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.