# HG changeset patch # User hyungrolee # Date 1402786842 14400 # Node ID 4ea2266383451202b2b4c47fee8fb287fe813e34 # Parent 803c7c39993e48f4459ca9790e000a2ddfbd0897 Deleted selected files diff -r 803c7c39993e -r 4ea226638345 mgescan.xml --- a/mgescan.xml Sat Jun 14 19:00:14 2014 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,101 +0,0 @@ - - - - - MGEScan - - - mgescan.sh $input '$input.name' 3 $output $program $clade $qvalue_en $qvalue_rt $ltr_gff3 $nonltr_gff3 - - - - - - - - - - - - - - program != "N" - - - program != "L" - - - program != "L" - - - program != "L" - - - program != "N" - - - program != "L" - - - - -Running the program -=================== - -To run MGEScan, select input genome data in From select box, and select program either LTR, nonLTR or both. - -Click 'Execute' button. - -If you like to have more options to run LTR or nonLTR progrma, use separated tools on the left panel. -In LTR > MGEScan-LTR, preprocessing by repeatmasker and setting other variables are available e.g. distance(bp) between LTRs. - -Output -============ -A. MGEScan_LTR: -Upon completion, MGEScan-LTR generates a file "ltr.out". This output file has information -about clusters and coordinates of LTR retrotransposons identified. Each cluster of LTR -retrotransposons starts with the head line of "[cluster_number]---------", followed by -the information of LTR retrotransposons in the cluster. The columns for LTR -retrotransposons are as follows. - -1. LTR_id: unique id of LTRs identified. It consist of two components, sequence file name and id in the file. For example, chr1_2 is the second LTR retrotransposon in the chr1 file. -2. start position of 5’ LTR. -3. end position of 5’ LTR. -4. start position of 3’ LTR. -5. end position of 3’ LTR. -6. strand: + or -. -7. length of 5’ LTR. -8. length of 3’ LTR. -9. length of the LTR retrotransposon. -10. TSD on the left side of the LTR retotransposons. -11. TSD on the right side of the LTR retrotransposons. -12. di(tri)nucleotide on the left side of 5’LTR -13. di(tri)nucleotide on the right side of 5’LTR -14. di(tri)nucleotide on the left side of 3’LTR -15. di(tri)nucleotide on the right side of 3’LTR - -B. MGEScan_nonLTR: - Upon completion, MGEScan-nonLTR generates the directory, "info" in the data directory you - specified. In this "info" directory, two sub-directories ("full" and "validation") are - generated. - - - The "full" directory is for storing sequences of elements. Each subdirectory in "full" - is the name of clade. In each directory of clade, the DNA sequences of nonLTRs identified - are listed. Each sequence is in fasta format. The header contains the position - information of TEs identified: - [genome_file_name]_[start position in the sequence] - - For example, >chr1_333 means that this element start at 333bp in the "chr1" file. - - - The "validation" directory is for storing Q values. In the files "en" and "rt", the first column corresponds to the element name and the last column Q value. - -License -============ -Copyright 2014 Mina Rho, Haixu Tang. -You may redistribute this software under the terms of the GNU General Public License. - - -