使用seqNdisplayR包生成可定制和可重复的测序覆盖数据图表的协议
Søren Lykke-Andersen1, Jérôme O Rouvière1, Manfred Schmid1
1Department of Molecular Biology and Genetics, Aarhus University, Universitetsbyen 81, 8000 Aarhus C, Denmark.
STAR protocols
|March 19, 2024
概括
seqNdisplayR是一个新的R包,用于可视化功能基因组学下一代测序数据覆盖范围. 它提供可定制和可重现的图案,即使是R初学者也可以通过Shiny应用程序界面访问.
科学领域:
- 基因组学就是基因组学.
- 生物信息学是一种生物信息学.
- 计算生物学 计算生物学
背景情况:
- 下一代测序 (NGS) 对功能基因组学至关重要.
- 需要标准化的数据可视化工具来进行一致的NGS分析.
- 现有的工具可能缺乏用户友好性或定制,用于基因组区域可视化.
研究的目的:
- 介绍seqNdisplayR,一个用于可视化测序数据覆盖范围的R包.
- 为绘制基因组数据提供一种可定制和可重复的方法.
- 为了使先进的测序数据可视化更广泛的受众,包括R初学者.
主要方法:
- 开发了一个名为seqNdisplayR.R的R包.
- 实现一个用户友好的"闪亮的应用程序"接口,以提高可访问性.
- 关于软件安装,数据准备和绘图选项的详细文档.
主要成果:
- seqNdisplayR可以绘制特定基因组区域内的标准测序数据覆盖范围.
- 该包提供可定制和可重现的可视化输出.
- 闪亮的应用程序界面简化了之前没有R经验的用户的过程.
结论:
- seqNdisplayR为功能基因组学研究提供了一个有价值的工具.
- 该软件包增强了测序数据可视化的标准化和一致性.
- seqNdisplayR促进了对复杂生物信息学工具的更广泛的访问.
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