Shinn-Ying Ho

Prof. Shinn-Ying Ho

Institute of Bioinformatics and Systems Biology, National Chiao Tung University, Hsinchu, 30068, Taiwan

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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28 November 2017 in Scientific Reports
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Journal Article
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WLWei-Hsiang Lee
Wei-Hsiang Lee
HCHui-Mei Chen
Hui-Mei Chen
SYShun-Fa Yang
Shun-Fa Yang
CLChao Liang
Chao Liang
CPChih-Yu Peng
Chih-Yu Peng
YJYuh-Jyh Jong
Yuh-Jyh Jong
Oral squamous cell carcinoma (OSCC) is the most common malignant neoplasm of the oral cavity and the fourth leading malignancy and cause of cancer-related death in the male population of Taiwan. Most cases are detected at advanced stages, resulting in poor prognosis. Therefore, improved detection of early oral health disorders is indispensable. The involvement of oral bacteria in inflammation and their association with OSCC progression provide a feasible target for diagnosis. Due to the nature of oral neoplasms, the diagnosis of epithelial precursor lesions is relatively easy compared with that of other types of cancer. However, the transition from an epithelial precursor lesion to cancer is slow and requires further and continuous follow-up. In this study, we investigated microbiota differences between normal individuals, epithelial precursor lesion patients, and cancer patients with different lifestyle habits, such as betel chewing and smoking, using next-generation sequencing. Overall, the oral microbiome compositions of five genera, Bacillus, Enterococcus, Parvimonas, Peptostreptococcus, and Slackia, revealed significant differences between epithelial precursor lesion and cancer patients and correlated with their classification into two clusters. These composition changes might have the potential to constitute a biomarker to help in monitoring the oral carcinogenesis transition from epithelial precursor lesion to cancer.

15 July 2008 in BMC Bioinformatics
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Chun-Wei TungChun-Wei Tung
Chun-Wei Tung
SHShinn-Ying Ho
Shinn-Ying Ho
Ubiquitylation plays an important role in regulating protein functions. Recently, experimental methods were developed toward effective identification of ubiquitylation sites. To efficiently explore more undiscovered ubiquitylation sites, this study aims to develop an accurate sequence-based prediction method to identify promising ubiquitylation sites.

3 March 2008 in IEEE Transactions on Systems, Man, and Cybernetics - Part A: Systems and Humans
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Journal Article
Closed access
SHShinn-Ying Ho
Shinn-Ying Ho
HLHung-Sui Lin
Hung-Sui Lin
WLWeei-Hurng Liauh
Weei-Hurng Liauh
SHShinn-Jang Ho
Shinn-Jang Ho
This paper proposes a novel variant of particle swarm optimization (PSO), named orthogonal PSO (OPSO), for solving intractable large parameter optimization problems. The standard version of PSO is associated with the lack of a mechanism responsible for the process of high-dimensional vector spaces. The high performance of OPSO arises mainly from a novel move behavior using an intelligent move mechanism (IMM) which applies orthogonal experimental design to adjust a velocity for each particle by using a systematic reasoning method instead of the conventional generate-and-go method. The IMM uses a divide-and- conquer approach to cope with the curse of dimensionality in determining the next move of particles. It is shown empirically that the OPSO performs well in solving parametric benchmark functions and a task assignment problem which is NP-complete compared with the standard PSO with the conventional move behavior. The OPSO with IMM is more specialized than the PSO and performs well on large-scale parameter optimization problems with few interactions between variables.

