Available Services
In this section, you may browse through all services available across all National Facilities. Use the filter function to filter services by National Facility, Infrastructural Unit or category of service. In addition, you may use the text search function to search across services using key words. Please note the system will search your chosen key word either in the service title or description.
Important: to activate the search remember to click on the magnifying glass icon.
Sequencing only with NovaSeq 6000 (Illumina)
The National Facility for Genomics will provide sequencing of pools of libraries prepared by the users with the NovaSeq6000 sequencing platform (Illumina).
The NovaSeq 6000 is a high-throughput sequencing platform developed by Illumina. It’s designed to handle a wide range of applications and large-scale genomic projects.
NovaSeq 6000 is commonly used for: Whole Genome Sequencing (WGS), Exome Sequencing (WES), Transcriptome Analysis (bulk RNA-Seq or single-cell RNAseq), Metagenomics, Epigenomics studies, Population Genomics.
Sequencing only with NextSeq 2000 (Illumina)
The National Facility for Genomics will provide sequencing of pools of libraries prepared by the users with the NextSeq2000 sequencing platform (Illumina).
The NextSeq 2000 is a next-generation sequencing platform developed by Illumina. It is designed to offer high-throughput sequencing with flexibility for various applications.
The NextSeq 2000 is commonly used for: Whole Genome Sequencing (WGS), RNA Sequencing (RNA-Seq and single-cell RNA-seq), Targeted Sequencing (amplicon sequencing), Exome Sequencing (WES), Metagenomics, ChIP-Seq and Epigenomics.
Sequencing only with MiSeq (Illumina)
The National Facility for Genomics will provide sequencing of pools of libraries prepared by the users with the MiSeq sequencing platform (Illumina).
the MiSeq is a benchtop next-generation sequencing platform developed by Illumina. It’s designed for smaller-scale sequencing projects and offers flexibility for various applications.
MiSeq is commonly used for: Targeted Sequencing (amplicon sequencing), Small Genomes Sequencing, Metagenomics, 16S rRNA Sequencing, Small RNA-Seq, Viral genomes Sequencing.