Header Leaderboard Ad

Collapse

Are the mate-pair reads always shadowed by their friends the paired-end (picture)

Collapse

Announcement

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

  • Are the mate-pair reads always shadowed by their friends the paired-end (picture)

    ** Title should be "Are the mate-pair reads always shadowed by their friends the paired-end reads (picture)"

    So, are the Illumina mate-pair reads always shadowed by their friends the paired-end reads ?

    See picture -> http://imgur.com/LNwws

    In the picture above, I can see two populations:

    - 250 +/- 25
    - 2250 +/- 225

    (approximations)

    What cause these during the library preparation ?

    I thought only the 2250 +/- 225 would be fished out by the biotin/streptavidin step.


    (data are from Assemblathon 2, this is the snake dataset)


    Thanks !

    Sébastien
    http://twitter.com/sebhtml
    Last edited by seb567; 07-14-2011, 07:01 AM. Reason: typo

  • #2
    Originally posted by seb567 View Post
    So, are the Illumina mate-pair reads always shadowed by their friends the paired-end reads ?
    In short, it seems yes.

    Originally posted by seb567 View Post
    In the picture above, I can see two populations:

    - 250 +/- 25
    - 2250 +/- 225

    (approximations)

    What cause these during the library preparation ?

    I thought only the 2250 +/- 225 would be fished out by the biotin/streptavidin step.
    Indeed - those fragments which span the splice are enriched, relative to those which come from a linear stretch of the original DNA. But the latter massively out-weigh the former (increasingly so at longer MP lengths - since there are more bad fragments, still only one good fragment), so the strep merely tilts the balance a bit in favour of the 'from the splice' fragments. The ratio can go from something like 10:1 against the spiced fragments to maybe 5:1 in favour - which isn't all that bad.

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Targeted Sequencing: Choosing Between Hybridization Capture and Amplicon Sequencing
      by seqadmin




      Targeted sequencing is an effective way to sequence and analyze specific genomic regions of interest. This method enables researchers to focus their efforts on their desired targets, as opposed to other methods like whole genome sequencing that involve the sequencing of total DNA. Utilizing targeted sequencing is an attractive option for many researchers because it is often faster, more cost-effective, and only generates applicable data. While there are many approaches...
      03-10-2023, 05:31 AM
    • seqadmin
      Expert Advice on Automating Your Library Preparations
      by seqadmin



      Using automation to prepare sequencing libraries isn’t a new concept, and most researchers are aware that there are numerous benefits to automating this process. However, many labs are still hesitant to switch to automation and often believe that it’s not suitable for their lab. To combat these concerns, we’ll cover some of the key advantages, review the most important considerations, and get real-world advice from automation experts to remove any lingering anxieties....
      02-21-2023, 02:14 PM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, 03-17-2023, 12:32 PM
    0 responses
    8 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 03-15-2023, 12:42 PM
    0 responses
    17 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 03-09-2023, 10:17 AM
    0 responses
    66 views
    1 like
    Last Post seqadmin  
    Started by seqadmin, 03-03-2023, 12:03 PM
    0 responses
    64 views
    0 likes
    Last Post seqadmin  
    Working...
    X