AI-MARRVEL (AIM) is an AI system for rare genetic disorder diagnosis
☆21May 12, 2026Updated last week
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:
- Distributed and cloud computing framework for vg☆23Apr 21, 2026Updated last month
- A phenotype-based tool for variant prioritization in WES and WGS data☆43Nov 21, 2022Updated 3 years ago
- Visualizing genetic sequence variation☆14Apr 27, 2020Updated 6 years ago
- Reference files for running HipSTR with various organisms☆17Feb 3, 2018Updated 8 years ago
- ☆21Aug 30, 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.
- SMN1 copy-number and sequence variant analysis from next generation sequencing data☆23Feb 20, 2026Updated 3 months ago
- A Snakemake pipeline for Quality Control of Whole Genome Sequencing data☆14Jan 18, 2022Updated 4 years ago
- Prioritizing Copy Number Variants (CNV) using Phenotype and Gene Functional Similarity☆18Mar 10, 2022Updated 4 years ago
- Robust detection of clinically relevant structural and copy number variation from whole genome sequencing data☆75Sep 4, 2024Updated last year
- omim database☆29Jun 13, 2024Updated last year
- Variant Graph Craft (VGC) is an interactive genomic variant visualization program.☆18May 17, 2024Updated 2 years ago
- reference implementation of GA4GH WGS Quality Control Standards☆11Nov 25, 2025Updated 6 months ago
- Classifier of pathogenic non-coding variants in Mendelian diseases☆11Feb 6, 2020Updated 6 years ago
- ☆12Dec 14, 2021Updated 4 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.
- Inferring multi-modality dynamics for single cell genomics data☆13Dec 18, 2025Updated 5 months ago
- A Girder plugin for exposing slicer execution model's CLI modules over the web☆18Feb 26, 2026Updated 2 months ago
- Software for analyzing high dimensional dose-response data☆19Mar 18, 2026Updated 2 months ago
- Config and setup to run nf-core/raredisease pipeline☆10Sep 11, 2025Updated 8 months ago
- An analysis pipeline for long-reads from both PacBio and Oxford Nanopore Technologies (ONT), written in Nextflow.☆66Updated this week
- SANEFALCON (Single reAds Nucleosome-basEd FetAL fraCtiON): Calculating the fetal fraction for noninvasive prenatal testing based on genom…☆14Jun 5, 2020Updated 5 years ago
- NiPTUNE. A Python library for NIPT analyses.☆11Nov 22, 2021Updated 4 years ago
- ☆17May 19, 2025Updated last year
- ☆13Jun 18, 2018Updated 7 years ago
- AI Agents on DigitalOcean Gradient AI Platform • AdBuild production-ready AI agents using customizable tools or access multiple LLMs through a single endpoint. Create custom knowledge bases or connect external data.
- Codes for the articles published in Towards Data Science, a journal of Medium.com☆11Jul 16, 2021Updated 4 years ago
- VPOT - Variant Prioritisation Ordering Tool. VPOT is a Python tool written to allow prioritisation of variants in ANNOVAR annotated VCF f…☆19Oct 27, 2021Updated 4 years ago
- New home of the Covid19-NP-Swab NP-swab manufacturing project☆16Jul 24, 2020Updated 5 years ago
- do some exercise☆14Dec 2, 2025Updated 5 months ago
- ☆14Dec 2, 2022Updated 3 years ago
- dv-trio provides a pipeline to call variants for a trio (father-mother-child) using DeepVariants [1]. Genomic Variant Calling Files (gVCF…☆11Feb 3, 2021Updated 5 years ago
- Package to design primers for MutaSeq and related methods☆11Jan 15, 2021Updated 5 years ago
- Granular Functional Filtering (Gruffi) to isolate stressed cells☆14Nov 7, 2024Updated last year
- Search your Paperpile library with Alfred☆10Feb 12, 2026Updated 3 months ago
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- Browser-based tool for visualizing and analyzing germline copy number variants in genomic data☆11Nov 7, 2024Updated last year
- Misc. documents for the Bioinformatics Open Source Conference (BOSC), https://www.open-bio.org/events/bosc/☆13Apr 6, 2026Updated last month
- TRGT Repeat expansion summary☆10Apr 10, 2023Updated 3 years ago
- ☆18Mar 27, 2024Updated 2 years ago
- Whole Slide Images Segmentation using Patch UNet☆17Mar 30, 2020Updated 6 years ago
- call copy number from WES(WXS)☆11May 10, 2021Updated 5 years ago
- Analysis of Multivariate Event Times https://kkholst.github.io/mets/☆14May 18, 2026Updated last week