KARR-seq reveals principles of high-order ribonucleoprotein structure assembly

Barcoded viral tracing of single-cell interactions in CNS inflammation

Genome-wide screening identifies Trim33 as an essential regulator of dendritic cell differentiation

A Quantitative Sequencing Method for 5-Formylcytosine in RNA

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

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

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

Transcriptome-wide profiling and quantification of N6-methyladenosine by enzyme-assisted adenosine deamination

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

De novo enhancer function in divergent hominin haplotypes

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

Dense, systematic mutagenesis to identify the features required for CSEs

Chamber selective enhancers identified in vivo by AAV-MPRA

Regulation of mouse chamber selective enhancers

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

Enhancer grammar of liver cell types and hepatocyte zonation states

Reconstructing regulative progenitor behaviors in synthetic embryos

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

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

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