I’m excited to share the first manuscript out of my PhD work with @NAltemose, in which we describe FiberFold: a deep learning tool that predicts cell-type-specific and haplotype-specific 3D genome organization from a single experiment!
https://t.co/FwJldYnCGe 1/
Mapping cancer somatic variants T2T. 16% of mutations occur in sequences missing from GRCh38. Satellites are UV-damage hotspots. Centromeres undergo extensive genetic and epigenetic remodeling. Somatic epimutations remodel cancer epigenomes. @SMaHTnetwork
https://t.co/vlkQKQnXNI
Plasmid-based reporter assays are the bedrock of regulatory genomics. But a basic question has gone unanswered for decades: Do chromatin architectures form on plasmids transfected into mammalian cells—and does it matter? We finally have answers.
https://t.co/34hcyRPN0z
(1/n) New preprint from @claricehongky Fan Fang @VarshiniRam23 in collab w Jie Liu
Q: How do we get ultra-high-res 3D genome maps?
A: New deep learning model, Cleopatra.
Cleo trains on Micro-C, fine-tunes on RCMC, and predicts genome-wide 3D maps
https://t.co/Wf7tppUk2p
Delighted to share our latest work deciphering the landscape of chromatin accessibility and modeling the DNA sequence syntax rules underlying gene regulation during human development! https://t.co/zIUjPy6ZLz. Read on for more 🧵 [1/16]
I’m excited to share the first manuscript out of my PhD work with @NAltemose, in which we describe FiberFold: a deep learning tool that predicts cell-type-specific and haplotype-specific 3D genome organization from a single experiment!
https://t.co/FwJldYnCGe 1/
FiberFold represents a major advance in genomic analysis: haplotype-specific 3D genome prediction from a single, accessible assay. By bridging single-molecule epigenomics and 3D genome modeling, we've created a powerful tool for both basic research and clinical applications. 16/