Luke Funk

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Luke Funk

Luke Funk

@lukebfunk

@CajalNeuro. Former: @BlaineyLab, @broadinstitute, @MIT_HST. Opinions my own. https://t.co/aDN2eJDKCK

Seattle, WA Katılım Eylül 2018
426 Takip Edilen185 Takipçiler
Luke Funk
Luke Funk@lukebfunk·
If the subject line includes the word "synergies" it's going straight to the trash
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Mohamad Ali Najia
Mohamad Ali Najia@MohamadNajia·
Excited to share how @jacobborrajo Anna Le and I are enabling the future of profiling dynamic cellular processes! We built a synthetic RNA export pathway for cells to "self-report" their transcriptional states in real-time. Big thanks to the entire team! biorxiv.org/content/10.110…
GIF
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Mark Kittisopikul
Mark Kittisopikul@markkitti·
Who is interested in microscopy and Zarr?
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Luke Funk
Luke Funk@lukebfunk·
Closest I have found to what I am looking for is MolArt (cusbg.github.io/MolArt/), but doesn't seem to allow custom annotations.
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Luke Funk
Luke Funk@lukebfunk·
Is there something like genome browser for protein structures? I would like an easy way to make custom annotations on specific amino acids and then see where those are in the 3D structure.
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Jan Funke
Jan Funke@janfunkey·
How can machine learning help you to analyze your microscopy images? Find out at the "Deep Learning for Microscopy Image Analysis" course at the @MBLScience in Woods Hole from Aug 21-Sep 5! Applications are due 🚨 May 18 🚨 Read on for more! 👇 mbl.edu/education/adva…
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Ben Barad
Ben Barad@benjaminbarad·
I am so excited to share that I will be starting a lab in January 2024 as an Assistant Professor at @OHSUSOM in Portland! I am building my team, so if you are interested in cellular cryoelectron tomography, computational structural biology, and working in PDX, hit me up!
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Seth Bannon
Seth Bannon@sethbannon·
Entrepreneur AI anxiety is real. Everything is moving so fast that many feel the ground is shifting under their feet. A 10x product of last month may be obsolete today. Many are asking the same question: Where is defensibility in the age of AI? 👇
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Wallace Marshall
Wallace Marshall@WallaceUcsf·
Sci Twitter help - why does differentiation of cells entail both cell fate determination AND arrest of division? Is continued division somehow incompatible with locking in a specific cell fate? Like by erasing chromatin state or something? Sorry if this is a dumb question
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Luke Funk
Luke Funk@lukebfunk·
Had conversations with two separate people this weekend who had never heard of CRISPR...I guess I am sufficiently getting out of my bubble?
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Ross D. Jones, PhD
Ross D. Jones, PhD@jonesr18·
@nika_shakiba @lukebfunk The v4 one already caused reduced growth rates - if Oct4 levels continue to go up, the efficiency would likely decrease due to this!
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Nika Shakiba
Nika Shakiba@nika_shakiba·
🚨 Check out our new preprint! Super excited to see this go over the finish line, thanks to a collaborative effort 📢 Katherine & Trevor! Tl;dr: #SynBio genetic circuits 🧬 + reprogramming to #iPSCs 🧫= robust cell fate control See thread for the story! biorxiv.org/content/10.110…
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Luke Funk
Luke Funk@lukebfunk·
@nika_shakiba Also, in the experiments in Fig. 4c & d, did you compare to a control without the miR casette? Wondering if the v4 miR-Oct4e with many mismatches is actually producing any repression? Or if the high & tight Oct4 distribution is driven primarily by the high MOI?
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Luke Funk
Luke Funk@lukebfunk·
@nika_shakiba In the final trajectory controller designs in Fig. 4a, it looks like the miR-Oct4e variants will target both the endogenous and exogenous OCT4 mRNA? Did you have a way to separately control and “overwrite” Oct4 levels in these experiments like earlier in the paper?
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Luke Funk
Luke Funk@lukebfunk·
@RecursionChris Also, how were the labeled genes chosen? Random subset? Intentionally selected for specific properties? What properties?
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Luke Funk
Luke Funk@lukebfunk·
@RecursionChris Totally agreed! Just not sure what to think of the 16k anonymized genes without any specific plans to de-anonymize in the future.
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