After electrophoresis, Data Collection software creates a sample file of the raw Sanger sequencing data. Using downstream software applications, further data analysis is required to translate the collected color-data images into the corresponding nucleotide bases.

Sanger sequencing primary analysis

The primary data analysis tools convert the images gathered during Data Collection into all four colors, representing the four corresponding nucleotide bases (Figure 1). For example, our sequencing analysis software is a primary analysis tool that must be used after collection is completed. The sequencing analysis software application allows users to basecall and re-basecall, trim data ends, display, edit and print sample files. Primary data analysis software processes your raw sequence data in an *.ab1 file using algorithms and applies the following analysis settings to the results:

  • Basecalling
    Figure 1: Primary Analysis Software results display each of the 4 bases as a different color.
    The selected basecaller processes the fluorescence signals, then assigns a base to each peak (A, C, G, T, or N). If the KB™ basecaller is used, it also provides per-base quality value predictions, optional mixed base calling, and automatic identification of failed samples (Figure 1).
  • Mobility Shift Correction
    The mobility file compensates for the change in DNA fragment mobility caused by the dye molecule attached to the DNA fragment and changes the color designation of bases depending on the type of chemistry used to label the DNA.
  • Quality Value (QV)
    If the KB basecaller is used for sequencing data analysis, the software assigns a QV for each base. The QV predicts the probability of a basecall error. For example, a QV of 20 predicts an error rate of 1%. The quality prediction algorithm is calibrated to return QVs that conform to the industry-standard relationship established by the Phred software. If your pipeline involves data analysis with Phred software to assign QVs after the data is basecalled, you can simplify your workflow and use the KB basecaller instead. The KB basecaller can perform basecalling and assign QVs. Then, you can generate *phd.1 or *.scf files using the KB basecaller to integrate with your downstream pipeline.

Sanger sequencing secondary analysis

These tools allow you to further refine your sequencing results. Algorithms in our secondary data analysis software products perform a number of functions supporting applications such as mutation detection and genotyping, and produce graphical outputs. 

Product selection guide: Sanger sequencing data analysis software

Software Type Features Applications
Minor Variant Finder Secondary analysis tool
  • 5 % somatic variant detection using Sanger sequencing
  • Sequence 1-96 amplicons/targets at the lowest cost
  • Confirm NGS findings in alignment view and Venn diagram
  • Oncology research
  • Resequencing
MicrobeBridge Secondary analysis tool
  • Assemble sequencing files into consensus sequence
  • One-click access to CDC MicrobeNet database for bacterial identification
  • Overview of read coverage shows the range of forward and reverse sequences in a specimen
    • Contig review highlights  discrepancies in the assembled contig sequence, and allows editing of the contig sequence
    • Quality status displays color-coded trace files based on user-settable quality ranges and provides thumbnail trace views to examine raw data
    • Export contig files  in FASTA format
  • 16S sequencing
  • Bacterial identification
Sequence Analysis Software v6.0

Primary analysis tool
  • Longer read lengths, including accuracy at 5' end
  • Low signal to noise
  • Basecalling quality values
  • Accurate mixed basecall
  • De novo sequencing
Sequence Scanner v2.0 Software (Download) Software viewing tool
  • Review traces in thumbnail format and sort by trace quality
  • Effective quality metrics
  • Simultaneously view raw and analyzed data
  • Results at a glance with Plate Report view
  • De novo sequencing
  • Quality control
SeqScape Software v3.0 Secondary analysis tool
  • Obtain quality values for each base pair, consensus sequence, and mutation
  • Automatically process raw data and generate reports with mutations linked to source electropherograms
  • Preconfigure templates
  • Custom data views
  • Resequencing
  • Medical sequencing
  • SNP/mutation detection
  • SNP/mutation/pathogen subtyping
Variant Reporter Software v2.0 Secondary analysis tool
  • Process >10 times more sample files than competing software products
  • Accelerate data review
  • Simple to learn
  • Robust data filtering with effective quality metrics
  • Resequencing
  • Comparative sequencing and direct sequencing
  • Medical sequencing
  • SNP/mutation detection