Pedigree drawing with ease
☆24Feb 10, 2022Updated 4 years ago
Alternatives and similar repositories for ped_draw
Users that are interested in ped_draw are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Graphite - Graph-based variant adjudication☆28Feb 9, 2021Updated 5 years ago
- Clin.iobio - Workflow and reporting for iobio variant analysis pipeline☆12Oct 7, 2025Updated 8 months ago
- Website to analyze conflicting assertions in ClinVar☆19Mar 16, 2026Updated 3 months ago
- A web tool for building pedigrees, https://ccge-boadicea.github.io/pedigreejs/☆74Jun 9, 2026Updated 3 weeks ago
- Client side iobio library for building and executing iobio commands☆10Dec 31, 2018Updated 7 years ago
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- Gene.iobio vue☆72Jun 4, 2026Updated 3 weeks ago
- Semantic data model of the set of common data elements for rare disease registration☆12Oct 26, 2023Updated 2 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆22Mar 25, 2022Updated 4 years ago
- A python tool for parsing pedigree files☆16Aug 29, 2017Updated 8 years ago
- StrVCTVRE, a structural variant classifier for exonic deletions and duplications☆19Dec 6, 2023Updated 2 years ago
- Jupyter notebook for the application of convolutional neural nets to toy DNA sequence data☆15Aug 25, 2021Updated 4 years ago
- Fast Structural Variation Detection Toolbox☆19Feb 16, 2015Updated 11 years ago
- Structural variant VCF annotation, duplicate removal and comparison☆38Oct 14, 2025Updated 8 months ago
- Computational Framework to reconstructing tumor clone structures☆15Mar 31, 2021Updated 5 years ago
- Simple, predictable pricing with DigitalOcean hosting • AdAlways know what you'll pay with monthly caps and flat pricing. Enterprise-grade infrastructure trusted by 600k+ customers.
- A python3 package for operations on pedigree and genotype data☆21Nov 13, 2017Updated 8 years ago
- GARFIELD-NGS: Genomic vARiants FIltering by dEep Learning moDels in NGS☆17Mar 4, 2019Updated 7 years ago
- Rails application for storing and parsing clinical exome VCF files. Gene annotations can be retrieved via Biomart integration from Ensemb…☆10May 7, 2017Updated 9 years ago
- VarFish: comprehensive DNA variant analysis for diagnostics and research☆53Updated this week
- A combined deep learning tool for automated recognition of human phenotype ontology☆27Nov 29, 2022Updated 3 years ago
- Phenotype driven gene prioritization for HPO☆52Jul 26, 2021Updated 4 years ago
- use the noise☆15Apr 15, 2020Updated 6 years ago
- Prediction of protein substitution impact using a directional substitution matrix and homolog alignments☆12Oct 25, 2021Updated 4 years ago
- A webtool for the clinical interpretation of CNVs in rare disease patients☆13Jun 10, 2022Updated 4 years ago
- Bare Metal GPUs on DigitalOcean Gradient AI • AdPurpose-built for serious AI teams training foundational models, running large-scale inference, and pushing the boundaries of what's possible.
- Whole Genome Sequenceing Structural Variation Pipelines☆18Apr 4, 2019Updated 7 years ago
- Human mitochondrial variants annotation using HmtVar.☆18Oct 16, 2023Updated 2 years ago
- ☆15Nov 22, 2022Updated 3 years ago
- C++ wrapper to tabix indexer☆17Jun 27, 2025Updated last year
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆43Jun 18, 2026Updated last week
- ☆13Oct 14, 2017Updated 8 years ago
- PharmGKB NGS Pipeline☆19Oct 2, 2018Updated 7 years ago
- Curated list of resources for variant prioritization☆15Nov 18, 2025Updated 7 months ago
- A phenotype-based tool for variant prioritization in WES and WGS data☆43Nov 21, 2022Updated 3 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.
- heuristics to merge structural variant calls in VCF format.☆38Oct 6, 2016Updated 9 years ago
- ☆36Mar 2, 2021Updated 5 years ago
- Structural variant detection and association testing☆109Feb 2, 2023Updated 3 years ago
- VariantToolChest (VTC) is intended to be a powerful tool chest to analyze VCF files. I encourage anyone to contribute their tools and hel…☆25Apr 8, 2016Updated 10 years ago
- repo for satRday Neuchâtel☆12Mar 21, 2020Updated 6 years ago
- What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.☆37Sep 13, 2023Updated 2 years ago
- The Madeline 2.0 Pedigree Drawing Engine (PDE) is a pedigree drawing program designed to handle large and complex pedigrees with an empha…☆21Feb 20, 2026Updated 4 months ago