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Thanks to everyone who gave us a follow — we’re proud to have been of service. So long, and thanks for all the FISH!
All your genetic data will be handled in accordance with Imputeme’s terms of service, so it has already been deleted.
We are undergoing an evolution to the next level of easy-to-access, high-quality genetic analysis. From now on, we’ll redirect to @nucleusgenomics, so we encourage you to follow that handle instead, as this profile is being closed down.
A Qualitative Study Exploring the Consumer Experience of Receiving Self-Initiated Polygenic Risk Scores from a Third-Party Website medrxiv.org/cgi/content/sh… #medRxiv
Version 1.0.7, "autumn 2021", is out now. What's new? Portability. Privacy. Ease-of-use. With @nextflowio it's just plug and play to get polygenic risk scores from any-format genetic data. Feedback and usage experience stories very welcome.
A new update has now been released. It's not a very big one, no new scores. Mostly improvement of containerized local running and documentation and generally making operation easier. It's called 1.0.5 👍
And lastly - please do participate in the surveys on reaction and motivations that users get after browsing a few scores - there’s a lot of heated debate in this field. But better data is always better.
Better @docker running, includes an ongoing drive towards more meaningful logs and usability, as well as now being (fully) tested on Windows-OS for the benefit of the citizen’s science initiatives out there, e.g. through @OSFramework
Spring 2021 update is now online. New scores, faster processing, and better docker-running. github.com/lassefolkersen…
(also - new @PGSCatalog-derived scores are in-processing to determine distributions. Stay tuned for next update.)
The detailed instructions for each use-case are found at: hub.docker.com/repository/doc… We hope that these new features will help improve understanding of genetic vulnerability as a continuous trait and further lower the bar for information access.
Winter 2021 release is ready (v1.0.3). Impute-me can now run from your own computer. This is done through a platform called Docker, which runs on both Linux, Mac and Windows.
Autumn 2020 update is now ready. Details are available at github.com/lassefolkersen…, but the main user-facing change is the work with DNA sequencing formats (vcfs)
Very happy that our paper on calculations and interpretations of polygenic risk scores (PRS) from direct-to-consumer (DTC) genetics is now published (frontiersin.org/articles/10.33…). A big thanks to my co-authors: @ollie_pain, Andrés Ingason, @thomas_werge, @cathrynlewis, @J9_Austin
If your data was processed before testing work on this update started, you may need to re-process from scratch, but the interface will tell you if it is missing novel SNPs for a trait. More details at github.com/lassefolkersen…
The previous calculations are not gone, you just have to switch off 'only show most recent study' if you want to find it.
Spring 2020 update is now available. The main interface change is that the variability explained pie-chart is now shown by default. It can still be switched-off under advanced options. This is done to highlight the relative prediction strength of the various scores.
Veera Rajagopal @doctorveera
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Eliezer de Souza da S... @sereliezer
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Laksman Research @LaksmanResearch
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grace or gabe or some... @viciousp0rkch0p
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Dr. Katharina Brosch @_kabro_
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665 Followers 5K Following For a moment in time, it really seemed like we could freeze the moment; and just for that, I know it was truly worth it...









