Sequencing only with NovaSeq 6000 (Illumina)

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The NF for Genomics will provide sequencing of pools of libraries prepared by the users with the NovaSeq6000 sequencing platform (Illumina).

The NovaSeq 6000 sequencing platform by Illumina offers high-throughput capabilities, making it ideal for diverse genomic studies. With its scalability and sequencing-by-synthesis technology, it efficiently generates large amounts of sequencing data. Its dual-flow cell design allows parallel sequencing of multiple samples, reducing turnaround times. Common applications include whole genome sequencing, exome sequencing, transcriptome analysis (bulk and single-cell RNA-Seq), metagenomics, epigenomics, and population genomics. This platform is pivotal for comprehensive genomic research, from understanding genetic variations to characterizing microbial communities and studying epigenetic modifications.