Illumina, 20040766, TruSight Oncology 500 DNA/RNA High-Throughput (72 Samples)

Name: TruSight Oncology 500 DNA/RNA High-Throughput (72 Samples)
Brand: Illumina
SKU: 20040766

Includes reagents for preparing and enriching up to 72 DNA and RNA samples. Purchase index anchors and NovaSeq 6000 sequencing reagents separately.

Catalog Number: 20040766

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Category

Target Enrichment Kits

Pack Sizebox of 96

TagsClinical research products

Description

Overview
TruSight Oncology 500 High-Throughput (HT) is a highly scalable pan-cancer, next-generation sequencing (NGS) assay that enables in-house comprehensive genomic profiling (CGP) from FFPE tissue.
Targets 523 genes to assess all DNA and RNA variant types (SNV, CNV, indels, fusions), plus MSI and TMB
Delivers accurate results with hybrid–capture chemistry and sophisticated bioinformatics
Reduces hands-on time and increases scalability with optional automation kits and methods*
Accommodates 8-36 samples with the NextSeq 1000 and NextSeq 2000 Systems , 16-192 samples with the NovaSeq 6000 System , and 32-960 samples with the NovaSeq X Series per run

Meaningful results
Evaluate > 500 pan-cancer biomarkers aligned with guidelines and clinical trials to increase chances of finding a positive biomarker with a single assay.

Streamlined workflow
Get results in 4–5 days using manual or automated workflows integrated with ready-to-use DRAGEN secondary analysis pipelines via on-premises server or in the cloud with Illumina Connected Analytics. Access an integrated interpretation report through Illumina Connected Insights † or Velsera Clinical Genomics Workspace (CGW ).
* Automation available on the Beckman Coulter iSeries or the Hamilton Microlab STAR . Contact Illumina Sales for more information.
† Not available in all countries. Illumina Connected Insights supports user-defined tertiary analysis through API calls to third-party knowledge sources.

Enable CGP with a comprehensive portfolio
Identify relevant biomarkers for clinical research with the TruSight Oncology 500 product line.
TruSight Oncology 500 High-Throughput
Batch up to 960 samples at a time while using the same panel content and tissue input type as TruSight Oncology 500.
TruSight Oncology 500
Assess relevant DNA and RNA cancer biomarkers from FFPE tumor tissue, now including HRD through an accessory kit to evaluate the Genomic Instability Score (GIS).‡
TruSight Oncology 500 ctDNA
Analyze circulating tumor DNA (ctDNA) in blood plasma via liquid biopsy with similar DNA panel content as TruSight Oncology 500.
‡ HRD is only available with the addition of the TruSight Oncology 500 HRD kit to TruSight Oncology 500. Not available in Japan.
§ The NextSeq 1000 System, NextSeq 2000 System, NovaSeq 6000Dx instrument (in Research Mode), and NovaSeq X Series require a separate, stand-alone DRAGEN server for secondary analysis.

Applications
TruSight Oncology 500 High-Throughput (HT) enables comprehensive genomic profiling of FFPE tumor samples to assess a wide range of biomarkers at increased scalability, from 8–480 samples per flow cell.

Example workflow
TruSight Oncology 500 High-Throughput assay
NextSeq 1000 & 2000 Systems
NovaSeq 6000 System
NovaSeq6000 Dx (in research mode)
NovaSeq X Series
Variant calling:
DRAGEN secondary analysis: on-premises via DRAGEN server
DRAGEN secondary analysis: cloud-based via Illumina Connected Analytics (ICA)
TruSight Oncology 500 Local App: Docker-based software
Insights and reporting:
Illumina Connected Insights**
** Not available in all countries. Illumina Connected Insights supports user-defined tertiary analysis through API calls to third-party knowledge sources.

