Phenome Exome Association and Correlation Of Key phenotypes
☆35Aug 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
Sorting:
- PHESANT - PHEnome Scan ANalysis Tool (pheWAS, Mendelian randomisation (MR)-pheWAS etc.) in UK Biobank☆157Oct 22, 2025Updated 4 months ago
- Suite of heritability and genetic correlation estimation tools for exome-sequencing data☆35Dec 5, 2025Updated 3 months ago
- Development for SAIGE and SAIGE-GENE(+)☆89Feb 12, 2026Updated 3 weeks ago
- Pipeline for multiplex computing of statistical colocalization via COLOC between GWAS and QTL data.☆21Aug 19, 2025Updated 6 months ago
- Divine: Prioritizing Genes for Rare Mendelian Disease in Whole Exome Sequencing Data☆13Apr 18, 2019Updated 6 years ago
- GENI plots to visualise results from genome-wide association studies☆31Oct 14, 2024Updated last year
- Heritability Estimation with high Efficiency using LD and Summary Statistics☆13Feb 14, 2024Updated 2 years ago
- An R package for plotting GWAS results from the GAPIT package☆14Oct 9, 2025Updated 4 months ago
- Make interactive LocusZoom plots from a local GWAS file☆10May 9, 2025Updated 9 months ago
- BrainSeq Phase II project lead by LIBD for the BrainSeq Consortium☆11Jan 7, 2024Updated 2 years ago
- Tests Allelic Expression data for extreme imbalance w.r.t. population☆11Oct 8, 2021Updated 4 years ago
- ☆12Jun 7, 2024Updated last year
- Counterfactual Inference by Machine Learning and Attribution Models☆14Aug 24, 2023Updated 2 years ago
- ☆12Dec 4, 2023Updated 2 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆22Mar 25, 2022Updated 3 years ago
- Software for estimating correlation of trait effect sizes across populations☆54May 30, 2025Updated 9 months ago
- Analysis of the genomic architecture and functional role of myocardial trabeculae☆13Apr 4, 2024Updated last year
- A curated list of monogenic epilepsy genes☆15Sep 4, 2025Updated 6 months ago
- Older repo for MRLocus. See new website for software usage guide:☆15Aug 17, 2023Updated 2 years ago
- The C. elegans transcriptome at single cell resolution☆11Mar 28, 2018Updated 7 years ago
- ☆13Jun 15, 2022Updated 3 years ago
- regenie is a C++ program for whole genome regression modelling of large genome-wide association studies.☆255Nov 13, 2025Updated 3 months ago
- The tutorial for performing single-/multi-trait association analysis of whole-genome/whole-exome sequencing (WGS/WES) studies using FAVOR…☆36Dec 3, 2024Updated last year
- A collection of commonly used formats for quick lookup.☆14Jan 12, 2026Updated last month
- Segmented HAPlotype Estimation and Imputation Tool☆96Dec 5, 2025Updated 3 months ago
- Sample code for ldsc analyses in UKBB☆33May 4, 2023Updated 2 years ago
- Hail helper functions for the gnomAD project and Translational Genomics Group☆100Updated this week
- Ultrafast GPU-enabled QTL mapper☆206Jun 29, 2025Updated 8 months ago
- ☆15Apr 10, 2024Updated last year
- ☆14Oct 26, 2017Updated 8 years ago
- Molecular Signatures Database (MSigDB) in a data frame☆16Dec 3, 2018Updated 7 years ago
- mity: A highly sensitive mitochondrial variant analysis pipeline for whole genome sequencing data☆40Sep 8, 2025Updated 5 months ago
- ☆16Dec 7, 2020Updated 5 years ago
- Fine-mapping with infinitesimal effects☆20May 27, 2025Updated 9 months ago
- Scripts for reproducing analyses of large RNA-seq datasets☆15May 22, 2019Updated 6 years ago
- Code for GBMI trans-ancestry proteome Mendelian randomization satellite paper☆18Dec 25, 2023Updated 2 years ago
- ☆196May 2, 2022Updated 3 years ago
- Scripts used for generating Neale Lab UKB results☆21Oct 11, 2022Updated 3 years ago
- Pairwise Hierarchical Model☆20Mar 11, 2022Updated 3 years ago