TruSight Oncology 500 v2

Enable CGP with a large pan-cancer panel covering all main variant classes plus key biomarkers (TMB, MSI, and HRD) from FFPE tissue.

3–4 days

Assay time

~7 hrs

Hands-on time

30 ng DNA (as low as 10 ng), 40 ng RNA (as low as 20 ng)

Input quantity

See full details in the specifications table

TruSight Oncology 500 v2 automation kits are coming soon. Contact an Illumina representative for more information.

Overview

TruSight Oncology 500 v2 is a pan-cancer next-generation sequencing (NGS) assay that enables in-house comprehensive genomic profiling (CGP) from formalin-fixed, paraffin-embedded (FFPE) tissue for oncology research.

  • Targets 523 genes to assess DNA and RNA variant types, including single nucleotide variants, copy number variants, indels, fusions, and large BRCA1/2 rearrangements

  • Includes analysis of microsatellite instability (MSI), tumor mutational burden (TMB), and homologous recombination deficiency (HRD) biomarkers

  • Achieves sensitive results from as little as 10 ng DNA or 20 ng RNA using advanced chemistry (30 ng DNA and 40 ng RNA recommended)

  • Enables rapid turnaround within 3–4 days from sample to results, with a streamlined workflow and automation kits and protocols

  • Performs fast, scalable variant calling with DRAGEN secondary analysis, available on-premises or via the cloud through Illumina Connected Analytics; enables reporting with Illumina Connected Insights* or Velsera Clinical Genomics Workspace (CGW)

  • Complements TruSight Oncology 500 ctDNA v2 liquid biopsy assay, with similar content and compatible platforms

Fully integrated HRD testing

HRD is a genomic signature linked to a cell’s inability to repair double-stranded DNA breaks, leading to genomic instability and tumorigenesis. HRD analysis is now integrated into the standard workflow, providing BRCA1/2 variant detection and genomic instability score (GIS) with no added time or complexity.

Automate for efficiency

Illumina has partnered with leading liquid-handling manufacturers to produce fully automated workflows that can reduce hand-on time by ~50%. This improves efficiency while achieving the same high-quality results produced by manual protocols.

*Illumina Connected Insights supports user-defined tertiary analysis through API calls to third-party knowledge sources.


Enable CGP with a comprehensive portfolio

Identify disease-relevant biomarkers for oncology research with the TruSight Oncology 500 product line.

Specifications

Required products

To run TruSight Oncology 500 v2 you need:

  • A TruSight Oncology 500 v2 library prep kit with a manual or automated workflow (note: DRAGEN variant calling pipeline included)
  • An index set:
    • For manual workflows: Illumina DNA/RNA UD indexes Sets A-D
    • For automated workflows: Illumina DNA/RNA UD indexes Set A-D v3, Auto
  • Reagent Kit if not included with library prep kit:
    • NextSeq 550 or NextSeq 550Dx Reagent Kit v2.5 for high-output flow cell, 300 cycles
    • NextSeq 1000 and 2000 XLEAP-SBS Reagent Kit with three flow cell options, 200 cycles
    • NovaSeq 6000 or NovaSeq 6000Dx v1.5 Reagent Kit with four flow cell options, 200 cycles
    • NovaSeq X Series Reagent Kit with three flow cell options, 200 cycles

To analyze with the DRAGEN variant calling pipeline you need:

  • A DRAGEN server for local analysis*, or
  • An Illumina Connected Analytics subscription with iCredits for cloud analysis

*NovaSeq 6000Dx paired DRAGEN server is enabled for TruSight Oncology 500 v2 local variant calling. All other instruments require a separate, stand-alone DRAGEN server for on-premise secondary analysis.

/ Results

Applications

TruSight Oncology 500 v2 enables comprehensive genomic profiling of FFPE tumor samples to assess a wide range of biomarkers using less sample, providing more informative results than single-gene or small panel assays.

