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  • Please click on the adjacent screen to view the detailed screenshot
  • Compatible with all sequencers
  • Easy handling and configuration
  • SeqPatient automatically uses all previously made analyses as controls for your actual samples and therefore is able to anticipate the shape of every peak in your electropherograms
  • Dissimilarity scores are calculated for every peak and are a measure for the deviation of the peak areas from the statistical average
  • Quick and simple download of any gene file
  • Configurable base caller with sequence dependent thresholds
  • Automatic joining of result files to patient-related orders
  • Automated documentation of amplification modules and sequencing primers for each result file
  • Easy editing in electropherogram view
  • Definition of reference electropherograms and management for known and pre-analyzed variations
  • Finds heterozygous positions by statistic warnings, peak height and area check
  • Easy installation of genomes like hg19 or hg38 for getting genomic coordinates
  • Direct access to SNP-databases like dbSNP, 1000 Genomes, COSMIC, ClinVar and CLINVITAE with individual filter functions
  • Data import / export from / to any LIMS system; connection to AlamutTM and Cartagenia; result export in vcf-file formate
  • Individually customizable patient reports

Would you like to try SeqPatient ?

Then get a free trial license. Find out how quick and easy sequence analysis can be.