The advent of next generation sequencing (NGS) platforms have opened exciting new avenues to life science researchers. Unfortunately, many researchers find themselves ill-prepared to handle the volume and nature of the resulting data, hindering their ability to capitalize on these new technologies.

The core has produced a series of analysis pipelines for common NGS data types to assist researchers. Additional pipelines are also under development.

  • RNAseq
  • miRNA
  • De Novo¬†Assembly
  • Reference Mapping
  • SNP/InDel
  • Copy Number Variation
  • Amplicon Library (e.g. 16S rRNA)
  • Metagenome
  • and more

Contact the Bioinformatics Core ( for more information.