Sharing this in case it's useful: I find that students often have a hard time conceptualizing quantitative parameters in genomics and popgen
Here's a cheat-sheet I put together for teaching. It's also part of a textbook I have been writing on human genetics (more on that below)
📣NEW TOOL! Wish there was a tool that made calculating existing #PolygenicScores and #PolygenicRiskScores in new datasets easier? We @PGSCatalog have made just that!
INTRODUCING pgsc_calc: an open-source pipeline to calculate PGS using nextflow https://t.co/ahsG91TiKV
Please RT: We are delighted to announce that the Department of Human Genetics at the University of Michigan is searching for a tenure-track faculty member at the Assistant Professor level! Please apply here: https://t.co/AEC3ZcBcUs.
🎉Final version of our dosage sensitivity study out today @CellCellPress!
https://t.co/2ST1FztGcl
Explored CNV associations across 54 phenotypes in ~1M genomes
Since @medrxivpreprint in 2021: added 200k samples & 22 phenotypes thanks to @GeneDx@ESTbiobank @vumcdbmi
🧵👇
1/6
Lovely weather in Vienna for some science! #ESHG2022
Two notes:
-I’m hiring! Please say hello if you’d like to chat about opportunities :)
-I’ll talk about some hot-off-the-cloud analyses of regional missense constraint on Monday (S22 session)
PRS-CSx has arrived. Congrats to @getian107@Yunfeng_Ruan@hailianghuang and colleagues
Improving polygenic prediction in ancestrally diverse populations
https://t.co/lta9r3bnob
I'm hiring postdocs to join my team at @CGM_MGH & Broad! We study patterns of rare variation in large genomic datasets (like gnomAD), and leverage those into insights about genetic risk for disease.
If you are interested, please reach out or apply here:
https://t.co/2MOkF3sij8
👇👇👇 most important advice to genomics trainees. To understand your data, and its error modes, find a simple informative plot of a slice of your data (read alignment etc) and plot for 100+ random instances. Use your brain’s pattern recognition. Takes minutes, saves months.
There are different versions of the human genome annotation but which do you use?
The Matched Annotation from @NCBI and EMBL-EBI (MANE) collaboration is the answer and brings new meaning to the phrase: two heads are better than one.
https://t.co/piRx08NP2b
Come and work with us! The Lindgren @ceclindgren Lab at the Big Data Institute @bdi_oxford in Oxford is looking to hire a junior statistical geneticist/bioinformatician (finished or about to finish undergrad/masters): https://t.co/uYgkbzIbO2. Please share!
Our lab is hiring! https://t.co/nPNeJO2wJX Come join our mission to cure prion disease through groundbreaking science. The folks who work here love our lab — you will too!
🚨 Last few days to apply for these posts - deadline is Thursday.
It am truly excited by this project and working with this awesome team (kick-ass female mentors anyone?)!
If you know anyone who might be interested, please please share! Thank you!
Join EMBL to complete your PhD at one of our six sites across Europe!
The EMBL International PhD Programme is open for applications until 19 April 2022. #PhD#research
Important information about the application process can be found here: https://t.co/PgpjqfcGL9
Stay at the forefront of rare disease genomics!
Register for #GRD22 by 21 March for an update on the latest approaches in common and rare variant research, as well as excellent international peer networking.
🌐https://t.co/HFAeWzQK8U
#RareDiseases#Mendelian@poseypod
Two amazing @CPMOxford talks over the next 2 weeks:
- 3rd Feb the incredible @HeidiRehm🤩 on a global ecosystem for genomic medicine
- 7th Feb the awesome @mkveerpn💪 on @covid19_hgi, diversity, collaboration and outreach
Sign up for both: https://t.co/PJ6ugA51n6
Please share!