Comments (3)
Thanks for the suggestion. Export of the recombination events is now supported in BED format. This option is activated using the argument "-chromosome_name" followed by the name of chromosome to use in the first column of the BED file, for example "-chromosome_name chr". If this argument is not used, the old recombination format is used for backward compatibility.
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Just noticed this after compiling and running on a dataset we had, BED files generally don't have header line. So bedtools complained about the header line. Can we remove it for BED output only? I can create another pull request if you want.
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Done (-:
Xavier
On 10 December 2015 at 17:39, alexjironkin [email protected] wrote:
Just noticed this after compiling and running on a dataset we had, BED
files generally don't have header line. So bedtools complained about the
header line. Can we remove it for BED output only? I can create another
pull request if you want.β
Reply to this email directly or view it on GitHub
#20 (comment)
.
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Related Issues (20)
- cfml_results.R error HOT 8
- xmfa format question; error: Segmentation fault (core dumped) HOT 1
- Question: xmfa format? HOT 7
- Recombination events total HOT 1
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- ERROR: incompatible with a bifurcating unrooted tree HOT 1
- node labels HOT 2
- ClonalFrameML for analyses of gene families HOT 2
- How to solve problems about "makefile", Thanks a lot! HOT 2
- input alignment for ClonalFrameML HOT 1
- segmentation fault (core dumped) HOT 1
- how to calculate the r/m value for subclade of a treeοΌ HOT 4
- R values for calculation of R*delta HOT 2
- Recombination filtered output vs importation_status.txt HOT 1
- why the r/m I calculated is so small using a subclone of subclone of klebsiella pneumoniae HOT 1
- Is it better to order genes by the reference genome for a xmfa file ??? HOT 2
- std::bad_alloc problem HOT 1
- Are there any detailed description of the output pdf from cfml_results.R? HOT 1
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