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关 键 词：sequencher正版软件学习班
行 业：IT 软件 实用工具软件
发布时间：2021-09-27
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Sequencher DNA序列分析软件是科学家们必备的工具。持续发展和改进超过25年，Sequencher提供了无与伦比的功能特征，成千上万的出版物都有相关的应用介绍。新手用户可以以少的时间投资产生结果，而有经验的用户会惊叹于功能的深度和控制。Sequencher自带各种专有算法，可以为Sanger, Next-Gen Sequencing (NGS)和RNA-Seq序列数据生成结果。
Sequencher通用装配工具应用如下
基因变异与参考序列的比较
确认向量构造
组装病毒和基因组
从cDNA库中集群数万个序列
将cDNA组合成基因组序列
创建引物图
组装参考
参考序列功能强大，它是测序和序列分析等的核心功能。无论您是从事法、系统研究、遗传学或人口研究，您都可能使用到参考序列功能。在GenBank格式中导入一个序列，将其特性表应用到序列中，并将其标记为一个引用序列。组装到参考序列意味着您可以将您的阅读和原型参考序列进行比较。如果您使用来自不同来源的多个示例，您甚至还可以按名称装配来自动化您的工作。
您甚至可以使用参考序列来去除您感兴趣区域之外的序列或者填补序列覆盖的空白。
Your results are important to you. Whether you work with Sanger Sequencing or Next-Gen Sequencing, you will want to compare your results with publically available data. Sequencher Connections is ideal for a quick search or a more detailed and prolonged analysis across multiple databases and with different parameters.
Working with core labs that use structured naming conventions to track data for individual clients, we developed the Assemble by Name strategy that has become such a powerful and popular tool for combining multiple sequencing projects into a single analysis run.
Sequencher makes traditional sequence assembly easy while keeping you in control.
Trim your sequences for poor quality data with ease. You can even maintain a library of trim criteria to make life even easier.
With intuitive controls you can select the best algorithm for your data including Assemble to Reference. And if you are working with multiple samples from different sources then automate the assembly using Assemble by Name.
Editing your data has never been simpler with tools to help you locate and deal with ambiguities, check for heterozygotes and move around your data.
Use confidence values to assist in trimming data, quality checks, and SNP detection to improve the quality of your results.
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