Bioinformatics Consulting Service

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Are you finalizing your PhD and need support on your material and methods chapter regarding NGS analysis? Paper is complete but need NGS data uploaded to a public repository? Do you want to analyze your own NGS data on a computer cluster but do not know where to start? Our Bioinformatics Consultancy Service offers support in those and the following areas:

  • Custom bioinformatics analysis and planning:
    • Single cell omics: 10x Genomics, Smart-Seq2.
    • Long read Pacbio, Oxford Nanopore: Denovo Assembly, ISO-Seq, Metagenomics, etc.
    • Short read Illumina: Variant calling, Somatic analysis, structural variants, Xenografts, etc.
    • RNA-Seq
  • Pathway and downstream analysis of RNA-Seq data
  • Support on High Performance Computing at the Flemish Super Computer
  • Paper and grant writing support
  • Data quality checks
  • Data curation and uploading to public repositories
  • NGS data analysis and interpretation
  • Training on NGS bioinformatics
Eligibility
  • The consulting service is open to the community in Belgium and abroad for researchers, infrastructures and industry.
Cost
  • First intake meeting is free.

Request a consulting service