☆40Jan 14, 2026Updated 5 months ago
Alternatives and similar repositories for Platinum-Pedigree-Datasets
Users that are interested in Platinum-Pedigree-Datasets are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- VNTR annotation using motif selection☆42May 25, 2026Updated last month
- Structural variant benchmark☆24Mar 4, 2025Updated last year
- Phased assembly variant caller☆141Dec 4, 2024Updated last year
- Improved structural variant discovery in accurate long reads using sample-specific strings (SFS)☆49Apr 20, 2026Updated 2 months ago
- A complete diploid human genome☆152Updated this week
- 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.
- Genotyping of copy number sensitive allele-specific haplotypes☆28Jun 18, 2026Updated last week
- Evaluating genome assemblies☆122Mar 3, 2026Updated 3 months ago
- bioinformatics toolkit in rust☆107May 14, 2026Updated last month
- vcfdist: Accurately benchmarking phased variant calls☆87Feb 23, 2026Updated 4 months ago
- Parakit is a tool to analyze the RCCX module, which contain the CYP21A2 gene, using long sequencing reads.☆15May 27, 2026Updated last month
- ☆17Aug 8, 2025Updated 10 months ago
- Tumor-normal variant calling workflow using HiFi reads☆31Mar 4, 2026Updated 3 months ago
- This repository contains the reference genome assembly Ash1, built from data collected from an Ashkenazi individual.☆12Feb 2, 2022Updated 4 years ago
- ☆129Updated this week
- 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.
- Copy number caller for long read data including SNV utilization☆69Mar 31, 2025Updated last year
- Telomere-to-Telomere diploid Indian Genome☆15Mar 5, 2026Updated 3 months ago
- Characterization of Structural Variation in Chinese samples☆17Dec 22, 2021Updated 4 years ago
- A toolkit for exploring regions of variation in pangenomes☆15Jun 12, 2026Updated 2 weeks ago
- Structural variant toolkit for VCFs☆417May 22, 2026Updated last month
- ☆67Apr 9, 2024Updated 2 years ago
- Lightweight mosaic/somatic SV caller for long reads (WIP)☆36Oct 27, 2025Updated 8 months ago
- Jasmine: SV Merging Across Samples☆255Dec 20, 2024Updated last year
- Functions to compare a SV call sets against a truth set.☆32Jun 18, 2025Updated last year
- 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.
- ☆85Mar 3, 2025Updated last year
- Toolkit for calling structural variants using short or long reads☆115Jun 15, 2026Updated 2 weeks ago
- ATaRVa - Analysis of Tandem Repeat Variation☆21Jun 16, 2026Updated last week
- Small variant, structural variant, and short tandem repeat phasing tool for PacBio HiFi reads☆86May 27, 2026Updated last month
- Rust library for processing sequencing reads.☆25Sep 2, 2024Updated last year
- General purpose utility related to GAF files☆29May 20, 2026Updated last month
- gpuPairHMM: Ultra-fast GPU-based PairHMM for DNA Variant Calling☆15Nov 6, 2025Updated 7 months ago
- LongcallD: joint calling and phasing of small, structural and mosaic variants from long reads☆105Updated this week
- Archived version 1.0.2☆16Nov 25, 2019Updated 6 years ago
- GPU virtual machines on DigitalOcean Gradient AI • AdGet to production fast with high-performance AMD and NVIDIA GPUs you can spin up in seconds. The definition of operational simplicity.
- A VCF comparison engine for structual variant benchmarking☆24Sep 26, 2025Updated 9 months ago
- Aligns short reads using dynamic seed size with strobemers☆202Updated this week
- HitSV: Maximizing discovery of structural variants across sequencing technologies☆26Updated this week
- VCF files of SVs using long-read sequencing (LRS).☆22Dec 17, 2021Updated 4 years ago
- Extract methylation calls from long reads (ONT/ PacBio)☆24Apr 30, 2026Updated last month
- Phase reads, assemble haplotypes and detect SVs☆19Nov 11, 2020Updated 5 years ago
- Tandem repeat genotyping and visualization from PacBio HiFi data☆139Jun 10, 2026Updated 2 weeks ago