Phenome Exome Association and Correlation Of Key phenotypes
☆36Aug 19, 2021Updated 4 years ago
Alternatives and similar repositories for PEACOK
Users that are interested in PEACOK are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Pipeline for multiplex computing of statistical colocalization via COLOC between GWAS and QTL data.☆21Aug 19, 2025Updated 9 months ago
- PHESANT - PHEnome Scan ANalysis Tool (pheWAS, Mendelian randomisation (MR)-pheWAS etc.) in UK Biobank☆163Oct 22, 2025Updated 6 months ago
- Suite of heritability and genetic correlation estimation tools for exome-sequencing data☆36Dec 5, 2025Updated 5 months ago
- Development for SAIGE and SAIGE-GENE(+)☆95Apr 6, 2026Updated last month
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Apr 18, 2019Updated 7 years ago
- Managed Kubernetes at scale on DigitalOcean • AdDigitalOcean Kubernetes includes the control plane, bandwidth allowance, container registry, automatic updates, and more for free.
- Make interactive LocusZoom plots from a local GWAS file☆10May 9, 2025Updated last year
- ☆26Oct 8, 2025Updated 7 months ago
- The C. elegans transcriptome at single cell resolution☆11Mar 28, 2018Updated 8 years ago
- A curated list of monogenic epilepsy genes☆17Mar 13, 2026Updated 2 months ago
- An R package for phenotype generation and association testing for phenome wide associations studies (PheWAS)☆14Jul 11, 2024Updated last year
- GENI plots to visualise results from genome-wide association studies☆32Oct 14, 2024Updated last year
- Tests Allelic Expression data for extreme imbalance w.r.t. population☆11Oct 8, 2021Updated 4 years ago
- Heritability Estimation with high Efficiency using LD and Summary Statistics☆13Feb 14, 2024Updated 2 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆22Mar 25, 2022Updated 4 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.
- ☆45May 13, 2026Updated last week
- Older repo for MRLocus. See new website for software usage guide:☆15Aug 17, 2023Updated 2 years ago
- An R package for plotting GWAS results from the GAPIT package☆14Oct 9, 2025Updated 7 months ago
- HAT is a set of tools for calling de novo variants from whole-genome sequencing data.☆24Nov 18, 2025Updated 6 months ago
- BrainSeq Phase II project lead by LIBD for the BrainSeq Consortium☆11Jan 7, 2024Updated 2 years ago
- Software for estimating correlation of trait effect sizes across populations☆56May 30, 2025Updated 11 months ago
- regenie is a C++ program for whole genome regression modelling of large genome-wide association studies.☆262Nov 13, 2025Updated 6 months ago
- ☆12Jun 7, 2024Updated last year
- Proportional Odds Logistic Mixed Model (POLMM) for ordinal categorical data analysis☆11Aug 26, 2022Updated 3 years ago
- Deploy to Railway using AI coding agents - Free Credits Offer • AdUse Claude Code, Codex, OpenCode, and more. Autonomous software development now has the infrastructure to match with Railway.
- ☆12Dec 4, 2023Updated 2 years ago
- Pairwise Hierarchical Model☆20Mar 11, 2022Updated 4 years ago
- mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data☆44Sep 8, 2025Updated 8 months ago
- Molecular Signatures Database (MSigDB) in a data frame☆16Dec 3, 2018Updated 7 years ago
- Ultrafast GPU-enabled QTL mapper☆210Jun 29, 2025Updated 10 months ago
- Hail helper functions for the gnomAD project and Translational Genomics Group☆100May 12, 2026Updated last week
- Sequence kernel association test (SKAT)☆54Aug 7, 2025Updated 9 months ago
- ☆13Jun 15, 2022Updated 3 years ago
- Tools for processing Nightingale NMR biomarker data in UK Biobank☆64Apr 13, 2026Updated last month
- 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.
- The tutorial for performing single-/multi-trait association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using FAVOR…☆37Dec 3, 2024Updated last year
- A python wrapper around SURVIVOR☆20Feb 15, 2024Updated 2 years ago
- ☆40Jan 24, 2018Updated 8 years ago
- Sample code for ldsc analyses in UKBB☆34May 4, 2023Updated 3 years ago
- A collection of commonly used formats for quick lookup.☆14Mar 26, 2026Updated last month
- ☆14Oct 26, 2017Updated 8 years ago
- ☆16Apr 10, 2024Updated 2 years ago