This package provides a function to reformat lists of genome coverage files, such as bigWig of bam files, into the directory structure of a UCSC Track Hub ready to be visualized in the genome browser. For details about it's use, please have a look at the vignette of the package.
☆28Apr 29, 2024Updated last year
Alternatives and similar repositories for easyTrackHubs
Users that are interested in easyTrackHubs are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ChIP-seq peak calling with GC effects adjustment☆10Jul 5, 2018Updated 7 years ago
- An R package to process and analyze transcriptomic data☆19Jun 18, 2025Updated 9 months ago
- Various multi-trait association tests in R☆11Oct 30, 2018Updated 7 years ago
- A library and tool for accessing remote BLOW5 files.☆24Feb 5, 2026Updated last month
- ☆25Feb 2, 2024Updated 2 years ago
- SNP and indel calls from multiple sequence alignment (MSA)☆13Nov 11, 2022Updated 3 years ago
- Plot bacterial gene maps and genome comparison plots from command line with genoPlotR and GenomeDiagram☆12Mar 10, 2026Updated last week
- ☆19Aug 8, 2023Updated 2 years ago
- Pipeline to analyse ChIP-Rx data, i.e ChIP-Seq with reference exogenous genome spike-in normalization☆15Sep 18, 2025Updated 6 months ago
- A segmentation approach to analyze DNA methylation patterns and identify differentially methylation regions from whole-genome datasets☆19Feb 16, 2026Updated last month
- Viola is a flexible and powerful python package designed specifically for analysis of genomic structural variant (SV) signatures.☆28Jul 26, 2024Updated last year
- ☆13Nov 15, 2017Updated 8 years ago
- Web-Application for the cross-visualization of HiC and ChIP-seq data.☆18Feb 17, 2026Updated last month
- Genomic Visualization Catalog☆13Oct 6, 2022Updated 3 years ago
- Generate IGV style locus tracks from bigWig files in R☆183Oct 28, 2024Updated last year
- Simplified odds ratio calculation of binomial GAM/GLM models☆30Oct 17, 2025Updated 5 months ago
- AirLift is a tool that updates mapped reads from one reference genome to another. Unlike existing tools, It accounts for regions not shar…☆28May 23, 2024Updated last year
- Mean Alterations Using Discrete Expression☆14Apr 9, 2024Updated last year
- A better, faster way to count guides in CRISPR screens.☆34Apr 11, 2025Updated 11 months ago
- Characterize gene dynamics over trajectories using GLMs, GEEs, & GLMMs.☆13Mar 3, 2026Updated 2 weeks ago
- ☆11Dec 7, 2022Updated 3 years ago
- ☆10May 31, 2022Updated 3 years ago
- CADD-SV – a framework to score the effect of structural variants☆18Feb 11, 2026Updated last month
- binned motif enrichment analysis and visualisation☆45Jan 27, 2026Updated last month
- ☆41Jun 16, 2025Updated 9 months ago
- Category-wide association study (CWAS) (Werling et al., 2018; An et al., 2018)☆10Dec 12, 2025Updated 3 months ago
- R package to wrap cBioPortal's API to pull data from public or private cBioPortal databases☆23Jan 30, 2026Updated last month
- TQSLE v1.0 released☆10Aug 29, 2023Updated 2 years ago
- Allo: a multi-mapped read rescue strategy for gene regulatory analyses☆24Sep 5, 2024Updated last year
- We present HRIBO (High-throughput annotation by Ribo-seq), a workflow to enable reproducible and high-throughput analysis of bacterial Ri…☆13May 22, 2025Updated 10 months ago
- ☆35Updated this week
- Tool comparison for detecting differentially expressed individual transposable elements☆11Jan 7, 2022Updated 4 years ago
- ☆10Jan 29, 2020Updated 6 years ago
- 🐶 hlabud: HLA genotype analysis in R☆17Apr 11, 2025Updated 11 months ago
- Tool for plotting sequencing data along genomic coordinates.☆336Dec 12, 2025Updated 3 months ago
- ☆352Apr 16, 2025Updated 11 months ago
- MetaSNV, a metagenomic SNV calling pipeline.☆21Mar 25, 2022Updated 3 years ago
- ☆18Apr 20, 2025Updated 11 months ago
- Bayesian mixed-effect model to test differences in cell type proportions from single-cell data, in R☆122Updated this week