GreenleafLab / NucleoATACLinks
nucleosome calling using ATAC-seq
☆106Updated 4 years ago
Alternatives and similar repositories for NucleoATAC
Users that are interested in NucleoATAC are comparing it to the libraries listed below
Sorting:
- HMMRATAC peak caller for ATAC-seq data☆99Updated 8 months ago
- A tool for bigWig files.☆119Updated 7 years ago
- Tools for processing UMI RNA-tag data☆131Updated 2 years ago
- A toolkit for QC and visualization of ATAC-seq results.☆70Updated 6 months ago
- ☆88Updated last month
- STAR based ENCODE Long RNA-Seq processing pipeline☆95Updated 4 years ago
- Analysis Workflow for Assay for Transposase-Accessible Chromatin using sequencing (ATAC-Seq)☆74Updated 2 years ago
- Pipeline for processing inDrops sequencing data☆76Updated 6 years ago
- Tool for the detection and quantification of alternative splicing events from RNA-Seq data.☆108Updated 2 weeks ago
- An R package for inferring the subclonal architecture of tumors☆122Updated last year
- WASP: allele-specific pipeline for unbiased read mapping and molecular QTL discovery☆105Updated 4 years ago
- A single cell RNA-seq workflow, including highly variable gene analysis, cell type assignment and differential expression analysis.☆103Updated 2 years ago
- AQUAS TF and histone ChIP-seq pipeline☆109Updated 3 years ago
- A modular, containerized pipeline for ATAC-seq data processing☆58Updated 2 months ago
- A toolset for profiling alternative splicing events in RNA-Seq data.☆81Updated 6 months ago
- ☆117Updated last year
- MOODS: Motif Occurrence Detection Suite☆105Updated 2 years ago
- ☆70Updated 2 years ago
- Tools for working with BUS files☆101Updated 2 months ago
- ATAC-seq snakemake pipeline☆89Updated 5 years ago
- Public repository containing research code for the TCGA PanCanAtlas Splicing project☆41Updated 4 years ago
- Inferring and visualizing clonal evolution in multi-sample cancer sequencing☆147Updated 4 years ago
- This package computes informative enrichment and quality measures for ChIP-seq/DNase-seq/FAIRE-seq/MNase-seq data. It can also be used to…☆59Updated 5 years ago
- Fast and accurate in silico inference of HLA genotypes from RNA-seq☆139Updated 11 months ago
- Transcript quantification import for modular pipelines☆141Updated last month
- Analysis of subclonal copy number alterations (CNA) and loss of heterozygosity (LOH) in cancer☆97Updated 4 years ago
- Create a *de novo* alternative splicing database, validate splicing events, and quantify percent spliced-in (Psi) from RNA seq data☆67Updated 5 years ago
- ENCODE Uniform processing pipeline for ChIP-seq☆124Updated 5 years ago
- mgatk: mitochondrial genome analysis toolkit☆108Updated 6 months ago
- Snakefiles for common RNA-seq data analysis workflows (STAR and Kallisto).☆93Updated 8 years ago