Zobrazeno 1 - 10
of 92
pro vyhledávání: '"Xuchao Li"'
Autor:
Yongming Liu, Tao Zhang, Honghong Zhang, Xing Jin, Xiaofei Ji, Xiaojing Li, Miaomiao Meng, Zengxue Li, Jiamin Liu, Xuchao Li
Publikováno v:
Energy Exploration & Exploitation, Vol 41 (2023)
The genetic relationships between the stratigraphic textures, thickness changes, burial depths, and the characteristics of the geothermal zoning of the Cenozoic in the northwestern Shandong region were analyzed in this study. Methods involving segmen
Externí odkaz:
https://doaj.org/article/c0a6436096e24960894d118b6131436d
Publikováno v:
Ecotoxicology and Environmental Safety, Vol 262, Iss , Pp 115203- (2023)
Evaluating the sublethal effects of insecticide is crucial for protecting and utilizing natural enemies. In this study, we determined the sublethal effects of acetamiprid and afidopyropen on Harmonia axyridis (Pallas) and explored the potential molec
Externí odkaz:
https://doaj.org/article/c1b7a181f2da4e0eb5fc5a9c15d6d3b9
Autor:
Haojun Jiang, Yifan Xie, Xuchao Li, Huijuan Ge, Yongqiang Deng, Haofang Mu, Xiaoli Feng, Lu Yin, Zhou Du, Fang Chen, Nongyue He
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0159385 (2016)
Short tandem repeats (STRs) and single nucleotide polymorphisms (SNPs) have been already used to perform noninvasive prenatal paternity testing from maternal plasma DNA. The frequently used technologies were PCR followed by capillary electrophoresis
Externí odkaz:
https://doaj.org/article/0d58f8ecfe6940aca4fe4293c8175279
Autor:
Xiongbin Kang, Jun Xia, Yicong Wang, Huixin Xu, Haojun Jiang, Weiwei Xie, Fang Chen, Peng Zeng, Xuchao Li, Yifan Xie, Hongtai Liu, Guodong Huang, Dayang Chen, Ping Liu, Hui Jiang, Xiuqing Zhang
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0161928 (2016)
With the speedy development of sequencing technologies, noninvasive prenatal testing (NIPT) has been widely applied in clinical practice for testing for fetal aneuploidy. The cell-free fetal DNA (cffDNA) concentration in maternal plasma is the most c
Externí odkaz:
https://doaj.org/article/b79b618f0cb345d5bf00349e04be9f85
Autor:
Xuchao Li, Shengpei Chen, Weiwei Xie, Ida Vogel, Kwong Wai Choy, Fang Chen, Rikke Christensen, Chunlei Zhang, Huijuan Ge, Haojun Jiang, Chang Yu, Fang Huang, Wei Wang, Hui Jiang, Xiuqing Zhang
Publikováno v:
PLoS ONE, Vol 9, Iss 1, p e85096 (2014)
BackgroundCopy number variations (CNVs) represent an important type of genetic variation that deeply impact phenotypic polymorphisms and human diseases. The advent of high-throughput sequencing technologies provides an opportunity to revolutionize th
Externí odkaz:
https://doaj.org/article/a735b02f41bf491b950a9345b85c6c80
Autor:
Shengpei Chen, Sheng Li, Weiwei Xie, Xuchao Li, Chunlei Zhang, Haojun Jiang, Jing Zheng, Xiaoyu Pan, Hancheng Zheng, Jia Sophie Liu, Yongqiang Deng, Fang Chen, Hui Jiang
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e92192 (2014)
Ultra-low coverage sequencing (ULCS) is one of the most promising strategies for sequencing based clinical application. These clinical applications, especially prenatal diagnosis, have a strict requirement of turn-around-time; therefore, the applicat
Externí odkaz:
https://doaj.org/article/46cc6597994c4ec383047512494bde66
Autor:
Chunlei Zhang, Chunsheng Zhang, Shengpei Chen, Xuyang Yin, Xiaoyu Pan, Ge Lin, Yueqiu Tan, Ke Tan, Zhengfeng Xu, Ping Hu, Xuchao Li, Fang Chen, Xun Xu, Yingrui Li, Xiuqing Zhang, Hui Jiang, Wei Wang
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e54236 (2013)
Copy number variations (CNVs), a common genomic mutation associated with various diseases, are important in research and clinical applications. Whole genome amplification (WGA) and massively parallel sequencing have been applied to single cell CNVs a
Externí odkaz:
https://doaj.org/article/aa8673d950e7437596d5a79a4d56784e
Autor:
Jing Zheng, Chenming Xu, Jing Guo, Yuan Wei, Huijuan Ge, Xuchao Li, Chunlei Zhang, Haojun Jiang, Ling Pan, Weiping Tang, Weiwei Xie, Hongyun Zhang, Yangyu Zhao, Fuman Jiang, Shengpei Chen, Wei Wang, Xun Xu, Fang Chen, Hefeng Huang, Hui Jiang
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e65050 (2013)
BACKGROUND: Currently very few noninvasive molecular genetic approaches are available to determine zygosity for twin pregnancies in clinical laboratories. This study aimed to develop a novel method to determine zygosity by using maternal plasma targe
Externí odkaz:
https://doaj.org/article/58eadf3154014a94a17bc9f827f8cd31
Autor:
Huijuan Ge, Xuan Huang, Xuchao Li, Shengpei Chen, Jing Zheng, Haojun Jiang, Chunlei Zhang, Xiaoyu Pan, Jing Guo, Fang Chen, Ning Chen, Qun Fang, Hui Jiang, Wei Wang
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e67464 (2013)
BACKGROUND: The discovery of cell free fetal DNA (cff-DNA) in maternal plasma has brought new insight for noninvasive prenatal diagnosis. Combining with the rapidly developed massively parallel sequencing technology, noninvasive prenatal detection of
Externí odkaz:
https://doaj.org/article/b815d170471b4159ba2eaee1557f533f
Autor:
Shan Dan, Fang Chen, Kwong Wai Choy, Fuman Jiang, Jingrong Lin, Zhaoling Xuan, Wei Wang, Shengpei Chen, Xuchao Li, Hui Jiang, Tak Yeung Leung, Tze Kin Lau, Yue Su, Weiyuan Zhang, Xiuqing Zhang
Publikováno v:
PLoS ONE, Vol 7, Iss 2, p e27835 (2012)
Fetal chromosomal abnormalities are the most common reasons for invasive prenatal testing. Currently, G-band karyotyping and several molecular genetic methods have been established for diagnosis of chromosomal abnormalities. Although these testing me
Externí odkaz:
https://doaj.org/article/14239b72586b46d39ba27a0b0717d209