violin plots representing atac-seq and gro-seq densities (GraphPad Software Inc)
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Violin Plots Representing Atac Seq And Gro Seq Densities, supplied by GraphPad Software Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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1) Product Images from "Lineage-determining transcription factor-driven promoters regulate cell type-specific macrophage gene expression"
Article Title: Lineage-determining transcription factor-driven promoters regulate cell type-specific macrophage gene expression
Journal: Nucleic Acids Research
doi: 10.1093/nar/gkae088
Figure Legend Snippet: Characterizing the major cistromes of BMDMs. (A-D) Cistromes of related TFs were filtered and united to aggregate cistromes; those of the ETS family with IRF8 ( A ) and the bZIP ( B ), bHLH ( C ) and MEF2 families ( D ). Heat maps represent the aggregate cistromes clustered and sorted based on TF densities (left). The scale of densities ranges from 0 to 3. The extent of DNA methylation (Bisulfite-seq, scale: 0–0.1) and chromatin openness (ATAC-seq, scale: 0–20) in 1-kb windows and nascent transcription (GRO-seq, scale: 0–20) in 2-kb windows for each region (middle) and the genomic distribution of the regions relative to the closest TSS (right) are depicted. For the latter, the average distance of 100 consecutive regions on the heat maps was calculated. ( E ) Violin plot represents the genomic distribution of the indicated cistromes relative to the closest TSS.
Techniques Used: DNA Methylation Assay, Bisulfite Sequencing
Figure Legend Snippet: Identification of macrophage-specific promoter classes. ( A ) Pie chart represents the ratio of putative promoters with the indicated composition. ( B ) Box plot represents the levels of nascent transcripts (GRO-seq) originating from the different classes of promoters indicated. Whiskers are plotted according to the Tukey method. ( C ) The distribution of TSSs (CAGE), the identified motifs, and CG sites and the extent of DNA methylation (Bisulfite-seq), chromatin openness (ATAC-seq), H3K27ac and H3K4me3 modifications (MC, MNase-ChIP-seq), and nascent transcription (GRO-seq) are depicted in 1-kb windows around the top TSSs at the indicated promoter classes (TSS selection is detailed in the Methods section). (D–I) Histograms show the distribution of CG sites ( D ), the extent of DNA methylation ( E ), the H3K27ac ( F ) and H3K4me3 modifications ( G ) and nascent transcription (H, I) around the top TSSs at the indicated promoter classes. ( J ) Line plots represent per-position nucleotide frequencies around the top TSSs at the promoters with distal elements only (left) or proximal elements only (right).
Techniques Used: DNA Methylation Assay, Bisulfite Sequencing, ChIP-sequencing, Selection
Figure Legend Snippet: Characteristics of LDTF-driven promoters. ( A ) Scatter plot represents correlations between the nascent (GRO-seq) and mature mRNA levels (RNA-seq) associated with LDTF-driven promoters. ( B ) GO terms (Biological processes) specific to LDTF-driven promoters are shown. ( C ) Putative models (top) and examples (bottom) for LDTF-driven (left) and CGI promoters (right) are shown. Model: Arrows represent TSSs and transcription initiation frequencies. Greyscale, white, red, and light gold boxes represent respectively methylatable, non-methylated, and prototypically TSS-distal or proximal non-methylatable elements. Black, greyscale and white circles represent respectively methylated, potentially methylated, and non-methylated cytosines. LDTF: lineage-determining TF, CBTF: CGI-binding TF. Genome browser views show the chromatin openness (dark olive), nascent transcription (light and dark green, strand specifically), mRNA level (dark grey), the density of CG (light blue) and methyl-CG dinucleotides (blue), and the distribution of elements (black and red boxes) of representative genes (middle) and promoters (bottom).
Techniques Used: RNA Sequencing, Methylation, Binding Assay