with annotations and epigenomic data.
This R package is part of the echoverse suite that supports
echolocatoR
: an automated
genomic fine-mapping pipeline.
If you use echoannot
, please cite:
if(!require("remotes")) install.packages("remotes")
remotes::install_github("RajLabMSSM/echoannot")
library(echoannot)
For more detailed information about each dataset, use ?
:
R library(echolocatoR) ?NOTT_2019.interactome # example dataset
-
Data from this publication contains results from cell type-specific (neurons, oligodendrocytes, astrocytes, microglia, & peripheral myeloid cells) epigenomic assays (H3K27ac, ATAC, H3K4me3) from human brain tissue.
-
For detailed metadata, see:
data("NOTT_2019.bigwig_metadata")
-
Built-in datasets:
- Enhancer/promoter coordinates (as GenomicRanges)
data("NOTT_2019.interactome") # Examples of the data nested in "NOTT_2019.interactome" object: NOTT_2019.interactome$`Neuronal promoters` NOTT_2019.interactome$`Neuronal enhancers` NOTT_2019.interactome$`Microglia promoters` NOTT_2019.interactome$`Microglia enhancers` ... ...
- PLAC-seq enhancer-promoter interactome coordinates
NOTT_2019.interactome$H3K4me3_around_TSS_annotated_pe NOTT_2019.interactome$`Microglia interactome` NOTT_2019.interactome$`Neuronal interactome` NOTT_2019.interactome$`Oligo interactome` ... ...
-
API access to full bigWig files on UCSC Genome Browser, which includes
- Epigenomic reads (as GenomicRanges)
- Aggregate epigenomic score for each cell type - assay combination
-
Data from this preprint contains results from bulk and single-cell chromatin accessibility epigenomic assays in 39 human brains.
data("CORCES_2020.bulkATACseq_peaks") data("CORCES_2020.cicero_coaccessibility") data("CORCES_2020.HiChIP_FitHiChIP_loop_calls") data("CORCES_2020.scATACseq_celltype_peaks") data("CORCES_2020.scATACseq_peaks")
- API access to a diverse library of cell type/line-specific epigenomic (e.g. ENCODE) and other genome-wide annotations.
- API access to cell type-specific epigenomic data.
- API access to various genome-wide SNP annotations (e.g. missense, nonsynonmous, intronic, enhancer).
- API access to known per-SNP QTL and epigenomic data hits.
Brian
M. Schilder, Bioinformatician II
Raj Lab
Department
of Neuroscience, Icahn School of Medicine at Mount Sinai