Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • jp.
    Senior Member
    • Jul 2013
    • 142

    #16
    Hi
    may I get your views on this thread of my question:
    Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc





    Originally posted by Helical View Post
    That is strange. When you run cufflinks, are you running it with -g (use reference transcripts and assemble new ones) or -G (only use reference transcripts)? I am no expert but I imagine this error could arise depending on how you mapped to the known transcripts.

    Comment

    • jp.
      Senior Member
      • Jul 2013
      • 142

      #17
      Hi all
      I am having the same problem...
      Warning: couldn't find fasta record for 'NT_166469'! This contig will not be bias corrected.
      Warning: couldn't find fasta record for 'X'!Warning: couldn't find fasta record for 'Y'! This contig will not be bias corrected.
      Initially, I used ensemble ref and got this warning and then I used UCSC genome.fa. Both gives me the same error.
      Why ??

      Originally posted by kmcarr View Post
      Psikon,

      Your hg19 reference file has chromosome names in the format 'chr1' so that is the format they would be in the BAM file(s) generated by TopHat. Whereas the Ensembl GTF you showed in the example has chromosome names as just the numbers (e.g. '11'). Since the alignments in your BAM file(s) are to references named 'chrN' and the annotations in the GTF file are to references named just 'N' Cufflinks naturally won't be able to match them. You need to ensure that the chromosome names in the reference FASTA you use to map exactly match the names in the annotation file. This is typically best done by getting your reference and annotation from the same source.

      Comment

      Latest Articles

      Collapse

      • 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
      • SEQadmin2
        New Genomics Technologies Take Aim at Long-Standing Limits
        by SEQadmin2


        Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

        We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
        ...
        09-28-2026, 10:25 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 10-15-2026, 10:52 AM
      0 responses
      15 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-14-2026, 05:39 AM
      0 responses
      21 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-13-2026, 09:56 AM
      0 responses
      20 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-09-2026, 11:14 AM
      0 responses
      27 views
      0 reactions
      Last Post SEQadmin2  
      Working...