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Nathan D Olson

Showing results (31-40 of 52) with videos related to

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Nature Communications|January 8, 2025
Small variant benchmark from a complete assembly of X and Y chromosomesJustin Wagner, Nathan D Olson, Jennifer McDaniel, et al.
Science (New York, N.Y.)|March 31, 2022
A complete reference genome improves analysis of human genetic variationSergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Nature Methods|August 4, 2025
The Platinum Pedigree: a long-read benchmark for genetic variantsZev Kronenberg, Cillian Nolan, David Porubsky, et al.
Microbiome|November 7, 2018
Current progress and future opportunities in applications of bioinformatics for biodefense and pathogen detection: report from the Winter Mid-Atlantic Microbiome Meet-up, College Park, MD, January 10, 2018Jacquelyn S Meisel, Daniel J Nasko, Brian Brubach, et al.
Cell Genomics|December 1, 2022
Benchmarking challenging small variants with linked and long readsJustin Wagner, Nathan D Olson, Lindsay Harris, et al.
Nature Biotechnology|February 8, 2022
Curated variation benchmarks for challenging medically relevant autosomal genesJustin Wagner, Nathan D Olson, Lindsay Harris, et al.
Cell Genomics|December 20, 2025
Characterization of subclonal variants in HG002 Genome in a Bottle reference material as a resource for benchmarking variant callersCamille A Daniels, Adetola A Abdulkadir, Megan H Cleveland, et al.
Biorxiv : the Preprint Server for Biology|December 16, 2024
A robust benchmark for detecting low-frequency variants in the HG002 Genome In A Bottle NIST reference materialCamille A Daniels, Adetola Abdulkadir, Megan H Cleveland, et al.
Nature Biotechnology|July 24, 2020
Author Correction: A robust benchmark for detection of germline large deletions and insertionsJustin M Zook, Nancy F Hansen, Nathan D Olson, et al.
Nature Biotechnology|June 17, 2020
A robust benchmark for detection of germline large deletions and insertionsJustin M Zook, Nancy F Hansen, Nathan D Olson, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Nature Communications|January 8, 2025
Small variant benchmark from a complete assembly of X and Y chromosomesJustin Wagner, Nathan D Olson, Jennifer McDaniel, et al.
Science (New York, N.Y.)|March 31, 2022
A complete reference genome improves analysis of human genetic variationSergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Nature Methods|August 4, 2025
The Platinum Pedigree: a long-read benchmark for genetic variantsZev Kronenberg, Cillian Nolan, David Porubsky, et al.
Microbiome|November 7, 2018
Current progress and future opportunities in applications of bioinformatics for biodefense and pathogen detection: report from the Winter Mid-Atlantic Microbiome Meet-up, College Park, MD, January 10, 2018Jacquelyn S Meisel, Daniel J Nasko, Brian Brubach, et al.
Cell Genomics|December 1, 2022
Benchmarking challenging small variants with linked and long readsJustin Wagner, Nathan D Olson, Lindsay Harris, et al.
Nature Biotechnology|February 8, 2022
Curated variation benchmarks for challenging medically relevant autosomal genesJustin Wagner, Nathan D Olson, Lindsay Harris, et al.
Cell Genomics|December 20, 2025
Characterization of subclonal variants in HG002 Genome in a Bottle reference material as a resource for benchmarking variant callersCamille A Daniels, Adetola A Abdulkadir, Megan H Cleveland, et al.
Biorxiv : the Preprint Server for Biology|December 16, 2024
A robust benchmark for detecting low-frequency variants in the HG002 Genome In A Bottle NIST reference materialCamille A Daniels, Adetola Abdulkadir, Megan H Cleveland, et al.
Nature Biotechnology|July 24, 2020
Author Correction: A robust benchmark for detection of germline large deletions and insertionsJustin M Zook, Nancy F Hansen, Nathan D Olson, et al.
Nature Biotechnology|June 17, 2020
A robust benchmark for detection of germline large deletions and insertionsJustin M Zook, Nancy F Hansen, Nathan D Olson, et al.
Pageof 6