☆84Mar 3, 2025Updated last year
Alternatives and similar repositories for princess
Users that are interested in princess are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ☆128May 4, 2026Updated 2 weeks ago
- Tools for the analysis of structural variation in genomes☆81Feb 23, 2026Updated 2 months ago
- ☆12Oct 13, 2021Updated 4 years ago
- Structural variation caller using third generation sequencing☆654Updated this week
- Combine structural variation outputs from long sequencing reads into a superior call set☆18Aug 6, 2025Updated 9 months 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.
- Long read aligner☆114May 26, 2023Updated 2 years ago
- ☆35Feb 20, 2020Updated 6 years ago
- Kmer Analysis of Pileups for Genotyping☆39Mar 6, 2026Updated 2 months ago
- Swipe your Structural Variants called on long (ONT/PacBio) reads with short exact (Illumina) reads.☆32Sep 19, 2022Updated 3 years ago
- Phylogenetic Analysis of Long Terminal Repeat Retrotransposons☆18Oct 4, 2022Updated 3 years ago
- Toolset for SV simulation, comparison and filtering☆417Dec 1, 2023Updated 2 years ago
- For bluntifying overlapped GFAs☆13Jul 26, 2024Updated last year
- Jasmine: SV Merging Across Samples☆252Dec 20, 2024Updated last year
- Structural variant caller☆55Dec 8, 2021Updated 4 years ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- Dynamic time warping of Oxford Nanopore squiggle data to characterize tandem repeats.☆32Jul 2, 2020Updated 5 years ago
- Clair: Exploring the limit of using deep neural network on pileup data for germline variant calling☆105Sep 1, 2022Updated 3 years ago
- A method for variant graph genotyping based on exact alignment of k-mers☆87Apr 1, 2019Updated 7 years ago
- Runs a combination of tools to generate structural variant calls on whole-genome sequencing data☆103Nov 5, 2020Updated 5 years ago
- DNA methylation analysis downstream to Nanopolish for Oxford Nanopore DNA sequencing datasets☆30Jul 3, 2023Updated 2 years ago
- Structural variant toolkit for VCFs☆410Mar 21, 2026Updated 2 months ago
- Archived version 1.0.2☆16Nov 25, 2019Updated 6 years ago
- Exact Tandem Repeat Finder (not a TRF replacement)☆51Oct 22, 2019Updated 6 years ago
- ☆42Dec 29, 2025Updated 4 months ago
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- Structural Variants Assessment Based on Haplotype-resolved Assemblies☆21Apr 28, 2023Updated 3 years ago
- Graph-based mapping of long sequences, noisy or HiFi.☆55Oct 5, 2020Updated 5 years ago
- pbsv - PacBio structural variant (SV) calling and analysis tools☆166Feb 26, 2025Updated last year
- Toolkit for VNTR genotyping and repeat-pan genome graph construction☆33Aug 18, 2025Updated 9 months ago
- assembly evaluation tool☆35May 11, 2022Updated 4 years ago
- Clair3 - Symphonizing pileup and full-alignment for deep learning-based long-read variant calling☆363May 4, 2026Updated 2 weeks ago
- ☆37Apr 13, 2024Updated 2 years ago
- A complete diploid human genome☆149May 7, 2026Updated 2 weeks ago
- SV genotyping with long reads☆40Jul 3, 2023Updated 2 years ago
- 1-Click AI Models by DigitalOcean Gradient • AdDeploy popular AI models on DigitalOcean Gradient GPU virtual machines with just a single click. Zero configuration with optimized deployments.
- A snakemake pipeline to assembly, polishing, correction and quality check from Oxford nanopore reads.☆36Apr 4, 2025Updated last year
- Toolkit for calling structural variants using short or long reads☆115Updated this week
- Set of tools to manipulate and visualize modified base bam files☆61Aug 2, 2022Updated 3 years ago
- ☆11Dec 9, 2022Updated 3 years ago
- Plotting tools for nanopore methylation data☆95Jul 28, 2025Updated 9 months ago
- Translocator: local realignment and global remapping enabling accurate translocation detection using single-molecule sequencing long read…☆12Jan 22, 2020Updated 6 years ago
- Long read based human genomic structural variation detection with cuteSV☆286Mar 26, 2026Updated last month