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Applied Biosystems™
Sequencing Analysis Software v7.0, Initial License
This software enables you to basecall, trim, display, edit, and print data from our entire line of capillary DNA sequencing深入閱讀
| 產品號碼 | Quantity |
|---|---|
| A38876 | 1 license |
產品號碼 A38876
價格 (HKD)Contact Us
-
Quantity:
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.
• 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.
規格
Data EntryCE Sequencing (.ab1 files)
LicenseInitial
Operating SystemWindows 10 Pro/IoT, Windows 7 Pro
Product TypeSequencing Analysis Software V7.0 Initial License
Quantity1 license
Software CategorySupports files from all AB Genetic Analyzers
Software TypeSequencing Data Analysis
Unit SizeEach
內容物與存放
Software/CD
Have questions about this product? Ask our AI assisted search.
Which instrument's data files can be analyzed using Sequencing Analysis Software v7.0?
In the Sequencing Analysis software, how do I display the data for select samples?
How do I change the Length of Read in the Sequencing Analysis software,?
What is an Analysis Protocol in the Sequencing Analysis software?
In the Sequencing Analysis software, what is entailed in Post Processing?
Show more FAQs for this product
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文件與下載
常見問答集 (常見問題)
The .ab1 files from a CD are locked (read-only), so you won't be able to analyze them. To work with files from a CD:
1. Drag the .ab1 files from the CD to the hard drive (not the desktop).
2. Select the files, right-click and select Properties.
3. De-select the Read Only check box and click OK.
4. The .ab1 files can now be added to Sequencing Analysis Software and analyzed.
Find additional tips, troubleshooting help, and resources within our Capillary Electrophoresis Software Support Center.
In the Sequencing Analysis software, after Analyzing your samples, the BC check box will change color, reflecting the status of the analysis.
Green: Analysis was successful.
Yellow: Poor quality data (if using KB Basecaller, a partial output file is available).
Red: Analysis Failed
The PP and P check boxes will only contain Green or Red status colors.
Find additional tips, troubleshooting help, and resources within our Capillary Electrophoresis Software Support Center.
In the Sequencing Analysis software, in order to display the data, the check box in the Show column needs to be checked next to the samples you wish to display. The "Show" button was designed to automatically check the show boxes for selected samples. You can select the samples by clicking on the row number. Holding down the shift key while clicking on the row number will allow you to select continuous samples, holding the control key while clicking the row number will allow you to select individual samples.
Find additional tips, troubleshooting help, and resources within our Capillary Electrophoresis Software Support Center.
Yes, bases can be edited in the Sequencing Analysis software. You can insert or delete bases in your electropherogram by simply typing in the change or highlighting the base and pressing the delete key. After making the changes, you must save the sample file in order for those changes to be reflected in your .seq files. Re-analyzing the samples after making any changes will remove the changes made to the sample file.
Find additional tips, troubleshooting help, and resources within our Capillary Electrophoresis Software Support Center.
In the Sequencing Analysis software, you can zoom in and out of the data or choose to view the full view of the samples by going to the View menu and selecting one of the display options or by clicking on the appropriate display button. When you zoom in or out, all samples that are being displayed at that time will be affected.
Find additional tips, troubleshooting help, and resources within our Capillary Electrophoresis Software Support Center.