adamewing / methylartistLinks
Tools for plotting methylation data in various ways
☆165Updated 2 weeks ago
Alternatives and similar repositories for methylartist
Users that are interested in methylartist are comparing it to the libraries listed below
Sorting:
- pbsv - PacBio structural variant (SV) calling and analysis tools☆159Updated 9 months ago
- ☆142Updated 2 weeks ago
- A tool for somatic structural variant calling using long reads☆155Updated last month
- ☆122Updated 4 months ago
- Tandem repeat genotyping and visualization from PacBio HiFi data☆129Updated this week
- Jasmine: SV Merging Across Samples☆232Updated 11 months ago
- ☆108Updated 2 weeks ago
- Wally: Visualization of aligned sequencing reads and contigs☆120Updated 2 months ago
- accurate LiftOver tool for new genome assemblies☆139Updated last year
- Pangenome-based genome inference☆149Updated last week
- A flexible, scalable, and reproducible pipeline to automate variant calling from raw sequence reads, with lots of bells and whistles - fo…☆110Updated 5 months ago
- Research release basecalling models and configurations☆117Updated 6 months ago
- Constructing a pangenome gene graph☆200Updated 4 months ago
- A tool to identify, orient, trim and rescue full length cDNA reads☆83Updated 3 years ago
- Hierarchical Alignment Format☆173Updated 3 months ago
- Transcriptome Annotation by Modular Algorithms (for long read RNA sequencing data)☆164Updated 2 years ago
- Pipeline for differential gene expression (DGE) and differential transcript usage (DTU) analysis using long reads☆108Updated 2 years ago
- BAM Statistics, Feature Counting and Annotation☆151Updated last week
- Pipeline for calling structural variations in whole genomes sequencing Oxford Nanopore data☆114Updated 4 years ago
- Meta-pipeline to identify transposable element insertions using next generation sequencing data☆105Updated 6 months ago
- Workflows and tutorials for LongRead analysis with specific focus on Oxford Nanopore data☆143Updated 4 months ago
- Phased assembly variant caller☆129Updated last year
- A *fast* tool for BAM/CRAM quality evaluation, intended for long reads☆163Updated this week
- A complete diploid human genome☆139Updated 2 months ago
- Structural Variant Identification Method using Long Reads☆179Updated 4 years ago
- Tandem repeat expansion detection or genotyping from long-read alignments☆134Updated 2 weeks ago
- Comprehensive TE insertion identification with WGS/WES data from multiple sequencing technics☆118Updated 5 months ago
- Collection of tools for the analysis of CpG data☆101Updated 5 months ago
- GenMap - Fast and Exact Computation of Genome Mappability☆113Updated last year
- Dfam Transposable Element Tools Docker container.☆101Updated last month