Tools for plotting methylation data in various ways
☆194Jun 13, 2026Updated last month
Alternatives and similar repositories for methylartist
Users that are interested in methylartist are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Set of tools to manipulate and visualize modified base bam files☆62Aug 2, 2022Updated 3 years ago
- DNA methylation analysis downstream to Nanopolish for Oxford Nanopore DNA sequencing datasets☆30Jul 3, 2023Updated 3 years ago
- A bioinformatics tool for working with modified bases☆271Jul 14, 2026Updated last week
- Identify and annotate TE-mediated insertions in long-read sequence data☆48Mar 25, 2026Updated 4 months ago
- ☆52Sep 27, 2025Updated 9 months ago
- Open source password manager - Proton Pass • AdSecurely store, share, and autofill your credentials with Proton Pass, the end-to-end encrypted password manager trusted by millions.
- Haplotype-specific somatic copy number aberrations/profiling from long reads sequencing data☆82Jul 17, 2026Updated last week
- Plotting tools for nanopore methylation data☆95Jul 28, 2025Updated 11 months ago
- Methylation Phasing for Nanopore Sequencing☆51Mar 5, 2023Updated 3 years ago
- ☆129Updated this week
- Methylation/modified base calling separated from basecalling.☆188Sep 17, 2024Updated last year
- ☆37Jul 3, 2026Updated 3 weeks ago
- Structural variation caller using third generation sequencing☆673Updated this week
- A bioinformatics tool for viewing and calculating base modification frequencies from BAM files☆46Jun 19, 2026Updated last month
- Oxford Nanopore's Basecaller☆854Updated this week
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- Tandem repeat expansion detection or genotyping from long-read alignments☆165Mar 25, 2026Updated 4 months ago
- Automatic DNA methylation detection from nanopore tools and their consensus model☆78May 22, 2023Updated 3 years ago
- A tool for somatic structural variant calling using long reads☆174Jun 8, 2026Updated last month
- ☆27Nov 14, 2025Updated 8 months ago
- Tandem repeat genotyping with long reads☆38Sep 23, 2025Updated 10 months ago
- Ultra-fast methylation calling and event alignment tool for nanopore sequencing data (supports CUDA acceleration)☆166Mar 19, 2026Updated 4 months ago
- SV calling for diploid assemblies☆32Mar 22, 2024Updated 2 years ago
- Comprehensive TE insertion identification with WGS/WES data from multiple sequencing technics☆126Apr 17, 2026Updated 3 months ago
- Clair3 - Symphonizing pileup and full-alignment for deep learning-based long-read variant calling☆383Jul 9, 2026Updated 2 weeks ago
- Deploy to Railway using AI coding agents - Free Credits Offer • AdUse Claude Code, Codex, OpenCode, and more. Autonomous software development now has the infrastructure to match with Railway.
- Copy number caller for long read data including SNV utilization☆69Mar 31, 2025Updated last year
- Read-based phasing of genomic variants, also called haplotype assembly☆423Jul 4, 2026Updated 3 weeks ago
- ☆14Sep 11, 2023Updated 2 years ago
- Long read based human genomic structural variation detection with cuteSV☆291Jul 12, 2026Updated last week
- Hybrid somatic SV caller using long reads and short-read refinement for tumor–normal sequencing.☆16May 14, 2026Updated 2 months ago
- PEPPER-Margin-DeepVariant