Genomics Research Services

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In evidence

Metagenomics and metatranscriptomics analysis

Concurrent analysis of whole microbial communities that may not be found using other available methods.

Sample all genes and transcripts in all organisms present in a given sample

16S & ITS Promotion


Efficient analysis of functional players

The exome, i.e. the protein-coding region of the genome, represents less than 1.5% of the genetic code, but contains ~85% of known disease-related variants. Exome-seq is a cost-effective alternative to whole-genome sequencing applied across a wide range of applications, including population genetics, genetic disease and cancer studies.

Examine virtually all protein-coding regions in the genome in a single test and capture the majority of the information related to genetic disease.


Focused assessment of key genes

Assess all clinically relevant genes in a single test. Eliminate the need for multiple costly single-gene sequencing tests and significantly improve the likelihood of identifying disease-causing and high-risk variants.

Converge time, expenses and data analysis on specific areas that are most likely to be involved in the phenotype under study.


Cutting-edge approaches

Our continuous commitment to follow and test the latest protocols and tools, as well as to develop new ones, assures the implementation of the state-of-the-art procedures and the optimization of the experimental design.

RNA-seq has now displaced microarrays as the preferred method for gene expression profiling.