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  • jaycee
    replied
    hi CNV boy, can you let me know why ssh -X works on yours? It's not working on mine. Thanks!

    Leave a comment:


  • clarissaboschi
    replied
    Bin size

    I know that there is information about the bin sizes in the supplemental material from CNVnator paper, and they recommend to test different sizes, and also higher the coverage, smaller the bin size.

    I tested 3 different bins: 100, 150 and 200, and I got very different number of CNVs.
    My coverage is about: 8-15X.

    I dont know which bin is better to use...
    Any suggestions??

    Leave a comment:


  • clarissaboschi
    replied
    I have solved my problem, I do not need to include the name of the fasta file for each chromosome....it worked!

    example
    HTML Code:
    cnvnator -root 1.root -genome /home/genomes/Ggallus.fa -chrom 1 -his 100
    Other comment I got much more deletions than duplications, is it the expected?

    Leave a comment:


  • clarissaboschi
    replied
    Dear members

    I am running CNVnator tool for chicken, but I am having some problems with step 2. I read many forums and also the manual and I did not get any solution for it.

    I ran the first step and it was ok. My command line was
    Code:
    cnvnator -root 1.root -genome /home/genomes/Ggallus.fa -tree /home/Sample_1/1sort.bam
    But in the second step I got the error message when I ran only for 1 chromosome (this fasta file file is in my current directory):
    Code:
    Can't determine length for 'chr1.fa'. No reference genome specified.
    I tried different command lines, and always the same error
    Code:
    cnvnator -root 1.root -genome /home/genomes/Ggallus.fa   -chrom  1 chr1.fa -his 100
    
    cnvnator -root 1.root -genome –d /home/genomes/Ggallus.fa  -chrom  1 chr1.fa -his 100
    
    cnvnator -root 1.root -genome /home/genomes/Ggallus.fa  -chrom  chr1 chr1.fa -his 100
    
    cnvnator -root 1.root -genome /home/genomes/Ggallus.fa  -chrom  chr1.fa -his 100

    Do you have any suggestion for it?

    Leave a comment:


  • SD2010Bioinfo
    replied
    hello CNVboy,

    I'm using Putty to log on our cluster. Could you tell me how to use ssh -X to visualising or genotyping the CNVnator result? Thanks

    Leave a comment:


  • bewlib
    replied
    I use ssh -X [email protected]…… ,but I can't see anything when I use
    [xug@pem610-006 src]$ ./cnvnator -root NA18507.root -view 100
    >chr12 11396601 11436500

    would you help me ??

    Leave a comment:


  • bewlib
    replied
    CNVnator

    Originally posted by gprakhar View Post
    Hello CNVboy,

    If you want to view anything other than text while using ssh, you will have to use the "-X" option.

    Regards,
    Prakhar Gaur

    Would you give me a detail description about hou to use ssh -X to view genotype ??

    Leave a comment:


  • jsbae
    replied
    Hello,

    I have two qestions to show output.root and -genotype command.
    1. After I sucessfully got a result by -call 100, I run -genotype. But I didn't show any result as following:
    (command -call) ./cnvnator -root my_output.root -chrom chr20 -call 100
    ... displayed calls result...
    (command -genotype) ./cnvnator -root my_output.root -chrom chr20 -genotype 100
    > (no result)

    Anyone know the reason? -view command also didn't give me any result.

    2. In my output.root, I wish to know copy number as 0x, 1x. How can I show it, please?

    Thanks your kind reply!!

    Leave a comment:


  • yeweijian
    replied
    Now i have already called CNV,but i don't know the format of CNV result.
    It does't look like "CNV_type coordinates CNV_size normalized_RD p-val1 p-val2"

    It likes "deletion chr1:1-10000 10000 0 1.59373e-11 0 1.99216e-11 5.41313e-300 -1"

    Why are my results a few more elements(columns)? And how to explain this situation?

    Leave a comment:


  • aaronh
    replied
    Check out the supplemental in the CNVnator paper for a discussion on bin sizes and sensitivity.

    Leave a comment:


  • Robby
    replied
    Hello,

    I am interested in the bin_size as well. Which bin_size do you use in the second step:

    ./cnvnator -root file.root -chrom ch1 -his bin_size

    And is the bin_size the same for the following steps?

    Thanks
    Robby

    Leave a comment:


  • dmacmillan
    replied
    Also does anyone know what bin_size refers to? There is a bin size as in the .BAM bin size, but there is also the genomic bin size...

    Leave a comment:


  • dmacmillan
    replied
    You have to "cd" into CNVnator/src/samtools and then "make", so libbam.a is created.

    Also remember to type

    Code:
    export LD_LIBRARY_PATH=${LD_LIBRARY_PATH}:${ROOTSYS}/lib
    Then type
    Code:
    cd ..
    to get back into your CNVnator/src directory and type
    Code:
    make
    again

    Leave a comment:


  • djeffares
    replied
    CNVnator, still not compiling

    Thanks for this, but still no luck. here is what I did:
    which root
    /usr/local/bin/root

    export ROOTSYS=/usr/local/bin/root
    cd software/CNVnator/src/
    make

    #And I still get this error.

    g++ -pthread -m64 -I/usr/local/bin/root/include -Isamtools -c cnvnator.cpp -o obj/cnvnator.o
    cc1plus: error: /usr/local/bin/root/include: Not a directory
    make: *** [obj/cnvnator.o] Error 1

    #thanks in advance for any ideas :-)

    Leave a comment:


  • dmacmillan
    replied
    Try simply by typing this:

    Code:
    export ROOTSYS=[path to root installed directory]
    replacing everything inside and including the square brackets by whatever directory you installed root to - e.g. /home/djaffares/root
    then type 'make' and hit enter and it should work! Good luck Dan!
    Last edited by dmacmillan; 01-06-2012, 02:45 PM.

    Leave a comment:

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