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TSDs are not identical #174
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Hi Jui-Hung, Sorry for the delayed response. "_INT" sequences are internal sequences of LTR retrotransposons. TSDs are found flanking LTR elements, so there won't be TSDs flanking "_INT" sequences. You will see "_INT" are flanked by CA and TG dinucleotides, becasuse they are motifs of the LTR regions. An intact LTR element looks like: Let me know if you have more questions! |
Hi Oushujun, Thank you for your reply. I’m interested in studying target sites, similar to the research in this study (https://academic.oup.com/plcell/article/15/8/1771/6010085). Thank you. Best, |
Yes, of course!
Shujun
…On Mon, Aug 26, 2024 at 8:21 AM ala98412 ***@***.***> wrote:
Hi Oushujun,
Thank you for your reply.
I’m interested in studying target sites, similar to the research in this
study (https://academic.oup.com/plcell/article/15/8/1771/6010085).
Could I directly use the TSD positions from the pass list to search for
patterns in the adjacent sequences?
Thank you.
Best,
Jui-Hung
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Hi,
I am trying to determine the insertion target site of my LTR/Gypsy elements. Using 10:22687853..22691116_INT as an example, I assume that:
scaffold name = 10
start_position = 22687853
end_position = 22691116
intact = INT
According to the manual, target site duplications (TSD) should be the same at both the 5' and 3' ends. However, in my genome, the 5' TSD and 3' TSD are not the same. I have noticed some patterns, but I believe they should be identical.
Did I misunderstand something? Sorry for my naive question.
This is my Python3 script:
seq[start_position -1-5:start_position -1], seq[end_position:end_position +5]
Here is my result table:
Best,
Jui-Hung
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