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A NEW DNA SEQUENCE ASSEMBLY PROGRAM

机译:一个新的DNA序列装配程序

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We describe the Genome Assembly Program (GAP), a new program for DNA sequence assembly, The program is suitable for large and small projects, a variety of strategies and can handle data from a range of sequencing instruments, It retains the useful components of our previous work, but includes many novel ideas and methods, Many of these methods have been made possible by the program's completely new, and highly interactive, graphical user interface, The program provides many visual clues to the current state of a sequencing project and allows users to interact in intuitive and graphical ways with their data, The program has tools to display and manipulate the various types of data that help to solve and check difficult assemblies, particularly those in repetitive genomes, We have introduced the following new displays: the Contig Selector, the Contig Comparator, the Template Display, the Restriction Enzyme Map and the Stop Codon Map, We have also made it possible to have any number of Contig Editors and Contig Joining Editors running simultaneously even on the same contig, The program also includes a new 'Directed Assembly' algorithm and routines for automatically detecting unfinished segments of sequence, to which it suggests experimental solutions.
机译:我们描述了基因组装配程序(GAP),这是一种用于DNA序列装配的新程序,该程序适用于大型和小型项目,各种策略,并且可以处理来自多种测序仪器的数据,它保留了我们的有用成分以前的工作,但包括许多新颖的思想和方法,这些方法中的许多已经通过程序的全新,高度交互的图形用户界面实现了。该程序提供了有关测序项目当前状态的许多视觉线索,并允许用户该程序具有显示和操纵各种类型的数据的工具,这些数据有助于解决和检查困难的装配,特别是重复基因组中的装配,我们引入了以下新显示:Contig Selector ,Contig比较器,模板显示,限制性酶图谱和终止密码子图谱,我们还可以使用任意数量的Co ntig编辑器和Contig联合编辑器即使在同一contig上也可以同时运行,该程序还包括新的“定向装配”算法和例程,用于自动检测未完成的序列片段,并建议采用实验性解决方案。

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