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BMC Genomics
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October 7, 2017
SVachra: a tool to identify genomic structural variation in mate pair sequencing data containing inward and outward facing reads
Oliver A Hampton, Adam C English, Mark Wang, et al.
Gigascience
|
January 16, 2023
xAtlas: scalable small variant calling across heterogeneous next-generation sequencing experiments
Jesse Farek, Daniel Hughes, William Salerno, et al.
Research Square
|
February 6, 2026
The Impact of Structural Variation on Alzheimer's Disease in the Alzheimer's Disease Sequencing Project
Songmi Lee, Adam C English, Gina M Peloso, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Enriching for Answers in Rare Diseases
Yilei Fu, Adam C English, Luis F Paulin, et al.
Nature Biotechnology
|
April 26, 2024
Analysis and benchmarking of small and large genomic variants across tandem repeats
Adam C English, Egor Dolzhenko, Helyaneh Ziaei Jam, et al.
Nature Communications
|
October 4, 2018
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects
Allison A Regier, Yossi Farjoun, David E Larson, et al.
Cell
|
March 5, 2019
Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2
Christine R Beck, Claudia M B Carvalho, Zeynep C Akdemir, et al.
BMC Genomics
|
April 19, 2015
Assessing structural variation in a personal genome-towards a human reference diploid genome
Adam C English, William J Salerno, Oliver A Hampton, et al.
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.
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of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
BMC Genomics
|
October 7, 2017
SVachra: a tool to identify genomic structural variation in mate pair sequencing data containing inward and outward facing reads
Oliver A Hampton, Adam C English, Mark Wang, et al.
Gigascience
|
January 16, 2023
xAtlas: scalable small variant calling across heterogeneous next-generation sequencing experiments
Jesse Farek, Daniel Hughes, William Salerno, et al.
Research Square
|
February 6, 2026
The Impact of Structural Variation on Alzheimer's Disease in the Alzheimer's Disease Sequencing Project
Songmi Lee, Adam C English, Gina M Peloso, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Enriching for Answers in Rare Diseases
Yilei Fu, Adam C English, Luis F Paulin, et al.
Nature Biotechnology
|
April 26, 2024
Analysis and benchmarking of small and large genomic variants across tandem repeats
Adam C English, Egor Dolzhenko, Helyaneh Ziaei Jam, et al.
Nature Communications
|
October 4, 2018
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects
Allison A Regier, Yossi Farjoun, David E Larson, et al.
Cell
|
March 5, 2019
Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2
Christine R Beck, Claudia M B Carvalho, Zeynep C Akdemir, et al.
BMC Genomics
|
April 19, 2015
Assessing structural variation in a personal genome-towards a human reference diploid genome
Adam C English, William J Salerno, Oliver A Hampton, et al.
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.
Page
of 3