Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • How to handle Ns in the middle of reads

    For my illumina data fastqc shows presence of N's at positions 13,14,15 in 101 bp longs reads. If i go for cropping first 15 bases by using trimmomatic, it solves the problem but i lose a lot of data. I wanted to know that if i retain the N's what sort of problems would they cause during alignment(bwa+stampy)/variant calling(unified genotyper) and how can i handle these problems?

    If any body faced a similar problem how did you handle it? Similar questions asked on different forums but none answered. Could not find a resourse on how variant calling programs handle N's. Do they ignore them? Or consider them as a variation with low confidence scores?
    Last edited by themysticgeek; 01-08-2014, 02:55 AM.

  • #2
    Are there N's at those positions in *all* reads? That would almost certainly indicate a technical problem of some kind with this run. In general your sequence provider should not have released this data if that is the case.

    Comment


    • #3
      The N's are in ~50% of the reads. I have attached the Fasqc image for per base n content. This is particular to this sequening run. Did not observe this problem in the other runs
      Last edited by themysticgeek; 01-08-2014, 05:45 AM.

      Comment


      • #4
        Similar problem

        I've just run FastQC on a published RNAseq dataset (SRX294957) and I see a very similar pattern:



        where on position 21-23, 80% of reads are N's. As I'm only interested in expression, I could accept the low read quality as long as the aligner accepts it. I'm using RSEM+bowtie for the purpose, so I'm wondering if bowtie will match NNN against anything in the reference?

        Comment


        • #5
          It will. You can alter the mismatch score due to an N and the maximum number of allowed Ns if you need to (you'll likely need to tweak the minimum allowable score if you do so).

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Current Approaches to Protein Sequencing
            by seqadmin


            Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
            04-04-2024, 04:25 PM
          • seqadmin
            Strategies for Sequencing Challenging Samples
            by seqadmin


            Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
            03-22-2024, 06:39 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, 04-11-2024, 12:08 PM
          0 responses
          25 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 10:19 PM
          0 responses
          28 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-10-2024, 09:21 AM
          0 responses
          24 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 04-04-2024, 09:00 AM
          0 responses
          52 views
          0 likes
          Last Post seqadmin  
          Working...
          X