Open kinerett opened 5 years ago
Do you have BLAT installed on your system?
No i didnt... i understod it latter... i instaled blat but had a problem with the huge memory missing error... do you have a code to use with the other aligning methods you mentioned? I saw they can be installed in r through bioconductor... ( im not a programer if its not clear 😊 just a desparet genetics student) thank you very much!
בתאריך יום שבת, 29 בדצמבר 2018, מאת Ge Tan notifications@github.com:
Do you have BLAT installed on your system?
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Kineret Taler Dr Adi Inbal's lab Department of Medical Neurobiology Institute for Medical Research – Israel-Canada The Hebrew University of Jerusalem Jerusalem 9112002, Israel Kineret.Taler@mail.huji.ac.il 0546356947
What's the specs of your machine? The example data should only needs small amount of memory. Other aligning methods are not implemented yet.
Dear Author, I am also facing the same issue.May I know if there is any fix for this error. I have installed BLAST and working on server with decent configuration. Although same function is running when just executed like: lavToPsl, axtChain, chainMergeSort, chainPreNet, chainNet, netSyntenic, netToAxt, axtSort
You installed BLAST
or BLAT
?
Typo error.. :D I installed both BLAT and ucsc-BLAT via anaconda.
It's hard for me to tell what exactly happened. When you run BLAT step in R, it simply calles the external BLAT program. Try to run the exact command on a shell and see what the error is. The exact commmand is shown as message in R.
In shell the command runs smoothly. I did able to get chain and net files but with little tweaks but still not able to figure out this R error.
Probably the BLAT installed by Anaconda is searchable in your R environment. Try
system("blat")
If it gives you the error of "sh: blat: command not found", you can use R package reticulate
to load your conda environment.
Hi @ge11232002 Thank you so much for providing such great software! But when I run it, there are some problems.
……
> lavs <- list.files(path="/data/CNEr/mm10vsgg6", pattern="\\.lav$")
> system("blat")
blat - Standalone BLAT v. 35 fast sequence search command line tool
usage:
blat database query [-ooc=11.ooc] output.psl
where:
database and query are each either a .fa , .nib or .2bit file,
or a list these files one file name per line.
……
> psls <- lavToPsl(lavs, removeLav=FALSE, binary="lavToPsl")
Run lavToPsl...
sh: lavToPsl: command not found
Warning message:
In system2(command = binary, args = arguments) : error in running command
The prompt says there is no such command. I have installed BLAT as discussed above, and also used system("blat"). My BLAT is installed with conda.What do I need to do next? And I want to know how to load the conda environment with R package reticulate.
Looking forward to your reply! Best wishes! DC
Hi,everyone
Sorry, I found that the error was caused by not installing UCSC Kent tools. I've tried to run the whole process, but I've found a puzzlement called "The scanning window size must be equal or larger than identity!" If so, then how to identify CNEs with 70% identity over 30bp.
Best wishes! DC
please help... i used the original files that come with the code, but when i use cneFinalListDanRer10Hg38 <- lapply(cneMergedListDanRer10Hg38, blatCNE)
it returns: Error in my.system(cmd) : res == 0 is not TRUE
why is that? how can i solve this? tnx