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Andrew Carroll

Showing results (101-110 of 119) with videos related to

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Nature Methods|August 4, 2025
The Platinum Pedigree: a long-read benchmark for genetic variantsZev Kronenberg, Cillian Nolan, David Porubsky, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 9, 2024
Genomic Determinants of Outcome in Acute Lymphoblastic LeukemiaTi-Cheng Chang, Wenan Chen, Chunxu Qu, 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|April 4, 2025
Severus detects somatic structural variation and complex rearrangements in cancer genomes using long-read sequencingAyse G Keskus, Asher Bryant, Tanveer Ahmad, et al.
The New England Journal of Medicine|January 12, 2022
Ultrarapid Nanopore Genome Sequencing in a Critical Care SettingJohn E Gorzynski, Sneha D Goenka, Kishwar Shafin, 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 Genetics|October 28, 2017
Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiologyJennifer A Brody, Alanna C Morrison, Joshua C Bis, et al.
Inflammatory Bowel Diseases|December 28, 2025
CRUCIAL Insights From a Decade Long Retrospective National Audit of Total Abdominal Colectomy Outcomes for Ulcerative ColitisIan J B Stephens, Brenda Murphy, Lucy Burns, et al.
Nature|May 19, 2026
Accelerating scientific discovery with Co-ScientistJuraj Gottweis, Wei-Hung Weng, Alexander Daryin, et al.
Pageof 12

Showing results (101-110 of 119) with videos related to

Sort By:
Pageof 12
Nature Methods|August 4, 2025
The Platinum Pedigree: a long-read benchmark for genetic variantsZev Kronenberg, Cillian Nolan, David Porubsky, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 9, 2024
Genomic Determinants of Outcome in Acute Lymphoblastic LeukemiaTi-Cheng Chang, Wenan Chen, Chunxu Qu, 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|April 4, 2025
Severus detects somatic structural variation and complex rearrangements in cancer genomes using long-read sequencingAyse G Keskus, Asher Bryant, Tanveer Ahmad, et al.
The New England Journal of Medicine|January 12, 2022
Ultrarapid Nanopore Genome Sequencing in a Critical Care SettingJohn E Gorzynski, Sneha D Goenka, Kishwar Shafin, 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 Genetics|October 28, 2017
Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiologyJennifer A Brody, Alanna C Morrison, Joshua C Bis, et al.
Inflammatory Bowel Diseases|December 28, 2025
CRUCIAL Insights From a Decade Long Retrospective National Audit of Total Abdominal Colectomy Outcomes for Ulcerative ColitisIan J B Stephens, Brenda Murphy, Lucy Burns, et al.
Nature|May 19, 2026
Accelerating scientific discovery with Co-ScientistJuraj Gottweis, Wei-Hung Weng, Alexander Daryin, et al.
Pageof 12