Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Ion Torrent adapter artefacts

    Hi guys!

    We recently began working with Ion Torrent PGM. At first we were thinking that server cuts off all adapters and barcodes and we are getting our clear and clean data out. Then we began noticing that sequences do have something in common at the end.

    Through the process of googling and brainsturming, we found that about 40% of all our output data has got REVERSE P1 + B adapters at the end of our sequences.

    P1: ATCACCGACTGCCCATAGAGAGG
    B: CTGAGACTGCCAAGGCACACAGGGGATAGG

    This is kinda wierd and we are not sure how to deal with that. We are thinking that this might have a negatine influence on our results increasing “unknown” and “unclassified” domens.

    Also, quite mysterious that we see a lot of REVERSE primers but very little FORWARD ones.

    Has anyone faced similar problems? What do you do about it?

    Will be very thankfull for any ideas/ thoughts/ advices!
    Kind regards,

    Alisa

  • #2
    First have a look at your library prep. Than on processing.

    First it would be help full if you could provide a bit more info about the sample/library prep used.

    Actually adapter artefacts can come in many variations, esp if you have a bit of nuclease activity during the library prep steps before/during the ligation steps (adapters may loose some of the 3'/5' nucleotides, form chimeras, ect.

    When they get sequenced, the instrument's data processing software is likely to miss them during processing, and they get into the downstream analysis...

    Some analysis (like mapping to a reference) would tolerate them, but other ones (de novo assembly) may be very sensitive to them.

    So convert the data to fastq format and run it through the fastqc (up a kmer size to 9 or 10 -k 9) and have a look on overrepresented sequences.

    Than grep out some reads with those sequence and and have a more detailed look.
    Use grep -c to get the number of matches

    Once you know your full contaminant sequence - remove it with cutadapt or trimmomatic.

    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
    18 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    22 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    16 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    46 views
    0 likes
    Last Post seqadmin  
    Working...
    X