RFK Jr. is apparently going to tell Congress today that HHS doesn't need much money.
The cuts have damaged important science. If he says it's all waste and duplication he's either lying or doesn't know his job.
@RepArrington@RepBrecheen@michaelcburgess@RepBuddyCarter
It comes down to the new algorithm. It shows you more of whatever you engage in. The trick is to not engage (not even pause scrolling) with content that you don't want to see a lot more of.
Another thing I do is bookmark in my browser specific people and go directly to their feed.
RNAseq is commonly performed. We compared N=30 wild-type Bl6 mice to an N=30 heterozygotic knockout with a phenotype, and then downsized. We found you need at least an N= 8-12 to avoid a >50% false positive rate. A 2nd line confirmed the finding.
https://t.co/wwKRUcdKmH
Fitbit users are unanimously opposed to removing the browser interface. Many of us feel strongly about it.
https://t.co/BMPMoxoJ3M
The claim that data and features of the dashboard are available in the app is a lie.
Why did they do this? It makes no sense.
#Fitbit is failing.
Rosaceae (berries, stone fruits, apples, and more) has amazing diversity in fruit development.
@BerryLab_UMD has vast omics data that captures much of this variation.
Now, Muzi Li has put it on a nice database.
https://t.co/aD6J4jPxhR
https://t.co/dX85LHl4O5
Glad to have helped.
Want to understand how splicing decisions are actually made in the cell based on pre-mRNA sequence? PhD student Kayla McCue has been hard at work modelling just that, & we're very excited to announce that now you can read about it in her new preprint! https://t.co/mU2rbjWhjo
Splicing variation shapes mammalian complex traits.
"more sVariants were called than eVariants, and ... multi-tissue sVariants alone explained a similarly large proportion (66%) of heritability to eVariants and sVariants jointly (69.2%)."
Also - many trans sVariants!
It's our pleasure to announce a new section, #RNA Bioinformatics, in Frontiers in Bioinformatics, led by Prof. Shuhui Song of the Beijing Institute of Genomics, Chinese Academy of Sciences.
This section is now open for submissions
Discover more: https://t.co/f1QZQiV3J5
Join ISMB/ECCB 2023 in Lyon, France, or virtually July 23-27!
I'm not going to make it this year, but ISMB is always a great conference.
Let's shape the future of our field together! https://t.co/4SVYlFFuGn
#ISMBECCB2023#ComputationalBiology#Bioinformatics#Conference
This is a nice story about genetic analysis leading to a cure. STAT4 variants contribute to disabling pansclerotic morphea, and it looks like JAK inhibitors are a potential treatment.
I've been hearing about it from @brynjmatt for a while now.
https://t.co/mThDjC8QGu
New preprint from us!
mRNAs act as chaperones for IDRs.
mRNAs often bind to IDRs. This changes their conformational ensembles to drive protein complex assembly, and controls protein activity.
Thank you @VickyLuo0223!
https://t.co/0LeTA2bjXv