harbourlab / SparKLinks
Publication quality NGS track plotting
☆113Updated 2 years ago
Alternatives and similar repositories for SparK
Users that are interested in SparK are comparing it to the libraries listed below
Sorting:
- HMMRATAC peak caller for ATAC-seq data☆100Updated 7 months ago
- Check strandedness of RNA-Seq fastq files☆124Updated 2 years ago
- An R package to Identify, Annoatate and Visialize Isoform Switches with Functional Consequences (from RNA-seq data)☆114Updated 4 months ago
- Allele-specific alignment sorting☆58Updated 2 years ago
- Generate IGV style locus tracks from bigWig files in R☆163Updated 7 months ago
- Fit-Hi-C is a tool for assigning statistical confidence estimates to chromosomal contact maps produced by genome-wide genome architecture…☆86Updated 2 years ago
- Tutorial Website☆59Updated 4 years ago
- Single Cell Long Read is a suite of tools dedicated to Cell barcode / UMI assignment and analysis of highly multiplexed single cell Nanop…☆73Updated 2 years ago
- Analysis pipeline for CUT&RUN and CUT&TAG experiments that includes QC, support for spike-ins, IgG controls, peak calling and downstream …☆92Updated 3 weeks ago
- Analysis Workflow for Assay for Transposase-Accessible Chromatin using sequencing (ATAC-Seq)☆75Updated last year
- fork of RSeQC python RNAseq metrics suit of tools☆48Updated 6 years ago
- A toolkit for QC and visualization of ATAC-seq results.☆70Updated 5 months ago
- Ultraperformant reimplementation of SICER☆56Updated 3 years ago
- ☆69Updated last year
- Software for Quantifying Interspersed Repeat Expression☆58Updated 3 years ago
- FEELnc : FlExible Extraction of LncRNA☆87Updated 9 months ago
- SEACR: Sparse Enrichment Analysis for CUT&RUN☆110Updated 2 years ago
- TAD calling, phase imputation, 3D modeling and more for diploid single-cell Hi-C (Dip-C) and general Hi-C☆109Updated 4 years ago
- Quantification of transposable element expression using RNA-seq☆71Updated last year
- Links to ATAC-seq analysis tools☆68Updated 3 years ago
- Extract 3D contacts (.pairs) from sequencing alignments☆113Updated this week
- Detecting sites of genomic enrichment☆192Updated 2 years ago
- SNV calling from single cell sequencing☆100Updated 7 months ago
- dcHiC: Differential compartment analysis for Hi-C datasets☆69Updated last year
- A single cell RNA-seq workflow, including highly variable gene analysis, cell type assignment and differential expression analysis.☆102Updated 2 years ago
- Estimate locus specific human LINE-1 expression.☆35Updated 2 years ago
- Tip and tricks for BAM files☆85Updated 6 years ago
- A package for quantifying transposable elements at a locus level for RNAseq datasets.☆27Updated 4 months ago
- A toolset for profiling alternative splicing events in RNA-Seq data.☆81Updated 5 months ago
- ☆62Updated last year