ATAC-seq peak-calling and QC analysis pipeline

A comprehensive tool for processing, analyzing and visulizing single cell chromatin accessibility sequencing data

Code for the paper "Integrating regulatory DNA sequence and gene expression to predict genome-wide chromatin accessibility across cellular contexts"

PECA is a software for inferring context specific gene regulatory network from paired gene expression and chromatin accessibility data

Big data Regression for predicting DNase I hypersensitivity

A python package for chromVAR

scNOVA : Single-Cell Nucleosome Occupancy and genetic Variation Analysis

A de novo prediction tool of chromatin accessible regions for plant genomes

Robust Open Chromatin Detection via Convex Optimization: Consensus Peak Calling across Multiple ATAC-seq signals

PECA is a software for inferring context specific gene regulatory network from paired gene expression and chromatin accessibility data

Analysis of Single Molecule Footprinting (SMF) data for the analysis of DNA methylation, chromatin accessibility and TF binding. The repository contains all primary code to reproduce the main analyses for the publication "Single molecule footprinting identifies context-dependent regulation of enhancers by DNA methylation" (Kreibich et al., 2023)

See the main fork of this repository here >>>

An R package designed to integrate and visualize various levels of epigenomic information, including but not limited to: ChIP, Histone, ATAC, and RNA sequencing. epiRomics is also designed to identify enhancer and enhanceosome regions from these data.

A robust statistical test for TF footprint data analyses

A two-step model that combines neural network and ensemble learning to predict OCR–mediated interactions.

Snakemake pipeline for analysis and normalization of ATAC-seq data starting from fastq.gz files.

Instructions on how to perform chromatin accessibility data pre-processing and analyses (focusing on bulk ATAC-seq)

A crash course in scATAC-seq data processing

Tool to analyze chromatin accessibility with long read sequencing technologies

Rapid diagnostic strategy for cardiomyopathy etiology