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ABI测序分析。对来自ABI DNA测序仪的序列数据进行处理。

ABI sequencing analysis. Manipulation of sequence data from the ABI DNA sequencer.

作者信息

Hagemann T L, Kwan S P

机构信息

Department of Pathological Sciences, Waisman Center, University of Wisconsin, Madison 53706, USA.

出版信息

Mol Biotechnol. 1999 Dec 1;13(2):137-52. doi: 10.1385/MB:13:2:137.

DOI:10.1385/MB:13:2:137
PMID:10934528
Abstract

The ABI Sequencing Analysis application is designed specifically for the analysis of data produced by the ABI DNA Sequencer. The ABI sequencer is a laser-based instrument that utilizes fluorescent labels to analyze the products of a sequencing reaction as they migrate through a gel. After the data are collected from a sequencing run, the Analysis program identifies and tracks the sample lanes of the gel and subsequently normalizes and integrates the raw data into a chromatogram of the final sequence. For the user, there are basically two types of files that can be manipulated to potentially improve the analysis results. The Gel File consists of a computer generated image of the sequencing gel with the fluorescent DNA banding patterns. This image allows the user to view and edit the tracking lines generated and used by Analysis to collect data points for each sample. Individual Sample Files are stored for each of the samples analyzed and include the chromatogram, raw data, and annotations and information regarding the sample and sequence run. Generally, the products of a sequencing reaction are easily resolved and the Analysis software interprets the correct nucleotide sequence. Ambiguous base calls tend to occur near the end of the sequence and may be either edited or deleted by the user before exporting the data for further comparisons or alignments. Occasionally the tracking lines within the gel image may need to be adjusted or moved. The sample data are then reextracted from the Gel File and analyzed again. This review explains the general operation of Analysis in terms of viewing and editing a chromatogram, retracking the lanes of a Gel File, and analyzing the final sample data. The three versions 1.2.1, 2.1.2, and 3.3 are discussed.

摘要

ABI测序分析应用程序是专门为分析ABI DNA测序仪产生的数据而设计的。ABI测序仪是一种基于激光的仪器,它利用荧光标记来分析测序反应产物在凝胶中迁移时的情况。从测序运行中收集数据后,分析程序会识别并跟踪凝胶的样品泳道,随后将原始数据进行归一化处理并整合到最终序列的色谱图中。对于用户来说,基本上有两种类型的文件可以进行操作,以潜在地改善分析结果。凝胶文件由测序凝胶的计算机生成图像以及荧光DNA条带模式组成。该图像允许用户查看和编辑分析程序生成并用于为每个样品收集数据点的跟踪线。为每个分析的样品存储单独的样品文件,其中包括色谱图、原始数据以及有关样品和测序运行的注释和信息。一般来说,测序反应的产物很容易分辨,分析软件会解读正确的核苷酸序列。在序列末尾附近往往会出现模糊的碱基调用,用户在导出数据进行进一步比较或比对之前,可以对其进行编辑或删除。偶尔可能需要调整或移动凝胶图像中的跟踪线。然后从凝胶文件中重新提取样品数据并再次进行分析。本综述从查看和编辑色谱图、重新跟踪凝胶文件的泳道以及分析最终样品数据等方面解释了分析程序的一般操作。文中讨论了1.2.1、2.1.2和3.3这三个版本。

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本文引用的文献

1
Consed: a graphical tool for sequence finishing.Consed:一种用于序列完成的图形工具。
Genome Res. 1998 Mar;8(3):195-202. doi: 10.1101/gr.8.3.195.
2
Base-calling of automated sequencer traces using phred. II. Error probabilities.使用Phred对自动测序仪追踪结果进行碱基识别。II. 错误概率。
Genome Res. 1998 Mar;8(3):186-94.
3
Base-calling of automated sequencer traces using phred. I. Accuracy assessment.使用Phred对自动测序仪轨迹进行碱基识别。I. 准确性评估。
Genome Res. 1998 Mar;8(3):175-85. doi: 10.1101/gr.8.3.175.