Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • seq_GA
    Senior Member
    • Feb 2009
    • 124

    #1

    Mapping reads with adapter sequences using MAQ

    I am trying to test pair end mapping with 3' adpter sequence and please let me know how the alogorithm handles the situation.

    The adapter sequence is stored in a text file. The adpter sequence is about 7 bps length. If the paired reads are mapped against the reference genome with option -d which contains 3' adapter, how does the algorithm handle the mapping situation.

    Will it just eliminate 7bps found in the reads as contaminants and eliminate the adpter portion of the reaad from mapping?

    What if both read1 and read2 does not contain the adapter sequence?

    If I am not concerned about the -a option (ie) Maximum outer distance for a correct read pair which has the default value as 250 is not of my concern and how to disable the -a option.

    Anyone can explain on how to interpret the outputdata?

    Thanks.
  • seq_GA
    Senior Member
    • Feb 2009
    • 124

    #2
    Hi Can anyone suggest a tool to map pair end reads with adpter sequence? Thanks.

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
      by SEQadmin2



      Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

      Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
      ...
      10-14-2026, 09:55 AM
    • SEQadmin2
      New Genomics Technologies Take Aim at Long-Standing Limits
      by SEQadmin2


      Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

      We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
      ...
      09-28-2026, 10:25 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, 10-22-2026, 11:13 AM
    0 responses
    30 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-22-2026, 10:48 AM
    0 responses
    22 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-15-2026, 10:52 AM
    0 responses
    39 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-14-2026, 05:39 AM
    0 responses
    45 views
    0 reactions
    Last Post SEQadmin2  
    Working...