Services

The MAD offers long-standing expertise in next-generation sequencing (NGS) to guide you through the complex world of genomics and transcriptomics. We have extra focus and expertise on smallRNA-seq. We have a strong focus and specialized expertise in small RNA sequencing (smallRNA-seq).

We provide genomics technologies services either in close collaboration or as affordable, stand-alone services.

  • RNA and DNA isolation from experimental samples
  • NGS short-read sequencing
    • Illumina  >> NextSeq 550 system
    • Specialized in small-RNAseq experiments
  • TGS ultra-long read sequencing
  • Single-Cell Sequencing 
    • 10X genomics  >> Chromium iX system
  • NGS specialized applications
    • Genome Lineup, a genotyping-by-sequencing method using whole-genome sequencing
    • ViSiR, a NGS method to detect known (plant) viruses and discover unknown (plant) RNA viruses
  • Flow cytometry analyses
    • Beckman Coulter  >> Gallios Flow Cytometer 
    • Becton Dickinson  >> FACSAria™ III Cell Sorter 

We are happy to discuss any questions you may have about these services and to help you design robust genomics experiments.

For assistance, support and advice, please contact us at: madinfo-fnwi [at] uva.nl.