Example workflow

Project recommendations

Instrument Recommended number of samples Read length
NextSeq 500 System, NextSeq 550Dx in Research Mode

8 samples per run (high output flow cell), 100M paired-end reads, 3,500× coverage 

2 × 101 bp

NextSeq 1000 System, NextSeq 2000 System

8 samples per run (P2 flow cell), 100M paired-end reads, 3,500× coverage

24 samples per run (P3 flow cell), 100M paired-end reads, 3,500× coverage

36 samples per run (P4 flow cell), 100M paired-end reads, 3,500× coverage

2 × 101 bp

NovaSeq X System

32 samples per run (1.5B flow cell), 100M paired-end reads, 3,500× coverage

192 samples per run (10B flow cell), 100M paired-end reads, 3,500× coverage

480 samples per run (25B flow cell), 100M paired-end reads, 3,500× coverage


*Throughput shown is for the single flow cell NovaSeq X Instrument. NovaSeq X Plus offers a dual flow cell system with twice the capacity listed.

2 × 101 bp

NovaSeq 6000 System, NovaSeq 6000Dx in Research Mode

16 samples per run (SP flow cell), 100M paired-end reads, 3,500x coverage

32 samples per run (S1 flow cell), 100M paired-end reads, 3,500x coverage

72 samples per run (S2 flow cell), 100M paired-end reads, 3,500x coverage

192 samples per run (S4 flow cell), 100M paired-end reads, 3,500x coverage

2 × 101 bp

Related applications and methods

Documentation

Product literature

Compare

TruSight Oncology 500 v2 TruSight Oncology 500 High-Throughput TruSight Oncology 500 ctDNA v2
Assay time 3–4 days from sample input to final results 4–5 days from sample to results 3–4 days from purified nucleic acid to variant report
Automation capability Liquid handling robot(s) Liquid handling robot(s) Liquid handling robot(s)
Automation details Explore available automation methods Explore available automation methods Explore available automation methods
Cancer type Pan-cancer, Solid tumor Pan-cancer, Solid tumor Pan-cancer, Solid tumor
Content specifications Targeted sequencing of DNA from 523 genes and RNA from 55 genes for a total of 1.94 Mb panel size. MSI and TMB measurement included.  The included HRD panel includes coverage of ~25K SNPs to assess homologous recombination deficiency through a comprehensive genomic instability score (LOH+TAI+LST) powered by Myriad Genetics. 

