An Efficient Multiple-Testing Adjustment for eQTL Studies that Accounts for Linkage Disequilibrium between Variants
☆14Oct 24, 2019Updated 6 years ago
Alternatives and similar repositories for eigenMT
Users that are interested in eigenMT are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ☆10Jan 20, 2023Updated 3 years ago
- Workflow and script for converting genomic coordinates using MUMmer output and CrossMap☆12Jun 15, 2026Updated last month
- Interactive eQTL visualizations☆14Dec 12, 2022Updated 3 years ago
- Draw the Gene structure based on the GFF and gene's ID☆10Jun 13, 2020Updated 6 years ago
- Toolkit for QTL mapping and meta-analysis.☆17May 24, 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.
- 3’ Tag RNA-seq pipeline (Work in progress)☆10Mar 14, 2021Updated 5 years ago
- eQTLHap: a comprehensive eQTL analysis tool.☆11Apr 15, 2021Updated 5 years ago
- Genotyping of segregating mobile elements insertions☆19Jul 29, 2021Updated 4 years ago
- This site provides information on conducting reproducible science using the R language.☆13Nov 2, 2016Updated 9 years ago
- ☆45Apr 15, 2026Updated 3 months ago
- ☆12Jan 9, 2023Updated 3 years ago
- Pipeline for genetic epidemiology projects at Univsersity of Bristol☆15Jul 15, 2026Updated last week
- Robust Allele Specific Quantification and quality controL☆42Dec 13, 2021Updated 4 years ago
- Learn tissue-specificity and tissue-sharing of genetic regulation across 49 tissues using constraint matrix factorization model☆22Oct 9, 2020Updated 5 years ago
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- A toolset to analyze genomic footprinting data☆20Updated this week
- Structural variant caller for low-depth long-read sequencing data☆31Jan 6, 2025Updated last year
- MPH is a C++ program for fast REML estimation of genetic (co)variance components.☆15Jan 5, 2026Updated 6 months ago
- Fine-mapping with infinitesimal effects☆20May 5, 2026Updated 2 months ago
- Partitioning algorithm developed for LAVA☆17May 17, 2024Updated 2 years ago
- Transposable element polymorphism identification☆34Jul 22, 2020Updated 6 years ago
- A collection of Python modules equivalent to R ReQTL Toolkit aims to identify the association between expressed SNVs with their gene expr…☆11Jan 20, 2022Updated 4 years ago
- Calculates allelic Fold Change (aFC) using standard input files for fastQTL.☆27Jun 30, 2022Updated 4 years ago
- Package to detect eQTLs jointly in multiple subgroups (e.g. tissues) via Bayesian Model Averaging.☆24Apr 16, 2018Updated 8 years ago
- End-to-end encrypted cloud storage - Proton Drive • AdSpecial offer: 40% Off Yearly / 80% Off First Month. Protect your most important files, photos, and documents from prying eyes.
- Dockerized Phoenix using docker-compose.☆10Jun 15, 2017Updated 9 years ago
- Post-GWAS enrichment, colocalization, TWAS and Mendelian Randomization to integrate molecular QTL and GWAS.☆37Updated this week
- xGAP is an efficient, modular, extensible and fault-tolerant pipeline for massively parallelized genomic analysis/variant discovery from …☆11Oct 21, 2020Updated 5 years ago
- scripts used for processing and analyzing data in the article.☆13Oct 31, 2019Updated 6 years ago
- Identify and annotate TE-mediated insertions in long-read sequence data☆48Mar 25, 2026Updated 3 months ago
- Visualization methods for omics dataset quality control☆10Jun 24, 2026Updated 3 weeks ago
- Network Visualization using both GUI and Programming☆29Jul 3, 2026Updated 2 weeks ago
- ☆10Sep 11, 2020Updated 5 years ago
- Detecting Archaic Introgression from Population Genetic Data with S*☆10Jul 10, 2026Updated last week
- End-to-end encrypted cloud storage - Proton Drive • AdSpecial offer: 40% Off Yearly / 80% Off First Month. Protect your most important files, photos, and documents from prying eyes.
- hot_scan is a free software to detect genomic regions unusually rich (hotspot) in a given pattern via scan statistics☆10Oct 17, 2013Updated 12 years ago
- A de novo prediction tool of chromatin accessible regions for plant genomes☆10Aug 12, 2021Updated 4 years ago
- Thesis template in Word | CC BY-NC-SA 4.0☆22Sep 29, 2025Updated 9 months ago
- Vector Approximate Message Passing inference framework for GWAS☆20Jun 12, 2026Updated last month
- ☆26Jun 9, 2026Updated last month
- This toolkit deals with GEnomic sequence and genome structure ANnotation files between inbreeding lines and species.☆45Mar 2, 2023Updated 3 years ago
- Machine learning workshop materials☆16Nov 19, 2024Updated last year