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 (help@bioinformatics.udel.edu) for more information.