TruSight Oncology 500 v2 is not available for sale in Japan
Targeted sequencing of DNA from 523 genes of interest and RNA from 55 genes, for a total of 1.94 Mb panel size. MSI and TMB measurement included. 
  • Immuno-oncology biomarker coverage: TMB and MSI
  • Guideline coverage: Broad coverage of key guidelines for multiple solid tumor types
  • Clinical trial coverage: Over 600 clinical trials (based on Velsera Knowledgebase, as of February 2023)
Description Enables comprehensive genomic profiling of solid tumors using DNA and RNA from FFPE tissue. Provides variant detection and biomarker assessment from a single sample for broad tumor characterization. A high-throughput comprehensive NGS assay to identify key biomarkers in guidelines and >1K clinical trials from a streamlined workflow using the NextSeq 1000 System, NextSeq 2000 System, NovaSeq 6000 System, NovaSeq 6000Dx instrument (in Research Mode), or NovaSeq X Series. Includes coverage of immuno-oncology biomarkers TMB and MSI. Provides a noninvasive research method for comprehensive genomic profiling of liquid biopsy samples (ctDNA from blood plasma). This liquid biopsy approach provides insights about intra- and inter-tumor heterogeneity using a minimally invasive sample collection approach to complement tissue-based CGP.
Hands-on time ~7 hrs for manual workflow ~2.5 hr for automated workflow
~10.5 hr for manual workflow
~1.5 hr for automated workflow
~2.5 hr for manual workflow
Input quantity 30 ng DNA (as low as 10 ng), 40 ng RNA (as low as 20 ng) 40 ng DNA and/or 40–80 ng RNA 20 ng cfDNA (4 ml of plasma)
Instruments NextSeq 550 System, NextSeq 2000 System, NextSeq 1000 System, NextSeq 550Dx in Research Mode, NovaSeq X System, NovaSeq 6000Dx in Research Mode, NovaSeq 6000 System, NovaSeq X Plus System NextSeq 2000 System, NextSeq 1000 System, NovaSeq X System, NovaSeq 6000Dx in Research Mode, NovaSeq 6000 System, NovaSeq X Plus System NovaSeq X System, NovaSeq 6000Dx in Research Mode, NovaSeq 6000 System, NovaSeq X Plus System
Method Targeted DNA sequencing, Targeted RNA sequencing, Target enrichment Targeted DNA sequencing, Targeted RNA sequencing, Target enrichment Targeted DNA sequencing, Target enrichment
Multiplexing NextSeq 550/Dx: 8 samples/run. NexSeq 1000 and 2000: P2 flow cell 8 samples, P3 flow cell 24 samples, P4 flow cell 36 samples. NovaSeq 6000/Dx: SP flow cell 16 samples, S1 flow cell 32 samples, S2 flow cell 72 samples, S4 flow cell 192 samples. NovaSeq X/X+: 1.5 B 32 samples, 10B 192 samples, 25B 480 samples. NextSeq 1000 and 2000: P2 flow cell 8 samples, P3 flow cell 24 samples, P4 flow cell 36 samples.
NovaSeq 6000/Dx: SP flow cell 16 samples, S1 flow cell 32 samples, S2 flow cell 72 samples, S4 flow cell 192 samples.
NovaSeq X Series*: 1.5B cartridge 32 samples, 10B cartridge 192 samples, 25B 480 samples.
NovaSeq X Series: 4 samples on 1.5B flow cell, 24 samples on 10B flow cell.
NovaSeq 6000 System: 8 samples on S2 flow cell, 24 samples on S4 flow cell, 192 indexes maximum.
Nucleic acid type DNA, RNA DNA, RNA DNA
Sample throughput 8–960 samples per run NextSeq 1000 and 2000: 8–36 samples/run. NovaSeq 6000/Dx: 16-192 samples/run. NovaSeq X: 32–480 samples/run. NovaSeq X Plus: 32-960 samples/run. 4-48 samples/run
Specialized sample types FFPE tissue FFPE tissue Circulating tumor DNA, Blood
Species category Human Human Human
Technology Sequencing Sequencing Sequencing
Variant class Gene fusions, Loss of heterozygosity (LOH), Somatic variants, Transcript variants, Single nucleotide variants (SNVs), Insertions-deletions (indels), Copy number variants (CNVs), Tumor mutational burden (TMB), Genomic instability score (GIS), Microsatellite instability (MSI), Novel transcripts, Single nucleotide polymorphisms (SNPs), Structural variants Gene fusions, Somatic variants, Novel transcripts, Structural variants, Transcript variants, Single nucleotide variants (SNVs), Insertions-deletions (indels), Copy number variants (CNVs) Single nucleotide variants (SNVs), Insertions-deletions (indels), Copy number variants (CNVs)

Figures

Improved exon coverage across tissue types and input level

TruSight Oncology 500 v2 showed improved median exon coverage compared to the original TruSight Oncology 500 across 13 cancer types for 10–40 ng DNA input. Improved exon coverage was observed across most conditions, particularly for lower input levels.

Increased coverage of the TERT promoter

TruSight Oncology 500 v2 has improved coverage of GC-rich regions, such as the TERT promoter, which are often difficult to amplify by PCR.

Variant detection performance for key genes in FFPE samples

TruSight Oncology 500 v2 showed accurate detection of single nucleotide variants (SNVs), multinucleotide variants (MNVs), and indels across input levels and reagent lots.

CNV detection by gene

TruSight Oncology 500 v2 demonstrated reliable copy number variant (CNV) detection, as indicated by mean fold change. Consistent performance was observed for 10–40 ng DNA input.

Gene fusion and splice variant detection across RNA input levels

TruSight Oncology 500 v2 showed sensitive gene fusion and splice variant detection across 20–80 ng RNA input.

Concordance of TruSight Oncology 500 v2 genomic instability score (GIS) with a reference standard

GIS results from TruSight Oncology 500 v2 using 30 ng DNA input showed high concordance to a reference test across 102 FFPE tissue samples.

