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Nathan D Olson

Showing results (41-50 of 52) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|March 18, 2024
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variationJonas A Gustafson, Sophia B Gibson, Nikhita Damaraju, et al.
Genome Research|October 2, 2024
High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variationJonas A Gustafson, Sophia B Gibson, Nikhita Damaraju, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
A complete diploid human genome benchmark for personalized genomicsNancy F Hansen, Nathan Dwarshuis, Hyun Joo Ji, et al.
Cell Genomics|June 20, 2022
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regionsNathan D Olson, Justin Wagner, Jennifer McDaniel, et al.
Biorxiv : the Preprint Server for Biology|September 30, 2024
Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pairJennifer H McDaniel, Vaidehi Patel, Nathan D Olson, et al.
Nature|October 19, 2022
Semi-automated assembly of high-quality diploid human reference genomesErich D Jarvis, Giulio Formenti, Arang Rhie, et al.
Biorxiv : the Preprint Server for Biology|May 18, 2026
A complete human pancreatic cancer genomeJustin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
Scientific Data|July 16, 2025
Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pairJennifer H McDaniel, Vaidehi Patel, Nathan D Olson, et al.
Scientific Data|August 8, 2025
Correction: Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pairJennifer H McDaniel, Vaidehi Patel, Nathan D Olson, et al.
Nature|August 23, 2023
The complete sequence of a human Y chromosomeArang Rhie, Sergey Nurk, Monika Cechova, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Medrxiv : the Preprint Server for Health Sciences|March 18, 2024
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variationJonas A Gustafson, Sophia B Gibson, Nikhita Damaraju, et al.
Genome Research|October 2, 2024
High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variationJonas A Gustafson, Sophia B Gibson, Nikhita Damaraju, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
A complete diploid human genome benchmark for personalized genomicsNancy F Hansen, Nathan Dwarshuis, Hyun Joo Ji, et al.
Cell Genomics|June 20, 2022
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regionsNathan D Olson, Justin Wagner, Jennifer McDaniel, et al.
Biorxiv : the Preprint Server for Biology|September 30, 2024
Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pairJennifer H McDaniel, Vaidehi Patel, Nathan D Olson, et al.
Nature|October 19, 2022
Semi-automated assembly of high-quality diploid human reference genomesErich D Jarvis, Giulio Formenti, Arang Rhie, et al.
Biorxiv : the Preprint Server for Biology|May 18, 2026
A complete human pancreatic cancer genomeJustin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
Scientific Data|July 16, 2025
Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pairJennifer H McDaniel, Vaidehi Patel, Nathan D Olson, et al.
Scientific Data|August 8, 2025
Correction: Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pairJennifer H McDaniel, Vaidehi Patel, Nathan D Olson, et al.
Nature|August 23, 2023
The complete sequence of a human Y chromosomeArang Rhie, Sergey Nurk, Monika Cechova, et al.
Pageof 6