3D GWAS across multiple phenotypes
☆13Oct 11, 2022Updated 3 years ago
Alternatives and similar repositories for PheGWAS
Users that are interested in PheGWAS are comparing it to the libraries listed below
Sorting:
- ☆21Nov 15, 2024Updated last year
- cEll tyPe enrIChment☆16Dec 11, 2022Updated 3 years ago
- Software to infer latent pleiotropic components from GWAS summary data☆15Jan 30, 2025Updated last year
- ☆15Apr 20, 2021Updated 4 years ago
- Integration of TWAS and Colocalization Analysis☆17Oct 29, 2024Updated last year
- ☆40Jan 13, 2026Updated last month
- Using real genotype data, simulate a complex trait as a function of latent expression, fit eQTL weights in independent data, and perform …☆29Jun 18, 2023Updated 2 years ago
- ☆20Sep 12, 2025Updated 5 months ago
- An R package for phenotype generation and association testing for phenome wide associations studies (PheWAS)☆15Jul 11, 2024Updated last year
- MR-link-2: pleiotropy robust cis MR☆21Aug 4, 2025Updated 7 months ago
- Fine-mapping method only using summary statistics☆20Mar 23, 2016Updated 9 years ago
- ☆57Jan 16, 2025Updated last year
- ☆14Jun 24, 2024Updated last year
- A statistical test of pleiotropic effect of a genetic variant on two traits using GWAS summary statistics☆39Sep 18, 2025Updated 5 months ago
- Code for multivariate genome wide association meta analysis☆25Aug 20, 2019Updated 6 years ago
- ☆35Jun 15, 2023Updated 2 years ago
- Estimate Bias Due To Sample Overlap In Mendelian Randomization Studies☆11Sep 1, 2022Updated 3 years ago
- Automated statistical and functional fine-mapping pipeline with extensive API access to datasets.☆43Jan 20, 2023Updated 3 years ago
- LOGODetect is a powerful tool to identify small segments that harbor local genetic correlation between two traits/diseases.☆28Jul 30, 2025Updated 7 months ago
- Leveraging functional information to improve GWAS summary statistic imputation☆19Aug 10, 2021Updated 4 years ago
- ☆24Jan 8, 2026Updated last month
- GWAS genetics Fine-mapping method☆26Oct 16, 2024Updated last year
- ☆11Mar 16, 2022Updated 3 years ago
- Summary-level Unified Method for Modeling Integrated Transcriptome☆10Jun 27, 2023Updated 2 years ago
- Obsolete!! Begin to turn to PrimerServer2☆10Jul 22, 2019Updated 6 years ago
- The local version of high-definition likelihood inference of genetic correlations (HDL-L)☆12Aug 8, 2025Updated 6 months ago
- EXpression PREdiction with Summary Statistics Only☆13Dec 10, 2025Updated 2 months ago
- A tool for detecting CNVs from WGS data☆11Jul 9, 2020Updated 5 years ago
- A tool for phasing and imputing haplotypes in 10k+ low coverage sequencing samples☆10Nov 20, 2020Updated 5 years ago
- An R package for plotting GWAS results from the GAPIT package☆14Oct 9, 2025Updated 4 months ago
- ☆11May 10, 2025Updated 9 months ago
- ☆11Oct 14, 2022Updated 3 years ago
- Causal Variant Evidence Mapping with Non-parametric resampling☆12Dec 16, 2020Updated 5 years ago
- Genotype-based Prediction (GenoPred)☆77Feb 20, 2026Updated 2 weeks ago
- Network representation of LDSC results☆31Mar 16, 2022Updated 3 years ago
- Create Regional Association Plots☆13Sep 7, 2025Updated 5 months ago
- Epigenomewide Association Studies (EWAS) with FUnctional Summary-based ImputatiON (FUSION)☆12Mar 24, 2023Updated 2 years ago
- Open4Gene, A Hurdle Model-based Method for Peak-to-Gene Linkage Analysis☆16Dec 1, 2025Updated 3 months ago
- An accurate and efficient colocalization method accounting for multiple causal signals☆13Jun 3, 2024Updated last year