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  • #16
    Originally posted by GenoMax View Post
    When you did QC/trimming of the data was a PE-read aware program used (to keep the pairs of reads in sync in both files) with the two data files at the same time (R1/R2)? It is possible that reads in your files went out of sync and this is resulting in the error above.

    Actually, I didn't do any thing with the files, I just got the .gtf file from The ucsc.
    and the .bam file from my advisor. and i am trying to get genes count from .bam file.

    is possible to let me know how i can check if the pairs of reads in sync in both files

    Thanks

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    • #17
      Do you know how the bam was generated (is there more than 1 bam per sample)? Do you have access to the original read files?

      Comment


      • #18
        I don't know how it has been generated, i have different samples and there is one bam file for every sample.

        I don't have access to the original read files.

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        • #19
          I got the solution I was using Wrong .gtf file.

          Thanks Geno for looking at this.

          Comment

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