Searching journal content for articles similar to Ramagopalan et al. 20 (10): 1352.

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  1. ...numbers of loci in a model that was then tractable for follow-up studies to dissect sequence requirements. In all, we tested 110 polymorphic Alu loci (Supplemental Table S1) selected because these are common variants, many of which map to Genome-Wide Association Studies (GWAS) signals and therefore may...
  2. ...to particular genomic regions.We first determined the location of ERVs based on RepeatMasker (Smit et al. 2013–2015) and their associated epigenetic marks by whole- bisulfite sequencing (WGBS) and H3K9me3 ChIP-seq in the human colon cancer cell line HCT116 (Fig. 1A). To simplify the epigenetic profiles, we...
  3. ...of specific biological pathways/functions. Results A large set of TRs share their recruitment sites with NR1H4 in the mouse liver , defining distinct classes of CRMs In order to define TRs interconnected with NR1H4, we used our chromatin immunoprecipitation-high throughput sequencing (ChIP-seq) data from Lien...
  4. ...perform a genome-wide scan of recent positive selection and identify hundreds of novel substrates of adaptive regulatory evolution that are enriched for biologically interesting pathways such as melanogenesis and adipocytokine signaling. These data and results provide new insights into patterns...
  5. ...regions and lineage-specific motifs associated with TF binding therein. To benchmark MEDEA, we used a panel of reference cell lines profiled by ENCODE and curated by the ENCODE Project Consortium for the ENCODE-DREAM Challenge. By comparing results with RNA-seq data, ChIP-seq peaks, and DNase...
  6. ...knockdown, ChIP-seq, and HiChIP experiments. After validating these key concepts, we will apply our method to study a time course of retinoic acid (RA)–induced differentiation of mouse embryonic stem cells (mESCs), in which gene expression and chromatin accessibility are measured at baseline (day 0...
  7. ...and BMS753 or RA and BMS961 and presenting a proximal FAIRE and RXRA binding site, stratified for the cell-specific (P19, F9) and common programs. (E) RT-qPCR revealing the temporal RA-induced mRNA expression profiles of bona fide RA target genes. (F ) FAIRE-seq, RXRA, and RNAPII ChIP-seq profiles...
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