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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
Variant Types
Single nucleotide variants (SNVs)
Insertions and deletions (Indels)
Structural variants (SVs)
Copy number variants (CNVs)
Repeat expansions
Mitochondrial DNA (mtDNA) variants
Paralogs
Economical GWAS Strategies
Access cost-effective approaches, including low-pass sequencing and imputation services, for conducting genome-wide association studies (GWAS) in large cohorts or complex disease research.
Enhanced Sequence Discovery
Efficient discovery of repeated sequences through next-generation sequencing
Reliable Bioinformatics Solutions
Utilize a top-tier bioinformatics pipeline and globally acclaimed software to ensure customers receive dependable, analysis-ready data.
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Biomarker Discovery & Translational Research
Clinical Trial Design & Patient Recruitment
Global Capabilities for Clinical Studies
CDx Development & Commercialization
Genomic Data Solutions
ctDNA Monitoring Portfolio
Other
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