Renato Santos

This study benchmarks TE detection tools on long-read data, showing significant variation in performance and highlighting tool-specific strengths and limitations.

This study compares Oxford Nanopore long-read sequencing with Illumina short-read sequencing and microarrays across 14 human genomes, finding LRS has competitive accuracy for SNVs and superior performance for structural variants.

This study uses low-coverage whole genome sequencing and imputation to analyze genetic variants in severe COVID-19 patients, showing high imputation accuracy and insights into clinical phenotypes.