NIH Websites Are Changing

Beginning in late July, NIH will start introducing a new website experience designed to make it easier to find health information, research, funding opportunities, and other resources. During the transition, you may notice changes to navigation, page layouts, and where some information is located.

 

Data Sharing

 *** In collaboration with the NICHD Bioinformatics & Scientific Programming Core (BSPC), we have developed multiome-wf, a Snakemake workflow that can be used to transform & combine raw data from scRNA-seq, scATAC-seq and scMultiome experiments into usable results for downstream analysis. multiome-wf can be found on github , with documentation located here . ***

*** Please visit our Embryonic Mouse Brain Epigenome Atlas at the UCSC Genome browser to explore our comprehensive characterization of the transcriptome (scRNA-seq), chromatin accessibility (snATAC-seq), histone modifications (H3K4me3, H3K27me3, H3K27ac) and higher order chromatin structure (Hi-C and Capture-C) in the E12.5 mouse brain (Rhodes et al., Nature Communications 2022). ***

Datasets from Reducing methylation of histone 3.3 lysine 4 in the medial ganglionic eminence and hypothalamus recapitulates neurodevelopmental disorder phenotypes (bioRxiv, 2025):

GSE293881 → Single cell Multiome reactions for all WT & H3.3K4M homozygous E13.5 (MGE & hypothalamus) and P60 (cortex & hypothalamus) samples used in this study. Separate subseries of snRNA-seq (GSE293751) & snATAC-seq (GSE293655) datasets.

Datasets from Loss of Ezh2 in the medial ganglionic eminence alters interneuron fate, cell morphology and gene expression profiles (Front Cell Neurosci, 2024):

GSE233153 → Single cell Multiome reactions for all E12.5 & E15.5 Nkx2.1-Cre;Ezh2 WT, heterozygous and homozygous samples used in this study. Separate subseries of snRNA-seq (GSE233151) and snATAC-seq (GSE233152) datasets.
GSE233190 → H3K27me3 CUT&Tag reactions of E12.5 and E15.5 MGE from Nkx2.1-Cre;Ezh2 WT, Het and Hom mouse.

Datasets from Transcriptional Heterogeneity of ventricular zone cell in the ganglionic eminences of the mouse forebrain (eLife, 2022):

GSE167013 → scRNA-seq of E12.5 WT MGE, LGE, CGE and cortex 
GSE190593 → (1) scRNA-seq of E12.5 Nes-dVenus MGE, LGE, CGE and cortex, (2) scRNA-seq of E14.5 WT MGE, LGE and CGE, (3) scRNA-seq of E14.5 Nes-dVenus MGE, LGE and CGE

Datasets from An epigenome atlas of neural progenitors within the embryonic mouse forebrain (Nat Comm, 2022):

GSE167050 → snRNA-seq and snATAC-seq of E12.5 WT MGE, LGE, CGE & cortex, and P30 Dlx6aCre;Sun1-GFP cortex & hippocampus samples used in this study. Separate subseries of E12.5 scRNA-seq (GSE167013), P30 snRNA-seq (GSE167016), E12.5 snATAC-seq (GSE167047) and P30 snATAC-seq (GSE167048) datasets.
GSE201494 → Cut&Tag and CUT&RUN reactions for E12.5 WT, MGE, LGE, CGE and cortex. Separate subseries of H3K4me3 CUT&Tag (GSE201487), H3K27me3 CUT&Tag (GSE201488) and H3K27ac CUT&RUN (GSE201400) datasets. 
GSE201186 → Hi-C reactions of E12.5 WT MGE, LGE, CGE and cortex
GSE201317 → Capture-C reactions of E12.5 WT MGE, LGE, CGE and cortex

 

Point of ContactPOC Email
Tim Petrostim.petros@nih.gov