Tjenester and Research
We are a research driven team which is one of our core interests. We are currently conducting research within cancer genomics and bioinformatics, and collaborating with academia. We always welcome research mind set and provide training to student and researchers within sensitive and non-sensitive genomic data management, bioinformatics of next generation sequencing output which lead us to cancer biomarker discovery. We are also open for research collaboration and training support across.
We provide various genomics and informatics solutions and services, hands-on trainings and consultation within cancer, genomics, bioinformatics, and related data science /AI fields including on Next Generation Sequencing (NGS) experimental design and bioinformatics analysis; e.g. Whole genome-, exome- and RNA-seq. This technical insight covers all the technical aspects starting from raw reads to variants discovery and annotations for precision medicine. Our bioinformatics training also consists of cloud and super computing, scripting/ programming for non-IT researchers which includes hands-on training on TSD (Tjenester for Sensitive Data infrastructure provided by University of Oslo).
Our Services :
Our Provide broad range of professional services within Cancer research including the followings :
NGS (Next Generation Sequencing)
- Best strategies to design NGS studies for you
- Recommending best options for your needs
Functional validation after NGS Discovery
- Concluding biological significance
- Best strategies and advice for the confirmation of bioinformatics discoveries
Bioinformatics cross check in NGS Discoveries
- Bioinformatics to get True Positive targets
- Cross checking the True Positive targets in NGS data
As required for your studies
- Biological significance for your needs
- Best strategies and advice to move further