NEWS

varSEAK Open offers full varSEAK functionality combined with an easy and automatable VCF file import for maximum platform flexibility.

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

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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...

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

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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...

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

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

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

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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!

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