Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • #31
    Originally posted by GenoMax View Post
    Is the bcftools executable in the directory you are currently in? Have you tried to "locate" it and provide the full path for it like you did for vcfutils.pl?

    Is your my.var.bcf file in the current directory?

    In future, start a new thread when you have a new question.
    1. bcftools is executable in my current directory.

    kurban@kurban-X550VC:~/Desktop/SNPs/CD$ bcftools

    Program: bcftools (Tools for data in the VCF/BCF formats)
    Version: 0.1.17-dev (r973:277)

    Usage: bcftools <command> <arguments>

    Command: view print, extract, convert and call SNPs from BCF
    index index BCF
    cat concatenate BCFs
    ld compute all-pair r^2
    ldpair compute r^2 between requested pairs


    2.i have tried to provide full path of bcftools:
    kurban@kurban-X550VC:~/Desktop/SNPs/CD$ /usr/bin/bcftools view my.var.bcf | /usr/share/samtools/vcfutils.pl varFilter - > my.var-final.vcf
    it says:
    open: No such file or directory
    and file my.var.bcf is in my current diractory.

    but it is still not working.

    Comment


    • #32
      Are you sure bcftools in in your current directory (~/Desktop/SNPs/CD from what I can see above)? You seem to be running the copy that is in /usr/bin (in the set of commands in #2).

      Have you verified that my.var.bcf file is non-zero bytes (i.e. there is something in it)?

      Can you use [ CODE] (remove the leading space before CODE) put your commands here [/CODE] to make the commands you are pasting clear (enclose them in CODE tags on both sides like I have shown). Otherwise it is difficult to decipher if there are spaces in wrong spot in your command line.
      Last edited by GenoMax; 08-08-2014, 04:31 AM.

      Comment


      • #33
        kurban910, I just ran
        Code:
        bcftools view jim.bcf
        and I don't have any file called jim.bcf. It gave me this:
        Code:
        open: No such file or directory
        This makes me think that you have the wrong name. Be careful with 1's and l's, -'s and _'s, etc -- it's easy to get these confused. Heck, I even get .'s and _'s confused sometimes. In the directory that the bcf file is located, can you execute:
        Code:
        ls $PWD/*.bcf
        and copy the bcf file's name exactly as it appears, including the full path, and then try running your command again?

        Comment


        • #34
          Originally posted by blakeoft View Post
          kurban910, are you sure that you have the right name for the bcf file? It looks to me like the command is correct.
          yes, i am sure the file name is right

          Comment


          • #35
            Originally posted by GenoMax View Post
            Are you sure bcftools in in your current directory (~/Desktop/SNPs/CD from what I can see above)? You seem to be running the copy that is in /usr/bin (in the set of commands in #2).

            Have you verified that my.var.bcf file is non-zero bytes (i.e. there is something in it)?

            Can you use [ CODE] (remove the leading space before CODE) put your commands here [/CODE] to make the commands you are pasting clear (enclose them in CODE tags on both sides like I have shown). Otherwise it is difficult to decipher if there are spaces in wrong spot in your command line.
            u r right ,thanks. i will put the commends in the code box next time. and yes, my.var.bcf file is around 7.6 BM.

            and for your first question, bcftools is not in the current directory i am in, but its executable from here.

            Comment


            • #36
              Originally posted by blakeoft View Post
              kurban910, I just ran
              Code:
              bcftools view jim.bcf
              and I don't have any file called jim.bcf. It gave me this:
              Code:
              open: No such file or directory
              This makes me think that you have the wrong name. Be careful with 1's and l's, -'s and _'s, etc -- it's easy to get these confused. Heck, I even get .'s and _'s confused sometimes. In the directory that the bcf file is located, can you execute:
              Code:
              ls $PWD/*.bcf
              and copy the bcf file's name exactly as it appears, including the full path, and then try running your command again?
              thank you for your time guys , now i find out not just this one, other commends also r not exacted in my terminal , ubuntu 12.04 some times isn’t stable . after i reinstall the system i will try again.

              Comment


              • #37
                Originally posted by maubp View Post
                If you did want to convert the FASTQ to an unaligned SAM or BAM file, try this:
                http://picard.sourceforge.net/comman...tml#FastqToSam
                I need to do this locally, and since we didn't have Picard installed but do have Biopython (yes, I'm biased ), I wrote a simple Python script to convert paired FASTQ files into unmapped SAM reads (which you can pipe into samtools to get as a BAM file):



                I would expect this to be slower than a dedicated tool, so probably not suitable for a high throughput pipeline - but it should be fine for a one-off analysis.

                Comment

                Latest Articles

                Collapse

                • seqadmin
                  Genetic Variation in Immunogenetics and Antibody Diversity
                  by seqadmin



                  The field of immunogenetics explores how genetic variations influence immune responses and susceptibility to disease. In a recent SEQanswers webinar, Oscar Rodriguez, Ph.D., Postdoctoral Researcher at the University of Louisville, and Ruben Martínez Barricarte, Ph.D., Assistant Professor of Medicine at Vanderbilt University, shared recent advancements in immunogenetics. This article discusses their research on genetic variation in antibody loci, antibody production processes,...
                  11-06-2024, 07:24 PM
                • seqadmin
                  Choosing Between NGS and qPCR
                  by seqadmin



                  Next-generation sequencing (NGS) and quantitative polymerase chain reaction (qPCR) are essential techniques for investigating the genome, transcriptome, and epigenome. In many cases, choosing the appropriate technique is straightforward, but in others, it can be more challenging to determine the most effective option. A simple distinction is that smaller, more focused projects are typically better suited for qPCR, while larger, more complex datasets benefit from NGS. However,...
                  10-18-2024, 07:11 AM

                ad_right_rmr

                Collapse

                News

                Collapse

                Topics Statistics Last Post
                Started by seqadmin, 11-08-2024, 11:09 AM
                0 responses
                35 views
                0 likes
                Last Post seqadmin  
                Started by seqadmin, 11-08-2024, 06:13 AM
                0 responses
                28 views
                0 likes
                Last Post seqadmin  
                Started by seqadmin, 11-01-2024, 06:09 AM
                0 responses
                32 views
                0 likes
                Last Post seqadmin  
                Started by seqadmin, 10-30-2024, 05:31 AM
                0 responses
                23 views
                0 likes
                Last Post seqadmin  
                Working...
                X