Whole Genome Sequencing

Overview:

Whole Genome Sequencing provides the complete DNA sequence of an organism, covering both coding and non-coding regions. Using short-read (Illumina) or long-read (Oxford Nanopore) platforms, it delivers high accuracy and uniform coverage.
Coverage depth can be adjusted depending on the application, typically from 30× to over 100×.
Applicable to genomic DNA extracted from blood, cells, fresh or FFPE tissues.
It enables comprehensive detection of single nucleotide variants (SNVs), indels, copy number variations (CNVs), and structural rearrangements. WGS supports population genomics, cancer genomics, microbial genome assembly, and full characterization of reference strains or cell lines, among other applications.

Workflow:

Genomic DNA extraction, fragmentation, library preparation, optional indexing/multiplexing, sequencing (short- or long-read)

Service options:

• Library prep only
• Library prep + sequencing
• Sequencing only