SeqNext Next generation sequencing


SEQUENCE Pilot 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. A warning is displayed for any peak with an abnormal high dissimilarity score. Deletions and insertions can be found be reduced fluorescense values.

10 arguments for SeqC

  • Configurable basecaller reaching callrates up to 99%.

  • Quick and simple download of any gene file.

  • Easily configurable for any chip (CDF-file). Gene grouping possible.

  • Choose from different master file formats the one that fits the needs of your laboratory best.

  • Detection of insertions/deletions by reduced fluorescense and heterozygous positions by fluorescense value and statistical evaluation.

  • Easy editing in electropherogram view, separate display for wildtype and mutation sequences.

  • Assembly and management / organization of a mutation database.

  • N-region statistics.

  • Check of PCR products for homologous regions (preventing the detection of false positive heterozygous positions).

  • Individually customizable patient reports.

Not convinced yet?

Then download SeqC without commitment. Install our demo data and analyze them with the corresponding step-by-step manual. Find out how quick and easy sequence analysis can be.