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
Sorting:
- Fast Structural Variation Detection Toolbox☆19Feb 16, 2015Updated 11 years ago
- Polygenic Risk Scores Pipeline to calculate genetic risk score for any given phenotype/trait (using PRSice)☆11Mar 30, 2023Updated 2 years ago
- Applying polygenic scores (PGS) on imputed genotypes☆31Oct 28, 2025Updated 4 months ago
- omim database☆27Jun 13, 2024Updated last year
- The Polygenic Score Catalog Calculator is a nextflow pipeline for polygenic score calculation☆157Dec 11, 2025Updated 2 months ago
- Interpretable prioritization of splice variants in diagnostic next-generation sequencing☆18May 9, 2024Updated last year
- Comprehensive Human Expressed SequenceS☆19Jul 13, 2025Updated 7 months ago
- Ancestry and haplotype aware simulation of genotypes and phenotypes for complex trait analysis☆24Dec 15, 2025Updated 2 months ago
- PacBio BAM C++ library☆20Aug 14, 2023Updated 2 years ago
- Variational Inference of Polygenic Risk Scores☆28Apr 22, 2025Updated 10 months ago
- Package for genetic network analysis of GWAS summary statistics☆15Aug 24, 2025Updated 6 months ago
- Identifying differentially methylated regions from MethylC-seq (bisulfite-sequencing) data☆28Jun 13, 2023Updated 2 years ago
- Research Methods in R☆31Nov 3, 2025Updated 4 months ago
- ☆10Jan 26, 2026Updated last month
- ☆12Oct 29, 2025Updated 4 months ago
- An approximate sequence pattern matcher for FASTQ/FASTA files.☆32Jan 22, 2016Updated 10 years ago
- A software package for calculating, applying, evaluating and plotting the results of polygenic risk scores☆202Aug 21, 2024Updated last year
- Structural variant VCF annotation, duplicate removal and comparison☆36Oct 14, 2025Updated 4 months ago
- pythonic wrapper for libhts (moved to: https://github.com/quinlan-lab/hts-python)☆49Mar 3, 2017Updated 9 years ago
- A tutorial on how to run basic polygenic risk score analysis☆84Jan 24, 2023Updated 3 years ago
- BS-seq analysis pipeline☆45Mar 28, 2023Updated 2 years ago
- Tool to annotate outfiles from ExpansionHunter and TRGT with the pathologic implications of the repeat☆39Dec 15, 2025Updated 2 months ago
- ☆39Jul 3, 2025Updated 8 months ago
- R codes and data for 'Smoking, Alcohol consumption, and 24 Gastrointestinal Diseases: Mendelian Randomization Analysis'☆11Mar 5, 2023Updated 3 years ago
- Simulate GWAS data from an arbitrary DAG☆11Oct 29, 2025Updated 4 months ago
- Scalable genomic analysis pipelines, written in WDL☆11Feb 24, 2026Updated last week
- ☆12Sep 20, 2020Updated 5 years ago
- Package to design primers for MutaSeq and related methods☆11Jan 15, 2021Updated 5 years ago
- Detecting recombination of viral lineages☆11Dec 23, 2025Updated 2 months ago
- ☆10Mar 7, 2023Updated 2 years ago
- R functions for automation of biomarker discovery based on processing downstream of large LC-MS datasets from any peak picking software☆10May 17, 2017Updated 8 years ago
- A high throughput GC-MS analysis pipeline built on the Python PyMS library☆11Feb 12, 2018Updated 8 years ago
- Super basic example for data joins in D3.js☆12Sep 7, 2018Updated 7 years ago
- ☆10Nov 23, 2018Updated 7 years ago
- ☆14Mar 26, 2024Updated last year
- Tracebacks for Humans (in Jupyter notebooks)☆12Dec 30, 2025Updated 2 months ago
- This is an R package to retrieve data from Open Target☆15Jul 25, 2025Updated 7 months ago
- pTFCE SPM Toolbox☆12Jan 2, 2020Updated 6 years ago
- The R/Python scripts for the analysis of single-cell RNA-seq data from COVID-19 patients☆10Dec 16, 2020Updated 5 years ago