Project recommendations
Instrument: Recommended number of samples
NextSeq 1000 System, NextSeq 2000 System: 8 samples per run (P2 flow cell), 800M paired-end reads, 3,500× coverage 24 samples per run (P3 flow cell), 2.4B paired-end reads, 3,500× coverage 36 samples per run (P4 flow cell), 3.6B paired-end reads, 3,500× coverage
8 samples per run (P2 flow cell), 800M paired-end reads, 3,500× coverage
24 samples per run (P3 flow cell), 2.4B paired-end reads, 3,500× coverage
36 samples per run (P4 flow cell), 3.6B paired-end reads, 3,500× coverage
2 x 101 bp
NovaSeq 6000 System: 16 samples per run (SP flow cell), 100M paired-end reads, 3,500× coverage 32 samples per run (S1 flow cell), 100M paired-end reads, 3,500× coverage 72 samples per run (S2 flow cell), 100M paired-end reads, 3,500× coverage 192 samples per run (S4 flow cell), 100M paired-end reads, 3,500× coverage
16 samples per run (SP flow cell), 100M paired-end reads, 3,500× coverage
32 samples per run (S1 flow cell), 100M paired-end reads, 3,500× coverage
72 samples per run (S2 flow cell), 100M paired-end reads, 3,500× coverage
192 samples per run (S4 flow cell), 100M paired-end reads, 3,500× coverage
2 × 101 bp
NovaSeq 6000Dx in Research Mode: 16 samples per run (SP flow cell), 100M paired-end reads, 3,500× coverage 32 samples per run (S1 flow cell), 100M paired-end reads, 3,500× coverage 72 samples per run (S2 flow cell), 100M paired-end reads, 3,500× coverage 192 samples per run (S4 flow cell), 100M paired-end reads, 3,500× coverage
NovaSeq X System: 32 samples per run (1.5B flow cell), 3.2B paired-end reads, 3,500× coverage 192 samples per run (10B flow cell), 20B paired-end reads, 3,500× coverage 480 samples per run (25B flow cell), 52B 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.
32 samples per run (1.5B flow cell), 3.2B paired-end reads, 3,500× coverage
192 samples per run (10B flow cell), 20B paired-end reads, 3,500× coverage
480 samples per run (25B flow cell), 52B 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.

Related applications and methods
Library prep automation
Reduce hands-on time and minimize errors with high- and low-throughput walk-away automation protocols available through Illumina automation partners.
Immuno-oncology research
Next-generation sequencing enables immuno-oncology researchers to gain insights into immunotherapy response factors and tumor immune evasion mechanisms.
Pathology and clinical cancer research
Our clinical cancer research solutions deliver accurate genomic information, and enable labs to analyze multiple genes in a single test.

Robust detection of fusions and splice variants
The information in this table shows examples of concordance between TruSight Oncology 500 and TruSight Oncology 500 High-Throughput and is not a comprehensive list of the fusions and splice variants detected. These data were generated with a Local App pipeline (not DRAGEN software).

CNV (Gene Amplification) Concordance
High concordance between NovaSeq X Series and NovaSeq 6000 for TSO 500 HT

Automation with TruSight Oncology 500 HT
Hear how customers at Intermountain Precision Genomics enabled CGP and scaled up their workflow with automation.
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How does TruSight Oncology 500 HT differ from the TruSight Oncology 500 assay?
The primary difference between the assays is scale. TruSight Oncology 500 HT runs on a variety of sequencers: NextSeq 1000 and 2000, NovaSeq 6000, NovaSeq 6000Dx (in Research Mode), and the NovaSeq X Series. Sample batching can range from 8-960 samples at a time, providing scalability to higher sample throughput. TruSight Oncology 500 runs on the NextSeq 550 System or NextSeq 550Dx Instrument (in Research Mode) and can batch up to 8 samples at a time. See the comparison table on this page for other differences.

Can I automate the TSO 500 HT workflow?
Yes, you can automate the TSO 500 HT workflow with Illumina Qualified automation methods . Illumina Qualified methods are available on the Beckman Coulter Life Sciences i7 and the Hamilton STAR (MOA configuration) liquid handling robots. Illumina Qualified methods are co-developed by Illumina and the automation partner. Automation specific library prep kits are offered by Illumina to accommodate the reagent volume required by automation platforms.

Can TSO 500 HRD be added to the TSO 500 HT library prep?
TruSight Oncology 500 HRD is not currently validated for use with TruSight Oncology 500 High-Throughput. Please reach out to your local Illumina sales or support representatives for information on alternative solutions. TruSight Oncology 500 HRD is not available in Japan.

What are the benefits of using DRAGEN for variant calling (secondary analysis)?
The Illumina DRAGEN secondary analysis platform delivers greater variant calling accuracy at twice the speed of non-DRAGEN options. 1 Increased accuracy provides better performance for sample QC, complex variants, small variants, fusions, and splice variants, as well as exon-level CNV calling for BRCA1/BRCA2. Illumina will continue to bring innovative features to DRAGEN TruSight Oncology 500 pipelines.

Can I analyze TruSight Oncology 500 HT data with my own software?
Yes, you can perform analysis with your own software. However, Illumina will not be able to directly provide technical support in this case.
Frequently purchased
Other products to consider
References
Data calculations on file. Illumina, Inc. 2023.

Specifications

General

Assay time	4–5 days from sample to results
Hands-on time	~2.5 hr for automated workflow ~10.5 hr for manual workflow
Input quantity	40 ng DNA and/or 40–80 ng RNA
Automation capability	Liquid handling robot(s)
Automation details	Explore available automation methods
Cancer type	Pan-cancer, Solid tumor
Content specifications	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.
Description	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.
Instruments	NextSeq 2000 System , NextSeq 1000 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

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