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Annotating 5'UTRs #3

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fulyataylan opened this issue Sep 22, 2021 · 4 comments
Open

Annotating 5'UTRs #3

fulyataylan opened this issue Sep 22, 2021 · 4 comments
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Enhancement New feature or request

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@fulyataylan
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Hi!

I have recently listened to an ESHG talk about annotating variants in 5'UTR. I found it very interesting and it is worth trying. Below you can find their GitHub page and publications.

https://github.com/ImperialCardioGenetics/UTRannotator

About the role of 5'UTR variants in human genetic disease:

Whiffin, N., Karczewski, K.J., Zhang, X. et al. Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals. Nat Commun 11, 2523 (2020). https://doi.org/10.1038/s41467-019-10717-9

About UTRannotator:

Annotating high-impact 5'untranslated region variants with the UTRannotator Zhang, X., Wakeling, M.N., Ware, J.S, Whiffin, N. Bioinformatics; doi: https://academic.oup.com/bioinformatics/advance-article/doi/10.1093/bioinformatics/btaa783/5905476

Kind regards,
Fulya

@jemten
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jemten commented Oct 13, 2021

First of all sorry about the late reply.
Indeed, this looks very interesting. We are currently in the process of rewriting MIP in nextflow which takes a lot of our resources and thus the work on MIP has been limited to maintenance mostly. However, we will try to include this in the nf-core pipeline :)

@jemten jemten added the Enhancement New feature or request label Oct 13, 2021
@henrikstranneheim
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Will not be done in MIP

@jemten jemten transferred this issue from Clinical-Genomics/MIP Mar 4, 2022
@jemten
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jemten commented Mar 4, 2022

Transferred this to our fork of the raredisease repo in order to not forget about it

@jemten jemten reopened this Mar 4, 2022
@jemten
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jemten commented Sep 25, 2023

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