Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • lingling huang
    Member
    • Mar 2016
    • 48

    How to find polycistronic transcripts in eukaryotes genomes

    Hi,there.
    I have got long, high-quality, consensus transcripts sequences, and I want to see weather there are polycistronic transcripts in my PacBia data.I have extracted the long open reading frames and predicted the likely coding regions by using TransDecoder.Then, I don't know how to calculate how many orfs in transcripts and filter for polycistronic candidates and get support from genome-based annotation. Any hints or links would be appreciated.Thank you!
  • Macspider
    Member
    • Feb 2016
    • 36

    #2
    I'm not an expert on PacBio data, but I think you can hardly determine if they are polycistronic or not without a reference genome.
    With coding region predictors you can only guess which parts of the sequence of your transcripts are translated and which not, but this makes sense only if you have primary transcripts sequenced and not mRNAs. In the latter case, you won't have any intron in your sequence and thus you will predict, for each transcript, a 5'UTR + a CDS + a 3'UTR.

    If you have time to spend on this, you will definitely benefit to map the reads to a reference.

    Are your PacBio data full length transcripts?
    Do you have a reference to align to?

    Comment

    • lingling huang
      Member
      • Mar 2016
      • 48

      #3
      Originally posted by Macspider View Post
      I'm not an expert on PacBio data, but I think you can hardly determine if they are polycistronic or not without a reference genome.
      With coding region predictors you can only guess which parts of the sequence of your transcripts are translated and which not, but this makes sense only if you have primary transcripts sequenced and not mRNAs. In the latter case, you won't have any intron in your sequence and thus you will predict, for each transcript, a 5'UTR + a CDS + a 3'UTR.

      If you have time to spend on this, you will definitely benefit to map the reads to a reference.

      Are your PacBio data full length transcripts?
      Do you have a reference to align to?
      Yes, my data are full-length non-chimeric transcripts and have a human reference. Therefore, I want to try to align them to human genome.

      Comment

      Latest Articles

      Collapse

      • GATTACAT
        Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
        by GATTACAT
        Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
        07-01-2026, 11:43 AM
      • SEQadmin2
        Nine Things a Sample Prep Scientist Thinks About Before Sequencing
        by SEQadmin2


        I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

        Here are nine questions we think about, in roughly the order they matter, before...
        06-18-2026, 07:11 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 07-02-2026, 11:08 AM
      0 responses
      16 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-30-2026, 05:37 AM
      0 responses
      17 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-26-2026, 11:10 AM
      0 responses
      20 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-17-2026, 06:09 AM
      0 responses
      54 views
      0 reactions
      Last Post SEQadmin2  
      Working...