Subset of genomic tumor profiling biomarkers for multiple cancer types

Pan-cancer: BRAF, NTRK1, NTRK2, NTRK3, RET, MSI, TMB and HRD
Genes with biomarkers of significance* Genes with biomarkers of potential significance
breast cancer
Breast
BRCA1 BRCA2 ERBB2 ESR1 PALB2 PIK3CA   180
colorectal cancer
Colorectal
ERBB2 KRAS NRAS         166
bone cancer
Bone
EGFR ERG ETV1 ETV4 EWSR1 FEV FLI1 140

FUS

H3F3A HEY1 IDH1 MDM2 NCOA2 SMARCB1
lung cancer
Lung
ALK EGFR ERBB2 KRAS MET NUTM1 ROS1 223
melanoma cancer
Melanoma
KIT NRAS ROS1         172
ovarian cancer
Ovarian
BRCA1 BRCA2 FOXL2         149
cns cancer
CNS
APC ATRX CDKN2A CDKN2B EGFR H3F3A HIST1H3B 140

HIST1H3C

IDH1 IDH2 MYCN PTCH1 RELA TERT

TP53

           
prostate cancer
Prostate
AR ATM BARD1 BRCA1 BRCA2 BRIP1 CDK12 151

CHEK1

CHEK2 FANCL FGFR2 FGFR3 PALB2 RAD51B

RAD51C

RAD51D RAD54L        
thyroid cancer
Thyroid
HRAS KRAS NRAS RET TERT     165
uterine cancer
Uterine & cervical
BRCA2 EPC1 ERBB2 ESR1 FOXO1 GREB1 JAZF1 138

NCOA2

NCOA3 NUTM2A NUTM2B PAX3 PAX7 PHF1

POLE

SMARCA4 SUZ12 TP53 YWHAE    
other solid cancer tumors
Other solid tumors
ALK APC ARID1A ASPSCR1 ATF1 ATIC BAP1 152

BCOR

BRCA1 BRCA2 CAMTA1 CARS CCNB2 CDK4

CDKN2A

CIC CITED2 CLTC COL1A1 COL6A3 CREB1

CREB3L1

CREB3L2 CSF1 CTNNB1 DDIT3 DDX3X DNAJB1

DUX4

EED EGFR ERBB2 ERG ETV1 ETV4

ETV6

EWSR1 FEV FGFR2 FGFR3 FLI1 FOXL2

FOXO1

FOXO4 FUS GLI1 HEY1 HGF HMGA2

IDH1

KRAS LEUTX MAML3 MDM2 MYB MYOD1

NAB2

NCOA2 NF1 NFATC2 NFIB NR4A3 NRAS

NUTMI

NUTM2A NUTM2B PALB2 PATZ1 PAX3 PAX7

PDGFB

PDGFRA PRKACA PRKD1 RANBP2 ROS1 SDHA

SDHB

SDHC SDHD SMARCB1 SS18 SSX1 SSX2

SSX4

STAT6 SUZ12 TAF15 TCF12 TERT TFE3

TFEB

TFG TP53 TPM3 TPM4 TRAF7 TSPAN31

VGLL2

WT1 WWTR1 YAP1 YWHAE ZC3H7B  

The genes and biomarkers listed in this table are a subset of all genes included in the panel. See the TruSight Oncology 500 data sheet for the full gene list.

* Genes with biomarkers of significance linked to current drug labels or guidelines.

Genes with biomarkers of potential significance based on presence in clinical trials.

CNS, central nervous system. 

References:

1. Data calculations on file. Illumina, Inc. 2023.

Resources

Video resources

Thumbnail

How TruSight Oncology 500 v2 is helping to advance cancer research at the Catalan Institute of Oncology

Learn how researchers at the Catalan Institute of Oncology are using TruSight Oncology 500 v2 to streamline their workflow and accelerate their research. In this video, scientists from the institute talk about the improved assay and share how faster results help to drive discovery.

Manual prep (18)

TruSight Oncology 500 v2 DNA/RNA Kit (24 samples)

20130527

Includes reagents for preparing and enriching up to 24 DNA and RNA samples. Purchase sequencing reagents and indexes separately.

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TruSight Oncology 500 v2 DNA Kit (48 samples)

20130528

Includes reagents for preparing and enriching up to 48 DNA samples. Purchase sequencing reagents and indexes separately.

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TruSight Oncology 500 v2 DNA/RNA Kit, For Use with NextSeq 550 (24 samples)

20130536

Includes reagents for preparing and enriching up to 24 DNA and RNA samples, and NextSeq 500/550 sequencing reagents. Purchase indexes separately.

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TruSight Oncology 500 v2 DNA Kit, For Use with NextSeq 550 (48 samples)

20130537

Includes reagents for preparing and enriching up to 48 DNA samples, and NextSeq 500/550 sequencing reagents. Purchase indexes separately.

