Identification of m6A residues at single nucleotide resolution using eCLIP and an accessible custom analysis pipeline

Integration of Hi-C and ChIP-seq data reveals distinct types of chromatin hubs

De novo mutations in the genome organizer CTCF cause Intellectual Disability

An AR-ERG co-mediated chromatin interactome defines the transcriptional network in prostate cancer cells

Argonaute-1 binds transcriptional enhancers and controls constitutive and alternative splicing in human cells

Evaluation of RNA amplification and RNA-Seq library preparation protocols for spermatozoa RNA profiling

Long non-coding RNAs display higher natural expression variation than protein-coding genes in healthy humans

E2F1 orchestrates transcriptomics and oxidative metabolism in Wharton’s jelly derived mesenchymal stem cells from growth-restricted neonates

miCLIP, RNA-Seq, and Ribo-Seq in MOLM13 cells

Intracranial aneurysm associated single-nucleotide polymorphisms alter regulatory DNA in the human circle of Willis

T-ALL

CRISPR-mediated deletion of prostate cancer risk-associated CTCF loop anchors identifies repressive chromatin loops

Multileveled reduction of p21 expression by Linc-ASEN represses cellular senescence

A predictable conserved DNA base composition signature defines human core DNA replication origins

m6A-Label-seq directly reports m6A methylome at base resolution

The chromatin landscape at the HIV-1 provirus integration site determines viral expression

In situ capture of global transcription dynamics and enhancer activity with high accuracy and sensitivity 

Suppression of MBD2 alternative splicing promotes breast cancer metastasis by activating FZD1 under hypoxia

Comparative 3D Genome Architecture in Vertebrates

RNA helicase DHX37 facilitates liver cancer progression by cooperating with PLRG1 to drive super enhancer-mediated transcription of cyclin D1