测序分析软件 v7.1,初始许可证
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Applied Biosystems™

测序分析软件 v7.1,初始许可证

使用此软件,您可以进行碱基识别、修剪、显示、编辑以及从我们的整个毛细管 DNA 测序仪器产品线中打印数据以进行数据分析和质量控制。• 读段长度、碱基质量以及 5'了解更多信息
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货号数量
A535511 license
货号 A53551
价格(CNY)
-
数量:
1 license
使用此软件,您可以进行碱基识别、修剪、显示、编辑以及从我们的整个毛细管 DNA 测序仪器产品线中打印数据以进行数据分析和质量控制。

• 读段长度、碱基质量以及 5' 端的准确度均增加
• 在信噪比低或存在异常信号伪影(如峰顶或染料团)的区域内的准确度提高
• 通过使用来自碱基识别质量值的卓越指标来确定数据质量
• 使用含分析统计数据的分析报告加快质量控制
• 通过序列剪切自动过滤出低质量序列末端

具有高质量碱基对的更长读段长度
KB 碱基识别算法是显著改进的碱基识别算法,目前,可让您得到比其他碱基识别算法多100个的高质量碱基。您还可以获得更长的读段长度和高质量碱基对、包括质量值的混合碱基识别率以及通常难以测序的短 PCR 片段的准确碱基检出率。

轻松查看带质量值的测序结果
该软件使您能够对代表低质量、中质量和高质量碱基的质量值范围进行自定义和颜色编码。这样,当 basecaller 识别每个碱基并为其分配质量值时,您只需查看颜色编码,以便轻松查看、丢弃或接受。此外,该软件还会剪切低质量碱基的末端,在用户界面上以灰色显示以便于识别,并计算样品分数,这是未剪切区域中所有碱基的平均质量值。

缩短数据筛选时间
无需手动检查批量测序数据。通过软件的质量控制 (QC) 报告,您可以获得每个样品文件的读段长度和样品分数(在明确范围内的碱基的平均 QV),使您能够按质量对数据进行排序。为了更容易查看数据,每份 QC 报告都通过添加超链接以便可返回其来源数据。
仅供科研使用。不可用于诊断程序。
规格
数据录入CE 测序(.ab1 文件)
许可证初始
操作系统Windows 10
产品类型测序分析软件 V7.0 初始许可
数量1 license
软件类别支持来自所有 AB 基因分析仪的文件
软件类型测序数据分析
Unit SizeEach
内容与储存
软件以 U 盘的形式提供。

常见问题解答 (FAQ)

Where can I download the Release Notes for Sequencing Analysis Software v7.1?

Please download this PDF (https://downloads.thermofisher.com/Sequencing_Analysis_Software_v7.1/100107870_SeqA_v7.1_Release_Notes.pdf).

Find additional tips, troubleshooting help, and resources within our Capillary Electrophoresis Software Support Center.

What has been updated in Sequencing Analysis Software v7.1?

The primary updates for Sequencing Analysis Software v7.1 (SeqA 7.1) are the following:

- Sequencing Analysis Software v7.1 (SeqA 7.1) is supported only on Microsoft Windows 10 Professional/Enterprise operating system
- Sequencing Analysis Software v7.1 (SeqA 7.1) supports data generated from SeqStudio Flex Series Genetic Analyzers
- Sequencing Analysis Software v7.1 (SeqA 7.1) uses KB Basecaller version 1.4.2.6 for basecalling
- Sequencing Analysis Software v7.1 (SeqA 7.1) supports upgrade from Sequencing Analysis Software v7.0

Find additional tips, troubleshooting help, and resources within our Capillary Electrophoresis Software Support Center.

Which instrument data does Sequencing Analysis Software v7.1 support?

Sequencing Analysis Software v7.1 supports data generated from the following Applied Biosystem instruments:

- SeqStudio Flex Series Genetic Analyzers
- SeqStudio Genetic Analyzer
- 3500 Genetic Analyzer
- 3500xL Genetic Analyzer
- 3130 Genetic Analyzer
- 3130xl Genetic Analyzer
- 3730 DNA Analyzer
- 3730xl DNA Analyzer
- 310 Genetic Analyzer

Find additional tips, troubleshooting help, and resources within our Capillary Electrophoresis Software Support Center.

In the Sequencing Analysis software, when I edit/re-analyze, how will my corresponding .seq files be affected?

When editing sample files by inserting or deleting bases in Sequencing Analysis software, the change will be reflected in the .seq file after the changes have been saved. It is not necessary to re-analyze the samples. In fact, re-analyzing the samples will remove any changes made to the sample file. If the changes had been made and saved and you inadvertently re-analyzed the samples, do not save the file. Remove it from the sample manager without saving and add it to the sample manager again to restore it to its last saved version.

Find additional tips, troubleshooting help, and resources within our Capillary Electrophoresis Software Support Center.

In the Sequencing Analysis software, what are .scf files?

In the Sequencing Analysis software, a standard chromatogram format (.scf) file is compatible with Staden package.

Note: When standard chromatogram file format is created, the .scf extension is not appended to the file name. However, the file format is correct.

Find additional tips, troubleshooting help, and resources within our Capillary Electrophoresis Software Support Center.