Genomic prevalence of heterochromatic H3K9me2 and transcription do not discriminate pluripotent from terminally differentiated cells (ChIP-seq)

Genomic prevalence of heterochromatic H3K9me2 and transcription do not discriminate pluripotent from terminally differentiated cells (RNA-seq)

DNA binding factors shape the mouse methylome at distal regulatory regions [BIS_seq]

DNA binding factors shape the mouse methylome at distal regulatory regions [ChIP-seq].

DNA binding factors shape the mouse methylome at distal regulatory regions [strand-specific-RNA-seq]

A chromatin-modifying function of JNK during stem cell differentiation

Chromatin based modeling of transcription rates identifies the contribution of different regulatory layers to steady-state mRNA levels

A comparative epigenomics approach reveals REST as a mediator of Polycomb reprogramming during neuronal differentiation

Methylation-dependent and -independent genomic targeting principles of the MBD protein family

Transcription factor occupancy is linked to DNA methylation turnover at active regulatory regions [Bisulfite-Seq]

Transcription factor occupancy is linked to DNA methylation turnover at active regulatory regions [MeDIP-Seq]

Identification of building principles of methylation states at CG rich regions by high-throughput editing of a mammalian genome

Genomic profiling of DNA methyltransferases reveals a role for DNMT3B in genic methylation [Bisulfite-Seq]

Genomic profiling of DNA methyltransferases reveals a role for DNMT3B in genic methylation [ChIP-Seq]

Cis-regulatory landscape of four cell types of the retina

Binding of High Mobility Group A proteins to the mammalian genome occurs as a function of AT-content [ChIP-Seq]

Binding of High Mobility Group A proteins to the mammalian genome occurs as a function of AT-content [RNA-Seq]

CG dinucleotides enhance promoter activity independent of DNA methylation

Mammalian ISWI and SWI/SNF selectively mediate binding of distinct groups of transcription factors (ATAC-seq data sets)

Mammalian ISWI and SWI/SNF selectively mediate binding of distinct groups of transcription factors (Bis-seq data sets)