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TruSight Oncology 500 v2 DNA/RNA Kit, For Use with NextSeq 1000/2000 P2 (24 samples)

20138676

Includes reagents for preparing and enriching up to 24 DNA and RNA samples, and NextSeq 1000/2000 P2 sequencing reagents. Purchase indexes separately.

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TruSight Oncology 500 v2 DNA Kit, For Use with NextSeq 1000/2000 P2 (48 samples)

20138677

Includes reagents for preparing and enriching up to 48 DNA samples, and NextSeq 1000/2000 P2 sequencing reagents. Purchase indexes separately.

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TruSight Oncology 500 v2 DNA/RNA Kit plus Velsera interpretation report (24 samples)

20138680

Includes reagents for preparing and enriching up to 24 DNA and RNA samples and data interpretation reports using Velsera Clinical Genomics Workspace. Purchase sequencing reagents and indexes separately.

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TruSight Oncology 500 v2 DNA Kit plus Velsera interpretation report (48 samples)

20138681

Includes reagents for preparing and enriching up to 48 DNA samples and data interpretation reports using Velsera Clinical Genomics Workspace. Purchase sequencing reagents and indexes separately.

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TruSight Oncology 500 v2 DNA/RNA Kit plus Velsera interpretation report, For Use with NextSeq 550 (24 samples)

20138686

Includes reagents for preparing and enriching up to 24 DNA and RNA samples and data interpretation reports using Velsera Clinical Genomics Workspace, and NextSeq 500/550 sequencing reagents. Purchase indexes separately.

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TruSight Oncology 500 v2 DNA Kit plus Velsera interpretation report, For Use with NextSeq 550 (48 samples)

20138687

Includes reagents for preparing and enriching up to 48 DNA samples and data interpretation reports using Velsera Clinical Genomics Workspace, and NextSeq 500/550 sequencing reagents. Purchase indexes separately.

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TruSight Oncology 500 v2 DNA/RNA Kit plus Velsera interpretation report, For Use with NextSeq 1000/2000 P2 (24 samples)

20138690

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TruSight Oncology 500 v2 DNA Kit plus Velsera interpretation report, For Use with NextSeq 1000/2000 P2 (48 samples) 

20138692

Includes reagents for preparing and enriching up to 48 DNA samples and data interpretation reports using Velsera Clinical Genomics Workspace, and NextSeq 1000/2000 P2 sequencing reagents. Purchase indexes separately.

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TruSight Oncology 500 v2 DNA/RNA Kit plus Illumina Connected Insights Software (24 samples)

20138695

Includes reagents for preparing and enriching up to 24 DNA and RNA samples and data interpretation reports using Illumina Connected Insights. Purchase sequencing reagents and indexes separately.

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TruSight Oncology 500 v2 DNA Kit plus Illumina Connected Insights Software (48 samples)

20138696

Includes reagents for preparing and enriching up to 48 DNA samples and data interpretation reports using Illumina Connected Insights. Purchase sequencing reagents and indexes separately.

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TruSight Oncology 500 v2 DNA/RNA Kit plus Illumina Connected Insights Software, For Use with NextSeq 550 (24 samples) 

20138775

Includes reagents for preparing and enriching up to 24 DNA and RNA samples and data interpretation reports using Illumina Connected Insights, and NextSeq 500/550 sequencing reagents. Purchase indexes separately.

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TruSight Oncology 500 v2 DNA Kit plus Illumina Connected Insights Software, For Use with NextSeq 550 (48 samples) 

20138776

Includes reagents for preparing and enriching up to 48 DNA samples and data interpretation reports using Illumina Connected Insights, and NextSeq 500/550 sequencing reagents. Purchase indexes separately.

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TruSight Oncology 500 v2 DNA/RNA Kit plus Illumina Connected Insights Software, For Use with NextSeq 1000/2000 P2 (24 samples) 

20138779

Includes reagents for preparing and enriching up to 24 DNA and RNA samples and data interpretation reports using Illumina Connected Insights, and NextSeq 1000/2000 P2 sequencing reagents. Purchase indexes separately.

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TruSight Oncology 500 v2 DNA Kit plus Illumina Connected Insights Software, For Use with NextSeq 1000/2000 P2 (48 samples) 

20138780

Includes reagents for preparing and enriching up to 48 DNA samples and data interpretation reports using Illumina Connected Insights, and NextSeq 1000/2000 P2 sequencing reagents. Purchase indexes separately.

