Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • mrfox
    Senior Member
    • Aug 2010
    • 103

    Tophat uniquely mapped reads

    I have just posted two questions but this time I would make it simpler and clearer. If I do not use "-g1" when running Tophat(i.e., allow multi-hits), then how can I identify uniquely mapped reads? My understanding is they are mapped reads with "NH:i:1", where NH is "Number of reported alignments that contains the query in the current record". Am I right?
    Thank you.
  • wisense
    Member
    • Sep 2011
    • 30

    #2
    Yes,you are right.When the 5 column of the bam file is 255,it also means it is an uniquely mapped read.

    Comment

    • rahilsethi
      Member
      • May 2010
      • 22

      #3
      NH:i:1 does not give uniquely mapped reads when TopHat run under default settings

      No, when running TopHat "NH:i:1" will not report uniquely mapped reads when run with default settings. This is because under default settings max no of reported primary alignments are 20 even when it is actually greater than 20. When I looked for max value of NH:i: in the output of whole transcriptome sequence it is 20. So some reads, in reality may contain more than 1 alignment NH:i: will give only the no. of reported alignment and in this case only primary alignments are reported. NH:i:1 for some reads may still give you 1 if only primary alignments are 1, even if the total alignments is greater than 1

      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, Yesterday, 11:08 AM
      0 responses
      6 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-30-2026, 05:37 AM
      0 responses
      11 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-26-2026, 11:10 AM
      0 responses
      19 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-17-2026, 06:09 AM
      0 responses
      53 views
      0 reactions
      Last Post SEQadmin2  
      Working...