Welcome to PhenoSystems

We develop software for the molecular genetics community since 2002, in close collaboration with leading European diagnostics laboratories, universities and public hospitals. We are regularly involved as active SME partners in European research projects funded by the European Community (FP6, FP7, Eureka).

Our products are targeted for the biologist, genetician or MD working on DNA sequences, whether it is human, viral or bacterial DNA, as well as for the biologists working in the veterinary field where DNA is used to diagnose diseases as well as for breeding purposes.


Wuhan COVID19 flu

As the coronavirus disease hits pandemic proportions we have included the current ASM985889v3 RefSeq to help support the research community in the field as well as technical improvements to our software to ease user inclusion of updates of this RefSeq that will certainly be deposited in the NCBI databases. Phenosystems SA has also committed to provide free of charge one year licenses to any laboratory, private or public, wishing to analyse SARS-CoV2 or other related coronaviruses in this fight against COVID-19. We will also provide support to these labs as far as possible during these difficult times.

You can download the application note here.

Please contact us for further information and the free licences.


Oracle Java licensing

Oracle has decided to change its licensing model with the end of Java 8: Java support roadmap info here.

If you are using Gensearch, you are not impacted by this change, as the Software is compiled to native code by us, and thus includes the relevant Java run-time packages, you don't need to even have Java installed on your machine.

If you are using GensearchNGS you either have opted for a native compiled version for Windows OS, in this case you are also not impacted by this change. The native compiled version has two disadvantages: you can't update it by using the built-in update system, and the native version runs only on single CPU systems, not servers or high-end Desktops with dual-CPUs.

In case you are using GensearchNGS as a Java class package (jar file) on a locally installed Java run-time, Oracle offers a license free drop in replacement with OpenJDK:

Info about Oracle releases for Java 11 and later here.

This OpenJDK JRE is functionally identical to the now license fee covered Oracle JDK (minus a few 'Enterprise' functionalities that are not used by GensearchNGS and thus not relevant in our case).

You can download the free drop-in replacement, OpenJDK 11 LTS (long term support) at the following link:

Download links for Java 11 here.

It will also explain you the installation process.

Translation of the Genetic Variant Interpretation Tool (ACMG/AMP)

With permission from Linda Jeng, MD, PhD, FACMG, (University of Maryland), and collaboration with molecular diagnostics partners in France and Czech Republic, we are now offering translations in French and Czech of their "Genetic Variant Interpretation Tool". We are open to collaborate with diagnostics laboratories in other countries to translate it into further languages.

You can find the French version here.

You can find the Czech version here.

Gensearch moves to 4.4 and provides submission tool to Clinvar

Gensearch latest release is now available with the 4.4 version. Germany has implement new regulations concerning reimbursement of genetic diagnostic tests, these include now a financial compensation for publication of novel clinically relevant variants to publicly accessible databases. Phenosystems has developed a module to submit variants to Clinvar to facilitate the work process and allow German labs to be reimbursed for this aspect in a user-friendly efficient way. Of course this module can be used by all our customers with current active support contract. In a second phase we will deploy this module also to GensearchNGS

Please contact us for more information.

New optional genotyping module

We have now released GT, an optional genotyping module for our classical Gensearch capillary DNA sequence software. It allows to quickly identify known SNPs in large batches of amplicons, and automatically generate the nomenclature such as for the APOE genotypes.

Share This
Follow Us