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Chuan Chang

Showing results (641-650 of 656) with videos related to

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Biorxiv : the Preprint Server for Biology|September 4, 2024
DeepSomatic: Accurate somatic small variant discovery for multiple sequencing technologiesJimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
Nature Biotechnology|March 29, 2022
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencingSneha D Goenka, John E Gorzynski, Kishwar Shafin, et al.
Diabetes Care|October 5, 2021
Genome-Wide Meta-analysis Identifies Genetic Variants Associated With Glycemic Response to SulfonylureasAdem Y Dawed, Sook Wah Yee, Kaixin Zhou, et al.
Nature Biotechnology|October 16, 2025
Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomaticJimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Severus: accurate detection and characterization of somatic structural variation in tumor genomes using long readsAyse Keskus, Asher Bryant, Tanveer Ahmad, et al.
Surgical Neurology|October 13, 2009
Clinical practice guidelines in severe traumatic brain injury in TaiwanKuo-Hsing Liao, Cheng-Kuei Chang, Hong-Chang Chang, et al.
Nature Methods|August 4, 2025
The Platinum Pedigree: a long-read benchmark for genetic variantsZev Kronenberg, Cillian Nolan, David Porubsky, 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.
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.
Pageof 66

Showing results (641-650 of 656) with videos related to

Sort By:
Pageof 66
Biorxiv : the Preprint Server for Biology|September 4, 2024
DeepSomatic: Accurate somatic small variant discovery for multiple sequencing technologiesJimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
Nature Biotechnology|March 29, 2022
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencingSneha D Goenka, John E Gorzynski, Kishwar Shafin, et al.
Diabetes Care|October 5, 2021
Genome-Wide Meta-analysis Identifies Genetic Variants Associated With Glycemic Response to SulfonylureasAdem Y Dawed, Sook Wah Yee, Kaixin Zhou, et al.
Nature Biotechnology|October 16, 2025
Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomaticJimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Severus: accurate detection and characterization of somatic structural variation in tumor genomes using long readsAyse Keskus, Asher Bryant, Tanveer Ahmad, et al.
Surgical Neurology|October 13, 2009
Clinical practice guidelines in severe traumatic brain injury in TaiwanKuo-Hsing Liao, Cheng-Kuei Chang, Hong-Chang Chang, et al.
Nature Methods|August 4, 2025
The Platinum Pedigree: a long-read benchmark for genetic variantsZev Kronenberg, Cillian Nolan, David Porubsky, 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.
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.
Pageof 66