All Projects → xqwen → fastenloc

xqwen / fastenloc

Licence: other
Colocalization analysis of genetic association signals

Programming Languages

C++
36643 projects - #6 most used programming language
r
7636 projects
perl
6916 projects
Makefile
30231 projects

Projects that are alternatives of or similar to fastenloc

GREIN
GREIN : GEO RNA-seq Experiments Interactive Navigator
Stars: ✭ 40 (+60%)
Mutual labels:  bioinformatics-analysis
sequencework
programs and scripts, mainly python, for analyses related to nucleic or protein sequences
Stars: ✭ 22 (-12%)
Mutual labels:  bioinformatics-analysis
Plant-Disease-Identification-using-CNN
Plant Disease Identification Using Convulutional Neural Network
Stars: ✭ 89 (+256%)
Mutual labels:  bioinformatics-analysis
galaksio
An easy-to-use way for running Galaxy workflows.
Stars: ✭ 19 (-24%)
Mutual labels:  bioinformatics-analysis
PBxplore
A suite of tools to explore protein structures with Protein Blocks 🐍
Stars: ✭ 21 (-16%)
Mutual labels:  bioinformatics-analysis
BioInstaller
A comprehensive R package to construct interactive and reproducible biological data analysis applications based on the R platform
Stars: ✭ 52 (+108%)
Mutual labels:  bioinformatics-analysis
bindSC
Bi-order integration (in silico multi-omics data) of single cell RNA sequencing, single cell ATAC sequencing, spacial transcriptomics and CyTOF data
Stars: ✭ 24 (-4%)
Mutual labels:  integrative-analysis
iSkyLIMS
is an open-source LIMS (laboratory Information Management System) for Next Generation Sequencing sample management, statistics and reports, and bioinformatics analysis service management.
Stars: ✭ 33 (+32%)
Mutual labels:  bioinformatics-analysis
bystro
Bystro genetic analysis (annotation, filtering, statistics)
Stars: ✭ 31 (+24%)
Mutual labels:  bioinformatics-analysis
pyrpipe
Reproducible bioinformatics pipelines in python. Import any Unix tool/command in python.
Stars: ✭ 53 (+112%)
Mutual labels:  bioinformatics-analysis
PHAT
Pathogen-Host Analysis Tool - A modern Next-Generation Sequencing (NGS) analysis platform
Stars: ✭ 17 (-32%)
Mutual labels:  bioinformatics-analysis
team-rosalind-project
This is the main repository for the HackBio'2020 Virtual Internship Experience ❤️
Stars: ✭ 22 (-12%)
Mutual labels:  bioinformatics-analysis
echolocatoR
Automated statistical and functional fine-mapping pipeline with extensive API access to datasets.
Stars: ✭ 13 (-48%)
Mutual labels:  colocalization
colocr
An R package for conducting co-localization analysis. Edit
Stars: ✭ 22 (-12%)
Mutual labels:  colocalization

fastENLOC: fast enrichment estimation aided colocalization analysis

Current release: version 2 (April, 2022)

This repository contains the software implementation of fastENLOC, which enables integrative genetic association analysis of molecular QTL data and GWAS data. The statistical model and the key computational procedures are described in [1], [2], [3], and [4].

For questions/comments regarding to the software package, please contact Xiaoquan (William) Wen (xwen at umich dot edu).

New features in version 2

  • Locus-level colcoalization analysis
  • Auto diagnosis of input files
  • Utility scripts for generating input files and computing gene-level colocalization probabilities (GLCP and GRCP).
  • Code optimization
  • Bug fix

License

Software distributed under the terms of the GNU General Public License as published by the Free Software Foundation, either version 3 of the License, or (at your option) any later version. See LICENSE for more details.

Tutorial and guideline

A detailed tutorial is provided in tutorial directory. Briefly, three main steps are required for a complete analysis

  1. Prepare eQTL annotation
  2. Prepare GWAS sumary (in term of posterior inclusion probabilities, or PIPs)
  3. Run fastenloc

We distribute pre-computed eQTL annotations from GTEx (v8) data. In the simplest case, the required GWAS PIPs can be computed from single-SNP association summary-statistics (e.g., z-scores and p-values) using torus

GTEx v8 multi-tissue eQTL annotations for fastENLOC

If you prefer to using newly released GTEx v8 eQTL annotation for analysis, please download the following vcf files

Citation

  1. Wen, X., Pique-Regi, R., Luca, F., 2017. Integrating Molecular QTL Data into Genome-wide Genetic Association Analysis: Probabilistic Assessment of Enrichment and Colocalization. PLOS Genetics, 13(3): e1006646.
  2. Pividori, M., et al., 2020. PhenomeXcan: Mapping the genome to the phenome through the transcriptome. Science Advances, 6(37), p.eaba2083.
  3. Hukku, A., Pividori, M., Luca, F., Pique-Regi, R., Im, H.K. and Wen, X., 2021. Probabilistic colocalization of genetic variants from complex and molecular traits: promise and limitations. The American Journal of Human Genetics, 108(1), pp.25-35.
  4. Hukku, A., Sampson, M.G., Luca, F., Pique-Regi, R. and Wen, X., 2022. Analyzing and Reconciling Colocalization and Transcriptome-wide Association Studies from the Perspective of Inferential Reproducibility. The American Journal of Human Genetics, (in press)
Note that the project description data, including the texts, logos, images, and/or trademarks, for each open source project belongs to its rightful owner. If you wish to add or remove any projects, please contact us at [email protected].