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Index adapters (8)

Illumina® DNA/RNA UD Indexes Set A, Tagmentation (96 Indexes, 96 Samples)

20091654

Illumina® DNA/RNA UD Indexes Set A, Tagmentation (96 Indexes, 96 Samples) Includes 96, 10 bp indexes sufficient for labeling 96 samples. Purchase library prep and enrichment reagents and probe panels separately.

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Illumina® DNA/RNA UD Indexes Set B, Tagmentation (96 Indexes, 96 Samples)

20091656

Illumina® DNA/RNA UD Indexes Set B, Tagmentation (96 Indexes, 96 Samples) Includes 96, 10 bp indexes sufficient for labeling 96 samples. Purchase library prep and enrichment reagents and probe panels separately.

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Illumina® DNA/RNA UD Indexes Set C, Tagmentation (96 Indexes, 96 Samples)

20091658

Illumina® DNA/RNA UD Indexes Set C, Tagmentation (96 Indexes, 96 Samples) Includes 96, 10 bp indexes sufficient for labeling 96 samples. Purchase library prep and enrichment reagents and probe panels separately.

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Illumina® DNA/RNA UD Indexes Set D, Tagmentation (96 Indexes, 96 Samples)

20091660

Illumina® DNA/RNA UD Indexes Set D, Tagmentation (96 Indexes, 96 Samples) Includes 96, 10 bp indexes sufficient for labeling 96 samples. Purchase library prep and enrichment reagents and probe panels separately.

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Illumina® DNA/RNA UD Indexes v3, Set A, Auto (96 Indexes 96 samples)

20141196

Includes one box of 96 Illumina DNA/RNA UD v3 Indexes Set A for labeling 96 samples sufficient for automation

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Illumina® DNA/RNA UD Indexes v3, Set B, Auto (96 Indexes 96 samples)

20141197

Includes one box of 96 Illumina DNA/RNA UD v3 Indexes Set B for labeling 96 samples sufficient for automation

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Illumina® DNA/RNA UD Indexes v3, Set C, Auto (96 Indexes 96 samples)

20141198

Includes one box of 96 Illumina DNA/RNA UD v3 Indexes Set C for labeling 96 samples sufficient for automation

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Illumina® DNA/RNA UD Indexes v3, Set D, Auto (96 Indexes 96 samples)

20141199

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Accessory products (1)

TruSight FFPE QC Kit

20139070

TruSight™ FFPE QC Kit uses a real-time PCR assay to evaluate the quality of prospective DNA samples.

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Software and informatics options (13)

Illumina DRAGEN Server v4

20051343

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ICA Basic Annual Subscription

20044874

Illumina Connected Analytics (ICA) Basic Annual Subscription. This product includes 1 year of access to ICA Basic, including sequencing instrument connectivity, data management capabilities, and access to pre-packaged analysis tools.

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ICA Enterprise Annual Subscription

20038994

Illumina Connected Analytics (ICA) Enterprise Annual Subscription. This product includes 1 year of access to ICA Enterprise, including sequencing instrument connectivity, data management capabilities, custom and pre-packaged analysis tools, and the Base module for data warehousing and mining. ICA Enterprise also includes optional HIPAA BAA (US-only), single sign-on (SSO), and a service level agreement (SLA).

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Illumina Connected Analytics (ICA) Compliance enables single sign-on (SSO), multi-factor authentication (MFA), HIPAA BAA (US-only), and a Service Level Agreement (SLA) for an ICA Basic Annual Subscription.

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Illumina Analytics - 1 iCredit

20042038

iCredits are used for data storage and analysis on either BaseSpace Sequence Hub or Illumina Connected Analytics.

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Illumina Analytics  Starter Pack - 1,000 iCredits

20042039

iCredits are used for data storage and analysis on either BaseSpace Sequence Hub or Illumina Connected Analytics.

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20042040

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20042041

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20042042

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20090137

Annual subscription to Illumina Connected Insights platform.

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Illumina Connected Insights – Trial Subscription

20112516

Free trial subscription for Illumina Connected Insights - for oncology.

