Next Generation Sequencing Services
At the Genomics Center, we specialize in Next Generation Sequencing. We are a one-stop service provider for all the aspects of NGS, from library preparation to data analysis. We routinely sequence DNA and RNA samples of all kinds and from various sources, using established as well as custom protocols.
DNA Sequencing
- Genomic DNA (small and large genomes)
- Ultra low input DNA
- Targeted (amplicon based)
- ChIP-Seq
- ATAC-Seq
- Methyl-Seq (RRBS)
- Methyl-Seq (WGS)
- 16S/18S ribosomal RNA genes (Bacterial/Fungal)
- Clinical diagnostic panels (see clinical genomics page for list of panels)
RNA Sequencing
- RNA w/poly A selection
- RNA w/RiboMinus
- Ultra low input RNA (RNA amplification)
- 3'READS
- Ribo-Seq
- Small RNA
- RIP-Seq
- CLIP-Seq
- Single Cell RNA-Seq (All 10X Chromium protocols)
Custom/New protocols
We will work with you to implement or develop new sequencing protocols for your research.
Data Management
Data Analysis
Basic and Advanced
- DNASeq
- RNASeq
- Single Cell Seq
- Microarrays
- Custom data analysis
- New pipelines
Data Storage
Large on-site, as well as cloud storage capabilities for data backup
Delivery of raw and/or analyzed data at the end of the project
Long-term storage available