Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • capricy
    Senior Member
    • Apr 2012
    • 125

    short reads clustering

    I have 20 million short reads: 25 bp each, and there is no genome reference available.

    I would like to examine the patterns of those reads, that is, some reads should be derived from the same gene locus.

    Any suggestions about a quick method to cluster them together so that I know how many loci they might be derived from?

    Thank you very much for any thoughts?
  • Brian Bushnell
    Super Moderator
    • Jan 2014
    • 2709

    #2
    I think you're asking for the impossible. Even if 25bp reads cluster together, that's not an indication they came from the same place. Clustering algorithms are pretty bad even with 150bp reads from different species, and clustering is notoriously bad at generating the correct number of clusters.

    I suggest mapping them to the reference of the most closely related organism you can find, or attempting assembly with K=21 with, say, Velvet. Then mapping them to the contigs you get, and blasting the contigs to see what they are. But it might be more cost-effective to sequence longer reads (150bp - 250bp) and make a good assembly than to waste your time on 25bp reads with no reference.

    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
    19 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 06-30-2026, 05:37 AM
    0 responses
    20 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 06-26-2026, 11:10 AM
    0 responses
    21 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...