☆14May 25, 2018Updated 8 years ago
Alternatives and similar repositories for mr-base-methods-paper
Users that are interested in mr-base-methods-paper are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Estimate Bias Due To Sample Overlap In Mendelian Randomization Studies☆12Sep 1, 2022Updated 3 years ago
- Repurposing antihypertensive drugs for the prevention of Alzheimer’s disease: a Mendelian Randomization study☆34Aug 25, 2020Updated 5 years ago
- Partitioning algorithm developed for LAVA☆17May 17, 2024Updated 2 years ago
- phenoscanner allows users to query the PhenoScanner database of genotype-phenotype associations from inside R☆56Jul 18, 2022Updated 4 years ago
- ☆29Jul 25, 2018Updated 7 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.
- Data objects for various sets of instruments☆48Jun 22, 2020Updated 6 years ago
- ☆16Feb 12, 2023Updated 3 years ago
- BWMR (Bayesian Weighted Mendelian Randomization)☆22Jun 14, 2023Updated 3 years ago
- Binaries for tools used in genetics in an R package☆12Apr 7, 2025Updated last year
- Connecting GWAS summary data to analytical tools☆24Mar 25, 2024Updated 2 years ago
- Analysis code for Olink CVD1 - HF analysis☆15Aug 14, 2024Updated last year
- Tutorial for running Mendelian Randomization analysis using R☆37Apr 29, 2024Updated 2 years ago
- Power calculations for Mendelian Randomisation☆23Sep 27, 2017Updated 8 years ago
- R package for epigraphdb☆31Jul 6, 2024Updated 2 years ago
- Managed Database hosting by DigitalOcean • AdPostgreSQL, MySQL, MongoDB, Kafka, Valkey, and OpenSearch available. Automatically scale up storage and focus on building your apps.
- R package for two-sample Mendelian randomization using the robust adjusted profile score☆42Oct 31, 2025Updated 8 months ago
- Mendelian Randomization with Biomarker Associations for Causality with Outcomes☆27Dec 7, 2018Updated 7 years ago
- Code to run Mendelian Randomization Analysis☆10Mar 14, 2022Updated 4 years ago
- Software implementing the Latent Causal Variable Model☆66Jun 30, 2020Updated 6 years ago
- finds rsid with genomic position for feasible input format.☆30Mar 26, 2024Updated 2 years ago
- ☆11Jan 30, 2025Updated last year
- ☆13Nov 30, 2018Updated 7 years ago
- This code relates to the project titled "Assessing the causal role of epigenetic clocks in the development of multiple cancers: a Mendeli…☆14Nov 22, 2021Updated 4 years ago
- Fine mapping of genes associated with Parkinson's Disease using a variety of methods☆11Mar 7, 2022Updated 4 years ago
- Open source password manager - Proton Pass • AdSecurely store, share, and autofill your credentials with Proton Pass, the end-to-end encrypted password manager trusted by millions.
- A repository on resources about Mendelian Randomization☆10Jul 9, 2018Updated 8 years ago
- user-friendly pipeline for GWAS fine-mapping☆14Mar 9, 2025Updated last year
- ☆10Jul 24, 2020Updated 5 years ago
- MR-link and genome integration. genome_integration is a repository for the analysis of genomic data. Specifically, the repository impleme…☆11Jul 8, 2022Updated 4 years ago
- ☆11Mar 16, 2022Updated 4 years ago
- this repository contains the code (not the data and the results) to reproduce the paper : Impact of the gut microbiota and associated met…☆15Jun 3, 2022Updated 4 years ago
- An R package for Mendelian Randomization☆40Mar 27, 2024Updated 2 years ago
- Application of the Simple Sum method for testing co-localization of GWAS with any other SNP-level data (e.g. eQTL data)☆10Jan 26, 2026Updated 5 months ago
- VarGen is an R package designed to get a list of variants related to a disease. It just need an OMIM morbid ID as input and optionally a…☆17Jan 28, 2024Updated 2 years ago
- Deploy open-source AI quickly and easily - Special Bonus Offer • AdRunpod Hub is built for open source. One-click deployment and autoscaling endpoints without provisioning your own infrastructure.
- BrainSeq Phase II project lead by LIBD for the BrainSeq Consortium☆11Jan 7, 2024Updated 2 years ago
- Create Regional Association Plots☆13May 27, 2026Updated last month
- ☆12Dec 4, 2023Updated 2 years ago
- Kidney Epigenome and Transcriptome-based multi-stage Prioritization☆17Oct 31, 2022Updated 3 years ago
- Workflow for performing cistrome-wide associations studies☆11Jul 25, 2022Updated 3 years ago
- Single cell Type Enrichment Analysis for Phenotypes (STEAP)☆14Jun 16, 2021Updated 5 years ago
- Epigenomewide Association Studies (EWAS) with FUnctional Summary-based ImputatiON (FUSION)☆12Mar 24, 2023Updated 3 years ago