A free and open-source pedigree tool by PhenoTips®
☆57Jan 10, 2024Updated 2 years ago
Alternatives and similar repositories for open-pedigree
Users that are interested in open-pedigree are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Repository for the family history/pedigree project☆13Jun 17, 2026Updated last month
- A web tool for building pedigrees, https://ccge-boadicea.github.io/pedigreejs/☆74Jun 9, 2026Updated last month
- Semantic data model of the set of common data elements for rare disease registration☆12Oct 26, 2023Updated 2 years ago
- Documentation for NCBI BLAST AMI☆11Feb 28, 2022Updated 4 years ago
- Process Illumina instrument data into SAM/BAM/CRAM files.☆10Jul 6, 2026Updated 2 weeks 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.
- Scotch pipeline for indel calling.☆10Nov 25, 2019Updated 6 years ago
- Pedigree drawing with ease☆24Feb 10, 2022Updated 4 years ago
- An online pedigree tool for research applications. Build pedigrees interactively and store as images or text files in ped format. QuickPe…☆31Jun 9, 2026Updated last month
- ☆26Aug 7, 2019Updated 6 years ago
- Design and implementation of FAIR Data Cube☆11Jun 2, 2025Updated last year
- Java library to map LOINC-encoded test results to Human Phenotype Ontology☆34Jan 16, 2024Updated 2 years ago
- ☆14Jun 15, 2026Updated last month
- A software toolkit for the interconversion of standard data models for phenotypic data☆16Updated this week
- The local version of high-definition likelihood inference of genetic correlations (HDL-L)☆14Aug 8, 2025Updated 11 months 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.
- Ontology for consent codes and data use requirements☆70Sep 21, 2022Updated 3 years ago
- A simple observation count database☆11Jan 13, 2026Updated 6 months ago
- Generate an enhanced VCF files from ClinVar XML Full releases☆17Feb 23, 2026Updated 4 months ago
- Multivariate Gaussian Models for Genomic and Pedigree Data☆14May 23, 2020Updated 6 years ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆44Jun 18, 2026Updated last month
- A MatchMaker Exchange server☆12Jun 1, 2026Updated last month
- R package for RNA-seq workflows at HCI☆15Nov 20, 2025Updated 8 months ago
- Ontoclick - A web browser extension to turn highlighted text into a proper Ontology term.☆13Jun 2, 2023Updated 3 years ago
- A python library for calculating semantic similarity between patients in N3C☆14Oct 5, 2022Updated 3 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.
- simulate sequence data and complicated pedigree structures☆16Apr 5, 2023Updated 3 years ago
- anor: an annotation and visualization system based on R and Shiny framework☆34Apr 20, 2020Updated 6 years ago
- A rules-based transformation engine that allows exporting data in REDCap as FHIR resources.☆12Apr 12, 2023Updated 3 years ago
- Simulation of rare and common variants based on 1000 genomes data☆19Sep 24, 2021Updated 4 years ago
- Calculates the Variant Allele Fraction of variants in VCF files☆19Nov 28, 2024Updated last year
- R packages for pedigree analysis☆16May 26, 2026Updated last month
- ☆15Feb 7, 2020Updated 6 years ago
- Python package for cancer early detection based on a model of cancer evolution and circulating tumor DNA (ctDNA) shedding☆13Jan 8, 2021Updated 5 years ago
- Tools for working with pedigrees in R☆28Jun 29, 2026Updated 3 weeks ago
- Serverless GPU API endpoints on Runpod - Get Bonus Credits • AdSkip the infrastructure headaches. Auto-scaling, pay-as-you-go, no-ops approach lets you focus on innovating your application.
- Platform for Oncogenomic Reporting and Interpretation (PORI)☆35Jan 10, 2026Updated 6 months ago
- An app and library for building, conversion, and validation of GA4GH Phenopackets.☆18Jun 15, 2026Updated last month
- ☆18Jul 3, 2020Updated 6 years ago
- PedigreeSim is software that generates simulated genetic marker data of individuals in pedigreed populations. A population can consist of…☆14Apr 13, 2021Updated 5 years ago
- Identification of Human Phenotype Entities☆11Nov 2, 2018Updated 7 years ago
- A3 - FHIR-native ETL+Q Prototype☆14Dec 14, 2020Updated 5 years ago
- The Rare Disease Registry Framework (RDRF) is an open source tool for the creation of web-based patient registries.☆18Jul 19, 2023Updated 3 years ago