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
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 5 months ago
- Website to analyze conflicting assertions in ClinVar☆19Mar 16, 2026Updated last week
- A web tool for building pedigrees, https://ccge-boadicea.github.io/pedigreejs/☆71Mar 3, 2026Updated 2 weeks ago
- Client side iobio library for building and executing iobio commands☆10Dec 31, 2018Updated 7 years ago
- Gene.iobio vue☆69Mar 13, 2026Updated last week
- 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 3 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☆36Oct 14, 2025Updated 5 months ago
- Computational Framework to reconstructing tumor clone structures☆15Mar 31, 2021Updated 4 years ago
- 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 8 years ago
- VarFish: comprehensive DNA variant analysis for diagnostics and research☆52Mar 14, 2026Updated last week
- Curated list of resources for variant prioritization☆14Nov 18, 2025Updated 4 months ago
- 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 5 years ago
- A webtool for the clinical interpretation of CNVs in rare disease patients☆13Jun 10, 2022Updated 3 years ago
- Prediction of protein substitution impact using a directional substitution matrix and homolog alignments☆12Oct 25, 2021Updated 4 years ago
- Whole Genome Sequenceing Structural Variation Pipelines☆18Apr 4, 2019Updated 6 years ago
- Human mitochondrial variants annotation using HmtVar.☆18Oct 16, 2023Updated 2 years ago
- ☆15Nov 22, 2022Updated 3 years ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆39Nov 19, 2025Updated 4 months ago
- C++ wrapper to tabix indexer☆17Jun 27, 2025Updated 8 months ago
- ☆13Oct 14, 2017Updated 8 years ago
- PharmGKB NGS Pipeline☆19Oct 2, 2018Updated 7 years ago
- A phenotype-based tool for variant prioritization in WES and WGS data☆42Nov 21, 2022Updated 3 years ago
- heuristics to merge structural variant calls in VCF format.☆38Oct 6, 2016Updated 9 years ago
- ☆35Mar 2, 2021Updated 5 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 9 years ago
- Structural variant detection and association testing☆108Feb 2, 2023Updated 3 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.☆36Sep 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 last month