Shawn Liu

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Shawn Liu

Shawn Liu

@ShawnLiu_Lab

Assistant Professor @Columbia | CRISPR-Epigenome-Editing-Brain | @DamonRunyon @WhiteheadInst @MIT @Stanford @Purdue alum | Recruiting postdoc and students

Manhattan, NY Katılım Mart 2017
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Shawn Liu
Shawn Liu@ShawnLiu_Lab·
Our In Vivo DNA methylation editing paper is finally published. Happy to share these two transgenic mouse lines to help investigate the function of DNA methylation at gene/locus of your interest! Happy holidays! #citeas" target="_blank" rel="nofollow noopener">nature.com/articles/s4146…
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棚哥说加密
棚哥说加密@LQP2021·
Anthropic 官方团队亲自演示了 Claude Code 的正确打开方式,这才是真正的高阶用法。 全程仅需30分钟,而且完全免费,主讲人就是 Claude Code 的核心开发者。 一定要去看这场工作坊,建议直接收藏。 它带来的价值,远比那些标价几百美元的付费课程要高得多。 你平时也在用 Claude,但大概率还不知道它藏着40个实用指令。
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Shawn Liu
Shawn Liu@ShawnLiu_Lab·
Dear @GenomeBiology, our manuscript submitted on Dec 23 2025 was with editor since Jan 6 2026. More than 3 months without any response from editor to our emails. Understandable not easy to find reviewers, but could you provide a simple update? We spent 4 years on this paper. 🙏
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Justin Eyquem
Justin Eyquem@j_eyquem·
I am so excited to share our new paper in @Nature: the first programmable, site-specific integration of a large DNA payload into T cells in vivo. A single IV injection results in therapeutic levels of TRAC-targeted CAR T cells in multiple models. #Ack1" target="_blank" rel="nofollow noopener">nature.com/articles/s4158… a 🧵
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UCSC Genome Browser
UCSC Genome Browser@GenomeBrowser·
We are excited to announce the release of the Human Methylation Atlas Summary and Signals tracks for hg38 and hg19. The tracks display genome-wide DNA methylation profiles across 39 primary human cell types from 205 healthy tissue samples. Learn more at bit.ly/humanMethylati…
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Lior Pachter
Lior Pachter@lpachter·
A new long-read preprint: run PIP-seq then PCR & put the library on ONT. Sadly, no data available so comparisons to other tech impossible (& scripts missing). Requires @FluentBio kits (they tried to reverse engineer the whitelist which seems to breach the @FluentBio EULA).
bioRxiv Genomics@biorxiv_genomic

BenchDrop-seq: a microfluidics-free platform for benchtop single-cell long-read RNA sequencing biorxiv.org/content/10.648… #biorxiv_genomic

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Adam.GPT
Adam.GPT@TheRealAdamG·
openai.com/index/new-ways… "Today, we’re making learning these [math and science] concepts in ChatGPT even more interactive with new dynamic visual explanations. Starting with more than 70 core math and science concepts, ChatGPT will guide learners by showing how formulas, variables, and relationships behave in real time. These experiences will be available globally across all plans starting today."
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Wert Laboratory
Wert Laboratory@WertLaboratory·
Kicked off with an excellent talk on epigenome editing by @ShawnLiu_Lab
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Ihtesham Ali
Ihtesham Ali@ihtesham2005·
🚨 Someone just turned Claude into a full AI research scientist. This GitHub repo called claude-scientific-skills just quietly changed what's possible with AI in science. Most people are using Claude to write emails and summarize docs. These researchers are using it to run actual drug discovery pipelines, analyze single-cell RNA sequencing data, interpret clinical variants, and generate publication-ready reports all from a single prompt. Here's how it works: You install one plugin in Claude Code. Claude automatically discovers and uses 140 scientific skills across every major research domain bioinformatics, cheminformatics, proteomics, clinical research, medical imaging, materials science, quantum computing, laboratory automation. The skills connect Claude directly to the databases and tools scientists actually use: → Query ChEMBL for bioactive compounds → Annotate variants with ClinVar and Ensembl → Dock molecules with DiffDock against AlphaFold structures → Analyze 10X genomics data with Scanpy → Search ClinicalTrials. gov and match patients to trials → Generate PDF clinical reports with ReportLab One prompt. Real scientific libraries. Live database APIs. Actual results. This is what happens when someone stops treating Claude like a chatbot and starts treating it like a research platform. /plugin install scientific-skills@claude-scientific-skills 100% Opensource. MIT License. (Link in the comments)
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Shawn Liu
Shawn Liu@ShawnLiu_Lab·
@jrblundell This is so cool. Lineage tracing is possible by methylation!
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Jamie Blundell
Jamie Blundell@jrblundell·
In 1999, Tom Maniatis discovered something remarkable: neurons achieve self-avoidance via stochastic methylation of the protocadherin gene cluster. We've just discovered this locus is an evolvable in-vivo barcode across the human tissues: biorxiv.org/cgi/content/sh… 🧵
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Shawn Liu
Shawn Liu@ShawnLiu_Lab·
@tangming2005 I love this case study to connect biology with bioinformatics. Pleased do more 🙏
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Ming "Tommy" Tang
Ming "Tommy" Tang@tangming2005·
🧵 That V-plot showing transcription factor binding? It might be an artifact. New research shows chromatin fragmentation methods create patterns even on naked DNA. Here's what went wrong.
Ming "Tommy" Tang tweet media
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Itai Yanai
Itai Yanai@ItaiYanai·
Papers submitted on Tuesdays are more likely to be accepted by Nature whereas Wednesdays seem the most likely day to submit and secure acceptance to PLOS ONE. For Cell, Mondays and Tuesdays seem the best submission days in case of accepted papers. link.springer.com/article/10.100…
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Shawn Liu
Shawn Liu@ShawnLiu_Lab·
@Mykalt45 Yes and can be done in a cell-type specific manner.
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Shawn Liu
Shawn Liu@ShawnLiu_Lab·
Our In Vivo DNA methylation editing paper is finally published. Happy to share these two transgenic mouse lines to help investigate the function of DNA methylation at gene/locus of your interest! Happy holidays! #citeas" target="_blank" rel="nofollow noopener">nature.com/articles/s4146…
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