Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • [question] reads detected sequences out of sequencing primer in the other direction

    Hi,

    I've got a pair-end illumina sequencing data (100bp each end) for Ago iClip in mouse ES cell.
    majority of read pairs show that the inserted fragments are very short. As shown in the following example:

    @DBRHHJN1:278:C11RFACXX:3:1101:1443:1167 1:N:0:
    ATAGGTATGCGCCACTGAGATCGGAAGAGCGGTTCAGCAGGAATGCCGAGACCGATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAAAAAAAAAGCACAC
    @DBRHHJN1:278:C11RFACXX:3:1101:1443:1167 2:N:0:
    CAGTGGCGCATACCTATAGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCGTATCATTAAAAAAAAAAAAAAACACAAGAGAG
    Above is one read pair. The underlined part of each read can be aligned with illumina PCR primers in the other end. And the 17bp part of each read is reverse complement to each other. This means that the insert fragment is only 17bp and the 100bp read go through the PCR primer (and sequencing primer) in the other end.

    Could any one explain me what is the "AAAAAAAAAAAAAAAAGCACAC" and "AAAAAAAAAAAAAAACACAAGAGAG" after the underlined sequences? How can I interpret them?
    The fastq score is low for these regions.

    Here is the same reads with fastq score:
    @DBRHHJN1:278:C11RFACXX:3:1101:1443:1167 1:N:0:
    ATAGGTATGCGCCACTGAGATCGGAAGAGCGGTTCAGCAGGAATGCCGAGACCGATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAAAAAAAAAGCACAC
    +
    @C@FFDDFHHHHHJJJJJIIJJJJJJJGHJJJJGIJJJJJJIJIJIIJIGHGGFC>ADBD@CDDDDDDDDDDDCCDCBDDDBDDDDB############
    @DBRHHJN1:278:C11RFACXX:3:1101:1443:1167 2:N:0:
    CAGTGGCGCATACCTATAGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCGTATCATTAAAAAAAAAAAAAAACACAAGAGAG
    +
    CCCFFFFFHHHHHJJIJJJJJJJJJIJIHGIJJJJJIDIIIJJJJJIHIJCHFHHHHHFFFDDEDDDDDDDDEEEDDCCCBDB#################
    Also, I am curious what will be the reason for these short insert fragments during sequencing. After library construction, the results of bioanalyzer show that the average length of insert fragment is ~100bp.

  • #2
    Originally posted by SF_mallish View Post
    Could any one explain me what is the "AAAAAAAAAAAAAAAAGCACAC" and "AAAAAAAAAAAAAAACACAAGAGAG" after the underlined sequences?
    After sequencing through the Illumina adapter the polymerase has literally reached the end of the line. There are physically no more bases being incorporated yet the software is "forced" to make a basecall. It's the equivalent of a wild guess.

    How can I interpret them?
    You can't, they're meaningless.

    Also, I am curious what will be the reason for these short insert fragments during sequencing. After library construction, the results of bioanalyzer show that the average length of insert fragment is ~100bp.
    It is very easy for peak of small/no insert fragments to hide in a BioAnalyzer trace. For extremely small library molecules like this a small physical amount of DNA can translate into a large molar amount.

    Comment


    • #3
      Thanks kmcarr for your quick reply!

      For the last point you mentioned,
      For extremely small library molecules like this a small physical amount of DNA can translate into a large molar amount
      Could you explain more detail about it, or do you have any reference for that?

      The experiment was done by my lab mate. Actually, he measured the length of the total fragment, which contain ~70bp adaptors (like sequences for PCR primers) flanking the inserted fragment in both end. The peak of bioanalyzer result is around 240bp, so we interpret the average inserted fragment size is ~100bp. Will the results of this protocol still be affected by the reason you mentioned?

      Thanks!

      Comment

      Latest Articles

      Collapse

      • seqadmin
        Advancing Precision Medicine for Rare Diseases in Children
        by seqadmin




        Many organizations study rare diseases, but few have a mission as impactful as Rady Children’s Institute for Genomic Medicine (RCIGM). “We are all about changing outcomes for children,” explained Dr. Stephen Kingsmore, President and CEO of the group. The institute’s initial goal was to provide rapid diagnoses for critically ill children and shorten their diagnostic odyssey, a term used to describe the long and arduous process it takes patients to obtain an accurate...
        12-16-2024, 07:57 AM
      • seqadmin
        Recent Advances in Sequencing Technologies
        by seqadmin



        Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.

        Long-Read Sequencing
        Long-read sequencing has seen remarkable advancements,...
        12-02-2024, 01:49 PM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, 12-17-2024, 10:28 AM
      0 responses
      33 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 12-13-2024, 08:24 AM
      0 responses
      49 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 12-12-2024, 07:41 AM
      0 responses
      34 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 12-11-2024, 07:45 AM
      0 responses
      46 views
      0 likes
      Last Post seqadmin  
      Working...
      X