Zobrazeno 1 - 10
of 167
pro vyhledávání: '"chuhsing kate hsiao"'
Autor:
Ting-Yi Lee, Ching-Hsuan Chen, I-Ming Chen, Hsi-Chung Chen, Chih-Min Liu, Shu-I Wu, Chuhsing Kate Hsiao, Po-Hsiu Kuo
Publikováno v:
Journal of Medical Internet Research, Vol 26, p e55635 (2024)
BackgroundAlthough significant research has explored the digital phenotype in mood disorders, the time-lagged and bidirectional relationship between mood and global positioning system (GPS) mobility remains relatively unexplored. Leveraging the wides
Externí odkaz:
https://doaj.org/article/d525d4b31a6a42f78025f6538aca2065
Publikováno v:
Journal of Medical Internet Research, Vol 26, p e59497 (2024)
BackgroundMonitoring free-living physical activity (PA) through wearable devices enables the real-time assessment of activity features associated with health outcomes and provision of treatment recommendations and adjustments. The conclusions of stud
Externí odkaz:
https://doaj.org/article/fe40a65de5f44a71abdc1dd9f1cd5517
Publikováno v:
BMC Public Health, Vol 22, Iss 1, Pp 1-10 (2022)
Abstract Background Preventive parental behavior may play an important role in the outcomes of children’s myopia. We investigated associations between parental behavior and children’s myopia status and daily activities using data from the most re
Externí odkaz:
https://doaj.org/article/6d862acaef004896aeaf220cd89a2cde
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Current algorithms for gene regulatory network construction based on Gaussian graphical models focuses on the deterministic decision of whether an edge exists. Both the probabilistic inference of edge existence and the relative strength of edges are
Externí odkaz:
https://doaj.org/article/eafac532acf74b5388e20ec7a0c68a80
Autor:
Jyh-Ming Jimmy Juang, Tzu-Pin Lu, Ming-Wei Su, Chien-Wei Lin, Jenn-Hwai Yang, Hou-Wei Chu, Chien-Hsiun Chen, Yi-Wen Hsiao, Chien-Yueh Lee, Li-Mei Chiang, Qi-You Yu, Chuhsing Kate Hsiao, Ching-Yu Julius Chen, Pei-Ei Wu, Chien-Hua Pai, Eric Y. Chuang, Chen-Yang Shen
Publikováno v:
Journal of Advanced Research, Vol 30, Iss , Pp 147-158 (2021)
Introduction: A population-specific genomic reference is important for research and clinical practice, yet it remains unavailable for Han Chinese (HC) in Taiwan. Objectives: We report the first whole genome sequencing (WGS) database of HC (1000 Taiwa
Externí odkaz:
https://doaj.org/article/9022988ea22547ef96ec142bdbfe0cc8
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/b5a542cd1e364db69531e413832f2203
Publikováno v:
BMC Bioinformatics, Vol 21, Iss 1, Pp 1-11 (2020)
Abstract Background To identify and prioritize the influential hub genes in a gene-set or biological pathway, most analyses rely on calculation of marginal effects or tests of statistical significance. These procedures may be inappropriate since hub
Externí odkaz:
https://doaj.org/article/a21111e4aa494588acef96ac91f1b64d
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 12, Iss 1 (2021)
AbstractGene-set analysis (GSA) is a standard procedure for exploring potential biological functions of a group of genes. The development of its methodology has been an active research topic in recent decades. Many GSA methods, when newly proposed, r
Externí odkaz:
https://doaj.org/article/6da10c1b32df414b828859df370081dc
Autor:
Qi-You Yu, Tzu-Pin Lu, Tzu-Hung Hsiao, Ching-Heng Lin, Chi-Yun Wu, Jung-Ying Tzeng, Chuhsing Kate Hsiao
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Genomic studies have been a major approach to elucidating disease etiology and to exploring potential targets for treatments of many complex diseases. Statistical analyses in these studies often face the challenges of multiplicity, weak signals, and
Externí odkaz:
https://doaj.org/article/26dec9d359274d64b573f8c6a9638280
Autor:
Amanda Brucker, Wenbin Lu, Rachel Marceau West, Qi-You Yu, Chuhsing Kate Hsiao, Tzu-Hung Hsiao, Ching-Heng Lin, Patrik K E Magnusson, Patrick F Sullivan, Jin P Szatkiewicz, Tzu-Pin Lu, Jung-Ying Tzeng
Publikováno v:
PLoS Computational Biology, Vol 16, Iss 5, p e1007797 (2020)
Copy number variants (CNVs) are the gain or loss of DNA segments in the genome that can vary in dosage and length. CNVs comprise a large proportion of variation in human genomes and impact health conditions. To detect rare CNV associations, kernel-ba
Externí odkaz:
https://doaj.org/article/88a8bc6a56c04085b78960c936494bce