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Pi-Chuan Chang

Showing results (31-40 of 39) with videos related to

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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.
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|May 18, 2026
A complete human pancreatic cancer genomeJustin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
The Complete Sequence and Comparative Analysis of Ape Sex ChromosomesKateryna D Makova, Brandon D Pickett, Robert S Harris, et al.
Nature|May 29, 2024
The complete sequence and comparative analysis of ape sex chromosomesKateryna D Makova, Brandon D Pickett, Robert S Harris, et al.
Nature|May 10, 2023
A draft human pangenome referenceWen-Wei Liao, Mobin Asri, Jana Ebler, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
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.
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|May 18, 2026
A complete human pancreatic cancer genomeJustin Wagner, Ayse G Keskus, Keisuke K Oshima, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
The Complete Sequence and Comparative Analysis of Ape Sex ChromosomesKateryna D Makova, Brandon D Pickett, Robert S Harris, et al.
Nature|May 29, 2024
The complete sequence and comparative analysis of ape sex chromosomesKateryna D Makova, Brandon D Pickett, Robert S Harris, et al.
Nature|May 10, 2023
A draft human pangenome referenceWen-Wei Liao, Mobin Asri, Jana Ebler, et al.
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