Illumina Accelerator

An assay for ctDNA samples demonstrating high performance on the NovaSeq X Series and NovaSeq 6000 System with significantly reduced run times.

Automation-compatible kit for library preparation and enrichment reagents for 64 DNA-only samples, optimized for cancer-related gene analysis from FFPE tissue samples.

Automation-compatible kit for library preparation and enrichment reagents for 32 DNA and 32 RNA samples, optimized for cancer-related gene analysis from FFPE tissue samples.

An NGS-based research assay that enables comprehensive genomic profiling (CGP) and homologous recombination deficiency (HRD) assessment simultaneously, analyzing 500+ genes and genomic signatures such as HRD, TMB, and MSI with a proprietary algorithm powered by Myriad Genetics.

A kit for library preparation and enrichment reagents for 24 DNA and RNA samples, optimized for cancer-related gene analysis from FFPE tissue samples.

Solid tumor assay for FFPE samples with DNA and RNA content. Compatible with NextSeq 500/550 and NextSeq 550Dx (in research mode) instruments only. This is the original release from the TruSight Oncology 500 product family.

A qualitative in vitro diagnostic test that uses targeted next-generation sequencing to assess Homologous Recombination Deficiency (HRD) using DNA from FFPE tumor tissue samples from ovarian cancer patients on the Illumina NextSeq 550Dx instrument. Detects variants in BRCA1 and BRCA2 genes and reports a Genomic Instability Score (GIS).

A pan-cancer panel with combined DNA/RNA content, utilizing the single-tube SLIMamp workflow for fast library prep and turnaround time. The assay combines DNA-based oncoReveal Multi-Cancer v4 with CNV Panel and RNA Fusion v2 Panel for joint sequencing, enabling variant detection as low as 1% VAF without UIDs, even with limited DNA input or poor sample quality.

Robust DNA NGS assay interrogating 48 genes across multiple solid tumor cancer types including NSCLC, colorectal, melanoma, endometrial, pancreatic, GIST, bladder, thyroid, and gliomas from FFPE samples. Includes genes important in immuno-oncology such as POLD1 and POLE.

The Pillar oncoReveal Fusion LBx Panel is a robust cfRNA liquid biopsy NGS assay that interrogates fusion transcripts from 18 driver genes with more than 80 partners relevant across multiple solid tumor types.

A 58-gene pan-cancer panel with combined DNA content, utilizing the single-tube SLIMamp workflow for fast library prep and turnaround time.

A robust NGS assay designed to interrogate 18 driver genes and 83 fusion partners relevant across multiple solid tumor types using RNA isolated from formalin-fixed, paraffin-embedded (FFPE) samples.

A qualitative in vitro diagnostic test using targeted next-generation sequencing to detect variants in 517 genes from FFPE tumor tissue samples of cancer patients with solid malignant neoplasms, using the Illumina NextSeq 550Dx instrument. Detects single nucleotide variants, multi nucleotide variants, insertions, deletions, RNA fusions in 24 genes, splice variants in one gene, and reports a Tumor Mutational Burden (TMB) score.

Software module for analyzing results from TruSight Oncology Comprehensive (EU) test on the instrument.

Targeted DNA and RNA research panel investigating variants across 161 genes associated with a range of cancer types. It covers key cancer genes including kinase domains and genes involved in DNA repair, suitable for somatic analysis research on hotspot and full-length targets of genes associated with solid tumor cancers.

Targeted resequencing assay for researching somatic mutations across hotspot regions of 50 genes with known associations to cancer, enabling sensitive variant detection in multiple cancer types including lung, colon, breast, ovarian, melanoma, and prostate.

Targeted custom research panels optimized for sequencing specific targets or genomic content of interest.

Targeted RNA expression panel investigating 395 genes involved in tumor-immune system interactions. It quantifies expression of cancer biomarkers indicative of immunotherapy response, enabling fast, streamlined library preparation from RNA or FFPE samples.

A library preparation kit for immune repertoire sequencing targeting T-cell receptor beta chains, used in immuno-oncology research to profile lymphocyte receptor variants.

A production-scale sequencing system with multiple flow cell options (SP, S1, S2, S4) delivering 65–800 Gb output range, 2 × 250 bp maximum read length, and run times from 13 to 38 hours, including onboard DRAGEN BCL Convert data analysis.

An in vitro diagnostic instrument with 1–2 Tb output range (S2 flow cell) or 3–6 Tb (S4 flow cell), 2 × 150 bp maximum read length, and run times up to 45 hours, including paired DRAGEN server data analysis.

A production-scale sequencing system with flow cell options delivering 165–716 Gb to 2.6–10.5 Tb output range, 2 × 150 to 2 × 300 bp maximum read length, and run times from 18 to 48 hours, including onboard DRAGEN BCL Convert data analysis.

This reagent kit provides one NovaSeq X Series 25B flow cell (with 8 lanes) and reagent consumables to support a single flow cell 200 cycles run on the NovaSeq X and NovaSeq X Plus systems.

