ERC Research, FensKavli Scholar.
Molecular basis of neuroplasticity.
New genomics technologies.
https://www.kitazawa-lab.com/home
We are thrilled to announce that our lab’s first preprint is out!
”Whole-genome single-cell multimodal history tracing to reveal cell identity transition”
We report HisTrac-seq, a multiomic single-cell molecular recording platform.
www.biorxiv.org/content/10.1...
Navigate challenges, sharpen leadership skills, make a roadmap together for generations of neuroscientists!
youngpisymposium2026.com
Check out our program and join us!
Our lab is now applying HisTrac to study id specification and plasticity (e.g., memory) and we look forward to sharing exciting results soon!
Our lab is now applying HisTrac to study id specification and plasticity (e.g., memory) and we look forward to sharing exciting results soon!
We are thrilled to announce that our lab’s first preprint is out!
”Whole-genome single-cell multimodal history tracing to reveal cell identity transition”
We report HisTrac-seq, a multiomic single-cell molecular recording platform.
www.biorxiv.org/content/10.1...
We are thrilled to announce that our lab’s first preprint is out!
”Whole-genome single-cell multimodal history tracing to reveal cell identity transition”
We report HisTrac-seq, a multiomic single-cell molecular recording platform.
www.biorxiv.org/content/10.1...
定期ゲスト北沢太郎さん(@kitazawa_taro) 回。直近に公開した自身のHisTrac-seqプレプリントと(と競合LagTagプレプリントの)解説回
#NeuroRadio
neuroradio.tokyo/2025/08/19/9...
定期ゲスト北沢太郎さん(@kitazawa_taro) 回。直近に公開した自身のHisTrac-seqプレプリントと(と競合LagTagプレプリントの)解説回
#NeuroRadio
neuroradio.tokyo/2025/08/19/9...
Indeed, your nanobody-Tn5 protocol is AMAZING!
We actually put some modifications, like sample-bcd implementation, as well as replacement of enzyme for 10x reaction, which may be interesting for you.
I look forward to discussing with you again!
Indeed, your nanobody-Tn5 protocol is AMAZING!
We actually put some modifications, like sample-bcd implementation, as well as replacement of enzyme for 10x reaction, which may be interesting for you.
I look forward to discussing with you again!
https://www.biorxiv.org/content/10.1101/2025.08.12.669973v1
https://www.biorxiv.org/content/10.1101/2025.08.12.669973v1
Our lab is now applying HisTrac to study id specification and plasticity (e.g., memory) and we look forward to sharing exciting results soon!
Our lab is now applying HisTrac to study id specification and plasticity (e.g., memory) and we look forward to sharing exciting results soon!
Using scHisTrac-seq to profile transcriptome, chromatin accessibility, and bivalency during neurodifferentiation, we analyzed over 90,000 single cells and uncovered drastic cell identity transitions—namely “identity jumps.
Using scHisTrac-seq to profile transcriptome, chromatin accessibility, and bivalency during neurodifferentiation, we analyzed over 90,000 single cells and uncovered drastic cell identity transitions—namely “identity jumps.
For the final form, we developed scHisTrac-seq, enabling simultaneous profiling of past and present multiomic states from the same single cells via a nanobody-mediated dual scCUT&Tag protocol (past = m6A, present = H3K27ac, transcription marker).
For the final form, we developed scHisTrac-seq, enabling simultaneous profiling of past and present multiomic states from the same single cells via a nanobody-mediated dual scCUT&Tag protocol (past = m6A, present = H3K27ac, transcription marker).
This captured neonatal epigenome and transcriptome in the adult brain, demonstrating that HisTrac-seq remains effective for at least two months in vivo!
This captured neonatal epigenome and transcriptome in the adult brain, demonstrating that HisTrac-seq remains effective for at least two months in vivo!
In addition, we extended the validation to the mesodermal cardiomyocyte lineage.
In addition, we extended the validation to the mesodermal cardiomyocyte lineage.
Because previously shown that m6A can persist for several hours until the next DNA replication, we expected it to serve as a long-term ”bookmark” in neurons, potentially for months.
Because previously shown that m6A can persist for several hours until the next DNA replication, we expected it to serve as a long-term ”bookmark” in neurons, potentially for months.