Genome access is transcription factor specific and defined by nucleosome position [NOMe-seq]

Genome access is transcription factor specific and defined by nucleosome position

Foxa-deficiency Restricts Hepatitis B Virus Biosynthesis Through Epigenic Silencing [Bisulfite-Seq]

Foxa-deficiency Restricts Hepatitis B Virus Biosynthesis Through Epigenic Silencing

Exploring the Stability of Genomic Imprinting and X-Chromosome Inactivation in the Aged Brain (IMPLICON-Seq)

Exploring the Stability of Genomic Imprinting and X-Chromosome Inactivation in the Aged Brain

guidedNOMe-seq quantifies chromatin states at single allele resolution for hundreds of custom regions in parallel [guidedNOMe-seq]

Epigenetic Modulation of GPER Expression in Gastric and Colonic Smooth Muscle of Male and Female Non-obese Diabetic (NOD) Mice: Insights into H3K4me3 and H3K27ac Modifications

Systematic assessment of ISWI subunits reveals that NURF creates local accessibility for CTCF [SMF]

Systematic assessment of ISWI subunits reveals that NURF creates local accessibility for CTCF

Durable and efficient gene silencing in vivo by hit-and-run epigenome editing [targeBSseq]

Durable and efficient gene silencing in vivo by hit-and-run epigenome editing

Durable and efficient gene silencing in vivo by hit-and-run epigenome editing [targetBSseq_CpG_Pcsk9_2]

Durable and efficient gene silencing in vivo by hit-and-run epigenome editing [targetBSseq_DMRs]

Durable and efficient gene silencing in vivo by hit-and-run epigenome editing [targetBSseq_DMRs_2]

Durable and efficient gene silencing in vivo by hit-and-run epigenome editing [targetBSseq_offTargets]

Durable and efficient gene silencing in vivo by hit-and-run epigenome editing [Bisulfite-seq]

Sex-specific epigenetics drive low GPER expression in gastrointestinal smooth muscles in Type 2 diabetic mice

Distinct disease mutations in DNMT3A result in a spectrum of behavioral, epigenetic, and transcriptional disruptions

TIME-Seq Enables Scalable and Inexpensive Epigenetic Age Predictions.