# HG changeset patch # User mrvollger # Date 1418442311 18000 # Node ID b28b80eb4b78808e7c1d1bc7505a15af633d922f # Parent 08bbc7ba8f21a4a5d6b04d7ba7371266079702dc Deleted selected files diff -r 08bbc7ba8f21 -r b28b80eb4b78 tool_depensencies.xml --- a/tool_depensencies.xml Fri Dec 12 17:55:32 2014 -0500 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,6 +0,0 @@ - - - - - - diff -r 08bbc7ba8f21 -r b28b80eb4b78 trtr.xml --- a/trtr.xml Fri Dec 12 17:55:32 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. - - -