Library preparation

Whole Genome Sequencing (WGS)

Whole genome sequencing is a powerful tool that determines the complete DNA sequence of human, mouse or other organisms. WGS can provide information about the variation, structure, function and evolution of an organism’s genetics.

Whole Exome Sequencing (WES)

Whole exome sequencing is a technique that determines the DNA sequence of all the protein-coding genes (exons) in humans or other organism’s genome. WES can reveal the genetic variants that affect the structure and function of proteins, which are often involved in diseases and traits.

WGS and WES have many applications such as:

• Population genetics/genomics
• Complex diseases
• Personalized medicine
• Drug development
• Mouse genomics

Ready to load sequencing (RtLseq)

Libraries prepared by users (WGS, WES, …) can be loaded in the NovaSeq X Plus System by purchasing single lanes or flowcells of any of the 3 flowcell available according to the size of the output:

• 1,5B – 1,6 billions of reads (only available in flowcell format)
• 10B – 10 billions of reads
• 25B – 26 billions of reads (only available in flowcell format)

For more information visit: https://emea.illumina.com/systems/sequencing-platforms/novaseq-x-plus/specifications.html?gclid=EAIaIQobChMIkYT2xu_8gQMVDIloCR2lGwNsEAAYASABEgK1hfD_BwE

Long read sequencing

Coming soon, H2

Other genomic applications

Other genomic applications based on NGS (gene panel sequencing, genotyping by sequencing,…) please contact with us: cegen@cnio.es