This reagent kit provides one NovaSeq X Series 10B flow cell (with 8 lanes) and reagent consumables to support a single flow cell 100 cycles run on the NovaSeq X and NovaSeq X Plus systems.

This reagent kit provides one NovaSeq X Series 25B flow cell (with 8 lanes) and reagent consumables to support a single flow cell 300 cycles run on the NovaSeq X and NovaSeq X Plus systems.

This reagent kit provides one NovaSeq X Series 25B flow cell (with 8 lanes) and reagent consumables to support a single flow cell 100 cycles run on the NovaSeq X and NovaSeq X Plus systems.

This reagent kit provides one NovaSeq X Series 10B flow cell (with 8 lanes) and reagent consumables to support a single flow cell 300 cycles run on the NovaSeq X and NovaSeq X Plus systems.

This reagent kit provides one NovaSeq X Series 10B flow cell (with 8 lanes) and reagent consumables to support a single flow cell 200 cycles run on the NovaSeq X and NovaSeq X Plus systems.

This reagent kit provides one NovaSeq X Series 5B flow cell (with 8 lanes) and reagent consumables to support a single flow cell 300 cycles run on the NovaSeq X and NovaSeq X Plus systems.

NovaSeq 6000 Xp Workflow delivers the flexibility of independent lane loading and high library multiplexing per flow cell, maximizing sample throughput on a single run.

Powered by XLEAP-SBS chemistry, provides kitted NextSeq 1000/2000 reagents for 600 cycles of sequencing, plus dual-indexing support (up to 100M single reads).

Powered by XLEAP-SBS chemistry, provides kitted NextSeq 1000/2000 reagents for 300 cycles of sequencing, plus dual-indexing support (up to 100M single reads).

Powered by XLEAP-SBS chemistry, provides kitted NextSeq 1000/2000 reagents for 100 cycles of sequencing, plus dual-indexing support (up to 100M single reads).

Powered by XLEAP-SBS chemistry, provides kitted NextSeq 1000/2000 reagents for 200 cycles of sequencing, plus dual-indexing support (up to 400M single reads).

Powered by XLEAP-SBS chemistry, provides kitted NextSeq 1000/2000 reagents for 600 cycles of sequencing, plus dual-indexing support (up to 400M single reads).

Powered by XLEAP-SBS chemistry, provides kitted NextSeq 1000/2000 reagents for 300 cycles of sequencing, plus dual-indexing support (up to 400M single reads).

Powered by XLEAP-SBS chemistry, provides kitted NextSeq 2000 reagents for 300 cycles of sequencing, plus dual-indexing support (up to 1.2B single reads).

Powered by XLEAP-SBS chemistry, provides kitted NextSeq 2000 reagents for 100 cycles of sequencing, plus dual-indexing support (up to 1.2B single reads).

Powered by XLEAP-SBS chemistry, provides kitted NextSeq 2000 reagents for 200 cycles of sequencing, plus dual-indexing support (up to 1.2B single reads).

Powered by XLEAP-SBS chemistry, provides kitted NextSeq 2000 reagents for 300 cycles of sequencing, plus dual-indexing support (up to 1.8B single reads).

Powered by XLEAP-SBS chemistry, provides kitted NextSeq 2000 reagents for 200 cycles of sequencing, plus dual-indexing support (up to 1.8B single reads).

A powerful, cost-effective genomic array with optimized, multiethnic, genome-wide content designed for clinical research and diverse population studies. It features broad coverage of clinical research variants associated with disease and pharmacogenomics and exome content representing diverse populations.

BeadChip combining exceptional coverage of clinical research variants with optimized multiethnic, genome-wide content for genotype screening.

The Infinium Global Diversity Array with Enhanced PGx is the most comprehensive genotyping microarray commercially available for pharmacogenomic (PGx) research, supporting disease and diversity studies and other applications.

The Global Screening Array-48 v4.0 Kit is a scalable, cost-effective solution designed to support high-volume genotyping studies.

Optimized reagent kit that provides increased cluster density and read length, improving sequencing quality scores compared to earlier versions.

A benchtop sequencing system offering scalable output, efficient runtimes, and high data quality with innovative patterned flow cell technology and XLEAP-SBS chemistry, supporting higher output reagents (P3 and P4).

A benchtop sequencing system with P1 flow cell delivering 10–60 Gb output range, 2 × 300 bp maximum read length, and run time of 8–34 hours, including onboard DRAGEN secondary analysis.

Includes four sets of AmpliSeq CD Indexes for Illumina, Set A, Set B, Set C and Set D. Each set contains 96, 8 bp indexes sufficient for labeling 96 samples. Requires separate purchase of library prep and probe panels.

Includes 96 indexes sufficient for labeling 96 samples. Requires separate purchase of library prep and enrichment reagents and probe panels.

An enrichment-based cancer research assay that interrogates both DNA and RNA, detecting small variants, gene amplifications, gene fusions, and splice variants.

Target 1385 cancer genes for gene expression, variant, and fusion detection studies in many RNA sample types, including blood, bone marrow, and FFPE tissue.

A product related to TruSight Oncology for connected run workflows.

