Trusted genomic ecosystem from sample to insight
Illumina delivers integrated genomic workflow solutions designed to help researchers move faster from sample to discovery. By combining industry-leading sequencing platforms, trusted assays, and advanced informatics, Illumina enables workflows that are scalable, efficient, and built to evolve with your research needs.
Genomics is transforming our understanding of cancer and genetic disease, yet many laboratories still rely on fragmented tools and disconnected analysis pipelines that slow discovery and increase complexity. Illumina workflow solutions address this challenge by unifying sequencing, analysis, and interpretation within a single, trusted ecosystem.
Illumina workflow solutions enable you to generate high-quality genomic insights efficiently and cost-effectively across a comprehensive portfolio of systems. From targeted panels to whole exome and whole genome sequencing, these workflows are supported by integrated data analysis capabilities that help identify relevant variants, biomarkers, and biological signals with confidence.
Most rare diseases and cancers have a genetic basis. As genomic applications expand and access to genomic data increases, laboratories require sequencing and informatics strategies that are streamlined, scalable, and flexible. The Illumina integrated ecosystem is designed to support and optimize genomic workflows across both oncology research and genetic disease research.
Illumina oncology research workflow solutions can deliver accurate, reproducible results across solid tumor and hematological cancer research. These integrated workflows enable rapid, comprehensive analysis to identify key variants and molecular signatures that support deeper biological insight.
Genetic disease research solutions
Molecular analysis is a critical step in understanding the genetic drivers of rare and inherited diseases. Optimized whole-exome and whole-genome sequencing workflows from Illumina provide researchers with comprehensive, high-resolution genomic insight, supported by trusted informatics to enable confident variant detection and interpretation.
Interested in a comprehensive genomic workflow solution that takes you from sample to discovery?
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