Run Only

Whole genome sequencing, RNA-Seq, bisulfite sequencing, large single-cell experiments. All data-intensive experiments are best suited on NovaSeq platform. Reserving dedicated lanes for your libraries will maximize the cost-effectiveness and ensure a fast track data delivery.

You need an urgent sequencing, you want it with with custom read length and throughput but you want to keep your budget under control.

A disruptive platform capable of read length up to million of bases, natively scanning both the genome and the epigenome of base modifications. Genome assembly, structural variation and phased epigenomes are readily accessible in a single experiment. While for transcriptomics studies you can choose between high-plex full-length cDNA sequencing and direct RNA sequencing to access epitranscriptome.