Genomic Profiling of Native R-Loops with a DNA-RNA Hybrid Recognition Sensor Protein

EWS/FLI mediated reprogramming of 3D chromatin promotes an altered transcriptional state in Ewing sarcoma (RNA-Seq)

Comparative epigenomics of human and mouse erythropoiesis

Identification of active transcriptional regulatory elements with GRO-seq

Identification of the long, edited dsRNAome in LPS-stimulated primary human peripheral blood monocytes

MYOD Remodeling of the Genome Architecture during Myogenic Conversion of Somatic Cells

Re-Wiring 3D Nuclear Architecture by a Single Transcription Factor during Somatic Cell Reprogramming

Allele-specific NKX2-5 binding underlies multiple genetic associations with human electrocardiographic traits

DONSON and FANCM associate with different replisomes distinguished by replication timing and chromatin domain

High dimensional association detection in large-scale genomic data

EWS/FLI mediated reprogramming of 3D chromatin promotes an altered transcriptional state in Ewing sarcoma (Cut&Tag III)

ETV6 Deficiency and Microsatellite Enhancers Drive Transcriptional Dysregulation in B-Lymphoblastic Leukemia: ChIP-Seq data

Shared patterns of glial transcriptional dysregulation link Huntington's disease and schizophrenia

ETV6 Deficiency Unlocks ERG-Dependent Microsatellite Enhancers to Drive Aberrant Gene Activation in B-Lymphoblastic Leukemia

Coronary artery disease genes SMAD3 and TCF21 promote opposing interactive genetic programs that regulate smooth muscle cell differentiation and disease risk [ChIP-seq]

Coronary artery disease genes SMAD3 and TCF21 promote opposing interactive genetic programs that regulate smooth muscle cell differentiation and disease risk

Targeted reprogramming of H3K27me3 resets epigenetic memory in plant paternal chromatin [sperm - third party reanalysis]

Shared patterns of glial transcriptional dysregulation link Huntington's disease and schizophrenia

Targeting DCAF5 suppresses SMARCB1-mutant cancer via stabilizing SWI/SNF

Reanalysis of white and brite adipocyte ChIP-Seq of PPARG and MED1 in the hg38 genome