Multi-application flexibility
Flexible read lengths allow an easy transition from small-scale DNA and RNA sequencing projects
Targeted DNA sequencing allows researchers to focus on a select set of genes or relevant gene regions using fixed panels of expert-selected content or custom, user-defined gene panels. By focusing the power of next-generation sequencing (NGS), targeted sequencing enables cost-effective and systematic variant detection with high accuracy and reproducibility.
AmpliSeq for Illumina Cancer HotSpot Panel v2
Targeted panel investigating hotspot regions of 50 genes with known associations to cancer.
AmpliSeq for Illumina Focus Panel
Targeted DNA and RNA panel investigating 52 genes with known relevance to solid tumors.
AmpliSeq for Illumina BRCA Panel
Targeted panel investigating somatic and germline variants in BRCA1 and BRCA2.
AmpliSeq for Illumina Immune Response Panel
Targeted RNA expression panel investigating 395 genes involved in tumor-immune system interactions.
AmpliSeq for Illumina Custom DNA Panel
Targeted custom panel optimized for specific targets or genomic content of interest.
Reagents include a flow cell and prefilled, ready-to-use cartridges containing clustering and sequencing reagents to support cycling runs on the iSeq 100 System.
Local Run Manager (DNA Amplicon Analysis Module)
An on-premises software solution for creating sequencing runs, monitoring run status, and analyzing data.
The Illumina genomics cloud-computing environment for NGS data analysis and management.
Bacterial sequencing enables comprehensive characterization of bacterial genomes, including antibiotic resistance, molecular epidemiology, and virulence. Using NGS, sequencing of bacterial genomes can be done quickly while producing highly accurate data.
Fast, integrated workflow for a wide range of applications, including sequencing whole human genomes, amplicons, plasmids, and microbial genomes.
Reagents include a flow cell and prefilled, ready-to-use cartridges containing clustering and sequencing reagents to support cycling runs on the iSeq 100 System.
Local Run Manager (Resequencing Analysis Module)
An on-premises software solution for creating sequencing runs, monitoring run status, and analyzing data.
The Illumina genomics cloud-computing environment for NGS data analysis and management.
Viral sequencing is a fast and effective tool for characterizing viral agents, studying viral variability, and identifying genetic markers associated with virulence.
Fast, integrated workflow for a wide range of applications, including sequencing whole human genomes, amplicons, plasmids, and microbial genomes.
Targeted RNA panel investigating 66 viruses that are of high risk to public health.
Reagents include a flow cell and prefilled, ready-to-use cartridges containing clustering and sequencing reagents to support cycling runs on the iSeq 100 System.
Local Run Manager (Resequencing Analysis Module)
An on-premises software solution for creating sequencing runs, monitoring run status, and analyzing data.
The Illumina genomics cloud-computing environment for NGS data analysis and management.
Sequencing entire bacterial, viral, and other microbial genomes is important for generating accurate reference genomes, microbial identification, and comparative genomic studies. Learn more about microbial whole-genome sequencing and the Illumina products that can make it happen.
Sequence the 16S ribosomal RNA (rRNA) gene with a culture-free method to identify and compare bacteria from complex, difficult-to-study microbiomes or environments.
Perform quality control (QC) applications for bioproduction studies or assess the quality of a sequencing library before committing it to a full-scale run.
Quality control and rebalancing of single-cell libraries
Evaluate the quality and enable accurate rebalancing of multiplexed single-cell libraries before committing it to a full-scale run.
Sequence the entire genome of a bacterium, virus, or other microbe for applications in public health, infectious disease surveillance, molecular epidemiology studies, and environmental metagenomics.
Select and sequence specific genes or genomic regions of interest using predesigned or custom designed panels for gene profiling studies.
Select and sequence specific transcripts of interest for gene expression profiling studies.
Environmental DNA (eDNA) sequencing offers a powerful lens to view changes in biodiversity
Researchers at Curtin University in Perth, Australia use the iSeq 100 System to analyze eDNA samples and monitor ecosystem changes over time.
The time is now for microbiome studies
Whole-genome shotgun sequencing and transcriptomics provide researchers and pharmaceutical companies with data to refine drug discovery and development.