Today I join @VesaliusTx as SVP Data Science. Our mission is to make progress in drug discovery for common disease. I’m excited to translate human genetics and genomics into action!
@StatGenDan I no longer bother re-formatting to journal style for a first submission, except bibs and any resources tables if mandatory. It either doesn’t matter or will be rearranged by the reviewers anyway.
@bvoight28 I now target 6/year (down from 10-12), in addition to AE duties @PLOSGenetics. For review I select for "important" or "I want to read in-depth" (otherwise I'd skim the pre-print and pretend I read it)
Do you read papers regularly? Contextually (writing grants/papers etc)? Rarely (who has the time)? I've gone from regular to rare over the last 10y and I'd like to change...
@alexisjbattle@Y_Gilad@yluo86@LB_Barreiro Went into this looking for a benchmark. Rather shocked at yield. I too suspect context (e.g. @kauralasoo enhancer priming) - but we do need to be thoughtful about current results, and about speculating w/out data. I'd also like to stop writing negative papers
@strnr I loved Ancillary Justice by Anne Leckie (first of three), and Gideon the Ninth by Tamsin Muir (also first of three). Both space operas, which aren't really my jam but these are great!
@WuTsaiYale postdoc fellowship now available to work on neuroticism genetics/genomics with @kristenbrennand and me at @Yale - apply by Aug 15th! https://t.co/rw69ZZ7eQc
@ceclindgren I like notability too - it's the only solution I've found that allows me to import an image and doodle on it to annotate. Still working out how to integrate with Bear (my main notes app) - don't want to ditch that one...
1/ Great to get this out there: we used mendelian randomisation to show that BMI during childhood and low vitamin D are causal risk factors for multiple sclerosis. Free to read here: https://t.co/AiuYuZzQtS