Our Whole Genome Sequencing (WGS) service is now available, using Oxford
Nanopore Technology (ONT) to provide real-time, long-read sequencing of complete
genomes. Unlike short-read sequencing, this platform enables researchers to capture
SNVs, SVs, indels, CNVs, STRs, and genome-wide methylation patterns, providing a
more complete view of genetic variation, including phasing.
Leveraging the latest ONT v14 chemistry and PromethION P24 platform, our WGS
service produces high-quality, amplification-free genomic data. Researchers receive a
full suite of customizable deliverables, including FASTA files, BAM files (upon request),
and detailed genome annotation reports covering SNVs, SVs, CNVs, and methylation
patterns. Typical turnaround time is 7 to 15 business days.