The sequencing field has experienced a major shift with the introduction of innovative, high-throughput sequencing technologies. The Genomics Unit at the CRG is presently equipped with Illumina sequencing technology.
Sequencing service is offered to the CRG, PRBB, and external users. We perform ChIP-Seq, mRNA-Seq, sequencing of small RNA molecules such as miRNA, amplicon sequencing, genome re-sequencing, and de novo sequencing.
Starting from DNA or RNA samples provided to us, the service includes:
Guidelines for ordering sequencing services of the Genomics Unit
1. Before bringing samples to the Unit, please discuss the project with the Unit leader. You can send an e-mail with an outline of your project or discuss it with us, so that we can design the experiments in detail and find the best strategy for dealing with your project.
2. Based on the agreed procedure, we will issue a quotation for the service.
3. Following your approval of the service quotation (please indicate which account can be charged for the work), please submit your samples to the Unit’s staff, along with the filled request form. In order to reduce interference with the Unit’s workflows, hand your samples over to lab staff only Monday, Wednesday, or Friday from 11 am to 1 pm.
4. Once your samples have arrived in the Unit, we can start planning with them (sample preparation; quality check; assigning the samples to sequencing runs).
5. If you have specific technical questions or concerns about your samples, contact us.
6. We are happy to assist in the analysis of the data together with the Bionformatics Unit.
7. Once you have analyzed your data, any feedback is welcome. The Unit depends on your input to improve the services that we offer!