Next up is MASTR-seq - a protocol for Cas9-based capture of target loci for multi-modal inquiry of short tandem repeat tracts and DNA methylation at single-allele resolution using Nanopore long read sequencing. Led by @chuanbin_su
We're excited to drop two new manuscripts on technologies for multi-modal single-allele or single-cell inquiry. First up: FISHnet - a computational method for finding domain-like chromatin structures in sequential Oligopaints imaging data. Led by @PatelRohanD and @KennethHPham
Howdy! I'm thrilled to introduce FISHnet, a computational tool designed to identify chromatin domains within sequential Oligopaints DNA FISH data.
Check it out on BioRxiv https://t.co/6Nn3DApYHr
🧵 ⬇️ ⬇️ ⬇️ (1/8).
Excited to introduce MASTR-seq, Multiplexed Analysis of Short Tandem Repeats, a multi-modal method for accurate sequencing of short tandem repeat tracts and DNA methylation across multiple samples. Now on biorxiv(https://t.co/08goWSzTl0). (1/6)
NIMH-supported research by @CreminsLab identified a widespread network of silenced gene locations that underly the onset of fragile X syndrome and related genetic disorders. https://t.co/OlR4SCp18N
Congrats to my colleagues @CreminsLab! If you want something to read for the holiday, don't miss this gorgeous work!
Spatially coordinated heterochromatinization of long synaptic genes in fragile X syndrome: Cell https://t.co/nUS43Rdiig
Spatially coordinated heterochromatinization of long synaptic genes in fragile X syndrome: Cell https://t.co/DgYTR5F49O Amazing paper showing that CGG repeat expansion causes heterochromatin assembly at FMR1, but also a plethora of other genes in TRANS!
Penn researchers have found new disrupted #genes and an unexpected molecular pattern—dubbed BREACHes—related to the genetic disorder Fragile X Syndrome #FXS. @PennGenetics@pennbioeng@CreminsLab https://t.co/OQk0etInGA
We are thrilled to share our latest work @CellCellPress on the discovery of BREACHes linking to long-range inter-chromosomal interactions, synaptic gene silencing, and instability of the repetitive genome in fragile X syndrome. @CreminsLab, @ericjoycelab, @FulcrumTx
We are very excited to share our findings on BREACHes using a human model of genome instability in fragile X syndrome with possible implications for other diseases with perturbations linked to genome instability! https://t.co/t68X7KxSUP. (1/18)
@etihad@EtihadHelp@EtihadPremium changing layover from 6hrs to 30 hrs that’s too much of wait time. I am not happy with this did not expected from @etihad this is very terrible experience I ever had..@EtihadHelp never respond to calls to resolve issue Frustrated
Happening today! Proudly presenting our work from
@CreminsLab at @KeystoneSymp#VKSChromatin22. Please stop by at our poster. We are here to help fight Alzheimer`s!!!