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Biorxiv : the Preprint Server for Biology
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January 23, 2024
Comprehensive and accurate genome analysis at scale using DRAGEN accelerated algorithms
Sairam Behera, Severine Catreux, Massimiliano Rossi, et al.
Nature Biotechnology
|
October 25, 2024
Comprehensive genome analysis and variant detection at scale using DRAGEN
Sairam Behera, Severine Catreux, Massimiliano Rossi, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 9, 2025
<i>Celeste</i>: A cloud-based genomics infrastructure with variant-calling pipeline suited for population-scale sequencing projects
Noora Siddiqui, Breanna Lee, Victoria Yi, et al.
Genome Medicine
|
October 1, 2015
A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases
Neil A Miller, Emily G Farrow, Margaret Gibson, et al.
Genome Biology
|
June 20, 2024
Evaluation of somatic copy number variation detection by NGS technologies and bioinformatics tools on a hyper-diploid cancer genome
Daniall Masood, Luyao Ren, Cu Nguyen, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 12, 2026
Scalable and comprehensive mosaic variant calling using DRAGEN
Sairam Behera, Massimiliano Rossi, Yina Wang, et al.
NPJ Genomic Medicine
|
April 10, 2026
Clinical validation of a high-performance somatic exome sequencing assay: from target-enrichment strategy to variant calling
Junko Tsuji, Micah Rickles-Young, Justin Abreu, 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.
Medrxiv : the Preprint Server for Health Sciences
|
December 17, 2025
Genomics of Acute Myeloid Leukemia at Diagnosis and Remission
Kai Yu, Laura W Dillon, Jesse M Tettero, et al.
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Search research articles
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Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Biorxiv : the Preprint Server for Biology
|
January 23, 2024
Comprehensive and accurate genome analysis at scale using DRAGEN accelerated algorithms
Sairam Behera, Severine Catreux, Massimiliano Rossi, et al.
Nature Biotechnology
|
October 25, 2024
Comprehensive genome analysis and variant detection at scale using DRAGEN
Sairam Behera, Severine Catreux, Massimiliano Rossi, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 9, 2025
<i>Celeste</i>: A cloud-based genomics infrastructure with variant-calling pipeline suited for population-scale sequencing projects
Noora Siddiqui, Breanna Lee, Victoria Yi, et al.
Genome Medicine
|
October 1, 2015
A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases
Neil A Miller, Emily G Farrow, Margaret Gibson, et al.
Genome Biology
|
June 20, 2024
Evaluation of somatic copy number variation detection by NGS technologies and bioinformatics tools on a hyper-diploid cancer genome
Daniall Masood, Luyao Ren, Cu Nguyen, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 12, 2026
Scalable and comprehensive mosaic variant calling using DRAGEN
Sairam Behera, Massimiliano Rossi, Yina Wang, et al.
NPJ Genomic Medicine
|
April 10, 2026
Clinical validation of a high-performance somatic exome sequencing assay: from target-enrichment strategy to variant calling
Junko Tsuji, Micah Rickles-Young, Justin Abreu, 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.
Medrxiv : the Preprint Server for Health Sciences
|
December 17, 2025
Genomics of Acute Myeloid Leukemia at Diagnosis and Remission
Kai Yu, Laura W Dillon, Jesse M Tettero, et al.
Page
of 2