Cambridge
Joined July 2012
Excellent work by @NadigAjay @Luke0connor !
How often is autism caused by de novo changes to the genome? What is the spectrum of penetrance across autism-associated genes? What can we expect from future autism gene discovery? I'm pleased to share a new preprint where we develop new statistical methods to answer these Qs.
1
173
Tushar Kamath retweeted
Spatial genomics has existed for many years, but it has often been limited by complex imaging systems, specialized equipment, and $$$. With IRISeq, we wanted to simplify this to a simple PCR rxn. nature.com/articles/s41593-0…
5
37
7
176
31,498
Tushar Kamath retweeted
2/8 Introducing Synapse-seq: our AAV-based tool for mapping brainwide presynaptic projections or postsynaptic distributions of molecularly-defined neurons, via protein-guided RNA barcoding & single-cell/spatial readouts: doi.org/10.64898/2026.02.26.…
1
4
16
1,259
We are thrilled to have the following superstars join our fellowship program in July 2026.  Congratulations to Erik, Wes, Tushar, Brian, May and Shawna, and congratulations to the MGH GI Division for recruiting such talent.  Welcome to the family!
2
6
1
84
7,694
A truly impressive synthesis of bio-psycho-social!
This Post is from an account that no longer exists. Learn more
2
203
Tushar Kamath retweeted
The first piece of work from my PhD has now been uploaded to biorXiv! Short 🧵below:
Hunger modulates exploration through suppression of dopamine signaling in the tail of striatum biorxiv.org/cgi/content/shor… #biorxiv_neursci
7
16
2
57
17,997
A particularly exciting way to look at transcriptional data using lessons learned from statistical genetics!
How do genetic perturbations change cells? How are these effects shaped by cell type and dosage? How do we best extract insight from modern massive perturbation atlases? Im pleased to share a new preprint where we develop a suite of statistical approaches to these Qs (link below)
1
11
442
Tushar Kamath retweeted
How do genetic perturbations change cells? How are these effects shaped by cell type and dosage? How do we best extract insight from modern massive perturbation atlases? Im pleased to share a new preprint where we develop a suite of statistical approaches to these Qs (link below)
8
76
7
293
101,862
What a fantastic presenter at SCGD!
Talk by @fluorocore on generalising single-cell analysis methods to spatial data #singlecellgenomicsday
4
482