
Nathanael Rollins
@_nathanrollins
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learning from evolution + synthesizing biology https://t.co/4R6uWsHqaL
Joined November 2016
RT @Mattmcpartlon1: It's been a privilege work alongside the most uniquely talented group of individuals I've ever encountered on this brea….
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RT @deboramarks: How can we use #GenerativeAI for #ProteinDesign? - check out work from our labs @deboramarks and @yaringal ..
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RT @NotinPascal: Want to catch up with the rapid progress in ML for functional protein design? Not sure where to start?.Check out our revie….
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RT @eLife: New microscopy technology enables nanoscale imaging of centimetre-scale tissues, making it possible to image the entire expanded….
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RT @kasiakready: New preprint out!. Babies are born to breastfeed. While 50% of lactating persons struggle to make enough milk, there are….
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RT @roseorenbuch: Announcing popEVE - a deep generative model of the human proteome that reveal over a hundred novel genes involved in rare….
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Excited to debut our work: ML methods that accelerate the development of proteins of interest into full-fledged therapeutics. By making proteins safer, faster, we hope to expand the space of therapies in the clinic!.
We're looking forward to presenting preclinical data describing the application of our IMPACT platform at PEGS Boston 2023 #PEGS23 next week, the world’s largest gathering of protein engineering and biotherapeutics experts. #WeAreSesimic.
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RT @ImranSHaque: But if we show all the gene knockouts ordered by genomic position, a curious pattern emerges: CRISPR knockouts look more s….
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RT @NthadaniN: We’ve updated our EVEscape paper with more SARS2 retrospective evaluation and potential use-cases! C….
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RT @NthadaniN: Can one anticipate viral evolution enough to support timely intervention? Check out our new preprint on forecasting antibody….
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RT @london_lab: Our new paper is out in @nchembio where we describe our journey from a #covalent fragment screen to an in vivo active Pin1….
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RT @davidrliu: Today we report the use of base editing in patient-derived cells and in mice to correct the most common cause of progeria, t….
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RT @Jonnygfrazer: 1/n I'm excited to share our preprint *Large-scale clinical interpretation of genetic variants using evolutionary data an….
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Natural seq models are good at predicting pathogenic mutants- often better than wet-lab assays! @Jonnygfrazer @MafaldaFigDias @NotinPascal @deboramarks classify 72,000 variants of unknown significance across human genome (& in total, 4x that in ClinVar!)
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