Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Zirui Dong

Showing results (41-50 of 66) with videos related to

Pageof 7
Sort By:
Frontiers in Cell and Developmental Biology|November 29, 2023
Single-cell analysis reveals specific neuronal transition during mouse corticogenesisZiheng Zhou, Yueyang Pan, Si Zhou, et al.
Nucleic Acids Research|November 9, 2022
TEDD: a database of temporal gene expression patterns during multiple developmental periods in human and model organismsZiheng Zhou, Cong Tan, Matthew Hoi Kin Chau, et al.
Current Protocols in Human Genetics|January 25, 2018
Balanced Chromosomal Rearrangement Detection by Low-Pass Whole-Genome SequencingZirui Dong, Lingfei Ye, Zhenjun Yang, et al.
Genes|April 3, 2021
Performance of Cell-Free DNA Screening for Fetal Common Aneuploidies and Sex Chromosomal Abnormalities: A Prospective Study from a Less Developed Autonomous Region in Mainland ChinaYunli Lai, Xiaofan Zhu, Sheng He, et al.
Science China. Life Sciences|April 14, 2026
Characterization of rare genomic structural variants across 2,981 genomes reveals significant involvements in recessive conditionsZirui Dong, Keying Li, Chi Chun Chan, et al.
Nature Biotechnology|February 14, 2012
Comprehensive analysis of RNA-Seq data reveals extensive RNA editing in a human transcriptomeZhiyu Peng, Yanbing Cheng, Bertrand Chin-Ming Tan, et al.
Nature Communications|January 11, 2025
An intelligent hybrid-fabric wristband system enabled by thermal encapsulation for ergonomic human-machine interactionAobo Cheng, Xin Li, Ding Li, et al.
HGG Advances|July 7, 2026
A personalized genomic medicine approach to rare genomic disorders associated with simple chromosomal structural variantsDezső David, Joana Fino, Márcia Rodrigues, et al.
Human Genetics|November 10, 2025
Clinical validation of artificial intelligence-assisted karyotyping on peripheral blood in a cytogenetic diagnostic laboratoryYujie Zhu, Matthew Hoi Kin Chau, Huilin Wang, et al.
Frontiers in Genetics|May 2, 2022
Investigation of Chromosomal Structural Abnormalities in Patients With Undiagnosed Neurodevelopmental DisordersYe Cao, Ho Ming Luk, Yanyan Zhang, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Frontiers in Cell and Developmental Biology|November 29, 2023
Single-cell analysis reveals specific neuronal transition during mouse corticogenesisZiheng Zhou, Yueyang Pan, Si Zhou, et al.
Nucleic Acids Research|November 9, 2022
TEDD: a database of temporal gene expression patterns during multiple developmental periods in human and model organismsZiheng Zhou, Cong Tan, Matthew Hoi Kin Chau, et al.
Current Protocols in Human Genetics|January 25, 2018
Balanced Chromosomal Rearrangement Detection by Low-Pass Whole-Genome SequencingZirui Dong, Lingfei Ye, Zhenjun Yang, et al.
Genes|April 3, 2021
Performance of Cell-Free DNA Screening for Fetal Common Aneuploidies and Sex Chromosomal Abnormalities: A Prospective Study from a Less Developed Autonomous Region in Mainland ChinaYunli Lai, Xiaofan Zhu, Sheng He, et al.
Science China. Life Sciences|April 14, 2026
Characterization of rare genomic structural variants across 2,981 genomes reveals significant involvements in recessive conditionsZirui Dong, Keying Li, Chi Chun Chan, et al.
Nature Biotechnology|February 14, 2012
Comprehensive analysis of RNA-Seq data reveals extensive RNA editing in a human transcriptomeZhiyu Peng, Yanbing Cheng, Bertrand Chin-Ming Tan, et al.
Nature Communications|January 11, 2025
An intelligent hybrid-fabric wristband system enabled by thermal encapsulation for ergonomic human-machine interactionAobo Cheng, Xin Li, Ding Li, et al.
HGG Advances|July 7, 2026
A personalized genomic medicine approach to rare genomic disorders associated with simple chromosomal structural variantsDezső David, Joana Fino, Márcia Rodrigues, et al.
Human Genetics|November 10, 2025
Clinical validation of artificial intelligence-assisted karyotyping on peripheral blood in a cytogenetic diagnostic laboratoryYujie Zhu, Matthew Hoi Kin Chau, Huilin Wang, et al.
Frontiers in Genetics|May 2, 2022
Investigation of Chromosomal Structural Abnormalities in Patients With Undiagnosed Neurodevelopmental DisordersYe Cao, Ho Ming Luk, Yanyan Zhang, et al.
Pageof 7