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一个新的DNA序列组装程序。

A new DNA sequence assembly program.

作者信息

Bonfield J K, Smith K f, Staden R

机构信息

MRC Laboratory of Molecular Biology, Cambridge, UK.

出版信息

Nucleic Acids Res. 1995 Dec 25;23(24):4992-9. doi: 10.1093/nar/23.24.4992.

Abstract

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.

摘要

我们描述了基因组组装程序(GAP),这是一个用于DNA序列组装的新程序。该程序适用于大小项目、各种策略,并且可以处理来自一系列测序仪器的数据。它保留了我们先前工作中的有用部分,但包含了许多新颖的想法和方法。这些方法中的许多都得益于该程序全新的、高度交互式的图形用户界面。该程序为测序项目的当前状态提供了许多视觉线索,并允许用户以直观的图形方式与他们的数据进行交互。该程序具有显示和操作各种类型数据的工具,有助于解决和检查困难的组装,特别是那些在重复基因组中的组装。我们引入了以下新的显示方式:重叠群选择器、重叠群比较器、模板显示、限制酶图谱和终止密码子图谱。我们还使得即使在同一重叠群上也可以同时运行任意数量的重叠群编辑器和重叠群连接编辑器。该程序还包括一种新的“定向组装”算法和用于自动检测未完成序列片段的例程,并为其提出实验解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa87/307504/2581ec81973c/nar00024-0068-a.jpg

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