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Nature Biotechnology
|
April 4, 2025
Severus detects somatic structural variation and complex rearrangements in cancer genomes using long-read sequencing
Ayse 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 Setting
John 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 callers
Camille 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 material
Camille 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 regions
Nathan D Olson, Justin Wagner, Jennifer McDaniel, 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.
Biorxiv : the Preprint Server for Biology
|
December 11, 2023
The Complete Sequence and Comparative Analysis of Ape Sex Chromosomes
Kateryna D Makova, Brandon D Pickett, Robert S Harris, et al.
Nature
|
May 29, 2024
The complete sequence and comparative analysis of ape sex chromosomes
Kateryna D Makova, Brandon D Pickett, Robert S Harris, et al.
Nature
|
May 10, 2023
A draft human pangenome reference
Wen-Wei Liao, Mobin Asri, Jana Ebler, et al.
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Search research articles
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Showing results (31-40 of 39) with videos related to
Sort By:
Page
of 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 sequencing
Ayse 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 Setting
John 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 callers
Camille 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 material
Camille 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 regions
Nathan D Olson, Justin Wagner, Jennifer McDaniel, 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.
Biorxiv : the Preprint Server for Biology
|
December 11, 2023
The Complete Sequence and Comparative Analysis of Ape Sex Chromosomes
Kateryna D Makova, Brandon D Pickett, Robert S Harris, et al.
Nature
|
May 29, 2024
The complete sequence and comparative analysis of ape sex chromosomes
Kateryna D Makova, Brandon D Pickett, Robert S Harris, et al.
Nature
|
May 10, 2023
A draft human pangenome reference
Wen-Wei Liao, Mobin Asri, Jana Ebler, et al.
Page
of 4