Scientific insight is a fundamental step in creating the best technologies for understanding life-science data.
Genomatix has been part of the scientific community since 1997 and continues to be an active player in research activities around the world.
Working with scientists and researchers outside the company has always been an important contribution to our aim to provide the best technologies for analyzing and interpreting biological data. Therefore we're always happy to collaborate in national and international scientific projects.
Our unique combination of algorithms and knowledge bases enable the efficient interpretation of life-science data.
From molecular data to medical relevance, our biological knowledge base will help you answer the complex questions of today's life science research.
Compiled from a multitude of public and proprietary sources, it provides information from 'a' like 'alternative transcripts' to 'z' like 'z-scores' for your individual field of research.
With the ever-increasing amount of biomedical data generated, the need for efficient analysis and comprehendible visualization has quickly become a major issue.
Genomatix offers online software and turnkey solutions for the analysis and interpretation in context with copious high-quality background data.
Complex challenges require complex thinking. Get assistance from our experts!
They will support your project every step of the way with their wealth of experience and expertise. In fact, this commitment to applying our skills to your individual scientific challenges lies at the heart of all our consulting activities.
More than a decade after sequencing the first human genome, genetic analysis has become routine in labs and hospitals around the world. Technologies like Genomatix GeneGrid™ software provide valuable clinical insights of your individual genomic setup.
While you can't change your genome, you can alter the way it is processed. This is where epigenetic mechanisms become important. Like a computer software they are adjustable and epigenetic changes can lead to effects e.g. on disease progression, obesity or aging.
GeneGrid annotates your variants with information from established sources. Moreover GeneGrid uses the richness of Genomatix' proprietary ElDorado genome annotation that combines RefSeq, Ensembl and GenBank for the most comprehensive transcript collection available.
Gene-to-disease associations from carefully-selected, curated resources like OMIM, ClinVar, COSMIC or Genomatix' proprietary LitInspector database make GeneGrid the tool of choice for clinical researchers.
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For variant visualization, GeneGrid integrates Genomatix' Genome Browser. All available genomic annotation in the immediate environment of any variant can be viewed.
Optionally, by importing the original BAM file, alignments can be explored down to single nucleotide level for inspecting aspects like coverage and read variability.
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The CLARITY Challenge 2012
INDUSTRIEPREIS 2013 
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