I guess I'll be here in the future:

RT @GeorgeMonbiot: This is my farewell post. I am not deleting this account, as I don’t want to lose the archive, and I don’t want my name…

RT @Q_StatGen: Our paper on misleading biases in AD GWAS-by-proxy is published @NatureGenet. We identify the source of biases and explore s…

RT @anthony_herzig: Save the date: European Mathematical Genetics Meeting (EMGM) 2025, 8-9 April, Brest, France

@mblum_g @felbalazard

@pp0196 No hyper-parameter I think. I just need to find a good way to choose the number of groups.

@pp0196 The goal would be to get ancestry proportions from automatic ancestry groups, based on PCA.

@pp0196 I guess PCA is not much sensitive to those, so it should be fine.

@pp0196 It is deterministic, if that's your question. If you meant whether I get the same results when e.g. subsetting, I'll need to test on some larger dataset.

RT @TimothyRaben: The UK Biobank (UKB) has been an amazing field changing resource for the past decade. Unfortunately, and very suddenly, t…

RT @WrayNaomi: New Oxford-Aarhus-Copenhagen collaboration - not yet launched - 2 postdocs, 2 senior postdocs and postdoc coordinator in…

@mblum_g . @antuki13 devrait savoir

@Rbn_Hfmstr I guess, if you have this, you can also report the r2(G_bgen, G_wgs) for each variant in the bgen data? This is really what I am looking for.

@AlexTISYoung Then we should talk :-)

@elonmuskADO No. Twitter.