8 June 2011 in BMC Bioinformatics
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SHShinn-Ying Ho
Shinn-Ying Ho
CCChih-Yuan Chao
Chih-Yuan Chao
HHHui-Ling Huang
Hui-Ling Huang
TCTzai-Wen Chiu
Tzai-Wen Chiu
PCPhasit Charoenkwan
Phasit Charoenkwan
EHERIC HWANG
ERIC HWANG
Background: Automatic quantification of neuronal morphology from images of fluorescence microscopy plays an increasingly important role in high-content screenings. However, there exist very few freeware tools and methods which provide automatic neuronal morphology quantification for pharmacological discovery. Results: This study proposes an effective quantification method, called NeurphologyJ, capable of automatically quantifying neuronal morphologies such as soma number and size, neurite length, and neurite branching complexity (which is highly related to the numbers of attachment points and ending points). NeurphologyJ is implemented as a plugin to ImageJ, an open-source Java-based image processing and analysis platform. The high performance of NeurphologyJ arises mainly from an elegant image enhancement method. Consequently, some morphology operations of image processing can be efficiently applied. We evaluated NeurphologyJ by comparing it with both the computer-aided manual tracing method NeuronJ and an existing ImageJ-based plugin method NeuriteTracer. Our results reveal that NeurphologyJ is comparable to NeuronJ, that the coefficient correlation between the estimated neurite lengths is as high as 0.992. NeurphologyJ can accurately measure neurite length, soma number, neurite attachment points, and neurite ending points from a single image. Furthermore, the quantification result of nocodazole perturbation is consistent with its known inhibitory effect on neurite outgrowth. We were also able to calculate the IC50 of nocodazole using NeurphologyJ. This reveals that NeurphologyJ is effective enough to be utilized in applications of pharmacological discoveries. Conclusions: This study proposes an automatic and fast neuronal quantification method NeurphologyJ. The ImageJ plugin with supports of batch processing is easily customized for dealing with high-content screening applications. The source codes of NeurphologyJ (interactive and high-throughput versions) and the images used for testing are freely available (see Availability).

25 September 2015 in PLOS ONE
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HCHsien-Yi Chiu
Hsien-Yi Chiu
HHHui-Ling Huang
Hui-Ling Huang
CLChien-Hsun Li
Chien-Hsun Li
HCHung-An Chen
Hung-An Chen
CYChia-Lun Yeh
Chia-Lun Yeh
SHShinn-Ying Ho
Shinn-Ying Ho
There have been few large population-based studies of the association between rheumatoid arthritis (RA) and chronic kidney disease (CKD) and glomerulonephritis. This nationwide cohort study investigated the risks of developing CKD and glomerulonephritis in patients with RA, and the associated risks for cardiovascular complications. From the Taiwan National Health Insurance Research Database, we identified a study cohort of 12,579 patients with RA and randomly selected 37,737 subjects without RA as a control cohort. Each subject was individually followed for up for 5 years, and the risk of CKD was analyzed using Cox proportional hazards regression models. During the follow-up period, after adjusting for traditional cardiovascular risk factors RA was independently associated with a significantly increased risk of CKD (adjusted hazard ratio [aHR] 1.31; 95% confidence interval [CI] 1.23–1.40) and glomerulonephritis (aHR 1.55; 95% CI 1.37–1.76). Increased risk of CKD was also associated with the use of non-steroidal anti-inflammatory drugs, cyclosporine, glucocorticoids, mycophenolate mofetil, and cyclophosphamide. Patients with comorbidities had even greater increased risk of CKD. Moreover, RA patients with concurrent CKD had significantly higher likelihood of developing ischemic heart disease and stroke. RA patients had higher risk of developing CKD and glomerulonephritis, independent of traditional cardiovascular risk factors. Their increased risk of CKD may be attributed to glomerulonephritis, chronic inflammation, comorbidities, and renal toxicity of antirheumatic drugs. Careful monitoring of renal function in RA patients and tight control of their comorbid diseases and cardiovascular risk factors are warranted.

31 October 2018 in Scientific Reports
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SSSrinivasulu Yerukala Sathipati
Srinivasulu Yerukala Sathipati
SHShinn-Ying Ho
Shinn-Ying Ho
Breast cancer is a heterogeneous disease and one of the most common cancers among women. Recently, microRNAs (miRNAs) have been used as biomarkers due to their effective role in cancer diagnosis. This study proposes a support vector machine (SVM)-based classifier SVM-BRC to categorize patients with breast cancer into early and advanced stages. SVM-BRC uses an optimal feature selection method, inheritable bi-objective combinatorial genetic algorithm, to identify a miRNA signature which is a small set of informative miRNAs while maximizing prediction accuracy. MiRNA expression profiles of a 386-patient cohort of breast cancer were retrieved from The Cancer Genome Atlas. SVM-BRC identified 34 of 503 miRNAs as a signature and achieved a 10-fold cross-validation mean accuracy, sensitivity, specificity, and Matthews correlation coefficient of 80.38%, 0.79, 0.81, and 0.60, respectively. Functional enrichment of the 10 highest ranked miRNAs was analysed in terms of Kyoto Encyclopedia of Genes and Genomes and Gene Ontology annotations. Kaplan-Meier survival analysis of the highest ranked miRNAs revealed that four miRNAs, hsa-miR-503, hsa-miR-1307, hsa-miR-212 and hsa-miR-592, were significantly associated with the prognosis of patients with breast cancer.