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Illumina Connected Insights – Oncology Genome Equivalent Sample - VCF

20090138

Illumina Connected Insights pre-paid oncology samples on per genome equivalent basis starting from VCF: one genome is equivalent to 2 exomes, 3 large and 6 small panel samples. Any unused samples will automatically roll over provided that the annual subscription to Illumina Connected Insights (20090137) is renewed on an annual basis. Access to a set of oncology knowledge bases is included.

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Services (5)

TruSight Oncology 500 Training (DNA and RNA, optional HRD) - Customer Site

20031668

3.5-day, hands-on instruction at customer site to familiarize users with the essential steps in the TruSight Oncology 500 workflow. Course provides hands-on training in sample and library preparation, enrichment, sequencing, and data analysis for a maximum of four trainees.

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TruSight Oncology 500 Training (DNA, optional HRD) - Customer Site

20031667

Three-day, hands-on instruction at customer site to familiarize users with the essential steps in the TruSight Oncology 500 workflow. Course provides hands-on training in sample and library preparation, enrichment, sequencing, and data analysis for a maximum of four trainees.

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Illumina Qualified Method Training - Customer Site

20091455

This 3.5 day course is designed to familiarize new users with the automated preparation of libraries using a supported Illumina Qualified method on a Hamilton or Beckman platform through detailed hands-on instruction. Participants will complete the entire automated workflow, including library preparation, enrichment, and sequencing. Prior experience with manual preparation of the library prep kit is highly recommended.

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Connected Insights Training - Remote

20092376

Illumina Connected Insights Training - Remote includes five (5) hours of product training delivered virtually.

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Informatics Professional Services - Remote

20071787

Professional services for Illumina informatics products and solutions including software implementations, pipelines and workflow development, integration, networking, migration, data ingestion projects and other informatics consultative, project-based services, performed remotely, and defined by a statement of work.

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v1 reagents (19)

TruSight Oncology 500 DNA Kit (48 samples)

20028213

Includes reagents for preparing and enriching up to 48 DNA samples and 16 indexes. Purchase NextSeq 500/550 sequencing reagents separately.

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TruSight Oncology 500 DNA Kit, For Use with NextSeq (48 samples)

20028214

Includes reagents for preparing and enriching up to 48 DNA samples, 16 indexes, and NextSeq 500/550 sequencing reagents.

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TruSight Oncology 500 DNA/RNA Bundle, (16 indexes, 24 samples)

20028215

Includes reagents for preparing and enriching up to 24 DNA and RNA samples and 16 indexes. Purchase NextSeq 500/550 sequencing reagents separately.

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TruSight Oncology 500 DNA/RNA Bundle, for use with NextSeq (16 indexes, 24 samples)

20028216

Includes reagents for preparing and enriching up to 24 DNA and RNA samples and 16 indexes and NextSeq 500/550 sequencing reagents.

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TruSight Oncology 500 DNA Kit plus Velsera interpretation report (16 indexes, 48 Samples)

20032624

Includes reagents for preparing and enriching up to 48 DNA samples, 16 indexes, and data interpretation reports using Pierian Clinical Genomics Workspace. Purchase NextSeq 500/550 sequencing reagents separately.

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TruSight Oncology 500 DNA Kit for Use with NextSeq plus Velsera interpretation report (16 indexes, 48 Samples)

20032625

Includes reagents for preparing and enriching up to 48 DNA samples and 16 indexes, data interpretation reports using Pierian Clinical Genomics Workspace, and NextSeq 500/550 sequencing reagents.

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TruSight Oncology 500 DNA/RNA Bundle plus Velsera interpretation report (16 indexes, 24 Samples) 

20032626

Includes reagents for preparing and enriching up to 24 DNA and RNA samples and 16 indexes and data interpretation reports using Pierian Clinical Genomics Workspace. Purchase NextSeq 500/550 sequencing reagents separately.

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TruSight Oncology 500 DNA/RNA Kit for Use with NextSeq plus Velsera interpretation report (16 indexes, 24 Samples) 

20032627

Includes reagents for preparing and enriching up to 24 DNA and RNA samples and 16 indexes, data interpretation reports using Pierian Clinical Genomics Workspace, and NextSeq 500/550 sequencing reagents.

