shifts hg19/38 genomic position for feasible input format.
☆12Jun 8, 2023Updated 3 years ago
Alternatives and similar repositories for easylift
Users that are interested in easylift are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- finds rsid with genomic position for feasible input format.☆30Mar 26, 2024Updated 2 years ago
- Genetic correlation calculation pipeline via summary statistics for PheWeb☆13Mar 22, 2019Updated 7 years ago
- ☆13Nov 30, 2018Updated 7 years ago
- ☆15Nov 12, 2017Updated 8 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
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- ☆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
- Code repository for Pietzner M, Wheeler E, et al. 2021 "Mapping the proteo-genomic convergence of human diseases"☆27Sep 2, 2021Updated 4 years ago
- R package for creating simulated summary statistics and testing MR methods☆12Sep 2, 2020Updated 5 years ago
- ☆10Jun 5, 2021Updated 5 years ago
- Analysis code for Olink CVD1 - HF analysis☆15Aug 14, 2024Updated last year
- GENetic Effect-Size distribution Inference from Summary-level data☆15Sep 6, 2020Updated 5 years ago
- Database for collecting and curating scientific papers related to single-cell and spatial transcriptomics sequencing.☆14Oct 5, 2025Updated 9 months ago
- An R package for testing high-dimensional covariance matrices☆11Oct 5, 2017Updated 8 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.
- ☆13Jun 26, 2026Updated last week
- This repository contains scripts related to Surendran P, Stewart I et al. Nature Medicine 2022 "Rare and common genetic causes of chemica…☆18Jul 15, 2022Updated 3 years ago
- Estimate local SNP heritability and genetic covariance from GWAS summary association statistics.☆43May 2, 2018Updated 8 years ago
- Pair-wise conditional analysis and colocalisation☆43May 2, 2024Updated 2 years ago
- gfftools - Galaxy toolshed repository☆15Sep 13, 2017Updated 8 years ago
- A Python module to calculate alignment between two sequences using EMBOSS' needle, stretcher, and water☆16Feb 27, 2025Updated last year
- Code for analyses in "Obesity and risk of female reproductive disorders: A Mendelian Randomisation Study"☆16Dec 19, 2024Updated last year
- Analysis code for applied UK Biobank analyses in Mendelian randomisation for mediation analysis and example code for MR and mediation ana…☆13May 11, 2020Updated 6 years ago
- TWAS-pipeline☆24Feb 21, 2021Updated 5 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 project to develop the R Shiny applications.☆12May 13, 2019Updated 7 years ago
- High-definition likelihood inference of genetic correlations (HDL)☆140May 8, 2026Updated 2 months ago
- Using real genotype data, simulate a complex trait as a function of latent expression, fit eQTL weights in independent data, and perform …☆32Jun 18, 2023Updated 3 years ago
- A python framework for inferring demography from tracts of identity by state as reported in PLoS Genetics by Harris and Nielsen (2013)☆15Aug 1, 2013Updated 12 years ago
- ☆11Jan 30, 2025Updated last year
- Software implementing the Latent Causal Variable Model☆65Jun 30, 2020Updated 6 years ago
- My configuration files☆11Updated this week
- R package for CAUSE☆59Dec 29, 2023Updated 2 years ago
- Filters for Next Generation Sequencing☆13Oct 31, 2024Updated last year
- 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.
- Instructions and analysis scripts for single cell Higher Order Testing (scHOT)☆10Oct 7, 2020Updated 5 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
- Fast and Efficient Tool to Simulate Summary Statistics from Genome-Wide Association Studies☆12May 21, 2024Updated 2 years ago
- ☆34Apr 3, 2026Updated 3 months ago
- Haplotype-based somatic genome simulator☆10Apr 20, 2026Updated 2 months 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