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A Unique tool for DNA Variant Analysis from Sanger Sequence Traces

Mutation Surveyor® is a DNA Sequencing analysis software capable of performing variant analysis of up to 2000 Sanger sequencing files (.ab1,.RSD,.ESD & .scf) generated by Applied Biosystems Genetic Analyzers, MegaBACE as well as Beckman CEQ electrophoresis systems in 15 minutes. Utilizing patented anti-correlation technology Mutation Surveyor delivers excellent accuracy, sensitivity, low false positive and negative rates in the analysis of DNA variants: SNPS, insertions and deletions (Indels), Somatic Mutations in direct sequencing, medical sequencing, PCR sequencing, Mitochondria sequencing, and resequencing projects. The software also provides superior basecalling; correcting N-calls of the KB Basecaller or Variant Reporter® software packages; sequence alignment and reference assembly, replacing such programs as DNAStar and Sequencher or SeqPilot. The package includes automated download of annotated GenBank files including amino acid sequence; de-convolution of heterozygous indels; DNA methylation detection, mitochondria DNA sequence analysis and quantification; customizable DNA variant coding; and reporting. Mutation Surveyor has been validated for use in clinical applications by NGRL, UK and University of Pittsburgh Medical Center.

Validations of Mutation Surveyor:
(National Genetics Reference Laboratory, Manchester UK) [pdf]

(University of Pittsburgh Medical Center) [pdf]

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Download/View Mutation Surveyor® Brochure

Mutation Surveyor Capabilities:
Detection Sensitivity & Accuracy
INDEL Detection
INDEL de-Convolution
Somatic Mutation Detection
Mutation Quantification
Methylation Analysis
Hypervariable Region Variant Detection
Reference Assembly
Custom Reporting Options
Alignment of Reads
Mitochondria DNA Sequence Analysis
Base Calling
Unattended Operation 

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