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    Showing items 131-140 of 1110. (111 Page(s) Totally)
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    DateTitleAuthors
    2021-12-21 臨床試驗設計及評估之創新統計方法-複合藥的調適性二階段前期臨床試驗設計(子計畫一);Adaptive Two-Stage Dose-Finding Designs for Combined Drugs 陳玉英
    2021-12-21 空間型態資料伴隨空間混淆效應之半母數研究;A Semiparametric Approach for Spatial Data with Spatial Confounding Effects 陳春樹
    2021-12-21 臨床試驗設計及評估之創新統計方法-對於研究目的為存活時間的三臂等效性試驗所需樣本數的計算(子計畫四);Sample Size Determination for Three-Arm Equivalence Trials with Survival Outcomes 曾議寬
    2021-12-21 可分析連續,分類與個數三種不同資料型態的R(個序列)與C(個時間點)的交叉設計的強韌概似推論法;Robust Likelihood Inference for Treatment Effects Comparison for General Continuous, Categorical and Count Data for Crossover Designs with R Sequences and C Periods 鄒宗山
    2021-12-21 鋰離子電池衰變數據的可靠度分析-鋰離子電池衰變數據的貝氏可靠度分析(子計畫一);Bayesian Reliability Analysis of Degradation Data of Lithium-Ion Battery 樊采虹
    2021-12-21 金融系統性風險與過度自信:強化學習框架下的隨機環境及部分資訊銀行借貸系統;Systemic Risk and Overconfidence Based on Interbank Network under Stochastic Enviroment with Partial Information: a Reinforcement Learning Framework 孫立憲
    2021-08-10 加速不變原則之偏斜-t過程;Skew-t Processes Based on the Acceleration Invariance Principle 黃鴻緒; Huang, Hung-Hsu
    2021-08-10 逆高斯過程之完整貝氏衰變分析;A Complete Bayesian Degradation Analysis under Inverse Gaussian Processes 古立丞; Ku, Li-Chen
    2021-08-03 根據毒性反應與疾病無惡化存活時間 建立之早期臨床試驗設計;Early clinical trial designs based on toxicity response and progression-free survival time 吳宥蓁; Wu, Yu-Jen
    2021-08-02 根據模型尋找混合藥物劑量之設計;Model-based designs for finding dose combinations 林羿州; Lin, Yi-Zhou

    Showing items 131-140 of 1110. (111 Page(s) Totally)
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