Whole Genome Sequencing (WGS)

From viral genomes less than 10kb to eukaryotic genomes consisting of billions of base pairs, whole genome sequencing (WGS) from short-read technologies, long-read technologies,  or a combination of both, can allow for de novo genome assembly and characterization of variation across genomes, including variation based on SNPs/SNVs, indels, and gene content and organization.

Need help performing a WGS study? Contact labservices@freegenllc.com for a free consult and/or quote.