Low-Pass Genome Sequencing-Based Detection of Paternity: Validation in Clinical Cytogenetics

por Li, Keying, Zhao, Yilin, Chau, Matthew Hoi Kin, Cao, Ye, Leung, Tak Yeung, Kwok, Yvonne K., Choy, Kwong Wai, Dong, Zirui
Publicado 2023

Trio-Based Low-Pass Genome Sequencing Reveals Characteristics and Significance of Rare Copy Number Variants in Prenatal Diagnosis

por Chau, Matthew Hoi Kin, Qian, Jicheng, Chen, Zihan, Li, Ying, Zheng, Yu, Tse, Wing Ting, Kwok, Yvonne K., Leung, Tak Yeung, Dong, Zirui, Choy, Kwong Wai
Publicado 2021

Investigation of the genetic etiology in male infertility with apparently balanced chromosomal structural rearrangements by genome sequencing

por Chau, Matthew Hoi Kin, Li, Ying, Dai, Peng, Shi, Mengmeng, Zhu, Xiaofan, Wah Chung, Jacqueline Pui, Kwok, Yvonne K, Choy, Kwong Wai, Kong, Xiangdong, Dong, Zirui
Publicado 2022

Low-pass genome sequencing-based detection of absence of heterozygosity: validation in clinical cytogenetics

por Dong, Zirui, Chau, Matthew Hoi Kin, Zhang, Yanyan, Yang, Zhenjun, Shi, Mengmeng, Wah, Yi Man, Kwok, Yvonne K., Leung, Tak Yeung, Morton, Cynthia C., Choy, Kwong Wai
Publicado 2021

TEDD: a database of temporal gene expression patterns during multiple developmental periods in human and model organisms

por Zhou, Ziheng, Tan, Cong, Chau, Matthew Hoi Kin, Jiang, Xiaosen, Ke, Ziyuan, Chen, Xiaoyan, Cao, Ye, Kwok, Yvonne K, Bellgard, Matthew, Leung, Tak Yeung, Choy, Kwong Wai, Dong, Zirui
Publicado 2022

Homology-independent multiallelic disruption via CRISPR/Cas9-based knock-in yields distinct functional outcomes in human cells

por Zhang, Chenzi, He, Xiangjun, Kwok, Yvonne K., Wang, Feng, Xue, Junyi, Zhao, Hui, Suen, Kin Wah, Wang, Chi Chiu, Ren, Jianwei, Chen, George G., Lai, Paul B. S., Li, Jiangchao, Xia, Yin, Chan, Andrew M., Chan, Wai-Yee, Feng, Bo
Publicado 2018

Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis

por Choy, Kwong Wai, Wang, Huilin, Shi, Mengmeng, Chen, Jingsi, Yang, Zhenjun, Zhang, Rui, Yan, Huanchen, Wang, Yanfang, Chen, Shaoyun, Chau, Matthew Hoi Kin, Cao, Ye, Chan, Olivia Y.M., Kwok, Yvonne K., Zhu, Yuanfang, Chen, Min, Leung, Tak Yeung, Dong, Zirui
Publicado 2019

Genome-Wide Cell-Free DNA Test for Fetal Chromosomal Abnormalities and Variants: Unrestricted Versus Restricted Reporting

por Kwan, Angel H. W., Zhu, Xiaofan, Mar Gil, Maria, Kwok, Yvonne K. Y., Wah, Isabella Y. M., Hui, Annie S. Y., Ting, Yuen-Ha, Law, Kwok-Ming, Lau, Doris, Xue, Shuwen, Choy, Kwong-Wai, Sahota, Daljit, Leung, Tak-Yeung, Poon, Liona C.
Publicado 2022

Identification of Balanced Chromosomal Rearrangements Previously Unknown Among Participants in the 1000 Genomes Project: Implications for Interpretation of Structural Variation in...

por Dong, Zirui, Wang, Huilin, Chen, Haixiao, Jiang, Hui, Yuan, Jianying, Yang, Zhenjun, Wang, Wen-Jing, Xu, Fengping, Guo, Xiaosen, Cao, Ye, Zhu, Zhenzhen, Geng, Chunyu, Cheung, Wan Chee, Kwok, Yvonne K, Yang, Huangming, Leung, Tak Yeung, Morton, Cynthia C., Cheung, Sau Wai, Choy, Kwong Wai
Publicado 2017

Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis

por Wang, Huilin, Dong, Zirui, Zhang, Rui, Chau, Matthew Hoi Kin, Yang, Zhenjun, Tsang, Kathy Yin Ching, Wong, Hoi Kin, Gui, Baoheng, Meng, Zhuo, Xiao, Kelin, Zhu, Xiaofan, Wang, Yanfang, Chen, Shaoyun, Leung, Tak Yeung, Cheung, Sau Wai, Kwok, Yvonne K., Morton, Cynthia C., Zhu, Yuanfang, Choy, Kwong Wai
Publicado 2019