Novaseq X

The Core Research Facility (CRF) offers comprehensive access to ultra-high-throughput sequencing on the Illumina NovaSeq X . This premium service is designed to make massive, data-intensive genomic projects highly accessible by offering unprecedented sequencing power at a drastically reduced cost per sample. Powered by Illumina’s high-fidelity XLEAP-SBS™ chemistry, our NovaSeq X service allows you to maximize your grant budget without compromising on data quality or turnaround time.

Supported Applications

 • Whole Genome Sequencing (WGS): Achieve high-depth sequencing for population-scale studies and complex trait analysis at a fraction of traditional costs.

• Deep Transcriptomics (RNA-Seq): Cost-effectively detect rare transcripts and alternative splicing across large sample cohorts.

• Single-Cell & Spatial Multi-Omics: Affordably generate the billions of reads required to power massive single-cell atlases and high-resolution spatial mapping.

• Epigenomics: High-throughput, budget-friendly support for ChIP-Seq, ATAC-Seq, and methylation profiling.

Why Use Our NovaSeq X Service?

• Highly Attractive Pricing: The immense data output of the NovaSeq X significantly drives down the price per gigabase, making deep-sequencing projects exceptionally affordable.

• End-to-End Convenience: We handle all the logistics. From initial sample QC and library prep in our core to the final sequencing run and data delivery, we streamline the entire process.

• Exceptional Accuracy: Next-generation chemistry delivers Q40+ scores, ensuring maximum read stability and precise variant detection

Novaseq 6000

The NovaSeq 6000 System leverages proven Illumina sequencing by synthesis (SBS) technology to deliver accurate data and robust performance. SBS chemistry uses reversible-terminator fluorescently labeled nucleotides. This method detects single bases as they are incorporated into growing DNA strands, reading billions of sequences in parallel.  

Patterned flow cell technology

The NovaSeq 6000 System incorporates patterned flow cell technology to generate an unprecedented level of throughput for a broad range of sequencing applications. Patterned flow cells contain billions of nanowells at fixed locations, a design that provides even spacing of sequencing clusters. This delivers significant increases in sequencing reads and total output of the system.

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