Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • shi
    Wei Shi
    • Feb 2010
    • 236

    <30% of reads mapped

    I tried using bowtie (0.12.2) to mapping Illumina GAII reads to human genome. However, the percentage of reads which were mapped (reads with at least one reported alignment) is less than 30%. The length of these reads is 100bp.

    I also have the GAII read data which included 50bp reads (same sample). More than 80% of reads can be mapped using bowtie.

    I used the default parameters to run bowtie. Should I adjust the parameter for aligning 100 bp or bowtie is not suitable for mapping reads longer than 50 bp?

    I notice that in Table 3 of the bowtie paper the percentage of mapped reads for 76 bp reads is 44.5% (31.7% if using option -v 2), which is much lower than the percentages for 50bp reads and 36 bp reads in the same table.


    Thanks,
    Wei
  • krobison
    Senior Member
    • Nov 2007
    • 734

    #2
    bowtie has options (--trim5 & --trim3) for removing N bases from the 5' or 3' end of read -- have you tried this to truncate your reads down to 50nt & see if you get much mapping.

    You might also take 10-20 reads or so with high quality scores & BLASTN them (easy to do at NCBI) against all known sequences -- this would check for a sample swap (to another species).

    Comment

    • dcfargo
      Member
      • Aug 2008
      • 22

      #3
      I'd drop the -v go with -n (perhaps make -l a little longer than default) and 'titrate' the -e value using a subset of the sequences.

      Comment

      Latest Articles

      Collapse

      • 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
      • SEQadmin2
        From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
        by SEQadmin2


        Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


        The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
        ...
        06-02-2026, 10:05 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 06-17-2026, 06:09 AM
      0 responses
      36 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-09-2026, 11:58 AM
      0 responses
      99 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-05-2026, 10:09 AM
      0 responses
      120 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 06-04-2026, 08:59 AM
      0 responses
      113 views
      0 reactions
      Last Post SEQadmin2  
      Working...