| dc.contributor.advisor | 謝明華<br>蔡瑞煌 | zh_TW |
| dc.contributor.advisor | <br> | en_US |
| dc.contributor.author (Authors) | 李大華 | zh_TW |
| dc.contributor.author (Authors) | Dai Hua, Lee | en_US |
| dc.creator (作者) | 李大華 | zh_TW |
| dc.creator (作者) | Dai Hua, Lee | en_US |
| dc.date (日期) | 2002 | en_US |
| dc.date.accessioned | 18-Sep-2009 14:21:59 (UTC+8) | - |
| dc.date.available | 18-Sep-2009 14:21:59 (UTC+8) | - |
| dc.date.issued (上傳時間) | 18-Sep-2009 14:21:59 (UTC+8) | - |
| dc.identifier (Other Identifiers) | G0089356020 | en_US |
| dc.identifier.uri (URI) | https://nccur.lib.nccu.edu.tw/handle/140.119/35176 | - |
| dc.description (描述) | 碩士 | zh_TW |
| dc.description (描述) | 國立政治大學 | zh_TW |
| dc.description (描述) | 資訊管理研究所 | zh_TW |
| dc.description (描述) | 89356020 | zh_TW |
| dc.description (描述) | 91 | zh_TW |
| dc.description.abstract (摘要) | 由於生物科技的蓬勃發展，加上人類基因體的序列草圖在電腦快速的運算能力配合之下已逐步完成，許多生物科技企業或生物學家，已早早開始投入生物資訊的領域中，而生物科技的領域是廣闊無垠的，只有在電腦的配合下，才能快速且準確的得到所想要的結果。而PCR技術的出現，對整個生物界可說是一埸不小的衝擊與革命。大大減少了以往所需的時間和資源。有鑒於以上的發展，本研究乃著手收集PCR相關文獻，整理分析相關知識及相關生技公司職員討論後作為研究基礎，本研究從資訊的角度切入，以Microsoft .Net為實作平台，C# 和ASP.Net 程式語言，提供生物學家一個方便使用的跨平台網路介面，並能讓生物學家從任何地方、任何時候來使用。並導入OOA/OOP的系統架構概念，將可以提高系統功能的再使用性與整體架構的擴充性。在本研究中以PCR(Polymerase Chain Reaction)中的引子設計為主要實作目標。且設計一個簡化版本的Multiplex PCR提供生物學家使用。而主要會影響Primer Design的優劣因素有以下這些：Melting Temperature, Annealing Score, GC content, Primer length,因此本研究使用這些因素來做為本研究選擇Primer的因素，並設計了Primer Design Algorithm來篩選出合適的引子。接著設計Primer Scoring Model用來評量引子的分數，並提供生物學家一個選擇的標準，也加入了權重的觀念，好讓使用者調整適合實驗的參數之重要性。 | zh_TW |
| dc.description.abstract (摘要) | The invention of PCR (Polymerase Chain Reaction) has revolutionized bioinformatics and molecular technology. PCR can amplify specific region of DNA sequence in few minutes. One of these critical parameters is the selection of short oligonucleotides, which called primer. To design the suitable primers is still not part of any standardized algorithm, and several different sets of rules or criteria have been proposed to control the selection of primer sequence.Our research results include the followings: we have created a general-purpose application that design for primer design with relative PCR domain knowledge. We have also implemented a prototype system with Microsoft new OOP language, C#. We also provide a simplify version of Multiple PCR, it could handle two DNA templates to produce qualified multiple primer sets. This program can scan entire gene sequences for all possible primer pairs obeying these primer design rules and displays information such as the length and melting temperature of each primer, which may be of additional help in choosing primers. This program allows the stringency of certain criteria to be varied for better suit the requirement of particular experiment. We try to provide a convenient computerized tool which has a friendly user interface for biologists or scientists to use easily. The design of our system is based on OOA (Object-Oriented Analysis) and OOP (Object-Oriented Programming). Therefore programmers can easily change some algorithm or updated biology data to improve the efficiency of our primer design system. | en_US |
| dc.description.tableofcontents | CHAPTER 1 INTRODUCTION 11.1 Research Motivation 11.2 Research Purpose 21.3 Research Process 21.4 Chapter Structure 3CHAPTER 2 CONCEPTS OF BIOINFORMATICS AND PROBLEM DESCRIPTION 42.1 Bioinformatics 42.2 Polymerase Chain Reaction (PCR) 52.2.1 Introduction of PCR 52.2.2 Process of PCR 72.3 The Problem of PCR 82.4 Multiplex PCR 10CHAPTER 3 PRIMER DESIGN CRITERIA 123.1 Melting Temperature 123.2 Self-Annealing and Self-end Annealing 143.3 Pairs Annealing and Pairs-end Annealing 163.4 GC Content 173.5 Primer Length 173.6 Introduction to Nearest-Neighbor Model 183.6.1 Nearest-Neighbor Model to Predict Stability 183.6.2 Components of Nearest-Neighbor Model 193.6.3 Improved Nearest-Neighbor Model to Predict Stability 19CHAPTER 4 PRIMER DESIGN SYSTEM MODEL AND DESIGN 234.1 Concepts of Primer Design Model 234.2 The Algorithm of Primer Design System 244.2.1 Primer Design Algorithm 254.2.2 Limitation of Primer Design algorithm 264.2 Primer Design Scoring Model 274.2.1 Single Primer Design Scoring Model 274.2.2 Multiplex PCR Primer Design Scoring Model 294.3Primer Design System Flow 344.3.1 Step1 Flow 354.3.2 Step2 Flow 384.3.3 Step3 Flow 384.4 Multiplex PCR Primer Design System Flow 394.4.1 Step1 Flow 404.4.2 Step2 Flow 424.4.3 Step3 Flow 454.5 System Development Environment 46CHAPTER 5 SYSTEM ANALYSIS AND DEMONSTRATION 485.1 System Analysis 485.1.1 Use Case Diagram 485.1.2 Class Diagram 495.1.3 Sequence Diagram 535.2 System Demonstration 575.3 Limitation of our primer design system 65CHAPTER 6 CONCLUSION AND SUGGESTIONS 666.1 Conclusion 666.2 Suggestions and Future Development 67REFERENCE 68 | zh_TW |
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| dc.language.iso | en_US | - |
| dc.source.uri (資料來源) | http://thesis.lib.nccu.edu.tw/record/#G0089356020 | en_US |
| dc.subject (關鍵詞) | 生物資訊 | zh_TW |
| dc.subject (關鍵詞) | 引子設計 | zh_TW |
| dc.subject (關鍵詞) | 聚合酶連鎖反應 | zh_TW |
| dc.subject (關鍵詞) | Bioinformatics | en_US |
| dc.subject (關鍵詞) | Primer Design | en_US |
| dc.subject (關鍵詞) | PCR | en_US |
| dc.title (題名) | 生物資訊引子設計系統之設計與實作 | zh_TW |
| dc.title (題名) | Bioinformatics Web-based Primer Design System: @Primer | en_US |
| dc.type (資料類型) | thesis | en |
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