a/trtr.xml Fri Dec 12 22:51:00 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. - - -