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TruSight Oncology 500 DNA Automation Kit (16 indexes, 64 Samples)

20045504

Includes reagents for preparing and enriching up to 64 DNA samples and 16 indexes. Purchase NextSeq 500/550 sequencing reagents separately. Intended for use with automation.

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TruSight Oncology 500 DNA Automation Kit, For Use with NextSeq (16 indexes, 64 Samples)

20045505

Includes reagents for preparing and enriching up to 64 DNA samples and 16 indexes and NextSeq 500/550 sequencing reagents. Intended for use with automation.

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TruSight Oncology 500 DNA Automation Kit plus Velsera interpretation report (16 indexes, 64 samples)

20045506

Includes reagents for preparing and enriching up to 64 DNA samples and 16 indexes and data interpretation reports using Pierian Clinical Genomics Workspace. Purchase NextSeq 500/550 sequencing reagents separately. Intended for use with automation.

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TruSight Oncology 500 DNA Automation Kit plus Velsera interpretation report, for Use with NextSeq (16 indexes, 64 samples

20045507

Includes reagents for preparing and enriching up to 64 DNA samples and 16 indexes, data interpretation reports using Pierian Clinical Genomics Workspace, and NextSeq 500/550 sequencing reagents. Intended for use with automation.

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TruSight Oncology 500 DNA/RNA Automation Kit (16 indexes, 32 Samples)

20045508

Includes reagents for preparing and enriching up to 32 DNA and RNA samples and 16 indexes. Purchase NextSeq 500/550 sequencing reagents separately. Intended for use with automation.

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TruSight Oncology 500 DNA/RNA Automation Kit plus Velsera interpretation report (16 indexes, 32 Samples)

20045509

Includes reagents for preparing and enriching up to 32 DNA and RNA samples and 16 indexes and data interpretation reports using Pierian Clinical Genomics Workspace. Purchase NextSeq 500/550 sequencing reagents separately. Intended for use with automation.

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TruSight Oncology 500 DNA/RNA Automation Kit, For Use with NextSeq (16 indexes, 32 Samples)

20045990

Includes reagents for preparing and enriching up to 32 DNA and RNA samples and 16 indexes and NextSeq 500/550 sequencing reagents. Intended for use with automation.

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TruSight Oncology 500 DNA/RNA Automation Kit plus Velsera interpretation report, For Use with NextSeq (16 indexes, 32 Samples) 

20045991

Includes reagents for preparing and enriching up to 32 DNA and RNA samples and 16 indexes, data interpretation reports using Pierian Clinical Genomics Workspace, and NextSeq 500/550 sequencing reagents. Intended for use with automation.

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TruSight Oncology 500 HRD Kit (24 samples)

20076480

TruSight Oncology 500 HRD Kit (includes HRD enrichment reagents. Does not include library prep or sequencing core reagents. HRD analysis license is required and sold separately.) Not available in Japan.

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TSO500 DNA/RNA Auto Kt NSQ(32) plus Illumina Connected Insights Software

20119459

Includes library prep, enrichment reagents and NextSeq reagents plus data interpretation reports (through ICI).

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TSO500 DNA/RNA Kit NextSeq (24) plus Illumina Connected Insights Software

20119462

Includes library prep, enrichment reagents and NextSeq reagents plus data interpretation reports (through ICI).

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FAQ

TruSight Oncology 500 v2 provides updated chemistry and a streamlined workflow that shortens turnaround time by 1–2 days. Key improvements include a single hybridization enrichment, increased DNA library coverage, better performance in GC-rich regions, more sensitive variant calling from lower input amounts, and integrated homologous recombination deficiency (HRD) analysis.

A separate high-throughput version is not needed. TruSight Oncology 500 v2 supports scalable testing with 384 unique dual indexes and broad compatibility across Illumina sequencing systems.

DRAGEN secondary analysis is required for variant calling. The DRAGEN TruSight Oncology 500 v2 analysis software is included with all TruSight Oncology 500 v2 library prep kits.

Both TruSight Oncology 500 v2 and TruSight Oncology 500 are available in manual and automated formats with third-party automation methods developed with Illumina.

Concordance data is available in the TruSight Oncology 500 v2 data sheet. Contact your local sales representative if you seek additional data beyond what is presented in the data sheet.

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Purchasing the Trusight Oncology 500 v2 kit for the first time?

Complete the form to receive information about the first-time TruSight Oncology 500 v2 purchase program.