Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Erh-Chan Yeh"'
Autor:
Hsiao-Jung Kao, Ting-Yi Lin, Feng-Jen Hsieh, Jia-Ying Chien, Erh-Chan Yeh, Wan-Jia Lin, Yi-Hua Chen, Kai-Hsuan Ding, Yu Yang, Sheng-Chu Chi, Ping-Hsing Tsai, Chih-Chien Hsu, De-Kuang Hwang, Hsien-Yang Tsai, Mei-Ling Peng, Shi-Huang Lee, Siu-Fung Chau, Chen Yu Chen, Wai-Man Cheang, Shih-Jen Chen, Pui-Yan Kwok, Shih-Hwa Chiou, Mei-Yeh Jade Lu, Shun-Ping Huang
Publikováno v:
npj Genomic Medicine, Vol 9, Iss 1, Pp 1-7 (2024)
Abstract Our study presents a 319-gene panel targeting inherited retinal dystrophy (IRD) genes. Through a multi-center retrospective cohort study, we validated the assay’s effectiveness and clinical utility and characterized the mutation spectrum o
Externí odkaz:
https://doaj.org/article/483be3c5b3ae4fb894f541f92bf270b0
Autor:
Chun-Yu Wei, Jenn-Hwai Yang, Erh-Chan Yeh, Ming-Fang Tsai, Hsiao-Jung Kao, Chen-Zen Lo, Lung-Pao Chang, Wan-Jia Lin, Feng-Jen Hsieh, Saurabh Belsare, Anand Bhaskar, Ming-Wei Su, Te-Chang Lee, Yi-Ling Lin, Fu-Tong Liu, Chen-Yang Shen, Ling-Hui Li, Chien-Hsiun Chen, Jeffrey D. Wall, Jer-Yuarn Wu, Pui-Yan Kwok
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-10 (2021)
Abstract Personalized medical care focuses on prediction of disease risk and response to medications. To build the risk models, access to both large-scale genomic resources and human genetic studies is required. The Taiwan Biobank (TWB) has generated
Externí odkaz:
https://doaj.org/article/3593b2764afa4ac58f96065a27161ace
Autor:
Karen H. Y. Wong, Walfred Ma, Chun-Yu Wei, Erh-Chan Yeh, Wan-Jia Lin, Elin H. F. Wang, Jen-Ping Su, Feng-Jen Hsieh, Hsiao-Jung Kao, Hsiao-Huei Chen, Stephen K. Chow, Eleanor Young, Catherine Chu, Annie Poon, Chi-Fan Yang, Dar-Shong Lin, Yu-Feng Hu, Jer-Yuarn Wu, Ni-Chung Lee, Wuh-Liang Hwu, Dario Boffelli, David Martin, Ming Xiao, Pui-Yan Kwok
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-11 (2020)
The human reference genome does not fully reflect human genetic diversity. Here, the authors analyse 338 human genome assemblies from diverse populations to identify missing sequences, define non-reference unique insertions and construct a Human Dive
Externí odkaz:
https://doaj.org/article/c8c00ea643e14a5fb06226803d1d0cb0
Autor:
Jenn-Hwai Yang, Saurabh Belsare, Yi-Ling Lin, Feng-Jen Hsieh, Ling-Hui Li, Jer-Yuarn Wu, Chen-Zen Lo, Wan-Jia Lin, Jeffrey D. Wall, C. M. Wei, Fu-Tong Liu, Hsiao-Jung Kao, Chien-Hsiun Chen, Te-Chang Lee, Anand Bhaskar, Pui-Yan Kwok, Lung-Pao Chang, Ming-Wei Su, Erh-Chan Yeh, Chen-Yang Shen, Ming-Fang Tsai
Publikováno v:
NPJ Genomic Medicine
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-10 (2021)
NPJ genomic medicine, vol 6, iss 1
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-10 (2021)
NPJ genomic medicine, vol 6, iss 1
Personalized medical care focuses on prediction of disease risk and response to medications. To build the risk models, access to both large-scale genomic resources and human genetic studies is required. The Taiwan Biobank (TWB) has generated high-cov
Autor:
Walfred Ma, Jen-Ping Su, Wan-Jia Lin, Wuh-Liang Hwu, Jer-Yuarn Wu, Ming Xiao, Yu-Feng Hu, Annie Poon, Catherine J. Chu, Hsiao-Jung Kao, Chi-Fan Yang, Pui-Yan Kwok, Dario Boffelli, Dar-Shong Lin, Hsiao-Huei Chen, Ni-Chung Lee, Eleanor Young, David I. K. Martin, C. M. Wei, Stephen K. Chow, Elin H. F. Wang, Erh-Chan Yeh, Karen H. Y. Wong, Feng-Jen Hsieh
Publikováno v:
Nature Communications
Nature Communications, Vol 11, Iss 1, Pp 1-11 (2020)
Nature communications, vol 11, iss 1
Nature Communications, Vol 11, Iss 1, Pp 1-11 (2020)
Nature communications, vol 11, iss 1
The current human reference genome is predominantly derived from a single individual and it does not adequately reflect human genetic diversity. Here, we analyze 338 high-quality human assemblies of genetically divergent human populations to identify
Autor:
Wan-Jia Lin, Yuan-Tsong Chen, Cheng-Yang Louis Tang, Fang-Chih Hsiao, Chih-Cheng Chen, Adam Yao, Huan-Chin Tseng, Erh-Chan Yeh, Yu-Chang Cheng, Hsing-Tsung Wu, Chuan-Kun Liu
Publikováno v:
Nucleic Acids Research
VarioWatch (http://genepipe.ncgm.sinica.edu.tw/variowatch/) has been vastly improved since its former publication GenoWatch in the 2008 Web Server Issue. It is now at least 10 000-times faster in annotating a variant. Drastic speed increase, through
Autor:
Yu-Chang Cheng, Fang-Chih Hsiao, Erh-Chan Yeh, Wan-Jia Lin, Cheng-Yang Louis Tang, Huan-Chin Tseng, Hsing-Tsung Wu, Chuan-Kun Liu, Chih-Cheng Chen, Yuan-Tsong Chen, Adam Yao
Publikováno v:
Nucleic Acids Research; 2012 Web Server issue, Vol. 40, pW76-W81, 6p, 2 Color Photographs, 1 Black and White Photograph