@SynBioGaoLab
Account based inUnited States
About this account
- Account based in
- United States
- Connected via
- United States App Store
Account-level information from X, not a live location or the device used for a specific post.
Assistant Professor @ Stanford ChemE synthetic biology, biomolecular engineering https://nitter.cf/t.co/KAajKt7YdT
Stanford, CA
Joined June 2019
- Tweets425
- Following847
- Followers3.1K
- Likes538
Congrats, Brian and team. It never ceases to amaze me what you guys can do with the language models!
As with biological design, AI can also accelerate biological discovery.
In new work led by @_David_Li and @garykbrixi with @mfgrp, we show how genome language models enable systematic discovery of genetic elements, revealing a new class of reverse-transcriptase mechanisms.
As with biological design, AI can also accelerate biological discovery.
In new work led by @_David_Li and @garykbrixi with @mfgrp, we show how genome language models enable systematic discovery of genetic elements, revealing a new class of reverse-transcriptase mechanisms.
Heading to mSBW? Check out work by @cnnrcall (Poster 47, genetically encoded urinary reporter to noninvasively monitor live molecular events), JS (Poster 46, efficient biophysical design of orthogonal DNA duplex libraries), and @mengzhang668 (talk, ablating cancer using RADAR).
Please RT: We're hiring! Computational postdoc for foundation model and sequence-structure-function studies of intrinsic disordered proteins through a consortium and unique large datasets. Ideal candidates have led ML/AI projects in protein design/analysis.
Xiaojing Gao retweeted
Efficient generation of epitope-targeted antibodies with Germinal - @BrianHie @SynBioGaoLab nature.com/articles/s41587-0…
Stop by our posters at SEED! @haoyu_dai_dhy on our latest efforts to improve ADAR-based sensors (Day 1, #24), @FloraHU8 on their application to cancer ablation (Day 1, #23), and @Xiaowei0402 on an efficient algorithm to refactor proteins for biomedical applications (Day 2, #136).
Xiaojing Gao retweeted
Nifty work on plasmid chromatinization from @stergachislab !
"plasmids are indeed capable of recapitulating nuclear genome-encoded chromatin architectures, ... However, plasmids consistently adopt a heterogeneous and incomplete chromatin architecture relative to nuclear-encoded chromatin fibers, and surrounding sequence context plays an integral role in modulating whether a plasmid-encoded regulatory element will recapitulate nuclear genome-encoded chromatin architectures."
Online Now: Chromatin architectures underlying plasmid-based assays for regulatory variant effects dlvr.it/TSkLhj
Xiaojing Gao retweeted
I have long written and spoken about the many ways US immigration policy harms international students and scholars. This has been true for as long as I can remember, including when I first came to the US on a single-entry student visa more than 20 years ago under a process formerly known as muslim registry program.
But the current administration has gone much further, through arbitrary policy changes, travel bans, and broad visa processing pauses that leave folks unable to work, travel, or train.
These policies affect a minority of scientists, and in the current state of the world they can be easy to overlook. But we should not let that happen.
I wrote about the quiet loss of Iranian scientific talent in US labs for @TheScientistLLC:
the-scientist.com/the-quiet-…
Xiaojing Gao retweeted
qPCR allowed us to measure transcripts, but just once, destructively, and only in post-mortem tissues. Here, we show we can record transcript level history in vivo and recover this information with a blood test to make a "noninvasive qPCR". nature.com/articles/s41467-0…
Xiaojing Gao retweeted
1/ Excited to share our new paper in Science: “Toward life with a 19-amino acid alphabet through generative artificial intelligence design.” @ColumbiaSysBio @ColumbiaBME @Columbia
science.org/doi/10.1126/scie… 🦠🧬🛠️🖥️💥
Xiaojing Gao retweeted
Excited to report the first de novo enzyme catalyzing two of the most energetically demanding reactions in biology—phosphomonoester and phosphodiester hydrolysis—with catalytic efficiencies comparable to natural enzymes! 🚀
desB was designed zero-shot with dEVA. No structure prediction, no pre-defined motif, no reaction-intermediates. 🧵
@StanfordBiosci @bioe_stanford @SLAClab
@EPFL @hes_so @simonduerr
Xiaojing Gao retweeted
Could the folding of synthetic gene circuits in 3D shape how genes are expressed? Today @ScienceMagazine we report on the role of gene syntax in shaping feedback between transcriptional activity and genome folding for advanced circuit design🧵 (1/n)
Xiaojing Gao retweeted
So you want to engineer your hiPSCs, but targeting DNA payloads requires multiple slow, inefficient steps for each construct. What if we could accomplish multi-site integration seamlessly? Come hear about STRAIGHT-IN Dual now out at Nature Biomedical Engineering! 🧵
Link at end!
Don't feel bad about missing the mSBW abstract deadline. We have extended it! We also keep the registration fee affordable ($150 for students) so that mammalian synbio-curious trainees can check it out, especially if you are in the Atlanta area. Meeting link below:
A neat amplification system to improve the limited sensitivity/dynamic range of RADAR pubs.acs.org/doi/10.1021/acs…
We just updated our Germinal preprint for de novo antibody-like binder design! Featuring additional scFv designs, extensive experimental validation of epitope specificity and polyreactivity, and CryoEM structure courtesy of Jim Zhang and Bing Rao from Feng Liang's lab.
Abstract due in two days!
Breakthroughs in mammalian synthetic biology happen when bold ideas meet the right audience. Could your research define the next frontier of medicine? Submit your abstract now: bit.ly/4jQmrFj #mSBW2026 #SyntheticBiology #MammalianSystems #CallForAbstracts
