
Benjamin Stewart
@drbstewart
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#singlecell #genomics 👨💻 🧬 | #kidneys 👨⚕️🏥
Cambridge, UK
Joined June 2014
(1/8) Excited to share our latest preprint introducing ACCESS-ATAC, a high-resolution approach to measure chromatin accessibility and transcription factor binding: https://t.co/C2opuEhn0Z
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V promising approach perturb multiome - effects of tf perturbations on chromatin accessibility and expression
pmc.ncbi.nlm.nih.gov
Single-cell CRISPR screens link genetic perturbations to transcriptional states, but high-throughput methods connecting these induced changes to their regulatory foundations are limited. Here we...
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Great collaboration between the @FoldingGenome and Watkins labs, reporting the first Gain of Function de novo enhancer causing Mendelian disease (ST Depression Syndrome), defining a multidisciplinary path with ML to solving non-coding clinical genetics. https://t.co/0ShPzik8Le
medrxiv.org
A substantial proportion of mutations underlying rare Mendelian diseases remain unknown, potentially because they lie in the non-coding genome. Here, we report the mapping of the causal mutation of...
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Every project is unique – like a ❄️– but after experiencing many projects it also gets pretty clear that there is pretty much a common way they unfold, once the initial idea happens:
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Very cool ancient genomics
It’s finally out! 🥳 Today @cellcellpress we report non-mineral fossils of ancient chromosomes in skin from a woolly mammoth that died in Siberia, 52,000 years ago. 🦣💨 Don’t miss our thread below! 🧵👇🏽
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Congratulations Asger This is very interesting and important work!
Mutant HSCs in human clonal haematopoiesis have an attenuated response to inflammation and ageing, which may give them a selective advantage. Happy to share our new paper published in @CellStemCell: https://t.co/TehWdhmkVw A thread below… /1
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amazing!
A first at Northwestern Medicine! Go inside the operating room and witness surgeons performing a #KidneyTransplant on a patient who was awake for the entire procedure. @NM_Transplant #NMBetter
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A privilege and honour to receive the Raine award and I hugely enjoyed sharing our science at #UKKW2024
Dame June Raine DBE, CEO of @MHRAgovuk presents @drbstewart with this years Raine Award (in memory of Tony Raine & awarded for significant contributions to renal research) at #UKKW2024 science session after the talk "Mapping immunity in the human kidney with single cell genomics"
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Making protein sequencing a nucleic acid sequencing problem seems to be the way this will be cracked
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this is a very interesting sequence-function association for the small number of enhancers that operate a large distances. Curious principle for gene regulation -
How do enhancers work over distances that sometimes exceed megabases? Excited to share our work led by @gracecbower where we uncover a unique sequence signature globally associated with long-range enhancer-promoter interactions in developing limb buds: https://t.co/n0p7BdxSdq 1/
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ribosomal DNA copy number variation as a potential genetic influence on CKD risk. https://t.co/e6SUvGl6kk Associates with creatinine, cystatin C, urea, microalbuminuria 'kidney failure' rather than glomerular disease or urolithiasis... what does rDNA copy number do to the kidney?
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It was a super cool pre-print. Now it's a super cool @Nature paper. Really innovative work The UMAP police are coming for Fig2c/d though...
GoT-ChA! I am thrilled to announce that our paper "Mapping Genotypes to Chromatin Accessibility Profiles in Single Cells" is now out in @Nature !! 👩🔬👨🔬🧬If you want to link somatic mutations to epigenetic changes directly in patient samples: https://t.co/M9Y3wEvpuW 👇🧵
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interesting clinical pearl on very very commonly prescribed drug.
1/15 Why are statins administered at night? In this tweetorial I'll discuss the mechanistic and historical reasons for the frequently used QHS dosing schedule. And why it's often unnecessary. But before we get there, I'm curious: when do you prescribe/order/take statins?
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