AI-MARRVEL (AIM) is an AI system for rare genetic disorder diagnosis
☆23May 12, 2026Updated 5 months ago
Alternatives and similar repositories for AI_MARRVEL
Users that are interested in AI_MARRVEL are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Rareservoir Database Tools☆15Mar 13, 2023Updated 3 years ago
- ☆11Feb 26, 2025Updated last year
- 3ASC: variant prioritization tool leveraging multiple instance learning for rare Mendelian disease genomic testing☆11Nov 11, 2024Updated last year
- ☆33Dec 6, 2024Updated last year
- Browser-based tool for visualizing and analyzing germline copy number variants in genomic data☆12Nov 7, 2024Updated last year
- 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.
- ☆11May 12, 2026Updated 5 months ago
- A machine learning tool to predict tandem repeat pathogenicity☆12Jan 2, 2024Updated 2 years ago
- NHC: A computational approach to detect physiological homogeneity in the midst of genetic heterogeneity☆12Feb 25, 2026Updated 8 months ago
- A Tool to Annotate and Prioritize Exome Variants☆268Aug 3, 2026Updated 3 months ago
- ☆23Sep 21, 2021Updated 5 years ago
- ☆23May 19, 2025Updated last year
- Pipeline to find aberrant events in RNA-Seq data, useful for diagnosis of rare disorders☆14Oct 26, 2026Updated last week
- ☆29Aug 25, 2025Updated last year
- A Mendelian approach to variant effect prediction built in keras☆22Aug 22, 2026Updated 2 months ago
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- Web app for interacting with Google DeepMind's AlphaGenome model — interval predictions, variant effect analysis, and visualization☆12Sep 19, 2026Updated last month
- Functional-trained variant effect predictor☆18Aug 27, 2026Updated 2 months ago
- Config and setup to run nf-core/raredisease pipeline☆10Sep 11, 2025Updated last year
- Variant Graph Craft (VGC) is an interactive genomic variant visualization program.☆19May 17, 2024Updated 2 years ago
- Distributed and cloud computing framework for vg☆23Apr 21, 2026Updated 6 months ago
- Long read sequencing pipeline to identify variants in patients with neurodevelopmental disorders☆13Oct 26, 2026Updated last week
- omim database☆31Jun 13, 2024Updated 2 years ago
- ☆12Sep 21, 2026Updated last month
- A Comprehensive Rare Disease Diagnostic Dataset with nearly 50,000 patients covering more than 4000 diseases☆53Mar 13, 2026Updated 7 months ago
- GPUs on demand by Runpod - Special Offer Available • AdRun AI, ML, and HPC workloads on powerful cloud GPUs—without limits or wasted spend. Deploy GPUs in under a minute and pay by the second.
- Variant catalogue pipeline☆26Jan 30, 2026Updated 9 months ago
- Basic UPD caller☆13Aug 23, 2021Updated 5 years ago
- A deep learning approach to de novo variant calling in next generation sequencing data☆21Jun 19, 2026Updated 4 months ago
- ☆19Mar 14, 2022Updated 4 years ago
- Automatic classification of sequence variants and CNVs according to ACMG criteria.☆34Sep 30, 2024Updated 2 years ago
- The present study is finalised to determine the most advanced models in the literature capable of producing new high-quality molecules st…☆10Aug 31, 2021Updated 5 years ago
- Reference files for running HipSTR with various organisms☆18Feb 3, 2018Updated 8 years ago
- mtDNA-Server 2: A web-service and Nextflow pipeline for mitochondrial genomes☆23May 19, 2026Updated 5 months ago
- genotype and visualize structural variants in the human pangenome graphs☆16Nov 21, 2025Updated 11 months 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.
- TAPES : a Tool for Assessment and Prioritisation in Exome Studies☆27Jun 22, 2026Updated 4 months ago
- A phenotype-based tool for variant prioritization in WES and WGS data☆41Nov 21, 2022Updated 3 years ago
- ☆28Updated this week
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆50Jun 18, 2026Updated 4 months ago
- First, Do NOHARM AI Benchmark Leaderboard☆13Feb 11, 2026Updated 8 months ago
- This is the repository for the Python based program for automated deep phenotype analysis of clinical information using large language mo…☆34Sep 30, 2025Updated last year
- Visualizing genetic sequence variation☆14Apr 27, 2020Updated 6 years ago