finds rsid with genomic position for feasible input format.
☆30Mar 26, 2024Updated 2 years ago
Alternatives and similar repositories for rsidmap
Users that are interested in rsidmap are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- shifts hg19/38 genomic position for feasible input format.☆12Jun 8, 2023Updated 3 years ago
- Analysis code for Olink CVD1 - HF analysis☆15Aug 14, 2024Updated last year
- Estimate Bias Due To Sample Overlap In Mendelian Randomization Studies☆12Sep 1, 2022Updated 3 years ago
- ☆10Jun 5, 2021Updated 5 years ago
- ☆14May 25, 2018Updated 8 years ago
- Managed Kubernetes at scale on DigitalOcean • AdDigitalOcean Kubernetes includes the control plane, bandwidth allowance, container registry, automatic updates, and more for free.
- ☆12Dec 4, 2023Updated 2 years ago
- Genetic correlation calculation pipeline via summary statistics for PheWeb☆13Mar 22, 2019Updated 7 years ago
- ☆13Nov 30, 2018Updated 7 years ago
- Connecting GWAS summary data to analytical tools☆24Mar 25, 2024Updated 2 years ago
- ☆23May 11, 2023Updated 3 years ago
- LOGODetect is a powerful tool to identify small segments that harbor local genetic correlation between two traits/diseases.☆29Jul 30, 2025Updated 11 months ago
- R package for epigraphdb☆31Jul 6, 2024Updated 2 years ago
- ☆120Nov 12, 2022Updated 3 years ago
- Partitioning algorithm developed for LAVA☆17May 17, 2024Updated 2 years ago
- 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.
- Software to infer latent pleiotropic components from GWAS summary data☆17Jan 30, 2025Updated last year
- Collaborative genetic studies of idiopathic pulmonary fibrosis☆22Jul 17, 2026Updated last week
- ☆11Jan 30, 2025Updated last year
- This repository contains scripts related to Surendran P, Stewart I et al. Nature Medicine 2022 "Rare and common genetic causes of chemica…☆19Jul 15, 2022Updated 4 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
- user-friendly pipeline for GWAS fine-mapping☆14Mar 9, 2025Updated last year
- cfdr.pleio is an R package implementing conditional and conjunctional false discovery rates for studying pleiotropic gene variants betwee…☆18Feb 9, 2023Updated 3 years ago
- A highly scalable and accurate inference of gene expression and structure for single-cell transcriptomes using semi-supervised deep learn…☆12May 19, 2021Updated 5 years ago
- Bare Metal GPUs on DigitalOcean Gradient AI • AdPurpose-built for serious AI teams training foundational models, running large-scale inference, and pushing the boundaries of what's possible.
- 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
- 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 6 months ago
- BrainSeq Phase II project lead by LIBD for the BrainSeq Consortium☆11Jan 7, 2024Updated 2 years 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…☆18Jan 28, 2024Updated 2 years ago
- A graph-based pipeline used to call/genotype snvs/indels/SVs from NGS data☆17Aug 30, 2025Updated 10 months ago
- Create Regional Association Plots☆13May 27, 2026Updated 2 months ago
- Cross-population fine-mapping☆46Dec 7, 2024Updated last year
- Workflow for performing cistrome-wide associations studies☆11Jul 25, 2022Updated 4 years ago
- Estimate local SNP heritability and genetic covariance from GWAS summary association statistics.☆43May 2, 2018Updated 8 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.
- Single cell Type Enrichment Analysis for Phenotypes (STEAP)☆14Jun 16, 2021Updated 5 years ago
- ☆31Feb 25, 2020Updated 6 years ago
- R package for CAUSE☆59Dec 29, 2023Updated 2 years ago
- Epigenomewide Association Studies (EWAS) with FUnctional Summary-based ImputatiON (FUSION)☆12Mar 24, 2023Updated 3 years ago
- ☆15Nov 12, 2017Updated 8 years ago
- Pair-wise conditional analysis and colocalisation☆43May 2, 2024Updated 2 years ago
- LocusCompareR is a R package with visualization tools for comparing two genetic association datasets.☆136Jul 8, 2026Updated 3 weeks ago