zack chiang
@zchiang.bsky.social
1.3K followers 970 following 22 posts
microscopy x epigenomics | buenrostro lab | harvard/broad
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zchiang.bsky.social
7 years ago, I met a junior fellow named Jason Buenrostro who blew me away with a vision of futuristic genomic technologies

Today, we (Ajay Labade, Caroline Comenho) are excited to share our first steps into that future: Expansion in situ genome sequencing

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zchiang.bsky.social
What do you do when grants are cancelled, faculty searches are frozen, and the ability to do the science you believe in is slipping out of reach?

I wrote an essay. On efforts to solve aging with reprogramming, the primacy of the epigenome, and the path to rewriting our future:
zchiang.bsky.social
maybe we just need more positive visions of what the future could look like if we develop mirror life
zchiang.bsky.social
nothing cooler than watching a friend literally turn science fiction into reality

it's been awe-inspiring to watch @andrewcpayne.bsky.social and co build E11 Bio and prove that the FRO model can produce amazing, unique science

also expansion + molecular barcoding <3
andrewcpayne.bsky.social
🧪 E11 Bio is excited to share a major step towards brain mapping at 100x lower cost, making whole-brain connectomics at human & mouse scale feasible (🧠→🔬→💻). Critical for curing brain disorders, building human-like AI systems, and even simulating human brains.

Read more: e11.bio/news/roadmap
zchiang.bsky.social
to be fair, it's been quite important to genome assembly and related areas for some time, but I think we're just scratching the surface with functional, multi-modal, and temporal readouts

combined with the speed and low cost, there's a lot of potential for both diagnostic and screening tech imo
zchiang.bsky.social
just a pic of my dog maple taking "be one with nature" a little too literally
zchiang.bsky.social
my friend Sai is a co-corresponding on this, so I suspect that's his doing!

critics normally complain single-cell atlases don't have any real biology, now they also gonna complain when it's too interventional, there's no winning I guess 😛
zchiang.bsky.social
when you temporarily have more followers than your PI

(anyway @jbuenrostro.bsky.social is here now)
zchiang.bsky.social
Happy to provide more info if needed! And thanks for pointing out the omission, we'll definitely add it to our methods section
Reposted by zack chiang
homeworld.bsky.social
New episode! This time on The Climate Biotech Podcast, Homeworld Collective co-founders Dan Goodwin and Paul Reginato sit down with the legendary George Church—a pioneer in genomics and synthetic biology.

Spotify: open.spotify.com/episode/6LfF...
Apple Podcasts: podcasts.apple.com/us/podcast/e...
"Inconvenient truths don't actually motivate people as much as convenient solutions. That’s what we should be seeking — and those solutions tend to be synthetic, and probably biological." – George Church, Ph.D. on The Climate Biotech Podcast
zchiang.bsky.social
Thanks! We add an oligo with an acrydite group to link it to the gel during polymerization, then use a complementary fluorescent oligo for visualization
zchiang.bsky.social
who knew it would be easier to get everyone to switch social media platforms than getting them to use hg38
Reposted by zack chiang
jobdekker.bsky.social
Leonid Mirny and I wrote this for all interested in chromosomes: "The chromosome folding problem and how cells solve it"

www.cell.com/action/showP...
www.cell.com
zchiang.bsky.social
seems like a fun game for all the scientists excited by the move but also mourning having to rebuild their following (it me)

I once made a meme to explain all of the drama surrounding the word "epigenetics" - to my horror, it is now used in at least several PhD classes
Reposted by zack chiang
zchiang.bsky.social
To show the power of this approach, we applied ExIGS to progeria cells with nuclear lamina abnormalities

By combining expansion and 3D genome sequencing in the same nucleus, we can literally see how the abnormal lamin topology changes the structure of chromosomes

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zchiang.bsky.social
In situ sequencing measures the 3D location and genomic position of each DNA fragment, letting us trace the path of every chromosome in the nucleus

We also do expansion IF imaging to measure which fragments co-localize with protein landmarks

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zchiang.bsky.social
Expanding the genome evenly is hard because DNA is a polymer, so here we use the Buenrostro lab's favorite enzyme Tn5 to make fragments beforehand

We then do Illumina sequencing, but instead of on a flowcell, all enzymatics are performed ~inside~ the expanded nucleus

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zchiang.bsky.social
Fortunately, we had Fei Chen & Ed Boyden, the inventors of expansion microscopy on board!

In ExM, samples are physically enlarged in gels, allowing superresolution imaging without fancy microscopes

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zchiang.bsky.social
In 2020, we (Andrew Payne, Paul Reginato) showed in situ genome sequencing, which we used to reveal the 3D genome at the very first stages of life: www.science.org/doi/10.1126/...

However, the resolution of IGS is capped by nuclear volume and the diffraction limit of light

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In situ genome sequencing resolves DNA sequence and structure in intact biological samples
A technical approach allows simultaneous sequencing and imaging of genomes in human fibroblasts and early mouse embryos.
www.science.org