PRSKB is a website and command-line interface tool for calculating polygenic risk scores using GWA studies from the NHGRI-EBI Catalog.
☆30Aug 22, 2024Updated last year
Alternatives and similar repositories for PolyRiskScore
Users that are interested in PolyRiskScore are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- An ensemble of functions for use analysing the UKBB records on DNA Nexus☆15Mar 2, 2026Updated 3 weeks ago
- Fine-tuning polygenic risk score models using GWAS summary statistics☆54Oct 19, 2025Updated 5 months ago
- The Polygenic Score Catalog Calculator is a nextflow pipeline for polygenic score calculation☆159Dec 11, 2025Updated 3 months ago
- Interpretable prioritization of splice variants in diagnostic next-generation sequencing☆18May 9, 2024Updated last year
- Fast Structural Variation Detection Toolbox☆19Feb 16, 2015Updated 11 years ago
- Proton VPN Special Offer - Get 70% off • AdSpecial partner offer. Trusted by over 100 million users worldwide. Tested, Approved and Recommended by Experts.
- Research Methods in R☆31Nov 3, 2025Updated 4 months ago
- A web app to search pubmed☆12Jul 8, 2024Updated last year
- Scalable genomic analysis pipelines, written in WDL☆12Mar 11, 2026Updated 2 weeks ago
- Comprehensive Human Expressed SequenceS☆19Jul 13, 2025Updated 8 months ago
- nf-core/references is a bioinformatics pipeline that build references, for multiple use cases☆19Jan 15, 2026Updated 2 months ago
- R codes and data for 'Smoking, Alcohol consumption, and 24 Gastrointestinal Diseases: Mendelian Randomization Analysis'☆11Mar 5, 2023Updated 3 years ago
- omim database☆27Jun 13, 2024Updated last year
- scikit-learn course for 2017 NGCM Summer Academy☆17Jun 30, 2017Updated 8 years ago
- Code for Hourly Temperature-Stroke Case-Crossover in NYS☆10May 21, 2021Updated 4 years ago
- 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.
- ClassifyCNV: a tool for clinical annotation of copy-number variants☆73Jun 26, 2023Updated 2 years ago
- Config files for my GitHub profile.☆14Mar 23, 2023Updated 3 years ago
- A software package for calculating, applying, evaluating and plotting the results of polygenic risk scores☆202Aug 21, 2024Updated last year
- Package for genetic network analysis of GWAS summary statistics☆17Aug 24, 2025Updated 7 months ago
- ☆15Sep 9, 2024Updated last year
- PacBio BAM C++ library☆20Aug 14, 2023Updated 2 years ago
- UKB Weekend Warrior MVPA Analysis☆12Apr 28, 2025Updated 10 months ago
- Steve's Miscellaneous Functions☆10Oct 21, 2025Updated 5 months ago
- ☆13Jul 17, 2024Updated last year
- Virtual machines for every use case on DigitalOcean • AdGet dependable uptime with 99.99% SLA, simple security tools, and predictable monthly pricing with DigitalOcean's virtual machines, called Droplets.
- Tracebacks for Humans (in Jupyter notebooks)☆12Dec 30, 2025Updated 2 months ago
- ☆14Jun 26, 2019Updated 6 years ago
- Association between physical frailty and incident depression☆14Apr 19, 2024Updated last year
- A tutorial on the case time series design for small-area analysis☆14Jul 14, 2024Updated last year
- Ancestry and haplotype aware simulation of genotypes and phenotypes for complex trait analysis☆24Dec 15, 2025Updated 3 months ago
- Identifying differentially methylated regions from MethylC-seq (bisulfite-sequencing) data☆28Jun 13, 2023Updated 2 years ago
- Tools for processing Nightingale NMR biomarker data in UK Biobank☆59Nov 28, 2025Updated 3 months ago
- Variational Inference of Polygenic Risk Scores☆28Apr 22, 2025Updated 11 months ago
- Genetic association studies☆16Oct 29, 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.
- Code and description to implement Bayesian Kernel Machine Regression-Causal Mediation Analysis by Devick et al. (arXiv: 1811.10453)☆15Dec 19, 2023Updated 2 years ago
- A script to run HLA typing tools from next generation sequencing data☆12Jan 4, 2023Updated 3 years ago
- Simulate GWAS data from an arbitrary DAG☆11Oct 29, 2025Updated 4 months ago
- Structural variant VCF annotation, duplicate removal and comparison☆37Oct 14, 2025Updated 5 months ago
- Adding random effects model to the METAL software☆15Jun 11, 2023Updated 2 years ago
- An R Interface to the SNOMED CT API <https://github.com/IHTSDO/snowstorm>☆12Dec 15, 2022Updated 3 years ago
- ☆15Dec 8, 2023Updated 2 years ago