Fully customizable methylation microarray for large, targeted epigenetic applications. The Infinium Custom Methylation Kit contains the Infinium HTS iSelect Methyl Custom BeadChip plus reagents to enable researchers and commercial users to develop groundbreaking assays for critical epigenetic research applications.

Highly accurate, comprehensive germline human whole-genome sequencing with only ~10 min of hands on time, without traditional library prep. Provides comprehensive genome with improved structural variant detection and phased reads and variant calls.

A single assay for comprehensive discovery of the 5-base genome (A, T, G, C, and 5mC), providing dual insights into the whole genome and methylome.

A CE-marked IVD instrument that enables clinical laboratories to develop and perform a wide range of applications including sequencing for tumor mutational burden testing.

Custom targeted enrichment sequencing panels enabling a fully customized enrichment solution.

A CE-marked (IVDR compliant) and FDA regulated library preparation and enrichment solution for diagnostic library preparation and enrichment applications. Supports various content types including fixed, custom, and exome panels. Optimized for Illumina IVD platforms for highly accurate data generation.

Infinium Exome-24 Kit arrays deliver exceptional coverage of putative functional exonic variants representing diverse populations and a range of common conditions.

A sensitive and comprehensive whole-exome sequencing solution that offers a tumor–normal workflow for detecting low-frequency variants from formalin-fixed, paraffin-embedded (FFPE) samples.

Robust methylation profiling microarray providing extensive coverage of CpG islands, genes, and enhancers. Ideal for genetic and rare disease research, cancer research, and classification.

Contains reagents to restore damaged FFPE DNA to an amplifiable state for genotyping using Illumina FFPE enabled Infinium BeadChips. Supplied with enough reagents to restore 24 FFPE DNA samples.

Web-based software tool for creating and optimizing custom sequencing or microarray projects, supporting custom microarray probes and sequencing panels for specific genomic content.

Benchtop sequencer designed for flexibility and operational simplicity, supporting exome and large panel sequencing, targeted gene sequencing, single-cell profiling, transcriptome sequencing, and liquid biopsy analysis.

Accessory product required to qualify FFPE samples with Nextera Flex for Enrichment. Library prep, enrichment, enrichment probe panel, and index adapter reagents need to be ordered separately.

A suite of bioinformatics pipelines to process NGS data and maximize genomic discovery, providing accurate, comprehensive, and highly efficient bioinformatics with multiple deployment options, applications, and pipelines.

High-precision, high-throughput array scanning for Illumina's expansive portfolio of genetic analysis assays.

An Illumina IVD sequencing instrument designed for clinical labs to perform accurate and reliable diagnostic testing, including NGS tests and predefined gene panels.

Reagent kit including reagents for preparing 384 libraries. Requires separate purchase of AmpliSeq for Illumina panel and index adapters.

A simple, cost-effective research solution for analysis of the coding transcriptome, generating mRNA-focused sequencing libraries from total RNA with enhanced multiplex capability and a simple workflow.

A fast and simple RNA sequencing library preparation workflow that supports low sample inputs and diverse sample types, including FFPE tissues, enabling high-quality RNA-Seq data generation in 6.5 hours with less than 1.5 hours hands-on time.

An accurate and efficient FASTQ to VCF secondary analysis solution for whole-exome and targeted panel NGS data, usable for both germline and somatic variant calling.

A benchtop sequencing system supporting 5M, 25M, 50M, and 100M flow cells, delivering 1.5–30 Gb output range with up to 2 × 500 bp maximum read length, including DRAGEN software for data analysis.

An integrated next-generation sequencing (NGS) solution for detection and characterization of SARS-CoV-2 RNA from nasopharyngeal, oropharyngeal, nasal swab, and mid-turbinate specimens for research applications, not for diagnostic use.

MiniSeq System Reagent kits have a ready-to-use cartridge with two-channel SBS chemistry for cost-efficient sequencing, even for low sample numbers.

A powerful and scalable analysis environment for interpreting and visualizing multiomic data, enabling seamless sample-to-insights workflows for multiomic and multimodal data analysis.

Index primer kit for multiplex sequencing on NextSeq 1000 and NextSeq 2000 Systems.

Cloud-based genomic run management and simplified bioinformatics for growing NGS operations. The software integrates with Illumina sequencing systems through an intuitive interface that allows users to streamline run setup and monitoring, providing access to push-button secondary analysis applications and enabling data sharing within a secure cloud ecosystem with expandable storage.

A library preparation kit for fast, reliable miRNA and small RNA sequencing from total RNA or isolated miRNA, optimized to prevent adapter dimers and improve quantification accuracy, suitable for various species and sample types including FFPE tissue and biofluids.

A library preparation kit for stranded total RNA sequencing with ribosomal RNA depletion, suitable for transcriptomic analysis in immuno-oncology research.

Accessible and highly scalable single-cell RNA-Seq solution for mRNA capture, barcoding, and library prep without complex workflows or microfluidics.

PhiX Control v3 is a ready-to-use control library for Illumina sequencing runs.