Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Chief_Lazy_Bison
    Junior Member
    • Dec 2014
    • 9

    #1

    bbmerge detects different adapters

    Hello,

    I have some bacterial genomes which were sequenced using the Nextera Flex library prep kit ( insert size ~350 bp) and MiSeq paired end reads (2x300). I want to merge these reads with bbmerge prior to adapter trimming and assembly.

    I have used bbmerge's adapter detection feature but have gotten some strange results.
    bbmerge seems to detect different adapters on each sample, and many have multiple N's.

    The first part of the detected adapter sequence is what Illumina provides as the Nextera Flex adapter sequence, but I'm not sure what the other stuff is.

    Here are some of the adapters that were detected:

    >Read1_adapter
    CTGTCNCTTATACACATCTCCGAGCCCACGAGACGGACTCCTANCTCGTATGCCGTCTTCTGCTTG

    >Read2_adapter
    CTGTCNCTTATACNCATCTGACGCTGCCGACGAAGAGGANAGNGNNNNNNNNGNNNGNNNC

    This is the Nextera Flex adapter sequence given by Illumina CTGTCTCTTATACACATCT

    as you can see the first part matches this except for an N stuck in.

    Across my 20 samples 16 unique Read1 adapters were detected and
    18 unique Read2 adapters were detected.

    Should I worry about this? should I feed the detected adapter sequences into bbmerge? should I just give bbmerge the Illumina provided sequence?

    Thanks!
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    I would suggest that you use the Illumina provided adapter sequence. BBMerge detection feature is good when you don't have that information a priori. There may be some sequencing errors in your reads which is leading to that N insertion.

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
      by SEQadmin2



      CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

      Despite this, “CRISPR helped turn genome editing from a specialized technique into
      ...
      07-31-2026, 11:01 AM
    • SEQadmin2
      Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
      by SEQadmin2


      Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

      The systematic characterization of the human proteome has
      ...
      07-20-2026, 11:48 AM
    • SEQadmin2
      Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
      by SEQadmin2



      Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
      ...
      07-09-2026, 11:10 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, Yesterday, 07:41 AM
    0 responses
    11 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-03-2026, 10:13 AM
    0 responses
    25 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-31-2026, 02:55 AM
    0 responses
    38 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-24-2026, 12:17 PM
    0 responses
    25 views
    0 reactions
    Last Post SEQadmin2  
    Working...