☆23May 19, 2025Updated last year
Alternatives and similar repositories for fast_hpo_cr
Users that are interested in fast_hpo_cr are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- This is the repository for the Python based program for automated deep phenotype analysis of clinical information using large language mo…☆35Sep 30, 2025Updated last year
- A software toolkit for the interconversion of standard data models for phenotypic data☆18Nov 2, 2026Updated last week
- Collections of GA4GH phenopackets that represent individuals with Mendelian diseases.☆43Updated this week
- Rareservoir Database Tools☆15Mar 13, 2023Updated 3 years ago
- An integrated ontology for Phenomics☆10Updated this week
- 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.
- An app and library for building, conversion, and validation of GA4GH Phenopackets.☆20Jun 15, 2026Updated 4 months ago
- Repository for the family history/pedigree project☆13Aug 26, 2026Updated 2 months ago
- Identification of Human Phenotype Entities☆11Nov 2, 2018Updated 8 years ago
- A package to convert cancer data to GA4GH phenopacket☆10Aug 5, 2025Updated last year
- ☆33Mar 15, 2025Updated last year
- Data ingest pipeline for OMIM.☆15Updated this week
- A Python library for discovery of genotype-phenotype associations☆12Oct 30, 2026Updated last week
- AI-MARRVEL (AIM) is an AI system for rare genetic disorder diagnosis☆23May 12, 2026Updated 5 months ago
- Ontoclick - A web browser extension to turn highlighted text into a proper Ontology term.☆13Oct 30, 2026Updated last week
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- Data ingest application for Monarch Initiative knowledge graph using Koza☆25Updated this week
- ☆11Oct 29, 2026Updated last week
- Misc. documents for the Bioinformatics Open Source Conference (BOSC), https://www.open-bio.org/events/bosc/☆13Apr 6, 2026Updated 7 months ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆50Jun 18, 2026Updated 4 months ago
- Intelligent APIs for a more connected web: https://smart-api.info☆24Updated this week
- AnModel Context Protocol (MCP) server for the Unpaywall API. Search article titles, fetch DOI metadata, retrieve best open‑access links, …☆12Apr 24, 2026Updated 6 months ago
- Connecting AI to biomedical data☆16Oct 6, 2026Updated last month
- ☆11Feb 26, 2025Updated last year
- ☆14Oct 4, 2022Updated 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.
- Medical action ontology☆66Oct 10, 2026Updated 3 weeks ago
- Diverse sampling for single-cell datasets☆17Mar 22, 2026Updated 7 months ago
- Fast Rust reimplementation of Ensembl VEP (Variant Effect Predictor): same flags and output formats, 100x+ faster☆48Updated this week
- First, Do NOHARM AI Benchmark Leaderboard☆13Feb 11, 2026Updated 8 months ago
- ☆35Jan 11, 2025Updated last year
- ☆14Oct 13, 2026Updated 3 weeks ago
- ☆12Sep 30, 2026Updated last month
- Bash scripts to bulk download full-text PDFs (or any other sources) from PubmedCentral OA articles☆11May 8, 2026Updated 6 months ago
- Human Phenotype Ontology Workbench☆22Sep 17, 2023Updated 3 years ago
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- For BioHackathon Europe 2021.☆30Nov 18, 2022Updated 3 years ago
- A Comprehensive Rare Disease Diagnostic Dataset with nearly 50,000 patients covering more than 4000 diseases☆53Mar 13, 2026Updated 7 months ago
- loinc2hpo Annotation Data☆26Aug 4, 2022Updated 4 years ago
- ☆12Aug 8, 2019Updated 7 years ago
- Ontology for the description of human clinical features☆381Updated this week
- 3ASC: variant prioritization tool leveraging multiple instance learning for rare Mendelian disease genomic testing☆11Nov 11, 2024Updated last year
- Create cell sentences from sequencing data☆23Aug 12, 2024Updated 2 years ago