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Neyra, J.

Publications and source records attributed to Neyra, J..

2 recordsLinked to original sources

GARSA: An integrative pipeline for genome wide association studies and polygenic risk score inference in admixed human populations

Genome-wide association studies (GWAS) and polygenic risk scores (PRS) are multistep analytical tools to identify genetic variants and to assess their contribution to phenotypes/diseases. These analyses are evolving and becoming instrumental to understand the genetic architecture of complex phenotypes/diseases. Nevertheless, to date, there is no single solution incorporating all major steps related to those analyses combined with robust populational bias correction. Here, we describe a semi-automated pipeline unifying steps involved in GWAS and PRS including widely used software. Our pipeline handles quality control (QC), GWAS, and PRS steps, managing different types of input/output files. Furthermore, it includes robust bias correction steps, such as inference of kinship matrix with correction for population structure, use of principal component analysis (PCA) with detection and removal of outlier variant followed by re-projection of related individuals (if desired), generation of PCA figures that assist in setting the best number of principal components (PCs) for association analysis, availability of mixed models, use of recommended software for GWAS based on population size, and a Markov chain Monte Carlo (MCMC) method to estimate best set of PRS parameters. Finally, we tested GARSA pipeline in a family-based Brazilian admixed population and demonstrated that the corrections implemented indeed mitigate bias in downstream analysis. The pipeline can be implemented on personal or server-side environments. AvailabilityThe development version (open-source) is available in https://github.com/LGCM-OpenSource/GARSA ContactFernando P. N. Rossi - fernando.rossi@hc.fm.usp.br; Jose S. L. Patane - jose.patane@hc.fm.usp.br Supplementary informationSupplementary tutorial.

bioinformatics↗

RaMP-DB 2.0: a renovated knowledgebase for deriving biological and chemical insight from genes, proteins, and metabolites

RaMP-DB 2.0 is a web interface, API, relational database and R package designed for straightforward and comprehensive functional interpretation of metabolomic and multi-omic data. Since its first release in 2018, RaMP-DB 2.0 has been upgraded with an expanded breadth and depth of functional and chemical annotation. Content from the source databases (Reactome, HMDB, and Wikipathways) has been updated, and new data types related to metabolite annotations have been incorporated. Structural information incorporated in RaMP-DB 2.0 includes SMILES strings, InChIs, InChIKeys. Chemical classes have been sourced from ClassyFire and LIPID MAPS. Accordingly, the RaMP-DB 2.0 R package has been updated and supports queries on pathways, common reactions, ontologies, chemical classes, and chemical structures. Additionally, RaMP-DB 2.0 now supports enrichment analyses on pathways and chemical classes. Our process for integrating annotations across resources has also been upgraded to lessen the burden of harmonization, thereby supporting more frequent updates. The code used to build all components of RaMP-DB 2.0 is freely available on GitHub at https://github.com/ncats/ramp-db and https://github.com/ncats/RaMP-Backend.

bioinformatics↗