Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • madsaan
    Member
    • Jan 2011
    • 26

    #1

    fold change value-cuffdiff

    Hi,

    I am trying to find the fold change between male and female gonad using cuffdiff.it seems to be working fine but am getting a value of -1.79769e+308.Now I need to find the top ten up and down regulated gene but not able to so because of the above value which appears for a significant number of genes.any help will be greatly appreciated.

    Thanks,
    Joji
  • dnusol
    Senior Member
    • Jul 2009
    • 136

    #2
    Hi Joji,

    If I am not wrong, the ln(fold_change) column in the gene_exp.diff file shows what you are after.
    By the way, did you manage to get gene information-annotation for your results using a genome .gtf file?
    Last edited by dnusol; 02-10-2011, 12:22 AM.

    Comment

    • madsaan
      Member
      • Jan 2011
      • 26

      #3
      thanks dnusol for your reply.I used a gene annotation.gtf file for cuffcompare.I am getting -1.79769e+308 in the ln(fold change) column so quite confused.

      Thanks,
      joji

      Comment

      • brachysclereid
        Member
        • Feb 2011
        • 32

        #4
        Trouble with GTF in Cufflinks

        Hi,
        I have seen something similar to what you are reporting when the FPKM in one sample is zero. In this case you can't compute a log fold change, but I am sure that you would have spotted that...

        I am having trouble getting Cufflinks to use my GTF also. Can anyone spot what's wrong with this? Everything looks ok to me, but I am just learning about this format:

        HTML Code:
        Un	protein_coding	exon	34432	34800	.	-	.	 gene_id "GSVIVG00013290001"; transcript_id "GSVIVT00013290001"; exon_number "1"; gene_name "D1J5D6_VITVI"; transcript_name "D1J5D6_VITVI";
        Un	protein_coding	CDS	34432	34800	.	-	0	 gene_id "GSVIVG00013290001"; transcript_id "GSVIVT00013290001"; exon_number "1"; gene_name "D1J5D6_VITVI"; transcript_name "D1J5D6_VITVI"; protein_id "GSVIVT00013290001";
        Un	protein_coding	start_codon	34798	34800	.	-	0	 gene_id "GSVIVG00013290001"; transcript_id "GSVIVT00013290001"; exon_number "1"; gene_name "D1J5D6_VITVI"; transcript_name "D1J5D6_VITVI";
        Un	protein_coding	exon	33789	34034	.	-	.	 gene_id "GSVIVG00013290001"; transcript_id "GSVIVT00013290001"; exon_number "2"; gene_name "D1J5D6_VITVI"; transcript_name "D1J5D6_VITVI";
        Un	protein_coding	CDS	33789	34034	.	-	0	 gene_id "GSVIVG00013290001"; transcript_id "GSVIVT00013290001"; exon_number "2"; gene_name "D1J5D6_VITVI"; transcript_name "D1J5D6_VITVI"; protein_id "GSVIVT00013290001";
        Un	protein_coding	exon	33058	33255	.	-	.	 gene_id "GSVIVG00013290001"; transcript_id "GSVIVT00013290001"; exon_number "3"; gene_name "D1J5D6_VITVI"; transcript_name "D1J5D6_VITVI";
        Un	protein_coding	CDS	33058	33255	.	-	0	 gene_id "GSVIVG00013290001"; transcript_id "GSVIVT00013290001"; exon_number "3"; gene_name "D1J5D6_VITVI"; transcript_name "D1J5D6_VITVI"; protein_id "GSVIVT00013290001";
        Un	protein_coding	exon	30354	30415	.	-	.	 gene_id "GSVIVG00013290001"; transcript_id "GSVIVT00013290001"; exon_number "4"; gene_name "D1J5D6_VITVI"; transcript_name "D1J5D6_VITVI";
        Un	protein_coding	CDS	30354	30415	.	-	0	 gene_id "GSVIVG00013290001"; transcript_id "GSVIVT00013290001"; exon_number "4"; gene_name "D1J5D6_VITVI"; transcript_name "D1J5D6_VITVI"; protein_id "GSVIVT00013290001";
        Un	protein_coding	exon	29264	29360	.	-	.	 gene_id "GSVIVG00013290001"; transcript_id "GSVIVT00013290001"; exon_number "5"; gene_name "D1J5D6_VITVI"; transcript_name "D1J5D6_VITVI";

        Comment

        • madsaan
          Member
          • Jan 2011
          • 26

          #5
          hi brachysclereid,

          You should put a chr in front of Un and other chromosome numbers as well.it should work after that.

          Thanks,
          Joji

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
            by SEQadmin2




            NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
            10-30-2026, 06:46 AM
          • SEQadmin2
            Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
            by SEQadmin2



            Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

            Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
            ...
            10-14-2026, 09:55 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 10-28-2026, 09:57 AM
          0 responses
          33 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-28-2026, 09:51 AM
          0 responses
          21 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-22-2026, 11:13 AM
          0 responses
          72 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-22-2026, 10:48 AM
          0 responses
          48 views
          0 reactions
          Last Post SEQadmin2  
          Working...