High Throughput Sequencing
The UiB Genomic Core Facility (GCF) offers a range of different NGS applications. The main volume of samples sequenced at GCF are mRNA-seq and Exome-seq. We sequence a range of different species, from whale, plants, fish to human samples. Our services are used in many research environments, from marine research, basic biology and biomedicine.
Hovedinnhold
High Throughput Sequencing Service
Sequencing systems available through the UiB Genomic Core Facility (GCF):
- Illumina NovaSeqX
- Illumina NovaSeq 6000
- Illumina NextSeq 500
- Illumina MiSeq
NGS applications* offered at UiB Genomic Core Facility
End-to-end solutions (from DNA/RNA library preparation, QC, sequencing and bioinformatics):
- Whole genome sequencing
- Exome sequencing
- Whole transcriptome sequencing (totRNA) for SNP detection, expression analysis, and splice variant detection
- mRNA sequencing
Sequencing service:
- 10X single cell sequencing
- Protein-DNA/RNA interactions (eg. ChIP-Seq etc.)
- Targeted sequencing
- Metagenomics
- Sequencing of ready-made libraries from users (quality checked by GCF)
*Please contact the UiB Genomic Core Facility if you would like to sequence any other type of application.
We can perform both single- or paired-end sequencing up to 300bp read lengths.
Please contact us regarding your research project so we can help you design your sequence experiment and discuss different solutions that could be applied to your project.
NGS Submission Guidelines
Please see our NGS submission guidelines for more information regarding different applications and how to submit samples for sequencing at GCF.
