Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • Break
    Junior Member
    • Mar 2012
    • 3

    Mapping reads from different genus

    Hi everyone!

    There are RNAseq reads for a mammalian specie with unsequenced genome. The most close mals genome that have been sequenced is related to the different genus. Did anyone try to map reads on so phylogenetically distant genomes (with bowtie/tophat)? Is there any sense to do this or it is better the de novo assemblie in this situation ? Thank you.
  • Break
    Junior Member
    • Mar 2012
    • 3

    #2
    PS: such a mapping is necessary for expression value calculations....

    Comment

    • ssing
      Member
      • Jan 2009
      • 21

      #3
      I have tried mapping to a genome from an organism about 15-20 mya from the organism of interest. I found that I only had a slight decrease in mapping efficiency (90 -> 80%) but that more divergent stuff didn't map well at all. I imagine you could try doing this iteratively, and map more stringently and then loosen the parameters and map again. FWIW, I ended up assembling de novo and then mapping.

      Good luck!

      Comment

      • Break
        Junior Member
        • Mar 2012
        • 3

        #4
        Thanks for the reply. De novo is a possibility. However, there is another question. I have several tissues. Is it better to pool all samples and map than reads to the reference contigs? Or it is better to do assembly for each tissue in separate because of presence tissue-specific isoforms?

        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, Today, 11:05 AM
        0 responses
        6 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-02-2026, 11:08 AM
        0 responses
        28 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-30-2026, 05:37 AM
        0 responses
        25 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-26-2026, 11:10 AM
        0 responses
        25 views
        0 reactions
        Last Post SEQadmin2  
        Working...