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Pi-Chuan Chang

Showing results (21-30 of 39) with videos related to

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Biorxiv : the Preprint Server for Biology|November 19, 2025
Rapid, accurate long- and short-read mapping to large pangenome graphs with vg GiraffeXian Chang, Adam M Novak, Jordan M Eizenga, et al.
Nature Biotechnology|September 1, 2022
DeepConsensus improves the accuracy of sequences with a gap-aware sequence transformerGunjan Baid, Daniel E Cook, Kishwar Shafin, et al.
Science (New York, N.Y.)|December 16, 2021
Pangenomics enables genotyping of known structural variants in 5202 diverse genomesJouni Sirén, Jean Monlong, Xian Chang, et al.
Nature Biotechnology|August 14, 2019
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genomeAaron M Wenger, Paul Peluso, William J Rowell, et al.
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.
Circulation. Genomic and Precision Medicine|February 8, 2022
Ultra-Rapid Nanopore Whole Genome Genetic Diagnosis of Dilated Cardiomyopathy in an Adolescent With Cardiogenic ShockJohn E Gorzynski, Sneha D Goenka, Kishwar Shafin, 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.
Nature Methods|August 4, 2025
The Platinum Pedigree: a long-read benchmark for genetic variantsZev Kronenberg, Cillian Nolan, David Porubsky, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Biorxiv : the Preprint Server for Biology|November 19, 2025
Rapid, accurate long- and short-read mapping to large pangenome graphs with vg GiraffeXian Chang, Adam M Novak, Jordan M Eizenga, et al.
Nature Biotechnology|September 1, 2022
DeepConsensus improves the accuracy of sequences with a gap-aware sequence transformerGunjan Baid, Daniel E Cook, Kishwar Shafin, et al.
Science (New York, N.Y.)|December 16, 2021
Pangenomics enables genotyping of known structural variants in 5202 diverse genomesJouni Sirén, Jean Monlong, Xian Chang, et al.
Nature Biotechnology|August 14, 2019
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genomeAaron M Wenger, Paul Peluso, William J Rowell, et al.
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.
Circulation. Genomic and Precision Medicine|February 8, 2022
Ultra-Rapid Nanopore Whole Genome Genetic Diagnosis of Dilated Cardiomyopathy in an Adolescent With Cardiogenic ShockJohn E Gorzynski, Sneha D Goenka, Kishwar Shafin, 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.
Nature Methods|August 4, 2025
The Platinum Pedigree: a long-read benchmark for genetic variantsZev Kronenberg, Cillian Nolan, David Porubsky, et al.
Pageof 4