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Medrxiv : the Preprint Server for Health Sciences
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January 13, 2025
Successful classification of clinical pediatric leukemia genetic subtypes via structural variant detection using HiFi long-read sequencing
Lisa A Lansdon, Byunggil Yoo, Ayse Keskus, et al.
NPJ Genomic Medicine
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April 9, 2026
Proof-of-concept study for the detection of somatic structural variant driver alterations using HiFi long-read sequencing in a pediatric leukemia cohort
Lisa A Lansdon, Byunggil Yoo, Ayse Keskus, et al.
Nature Communications
|
May 29, 2023
Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort
Warren A Cheung, Adam F Johnson, William J Rowell, et al.
Biorxiv : the Preprint Server for Biology
|
September 4, 2024
DeepSomatic: Accurate somatic small variant discovery for multiple sequencing technologies
Jimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
Nature Biotechnology
|
October 16, 2025
Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomatic
Jimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
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.
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Showing results (21-30 of 26) with videos related to
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Page
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This site can display upto 26 results.
Medrxiv : the Preprint Server for Health Sciences
|
January 13, 2025
Successful classification of clinical pediatric leukemia genetic subtypes via structural variant detection using HiFi long-read sequencing
Lisa A Lansdon, Byunggil Yoo, Ayse Keskus, et al.
NPJ Genomic Medicine
|
April 9, 2026
Proof-of-concept study for the detection of somatic structural variant driver alterations using HiFi long-read sequencing in a pediatric leukemia cohort
Lisa A Lansdon, Byunggil Yoo, Ayse Keskus, et al.
Nature Communications
|
May 29, 2023
Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort
Warren A Cheung, Adam F Johnson, William J Rowell, et al.
Biorxiv : the Preprint Server for Biology
|
September 4, 2024
DeepSomatic: Accurate somatic small variant discovery for multiple sequencing technologies
Jimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
Nature Biotechnology
|
October 16, 2025
Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomatic
Jimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
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.
Page
of 3