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  • zjrouc
    Member
    • Sep 2010
    • 25

    #1

    Is there anyone knows how to calculate FPKM for specific UTR region?

    Is there anyone knows how to calculate FPKM for specific UTR region or just specif exon?
    Last edited by zjrouc; 07-27-2015, 05:53 PM.
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    The same as you would for anything else. You take the number of fragments mapping to each region, divide that by the length of each region in kilobases, and then divide the results by a million.

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    • zjrouc
      Member
      • Sep 2010
      • 25

      #3
      Then how do you count reads in that region? Manually?

      Comment

      • dpryan
        Devon Ryan
        • Jul 2011
        • 3478

        #4
        You have a plethora of choices: htseq-count, featurecounts, summarizeOverlaps (in R), bedtools intersect, samtools view (note the -c option), etc.

        Comment

        • zjrouc
          Member
          • Sep 2010
          • 25

          #5
          So if i want to use htseq to count reads for this specif region. i need to generate a gtf file for this region, right? now i have problem with that. my htseq or cufflink results from using this own gtf file were empty. i am wondering if there are other easier ways

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          • dpryan
            Devon Ryan
            • Jul 2011
            • 3478

            #6
            Yes, htseq-count requires a GTF file. If you can see alignments in IGV and you don't get any with the GTF file and htseq-count then you're probably doing something wrong. Try making a BED file and use bedtools intersect with that and the GTF file separately. If they both work and give approximately the same results then you know that you were using htseq-count wrong. If they give vastly different results then there's likely something wrong with the GTF file. If they don't give any alignments then you've screwed up specifying the region.

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