# yQTL Pipeline: A structured computational workflow for large scale quantitative trait loci discovery and downstream visualization

**Authors:** Mengze Li, Zeyuan Song, Anastasia Gurinovich, Nicholas Schork, Paola Sebastiani, Stefano Monti, Chunyu Liu, Chunyu Liu, Chunyu Liu

PMC · DOI: 10.1371/journal.pone.0298501 · PLOS ONE · 2024-06-04

## TL;DR

The yQTL Pipeline is a computational tool that automates and speeds up QTL analysis, helping researchers find DNA regions linked to traits like metabolite levels.

## Contribution

The yQTL Pipeline introduces a reproducible, parallelized workflow for large-scale QTL discovery with integrated visualization tools.

## Key findings

- The pipeline reduced analysis run time from ~90 min to ~26 min using parallelization.
- 14,983 metabolite QTLs (mQTLs) were identified across 312 metabolites in a study of 194 participants.
- Visualization tools revealed multiple mQTLs shared across multiple metabolites.

## Abstract

Quantitative trait loci (QTL) denote regions of DNA whose variation is associated with variations in quantitative traits. QTL discovery is a powerful approach to understand how changes in molecular and clinical phenotypes may be related to DNA sequence changes. However, QTL discovery analysis encompasses multiple analytical steps and the processing of multiple input files, which can be laborious, error prone, and hard to reproduce if performed manually. To facilitate and automate large-scale QTL analysis, we developed the yQTL Pipeline, where the ‘y’ indicates the dependent quantitative variable being modeled. Prior to the association test, the pipeline supports the calculation or the direct input of pre-defined genome-wide principal components and genetic relationship matrix when applicable. User-specified covariates can also be provided. Depending on whether familial relatedness exists among the subjects, genome-wide association tests will be performed using either a linear mixed-effect model or a linear model. The options to run an ANOVA model or testing the interaction with a covariate are also available. Using the workflow management tool Nextflow, the pipeline parallelizes the analysis steps to optimize run-time and ensure results reproducibility. In addition, a user-friendly R Shiny App is developed to facilitate result visualization. It can generate Manhattan and Miami plots of phenotype traits, genotype-phenotype boxplots, and trait-QTL connection networks. We applied the yQTL Pipeline to analyze metabolomics profiles of blood serum from the New England Centenarians Study (NECS) participants. A total of 9.1M SNPs and 1,052 metabolites across 194 participants were analyzed. Using a p-value cutoff 5e-8, we found 14,983 mQTLs associated with 312 metabolites. The built-in parallelization of our pipeline reduced the run time from ~90 min to ~26 min. Visualization using the R Shiny App revealed multiple mQTLs shared across multiple metabolites. The yQTL Pipeline is available with documentation on GitHub at https://github.com/montilab/yQTLpipeline.

## Full-text entities

- **Genes:** SNORA74A (small nucleolar RNA, H/ACA box 74A) [NCBI Gene 26821] {aka RNU19, U19}
- **Chemicals:** N2-acetyl,N6,N6-dimethyllysine (-), orotidine (MESH:C008714), PS (MESH:D010758), SM (MESH:D012493), N6-methyllysine (MESH:C005205)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs4539242, rs541005701, rs768854100, rs192581407
- **Cell lines:** UH3 — Homo sapiens (Human), Diffuse large B-cell lymphoma, Cancer cell line (CVCL_A1JU), U19- — Mus musculus (Mouse), Hybridoma (CVCL_VI33), U19-AG023122 — Homo sapiens (Human), Sacral chordoma, Cancer cell line (CVCL_A5IF)

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## Figures

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## References

13 references — full list in the complete paper: https://tomesphere.com/paper/PMC11149833/full.md

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Source: https://tomesphere.com/paper/PMC11149833