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Aaron M Wenger

Showing results (41-50 of 49) with videos related to

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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.
Science (New York, N.Y.)|February 26, 2021
Haplotype-resolved diverse human genomes and integrated analysis of structural variationPeter Ebert, Peter A Audano, Qihui Zhu, 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.
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.
Biorxiv : the Preprint Server for Biology|May 18, 2026
A complete human pancreatic cancer genomeJustin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
Nature|August 23, 2023
The complete sequence of a human Y chromosomeArang Rhie, Sergey Nurk, Monika Cechova, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2022
Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomesAna S A Cohen, Emily G Farrow, Ahmed T Abdelmoity, et al.
Nature Communications|April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomesMark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
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Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
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.
Science (New York, N.Y.)|February 26, 2021
Haplotype-resolved diverse human genomes and integrated analysis of structural variationPeter Ebert, Peter A Audano, Qihui Zhu, 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.
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.
Biorxiv : the Preprint Server for Biology|May 18, 2026
A complete human pancreatic cancer genomeJustin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
Nature|August 23, 2023
The complete sequence of a human Y chromosomeArang Rhie, Sergey Nurk, Monika Cechova, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2022
Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomesAna S A Cohen, Emily G Farrow, Ahmed T Abdelmoity, et al.
Nature Communications|April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomesMark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
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