PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regionsNathan D. Olson, Ivan J. Johnson, Justin Wagner et al.|Cell Genomics|2022Cited by 209
precisionFDA Truth Challenge V2: Calling variants from short- and long-reads in difficult-to-map regionsNathan D. Olson, Ivan J. Johnson, Justin Wagner et al.|bioRxiv (Cold Spring Harbor Laboratory)|2020Cited by 67
A genome-wide association study of survival in patients with sepsisTamara Hernández-Beeftink, Miryam Prieto-González, Aurelio Rodríguez et al.|Critical Care|2022Cited by 40
A robust benchmark for detecting low-frequency variants in the HG002 Genome In A Bottle NIST reference material.Camille Daniels, Nathan D. Olson, Adetola Abdulkadir et al.|bioRxiv (Cold Spring Harbor Laboratory)|2024Cited by 5
A Genome-Wide Association Study of Survival in Patients with SepsisTamara Hernández-Beeftink, Beatriz Guillén‐Guío, José M. Lorenzo-Salazar et al.|medRxiv|2022Cited by 2