A Quantitative Sequencing Method for 5-Formylcytosine in RNA

BID-seq for transcriptome-wide quantitative sequencing of mRNA pseudouridine at base resolution

CRISPR and biochemical screens identify MAZ as a co-factor in CTCF-mediated insulation at Hox clusters

Chamber selective enhancers identified in vivo by AAV-MPRA

De novo enhancer function in divergent hominin haplotypes

Dense, systematic mutagenesis to identify the features required for CSEs

Distal and proximal cis-regulatory elements sense X-dosage and developmental state at the Xist locus

Enhancer grammar of liver cell types and hepatocyte zonation states

High resolution spatially resolved transcriptomic atlas of kidney injury and repair by RNA hybridization-based in situ sequencing

Identifying non-genetic determinants of malignant clonal fitness at single cell resolution

Impact of a gain of function mutation in Fgfr3 gene on mandibular bone repair in a mouse model of hypochondroplasia, Fgfr3N534K/+

Mesenchymal glioma stem cells trigger vasectasia, a distinct neovascularization process mediated by extracellular vesicles carrying EGFR [scRNA-seq]

Missense mutations in CRX homeodomain cause dominant retinopathies through two distinct mechanisms

Open-ST: High-resolution spatial transcriptomics in 3D

Paired single-cell host profiling with multiplex-tagged bacterial mutants reveals intracellular virulence-immune networks

Reconstructing regulative progenitor behaviors in synthetic embryos

Regulation of mouse chamber selective enhancers

Sequencing of N6-methyl-deoxyadenosine at single-base resolution across the mammalian genome

The effect of MPC EV on myotubes

Therapeutic application of circular RNA aptamers in a mouse model of psoriasis