NEWS

We are happy to announce that SEQNEXT Version 5.2.0 has been improved for analysis of Virus NGS data.

The improved algorithm has an accuracy of 96.4%, which was trained on approximately 200.000 real splice sites taken from GRCh37 and 300.000 false...

Some of the highlights: Trioanalysis, jumping option to varSEAK and all available public SNP databases, Sequence Ontology Annotations...

Stop by at our booth number 638 and we can show you our newest feature TRIOANALYSIS integrated in the module SEQNEXT and our newest product SEQARRAY...

Looking back at the GfH and BeSHG 2019: Presentation of our newest SEQUENCE PILOT family member SEQARRAY...

Some of the highlights: analysis of Whole Exome Sequencing data, easy and fast definition of big panels...

We are happy to announce that starting Summer 2018, we have now joined efforts with Roche to offer you the best NGS solution...

Stop by at our stand 260 and we can present our products and if you are interested, we will offer you a special conference price!

varSEAK is a fast and reliable tool to manage and interpret sequencing data, offering conveniently aggregated information from public databases. These...