REEV: Explanation and Evaluation of Variants
☆11Apr 27, 2026Updated 4 months ago
Alternatives and similar repositories for reev
Users that are interested in reev are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- SODAR Core: A Django-based framework for building scientific data management web apps☆13Aug 26, 2026Updated last week
- ☆21Aug 30, 2022Updated 4 years ago
- VarFish: comprehensive DNA variant analysis for diagnostics and research☆53Updated this week
- BIH Cluster Wiki☆19Aug 24, 2026Updated 2 weeks ago
- Curated most up-to-date list of AI Agent Frameworks☆37Sep 22, 2025Updated 11 months ago
- Managed Kubernetes at scale on DigitalOcean • AdDigitalOcean Kubernetes includes the control plane, bandwidth allowance, container registry, automatic updates, and more for free.
- This tools counts the number of specific k-mers within sequence data. The counts can then be compare to other counts to determine to comp…☆32Nov 25, 2024Updated last year
- ☆42Jul 3, 2025Updated last year
- Automatic classification of sequence variants and CNVs according to ACMG criteria.☆33Sep 30, 2024Updated last year
- Command line tool to predict phenotype from VCF (gets models from pheno-server-21)☆16Jan 1, 2016Updated 10 years ago
- Automated ACMG/AMP classification for human variants associated with congenital hearing loss☆11May 14, 2025Updated last year
- ☆26Updated this week
- This plugin enables fast translations using deepl.com☆10Nov 10, 2020Updated 5 years ago
- Statistical comparison study of valence-arousal classifiers from EEG signals on DEAP and MANHOB datasets☆12Sep 28, 2022Updated 3 years ago
- UMCU Genetics Nextflow modules☆30Oct 25, 2024Updated last year
- 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.
- emotion recognition through eeg by using HOS method☆10Dec 29, 2021Updated 4 years ago
- A web-browser app to visualise, interpret and prioritise genomic/transcriptomic structural variations (SVs) of multiple samples.☆14May 16, 2026Updated 3 months ago
- Bitscopic Interpreting ACMG Standards 2015☆36Updated this week
- Human mitochondrial variants annotation using HmtVar.☆18Oct 16, 2023Updated 2 years ago
- Example of Empirical Mode Decomposition algorithm☆14Mar 25, 2021Updated 5 years ago
- ☆28Mar 31, 2026Updated 5 months ago
- Recommendations to contenarized your bioinformatics software☆12May 30, 2018Updated 8 years ago
- ☆13Dec 7, 2021Updated 4 years ago
- SUmmarizing Multiple Enrichment analysis Results☆10Nov 14, 2024Updated last year
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- ☆12Mar 3, 2026Updated 6 months ago
- Python 3 library with good support for both reading and writing VCF☆112Oct 2, 2025Updated 11 months ago
- ☆17Jan 24, 2023Updated 3 years ago
- A nextflow pipeline which integrates multiple omic data streams and performs coordinated analysis☆11Jul 29, 2026Updated last month
- A Xojo/python tool for identification and annotation of transcription factor binding sites in bacterial genomes☆19Aug 8, 2026Updated 3 weeks ago
- Pipeline for RNA and DNA integrated analysis for somatic mutation detection☆13Updated this week
- (current) A NGS analysis framework for WGS data, which automates the entire process of spinning up AWS EC2 spot instances and processing …☆22Updated this week
- SODAR: System for Omics Data Access and Retrieval☆23Updated this week
- Phenotype-based Diagnosis Tool for Rare Diseases☆13Mar 2, 2026Updated 6 months 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.
- ☆14Aug 31, 2016Updated 10 years ago
- Phenotype and genotype-based patient similarity☆13Oct 2, 2025Updated 11 months ago
- Config and setup to run nf-core/raredisease pipeline☆10Sep 11, 2025Updated 11 months ago
- Generating tool descriptors from bio.tools☆10Jun 13, 2018Updated 8 years ago
- python scripts for proteogenomics analysis☆10Oct 17, 2019Updated 6 years ago
- Variant Interpretation Pipeline☆51Updated this week
- Linear Regression From Scratch☆15Jul 20, 2018Updated 8 years ago