Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Shoufang Qu"'
Autor:
Weihua Zhao, Yanyan Song, Chuanfeng Huang, Shan Xu, Qi Luo, Runsi Yao, Nan Sun, Bo Liang, Jia Fei, Fangfang Gao, Jie Huang, Shoufang Qu
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-8 (2024)
Abstract Objective Preimplantation genetic testing for monogenic disorders (PGT-M) has been used for over 20 years to detect many serious genetic conditions. However, there is still a lack of reference materials (RMs) to validate the test performance
Externí odkaz:
https://doaj.org/article/16fcad30e8ee4b12b1a66c58c29e0149
Autor:
Xiaofei Yang, Xixi Zhao, Shoufang Qu, Peng Jia, Bo Wang, Shenghan Gao, Tun Xu, Wenxin Zhang, Jie Huang, Kai Ye
Publikováno v:
Fundamental Research, Vol 2, Iss 6, Pp 946-953 (2022)
The advantages of both the length and accuracy of high-fidelity (HiFi) reads enable chromosome-scale haplotype-resolved genome assembly. In this study, we sequenced a cell line named HJ, established from a Chinese Han male individual by using HiFi an
Externí odkaz:
https://doaj.org/article/b8ae0c4e73e84c55b8804e590dd9d82a
Autor:
Min Zhang, Kun Li, Shoufang Qu, Zhiwei Guo, Yuanli Wang, Xu Yang, Junhua Zhou, Guojun Ouyang, Rongtao Weng, Fenxia Li, Yingsong Wu, Xuexi Yang
Publikováno v:
Journal of Translational Medicine, Vol 20, Iss 1, Pp 1-12 (2022)
Abstract Background Chromosomal aneuploidy is the most common birth defect. However, the developmental mechanism and gene expression profile of fetuses with chromosomal aneuploidy are relatively unknown, and the maternal immune changes induced by fet
Externí odkaz:
https://doaj.org/article/d5ae43a9500c41b08bad696e989acea9
Autor:
Xiao Du, Lili Li, Fan Liang, Sanyang Liu, Wenxin Zhang, Shuai Sun, Yuhui Sun, Fei Fan, Linying Wang, Xinming Liang, Weijin Qiu, Guangyi Fan, Ou Wang, Weifei Yang, Jiezhong Zhang, Yuhui Xiao, Yang Wang, Depeng Wang, Shoufang Qu, Fang Chen, Jie Huang
Publikováno v:
Genomics, Proteomics & Bioinformatics, Vol 20, Iss 1, Pp 192-204 (2022)
The importance of structural variants (SVs) for human phenotypes and diseases is now recognized. Although a variety of SV detection platforms and strategies that vary in sensitivity and specificity have been developed, few benchmarking procedures are
Externí odkaz:
https://doaj.org/article/479691735ac349b781de159587e94e9d
Autor:
Dengwei Zhang, Si Zhou, Ziheng Zhou, Xiaosen Jiang, Dongsheng Chen, Hai-Xi Sun, Jie Huang, Shoufang Qu, Songchen Yang, Ying Gu, Xiuqing Zhang, Xin Jin, Ya Gao, Yue Shen, Fang Chen
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-10 (2021)
Abstract Background Birth defects pose a major challenge to infant health. Thus far, however, the causes of most birth defects remain cryptic. Over the past few decades, considerable effort has been expended on disclosing the underlying mechanisms re
Externí odkaz:
https://doaj.org/article/b6a4d6d5fc68481f94d235876c9789e7
Autor:
Wenxin Zhang, Ruixia Wang, Huan Fang, Xiangyuan Ma, Dan Li, Tao Liu, Zhenxi Chen, Ke Wang, Shiguang Hao, Zicheng Yu, Zhili Chang, Chenglong Na, Yin Wang, Jian Bai, Yanyan Zhang, Fang Chen, Miao Li, Chao Chen, Liangshen Wei, Jinghua Li, Xiaoyan Chang, Shoufang Qu, Ling Yang, Jie Huang
Publikováno v:
Clinical and Translational Medicine, Vol 11, Iss 5, Pp n/a-n/a (2021)
Abstract Background Tumor mutational burden (TMB) is a promising biomarker for stratifying patient subpopulation who would benefit from immune checkpoint blockade (ICB) therapies. Although great efforts have been made for standardizing TMB measuremen
Externí odkaz:
https://doaj.org/article/4ed20a23b2154d3eb3ae4136989e3def
Autor:
Zheng Jia, Junju Huang, Ying Yang, Yong Yang, Wei Lin, Shoufang Qu, Nan Sun, Wenxin Zhang, Lulu Han, Jie Huang
Publikováno v:
Pharmacogenetics & Genomics; Aug2024, Vol. 34 Issue 6, p175-183, 9p
Autor:
Wenxin, Zhang, Shoufang, Qu, Qiong, Chen, Xuexi, Yang, Jing, Yu, Shuang, Zeng, Yuxing, Chu, Hao, Zou, Zhihong, Zhang, Xiaowen, Wang, Ruilin, Jing, Yingsong, Wu, Zhipeng, Liu, Ren, Xu, Chunyan, Wu, Chuanfeng, Huang, Jie, Huang
Publikováno v:
Technology and Health Care. 31:485-495
BACKGROUND: Along with the dramatic development of molecular diagnostic testing for the detection of oncogene variations, reference materials (RMs) have become increasingly important in performance evaluation of genetic testing. OBJECTIVE: In this st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a2fa5e19784b9dc7814443c59d1f3e1
https://doi.org/10.3233/thc-220102
https://doi.org/10.3233/thc-220102
Autor:
Weilun Huang, Shoufang Qu, Qiongzhen Qin, Xu Yang, Wanqing Han, Yongli Lai, Jiaqi Chen, Shihao Zhou, Xuexi Yang, Wanjun Zhou
Publikováno v:
Clinical Chemistry; Sep2023, Vol. 69 Issue 9, p1062-1071, 10p
Autor:
Sanyang Liu, Yuhui Sun, Fan Liang, Linying Wang, Yuhui Xiao, Shoufang Qu, Jiezhong Zhang, Xiao Du, Xinming Liang, Shuai Sun, Yang Wang, Fei Fan, Jie Huang, Fang Chen, Wenxin Zhang, Depeng Wang, Weifei Yang, Li-Li Li, Ou Wang, Guangyi Fan, Weijin Qiu
Publikováno v:
Genomics, Proteomics & Bioinformatics. 20:192-204
The importance of structural variants (SVs) for human phenotypes and diseases is now recognized. Although a variety of SV detection platforms and strategies that vary in sensitivity and specificity have been developed, few benchmarking procedures are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70bbbea831ae1ea4404594ad0039b1e3
https://doi.org/10.1016/j.gpb.2020.10.006
https://doi.org/10.1016/j.gpb.2020.10.006