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author | Petar Petrov <petar.petrov@student.oulu.fi> | 2014-06-09 01:01:54 +0700 |
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committer | Willy Sudiarto Raharjo <willysr@slackbuilds.org> | 2014-06-12 06:51:45 +0700 |
commit | f8fb5e97dfa1dabbf7808f259e3bd9796f3e098c (patch) | |
tree | 4378038e032bf4899317c0808eea0e40d8152617 /academic/geneconv/README | |
parent | 9ae03e0d3cb2e36223b59c65ec3d61d972a873d8 (diff) |
academic/geneconv: Added (Statistical Tests).
Signed-off-by: Willy Sudiarto Raharjo <willysr@slackbuilds.org>
Diffstat (limited to 'academic/geneconv/README')
-rw-r--r-- | academic/geneconv/README | 27 |
1 files changed, 27 insertions, 0 deletions
diff --git a/academic/geneconv/README b/academic/geneconv/README new file mode 100644 index 0000000000000..885f156f08cbe --- /dev/null +++ b/academic/geneconv/README @@ -0,0 +1,27 @@ +GENECONV: Statistical Tests for Detecting Gene Conversion + +Gene conversion is any process that causes a segment of DNA to be +copied onto another segment of DNA, or else appears to act in this +way. The target segment can be on the same chromosome, on a different +chromosome, or in a different organism. Short-segment gene conversion +is an important force in evolution, and often takes place at a higher +frequency than does point mutation. + +Given an alignment of DNA or protein sequences, GENECONV finds the +most likely candidates for aligned gene conversion events between +pairs of sequences in the alignment. The program can also look for +gene conversion events from outside of the alignment. Candidate events +are ranked by multiple-comparison corrected P-values and listed to a +spreadsheet-like output file. + +IMPORTANT: +You may get a "Segmentation fault" when running the program; the +problem arises only when GENECONV writes to its log file (e.g. +myfile.nex.sum), as opposed to its main output file myfile.nex.frags; +the easiest workaround is to run GENECONV with the -nolog option: + +geneconv myfile.nex -nolog + +CITING: +For references and citation information, check the documentation +folder of the package. |