Sequencing Analysis Software v7.1, initial license
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Applied Biosystems™

Sequencing Analysis Software v7.1, initial license

This software enables you to basecall, trim, display, edit, and print data from our entire line of capillary DNA sequencing詳細を見る
製品番号(カタログ番号)数量
A535511 license
製品番号(カタログ番号) A53551
価格(JPY)
Each
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数量:
1 license
This software enables you to basecall, trim, display, edit, and print data from our entire line of capillary DNA sequencing instruments for data analysis and quality control.

• Obtain longer read lengths, more high-quality bases, and increased accuracy at the 5' end
• Get increased accuracy in regions with low signal-to-noise ratios or with anomalous signal artifacts such as spikes or dye blobs
• Determine the quality of your data using superior metrics from basecalling quality values
• Accelerate quality control using analysis reports with analysis statistics
• Filter out low-quality sequence ends automatically with sequence trimming

Longer Read Lengths with High-Quality Base Pairs
Our significantly improved basecalling algorithm, the KB basecaller, now gives you up to 100 more high-quality bases than other basecalling algorithms. You also get longer read lengths with high-quality base pairs, mixed basecalling with quality value, and accurate basecalling of usually difficult-to-sequence short PCR fragments.

Easily Review Sequencing Results with Quality Values
This software enables you to customize and color code the range of the quality values to represent low-, medium-, and high-quality bases. This way, when the basecaller identifies each base and assigns it a quality value, all you have to do is look at the color coding to easily review, discard, or accept it. In addition, the software trims the ends of low-quality bases, grays them out on the user interface for easy identification, and calculates a sample score, which is the average quality value for all the bases in the untrimmed region.

Reduce Data Screening Time
Eliminate manual review of sequencing data batches. With the software's Quality Control (QC) reports, you get read length and sample score (average QV of bases in the clear range) for each sample file, enabling you to sort data by quality. And to make reviewing data even easier, each QC report is hyperlinked back to its source data.
研究用途にのみご使用ください。診断目的には使用できません。
仕様
データ入力CE Sequencing (.ab1 files)
ライセンスInitial
動作システムWindows 10
製品タイプSequencing Analysis Software V7.0 Initial License
数量1 license
ソフトウェアカテゴリSupports files from all AB Genetic Analyzers
Software TypeSequencing Data Analysis
Unit SizeEach
組成および保存条件
The software is provided in the form of a USB stick.

よくあるご質問(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.