生产级通量和低廉成本的组合，可支持对更大样本队列进行更深入的测序。NovaSeq X Plus基因测序仪的输出量可达16 Tb，每次双25B流动槽运行能够以30×覆盖度对128个人类基因组进行测序或以40×覆盖度对96个人类基因组进行测序。
Illumina Complete Long Reads能够在同一仪器上生成长read和短read，适用于可扩展度更高、更全面的全基因组测序。
NovaSeq X系列应用和方法
超乎想象的实验，更具成本效益
NovaSeq X系列具有广泛的应用范围，支持生产级的数据密集型方法
主要应用和方法
制备
高性能、快速、集成化的工作流程，适用于全基因组测序或tumor-normal配对样本测序等应用。
Illumina Complete Long Read Prep
Illumina Complete Long Read Prep，Human设计用于人类全基因组测序（WGS）。
测序
将XLEAP-SBS化学技术的强大功能与灵活、高效、可持续的工作流程相结合，助力变革性的大规模基因组学研究。
25B流动槽为因美纳测序仪的测序运行扩展了更高通量。拥有8条可独立上样的通道，并且每次运行的输出比NovaSeq 6000基因测序仪高2.5倍，25B显著扩展了测序规模和多重分析，使测序项目能够获得更深、更广和更高的成本效益。
分析
DRAGEN ICLR WGS (Illumina Complete Long Reads)
使用DRAGEN和Illumina Complete Long Read生成最准确、最全面的全人类基因组数据。
Representing less than 2% of the genome, WES is a cost-effective alternative to WGS. The NovaSeq X Plus system offers sequencing of ~1500 exomes in a single run using a dual 25B flow cell run.
Prep
Illumina DNA Prep with Enrichment
This kit uses a fast, user-friendly workflow. On-bead tagmentation chemistry is combined with a simplified, single hybridization protocol to reduce total workflow time.
Sequence
The power of XLEAP-SBS chemistry combined with flexible, efficient, and sustainable workflows for transformational genomics at scale.
Analyze
Exome analysis for variant detection, including a full suite of enrichment metrics and reporting.
Analyze coding plus multiple forms of noncoding RNA for a comprehensive picture of the transcriptome. With the NovaSeq X Plus system, you can sequence over 1000 transcriptomes in a single run using a dual 25B flow cell run.
Prep
Illumina Stranded Total RNA Prep
Rapid library preparation from a broad range of sample types for studying the coding and non-coding transcriptome with unparalleled study flexibility.
Sequence
The power of XLEAP-SBS chemistry combined with flexible, efficient, and sustainable workflows for transformational genomics at scale.
Analyze
解锁新一轮基因组学发现
发现能力的提升将来自于更大规模的研究、更深入的测序以识别罕见遗传事件，并借助更广泛的测序方法和多组学来更全面地了解细胞活动。了解如何使用NovaSeq X系列开展更广泛、更深入的测序并承接以前无法企及的项目。
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