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Xuefang Zhao

Showing results (41-50 of 48) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Integrating 730,947 exome sequences with clinical literature improves gene discoveryJeremy Guez, Julia K Goodrich, Mikhail A Moldovan, et al.
Cell Genomics|June 30, 2023
Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementiasKarri Kaivola, Ruth Chia, Jinhui Ding, et al.
Biorxiv : the Preprint Server for Biology|October 7, 2024
Complex genetic variation in nearly complete human genomesGlennis A Logsdon, Peter Ebert, Peter A Audano, et al.
Nature|July 23, 2025
Complex genetic variation in nearly complete human genomesGlennis A Logsdon, Peter Ebert, Peter A Audano, et al.
Science (New York, N.Y.)|February 26, 2021
Haplotype-resolved diverse human genomes and integrated analysis of structural variationPeter Ebert, Peter A Audano, Qihui Zhu, et al.
Nature|August 26, 2025
Author Correction: Complex genetic variation in nearly complete human genomesGlennis A Logsdon, Peter Ebert, Peter A Audano, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencingAlba Sanchis-Juan, Yulia Mostovoy, Sarah L Stenton, et al.
Nature Communications|April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomesMark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Integrating 730,947 exome sequences with clinical literature improves gene discoveryJeremy Guez, Julia K Goodrich, Mikhail A Moldovan, et al.
Cell Genomics|June 30, 2023
Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementiasKarri Kaivola, Ruth Chia, Jinhui Ding, et al.
Biorxiv : the Preprint Server for Biology|October 7, 2024
Complex genetic variation in nearly complete human genomesGlennis A Logsdon, Peter Ebert, Peter A Audano, et al.
Nature|July 23, 2025
Complex genetic variation in nearly complete human genomesGlennis A Logsdon, Peter Ebert, Peter A Audano, et al.
Science (New York, N.Y.)|February 26, 2021
Haplotype-resolved diverse human genomes and integrated analysis of structural variationPeter Ebert, Peter A Audano, Qihui Zhu, et al.
Nature|August 26, 2025
Author Correction: Complex genetic variation in nearly complete human genomesGlennis A Logsdon, Peter Ebert, Peter A Audano, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Structural variant discovery and diagnostic impact in rare diseases from short-read and long-read sequencingAlba Sanchis-Juan, Yulia Mostovoy, Sarah L Stenton, et al.
Nature Communications|April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomesMark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
Pageof 5