Whole genome sequencing is the most comprehensive application for detecting all of these variant types in a single assay.
High-quality data to cover whole human genomes for documentation of SNVs, Indels, SVs, and CNVs.
Product Introduction
Low-pass WGS (~3x)
Copy Number Variants (CNV) . Chromosomal Instability (CIN) analysis.
Customized High-Resolution WGS
(>50× Coverage)
Detects copy number variants (CNVs). Enables chromosomal instability (CIN) analysis. Identifies single nucleotide variants (SNVs), insertions, and deletions (Indels), among others.
Optimized for FFPE and Liquid Biopsy Samples
Supports both FFPE-derived DNA and plasma-derived cfDNA. Works with low input amounts: 30–200 ng of DNA.
Broad Research Applications and Integration
Supports genome-wide association studies (GWAS). Easily integrates with RNA sequencing for comprehensive transcriptomic and genomic profiling. Compatible with methylation sequencing for advanced multi-omics analysis.
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