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Nature Biotechnology
|
July 24, 2020
Author Correction: A robust benchmark for detection of germline large deletions and insertions
Justin 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 insertions
Justin 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 variation
Peter 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 pair
Jennifer 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 pair
Jennifer H McDaniel, Vaidehi Patel, Nathan D Olson, et al.
Biorxiv : the Preprint Server for Biology
|
May 18, 2026
A complete human pancreatic cancer genome
Justin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
Nature
|
August 23, 2023
The complete sequence of a human Y chromosome
Arang 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 genomes
Ana 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 genomes
Mark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
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Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 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 insertions
Justin 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 insertions
Justin 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 variation
Peter 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 pair
Jennifer 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 pair
Jennifer H McDaniel, Vaidehi Patel, Nathan D Olson, et al.
Biorxiv : the Preprint Server for Biology
|
May 18, 2026
A complete human pancreatic cancer genome
Justin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
Nature
|
August 23, 2023
The complete sequence of a human Y chromosome
Arang 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 genomes
Ana 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 genomes
Mark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
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of 5